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Dayang Chem (Hangzhou) Co.,Ltd.

As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch

(S,S)-2,8-Diazabicyclo[4,3,0]nonane Manufacturer/High quality/Best price/In stock

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

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Simagchem Corporation

Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our

High quality (S,S)-2,8-Diazabicyclo[4,3,0]Nonane supplier in China

Cas:151213-42-2

Min.Order:0 Metric Ton

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Type:Manufacturers

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Wuhan Fortuna Chemical Co.,Ltd

Unique advantages Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Colorless to light brown liquid Storage:Cool dry place Package:1kg/foill bag;25kg/drum Appli

High quality (S,S)-2,8-Diazabicyclo[4,3,0]nonane Cas 151213-42-2 with best price

Cas:151213-42-2

Min.Order:1 Kilogram

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Type:Trading Company

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Henan Allgreen Chemical Co.,Ltd

T he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality service Appearance:White

151213-42-2

Cas:151213-42-2

Min.Order:1 Kilogram

Negotiable

Type:Manufacturers

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EAST CHEMSOURCES LIMITED

(S,S)-2,8-Diazabicyclo[4.3.0]nonane [Chemical Name]: (S,S)-2,8-Diazabicyclo[4,3,0]nonane [CAS No.]: 151213-42-2 [Structure Formula]: [Molecular For

(S,S)-2,8-Diazabicyclo[4.3.0]nonane

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $2.0 / 3.0

Type:Manufacturers

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Xi'an Xszo Chem Co., Ltd.

1. Factory price and high quality must be guaranteed, base on 8 years of production and R&D experience2. Free samples will be provided,ensure specifications and quality are right for customer3. Customers will receive the most professional technical s

High Quality 99% 1H-Pyrrolo[3,4-b]pyridine,octahydro-, (4aR,7aR)- 151213-42-2 ISO Producer

Cas:151213-42-2

Min.Order:1 Gram

FOB Price: $0.1

Type:Manufacturers

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Enke Pharma-tech Co.,Ltd. (Cangzhou, China )

Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new ap

(1R,6R)-2,8-Diazabicyclo[4,3,0]nonane

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $1.0

Type:Manufacturers

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Chemwill Asia Co., Ltd.

Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block

(R,R)-2,8-Diazabicyclo[4.3.0]nonane

Cas:151213-42-2

Min.Order:5 Kiloliter

FOB Price: $1.2 / 5.0

Type:Manufacturers

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Leader Biochemical Group

About Product Technical Details (S,S)-2,8-Diazabicyclo[4,3,0]nonane Chemical Properties Boiling point 198.5±8.0 °C(Predicted) density 0.950±0.06 g/cm3(Predicted)

China Largest factory Manufacturer Supply (S,S)-2,8-Diazabicyclo[4,3,0]nonane CAS 151213-42-2

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $1.0 / 3.0

Type:Lab/Research institutions

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Ality Chemical Corporation

(S,S)-2,8-Diazabicyclo[4,3,0]nonane Basic information Product Name: (S,S)-2,8-Diazabicyclo[4,3,0]nonane Synonyms: [S,S]-2,8-Diazabicyclo[4.3.0]Nonane98%;(S,S)-2,8-Diazabicyclo[4,3,0]onoane;(S,S)-2,8-DIAZABICYCLO[4,3,0]NONANE [FOR MOXIFLOXACIN];(

Factory Supply cis-Octahydropyrrolo[3,4-b]pyridine

Cas:151213-42-2

Min.Order:1 Gram

Negotiable

Type:Other

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Hebei Nengqian Chemical Import and Export Co., LTD

Our advantages: 1. High quality and competitive price: 1) Standard: BP/USP/EP/ enterprise standard 2) All purity 鈮 9% 3) We are manufacturers and can provide high quality products at factory prices. 2. Fast and safe delivery 1) The package can

(S,S)-2,8-Diazabicyclo[4,3,0]nonane CAS 151213-42-2

Cas:151213-42-2

Min.Order:1 Metric Ton

FOB Price: $5.0 / 10.0

Type:Trading Company

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Henan Tianfu Chemical Co., Ltd.

TIANFUCHEM--151213-42-2--High purity (S,S)-2,8-Diazabicyclo[4,3,0]nonane factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had est

TIANFUCHEM--151213-42-2--High purity (S,S)-2,8-Diazabicyclo[4,3,0]nonane factory price

Cas:151213-42-2

Min.Order:1 Metric Ton

FOB Price: $2000.0

Type:Lab/Research institutions

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Zhuozhou Wenxi import and Export Co., Ltd

WITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et

Pharmaceutical Grade CAS 151213-42-2 with competitive price

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $139.0 / 210.0

Type:Trading Company

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LIDE PHARMACEUTICALS LIMITED

Advantage : LIDE PHARMACEUTICALS LTD. is a mid-small manufacturing-type enterprise, engaged in pharmaceutical intermediates of R&D, custom-made and production, and also involving trading chemicals for export. We have established the R&amp

(S,S)-2,8-Diazabicyclo[4,3,0]nonane/ LIDE PHARMA- Factory supply / Best price

Cas:151213-42-2

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Hebei Sankai Chemical Technology Co., Ltd

1. Product advantages ♦ High purity, all above 98.5%, no impurities after dissolution ♦ We will test each batch to ensure quality ♦ OEM and private brand services designed for free ♦ Various cap colors available ♦ W

(S,S)-2,8-Diazabicyclo[4,3,0]nonane CAS151213-42-2

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $7.0 / 9.0

Type:Trading Company

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Henan Sinotech Import&Export Corporation

Product name: 2,8-Diazabicyclo[4.3.0]nonane CAS No.: 151213-42-2, 151413-40-0 Molecular weight: 199.1213 Useing: Pharmaceutical intermediate Appearance: white powder Storage:Store in cool and dry

2,8-Diazabicyclo[4.3.0]nonane CAS:151213-42-2

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $1.0

Type:Other

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Hangzhou Think Chemical Co. Ltd

Moxifloxacin intermediate:(S,S)-2,8-Diazabicyclo[4,3,0]nonane[CAS:151213-42-2] Name (1R,6R)-2,8-Diazabicyclo[4,3,0]nonane Molecular Structure Molecular Formula C7H14N2

(S,S)-2,8-Diazabicyclo[4,3,0]nonane for Moxifloxacin

Cas:151213-42-2

Min.Order:1 Kilogram

Negotiable

Type:Other

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Hubei Langyou International Trading Co., Ltd

1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:Clear light red liquid Storage:Store in sealed contain

best price of(S,S)-2,8-Diazabicyclo[4,3,0]Nonane/ Cas no:151213-42-2

Cas:151213-42-2

Min.Order:10 Gram

Negotiable

Type:Other

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Shanghai Upbio Tech Co.,Ltd

1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized

1H-Pyrrolo[3,4-b]pyridine,octahydro-, (4aR,7aR)- 151213-42-2

Cas:151213-42-2

Min.Order:1 Kilogram

Negotiable

Type:Lab/Research institutions

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Baoji Guokang Healthchem co.,ltd

Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese

Pharmaceutical Intermediate, (S,S)-2,8-Diazabicyclo[4,3,0]nonane CAS:151213-42-2

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $248.0 / 256.0

Type:Trading Company

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Qingdao Beluga Import and Export Co., LTD

(S,S)-2,8-Diazabicyclo[4,3,0]nonane CAS: 151213-42-2 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high qu

(S,S)-2,8-Diazabicyclo[4,3,0]nonane CAS: 151213-42-2

Cas:151213-42-2

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

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Shandong Hanjiang Chemical Co., Ltd.

Hello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai

1H-Pyrrolo[3,4-b]pyridine,octahydro-, (4aR,7aR)-

Cas:151213-42-2

Min.Order:1 Kilogram

Negotiable

Type:Lab/Research institutions

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Henan Wentao Chemical Product Co., Ltd.

Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod

CAS NO.:151213-42-2

Cas:151213-42-2

Min.Order:0

Negotiable

Type:Lab/Research institutions

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Hebei Mojin Biotechnology Co.,Ltd

Product quality: Our company have high quality product , and also the product we have good manufacture . First of all, this product is of fine quality. Every finish should be checked by quality inspection system.And every one should be also tried

(S,S)-2,8-Diazabicyclo[4,3,0]Nonane CAS NO.151213-42-2

Cas:151213-42-2

Min.Order:1 Kilogram

FOB Price: $20.0 / 30.0

Type:Trading Company

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Xiamen Hisunny Chemical Co.,Ltd

Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia

(S,S)-2,8-Diazabicyclo[4,3,0]Nonane

Cas:151213-42-2

Min.Order:0

Negotiable

Type:Manufacturers

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Triumph International Development Limilted

Appearance:white or light yellow crystalline powder Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:By

(S,S)-2,8-Diazabicyclo[4.3.0]nonane

Cas:151213-42-2

Min.Order:100 Gram

Negotiable

Type:Lab/Research institutions

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Afine Chemicals Limited

1. "Top 100 innovation-oriented export enterprises Of Hangzhou" honored by Hangzhou government 2. Specialized in the fine chemicals and pharmaceuticals 3. A leading manufacturer and trader of APIs in Chin

Hangzhou J&H Chemical Co., Ltd.

J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia

(S,S)-2,8-Diazabicyclo[4,3,0]nonane

Cas:151213-42-2

Min.Order:0

Negotiable

Type:Lab/Research institutions

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SHANGHAI T&W PHARMACEUTICAL CO., LTD.

A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc

(S,S)-2,8-Diazabicyclo[4,3,0]nonane

Cas:151213-42-2

Min.Order:4 Kilogram

Negotiable

Type:Lab/Research institutions

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Hangzhou Fonlynn Health Technology Co., Ltd.

Packing: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once Transportation:Express/Sea/Air Port:Ningbo/Shanghai/Qingd

(S,S)-2,8-Diazabicyclo[4,3,0]nonane

Cas:151213-42-2

Min.Order:0

Negotiable

Type:Trading Company

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Synthetic route

[R,R]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane
151213-43-3

[R,R]-8-benzyl-2,8-diazabicyclo[4.3.0]nonane

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
With hydrogen; 5%-palladium/activated carbon In methanol at 90℃; under 67506.8 Torr; for 5h;85%
9.61 g (85%)
9.61 g (85%)
With palladium on activated charcoal; hydrogen In methanol
(R,R)-6-(toluene-4-sulfonyl)-octahydro-pyrrolo[3,4-b]pyridine
1038923-76-0

(R,R)-6-(toluene-4-sulfonyl)-octahydro-pyrrolo[3,4-b]pyridine

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
Stage #1: (R,R)-6-(toluene-4-sulfonyl)-octahydro-pyrrolo[3,4-b]pyridine With hydrogen bromide; propionic acid; phenol In water for 6 - 7h; Heating / reflux;
Stage #2: With sodium hydroxide In water pH=11 - 12;
80.1%
8-benzyl-2,8-diazabicyclo[4.3.0]nonane

8-benzyl-2,8-diazabicyclo[4.3.0]nonane

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: D-tartaric acid / N,N-dimethyl-formamide; 2-methoxy-ethanol
2: palladium on activated charcoal; hydrogen / methanol
View Scheme
6,7-dihydro-5H-pyrrolo[3,4-b]pyridine hydrochloride salt

6,7-dihydro-5H-pyrrolo[3,4-b]pyridine hydrochloride salt

A

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

B

(1S,6S)-2,8-diazabicyclo[4.3.0]nonane
151213-40-0

(1S,6S)-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 25 - 35 °C
2.1: hydrogen; 5%-palladium/activated carbon / toluene / 24 h / 80 °C / 6000.6 Torr
2.2: Reflux
View Scheme
(S)-2-(6-methoxynaphthalen-2-yl)-1-(5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)propan-1-one
1558014-39-3

(S)-2-(6-methoxynaphthalen-2-yl)-1-(5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)propan-1-one

A

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

B

(1S,6S)-2,8-diazabicyclo[4.3.0]nonane
151213-40-0

(1S,6S)-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
Stage #1: (S)-2-(6-methoxynaphthalen-2-yl)-1-(5H-pyrrolo[3,4-b]pyridin-6(7H)-yl)propan-1-one With 5%-palladium/activated carbon; hydrogen In toluene at 80℃; under 6000.6 Torr; for 24h;
Stage #2: With hydrogen bromide; phenol In acetic acid; propionic acid Reflux;
A n/a
B n/a
6-(2,4-dimethoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-b]pyridine
1257241-37-4

6-(2,4-dimethoxybenzyl)-6,7-dihydro-5H-pyrrolo[3,4-b]pyridine

A

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

B

(1S,6S)-2,8-diazabicyclo[4.3.0]nonane
151213-40-0

(1S,6S)-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: trifluoroacetic acid; triethylsilane / 4 h / 60 - 65 °C
1.2: 20 °C
2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 25 - 35 °C
3.1: hydrogen; 5%-palladium/activated carbon / toluene / 24 h / 80 °C / 6000.6 Torr
3.2: Reflux
View Scheme
C14H16N2O

C14H16N2O

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: sodium tetrahydroborate; boron trifluoride-tetrahydrofuran complex / tetrahydrofuran / -5 - 20 °C
2: palladium 10% on activated carbon; hydrogen / ethanol / 40 °C / 2250.23 - 3750.38 Torr
3: L-Tartaric acid / isopropyl alcohol; water / 20 - 80 °C
View Scheme
2,8-diazabicyclo-[4.3.0]-nonane
5654-94-4

2,8-diazabicyclo-[4.3.0]-nonane

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
With L-Tartaric acid In water; isopropyl alcohol at 20 - 80℃;3.8 g
C18H25N3O

C18H25N3O

[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: ethyl acetate / 70 °C
2: sodium tetrahydroborate; boron trifluoride-tetrahydrofuran complex / tetrahydrofuran / -5 - 20 °C
3: palladium 10% on activated carbon; hydrogen / ethanol / 40 °C / 2250.23 - 3750.38 Torr
4: L-Tartaric acid / isopropyl alcohol; water / 20 - 80 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid
112811-72-0

1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid

moxifloxacin

moxifloxacin

Conditions
ConditionsYield
With nano iron oxide on ZrO2 coated sulfonic acid In water for 0.416667h; Reflux;96%
at 150℃; Microwave irradiation;83%
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

N-[2-amino-6-chloro-4-pyrimidinyl]-N-[3-fluoro-4-(1H-indazol-5-yloxy)phenyl]amine
688779-61-5

N-[2-amino-6-chloro-4-pyrimidinyl]-N-[3-fluoro-4-(1H-indazol-5-yloxy)phenyl]amine

6-[(4aR,7aR)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-N4-[3-fluoro-4-(1H-indazol-5-yloxy)phenyl]-2,4-pyrimidinediamine

6-[(4aR,7aR)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-N4-[3-fluoro-4-(1H-indazol-5-yloxy)phenyl]-2,4-pyrimidinediamine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In 2-Ethylhexyl alcohol at 150℃;93%
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

levofloxacin Q-acid
100986-89-8

levofloxacin Q-acid

(3S)-9-fluoro-10-{(4aR,7aR)-hexahydro-1H-pyrrolo[3,4-b]-pyridin-6(2H)-yl}-3-methyl-7-oxo-3,7-dihydro-2H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid

(3S)-9-fluoro-10-{(4aR,7aR)-hexahydro-1H-pyrrolo[3,4-b]-pyridin-6(2H)-yl}-3-methyl-7-oxo-3,7-dihydro-2H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid

Conditions
ConditionsYield
With nano iron oxide on ZrO2 coated sulfonic acid In water for 0.45h; Reflux;93%
at 150℃; Microwave irradiation;89%
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acid
86393-33-1

7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acid

1-cyclopropyl-6-fluoro-7-{(4aR,7aR)-hexahydro-1H-pyrrolo[3,4-b]pyridin-6(2H)-yl}-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

1-cyclopropyl-6-fluoro-7-{(4aR,7aR)-hexahydro-1H-pyrrolo[3,4-b]pyridin-6(2H)-yl}-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Conditions
ConditionsYield
With nano iron oxide on ZrO2 coated sulfonic acid In water for 0.3h; Reflux;91%
at 150℃; Microwave irradiation;84%
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinoline carboxylic acid-O3,O4(bis(acyloxy-O)) borate
139693-52-0

1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinoline carboxylic acid-O3,O4(bis(acyloxy-O)) borate

moxifloxacin hydrochloride
1394029-14-1

moxifloxacin hydrochloride

Conditions
ConditionsYield
Stage #1: [R,R]-2,8-diazabicyclo[4.3.0]nonane; 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinoline carboxylic acid-O3,O4(bis(acyloxy-O)) borate With triethylamine In acetonitrile at 15 - 30℃; for 8h;
Stage #2: With hydrogenchloride In methanol at 15 - 20℃; Temperature;
71%
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

N-{4-[(3-amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}-N-(2-amino-6-chloro-4-pyrimidinyl)amine

N-{4-[(3-amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}-N-(2-amino-6-chloro-4-pyrimidinyl)amine

4-[(4aR,7aR)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-6-({4-[(3-amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}amino)-2-pyrimidinylamine

4-[(4aR,7aR)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-6-({4-[(3-amino-1,2-benzisoxazol-4-yl)oxy]-3-fluorophenyl}amino)-2-pyrimidinylamine

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In 2-Ethylhexyl alcohol at 150℃; for 3h;14%
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

2-Amino-4,6-dichloropyrimidine
56-05-3

2-Amino-4,6-dichloropyrimidine

C11H16ClN5

C11H16ClN5

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In ethanol at 60℃; for 2h;
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

1-cyclopropyl-6,7-difluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinoline carboxylic acid (O3,O4)bis(acyloxy-O)borate
139678-43-6

1-cyclopropyl-6,7-difluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinoline carboxylic acid (O3,O4)bis(acyloxy-O)borate

(4aS-cis)-1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid (O3,O3)bis(acyloxy-O)borate

(4aS-cis)-1-cyclopropyl-7-(2,8-diazabicyclo[4.3.0]non-8-yl)-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid (O3,O3)bis(acyloxy-O)borate

Conditions
ConditionsYield
With triethylamine In acetonitrile for 1h; Heating / reflux;
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

(R,R)-2,8-diazabicyclo[4.3.0]nonane dihydrobromide

(R,R)-2,8-diazabicyclo[4.3.0]nonane dihydrobromide

Conditions
ConditionsYield
With hydrogen bromide In ethanol
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

2,4,8-trichloro-benzo[4,5]furo[3,2-d]pyrimidine
160199-00-8

2,4,8-trichloro-benzo[4,5]furo[3,2-d]pyrimidine

C17H16Cl2N4O
1345538-56-8

C17H16Cl2N4O

Conditions
ConditionsYield
In ethanol
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

trityl chloride
76-83-5

trityl chloride

C26H28N2

C26H28N2

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 20℃; for 3h; Cooling with ice;
With triethylamine In N,N-dimethyl-formamide at 20℃; for 3h; Cooling with ice;
With triethylamine In N,N-dimethyl-formamide at 20℃; for 3h; Cooling with ice;
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

Reaxys ID: 29971796

Reaxys ID: 29971796

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
4: dicyclohexyl-carbodiimide
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C25H30ClN3O3

C25H30ClN3O3

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
4: dicyclohexyl-carbodiimide; dmap / tetrahydrofuran / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C35H37N3O

C35H37N3O

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
View Scheme
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Reflux; Inert atmosphere
View Scheme
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
View Scheme
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
View Scheme
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C
2: N,N-dimethyl-formamide / 1 h / Reflux; Inert atmosphere
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C16H23N3O

C16H23N3O

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Reflux; Inert atmosphere
3: hydrogenchloride / methanol / 5 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / water; methanol / 5 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C
2: N,N-dimethyl-formamide / 1 h / Reflux; Inert atmosphere
3: hydrogenchloride / methanol; water / 5 h / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C23H27N3O2

C23H27N3O2

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
4: dicyclohexyl-carbodiimide; dmap / tetrahydrofuran / 20 °C
View Scheme
Multi-step reaction with 4 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Reflux; Inert atmosphere
3: hydrogenchloride / methanol / 5 h / 20 °C
4: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
View Scheme
Multi-step reaction with 4 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
4: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C35H36ClN3O

C35H36ClN3O

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
View Scheme
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
View Scheme
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C
2: N,N-dimethyl-formamide / 1 h / Reflux; Inert atmosphere
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C16H22ClN3O

C16H22ClN3O

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C
2: N,N-dimethyl-formamide / 1 h / Reflux; Inert atmosphere
3: hydrogenchloride / methanol; water / 5 h / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C24H28ClN3O3

C24H28ClN3O3

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: N,N-dimethyl-formamide / 1 h / Inert atmosphere; Reflux
3: hydrogenchloride / methanol; water / 5 h / 20 °C
4: dicyclohexyl-carbodiimide; dmap / tetrahydrofuran / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C12H15FN2OS

C12H15FN2OS

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
3: hydrogenchloride / water; methanol / 5 h / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C20H27FN2O2S

C20H27FN2O2S

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
3: hydrogenchloride / water; methanol / 5 h / 20 °C
4: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C31H29FN2OS

C31H29FN2OS

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C13H18N2OS

C13H18N2OS

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
3: hydrogenchloride / water; methanol / 5 h / 20 °C
View Scheme
[R,R]-2,8-diazabicyclo[4.3.0]nonane
151213-42-2

[R,R]-2,8-diazabicyclo[4.3.0]nonane

C21H30N2O2S

C21H30N2O2S

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / N,N-dimethyl-formamide / 3 h / 20 °C / Cooling with ice
2: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
3: hydrogenchloride / water; methanol / 5 h / 20 °C
4: dmap; dicyclohexyl-carbodiimide / tetrahydrofuran / 20 °C
View Scheme

Raw Materials

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