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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

Benzeneethanamine,3-methoxy-4-(phenylmethoxy)-, hydrochloride (1:1)

Cas:1860-57-7

Min.Order:1 Kilogram

FOB Price: $3.0

Type:Lab/Research institutions

inquiry

Hebei Nengqian Chemical Import and Export Co., LTD

Our Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con

3-Methoxy-4-(benzyloxy)phenethylamine Hydrochloride CAS 1860-57-7

Cas:1860-57-7

Min.Order:1 Kilogram

FOB Price: $1.0 / 10.0

Type:Trading Company

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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 1860-57-7 with competitive price

Cas:1860-57-7

Min.Order:1 Kilogram

FOB Price: $139.0 / 210.0

Type:Trading Company

inquiry

Shanghai Upbio Tech Co.,Ltd

1.In No Less 10 years exporting experience. you 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 Specializ

Benzeneethanamine,3-methoxy-4-(phenylmethoxy)-, hydrochloride (1:1)

Cas:1860-57-7

Min.Order:1 Gram

Negotiable

Type:Lab/Research institutions

inquiry

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

Benzeneethanamine,3-methoxy-4-(phenylmethoxy)-, hydrochloride (1:1)

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

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

Benzeneethanamine,3-methoxy-4-(phenylmethoxy)-, hydrochloride (1:1)

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Xi`an Eastling Biotech Co., Ltd.

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou

3-Methoxy-4-(benzyloxy)phenethylamine Hydrochloride

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Antimex Chemical Limied

Benzeneethanamine,3-methoxy-4-(phenylmethoxy)-, hydrochloride (1:1)Appearance:detailed see specifications Storage:Keep away of light, cool place Package:25kg/drum;200kg/drum Application:It is an important raw material and intermediate used in Organic

Benzeneethanamine,3-methoxy-4-(phenylmethoxy)-, hydrochloride (1:1)

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

Henan Tianfu Chemical Co., Ltd.

Benzeneethanamine,3-methoxy-4-(phenylmethoxy)-, hydrochloride (1:1) Application:Organic Chemicals

1860-57-7

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Lab/Research institutions

inquiry

BOC Sciences

We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:white powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as primary a

3-Methoxy-4-(benzyloxy)phenethylamine

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Hangzhou Fandachem Co.,Ltd

Benzeneethanamine,3-methoxy-4-(phenylmethoxy)-, hydrochloride (1:1) cas 1860-57-7Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

Shanghai Chinqesen Biotechnology Co., Ltd.

Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen

1860-57-7

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

ZHEJIANG JIUZHOU CHEM CO.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

3-Methoxy-4-(benzyloxy)phenethylamine Hydrochloride

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

HWRK Chem

in storeAppearance:Pale Beige Solid Package:100g Application:Organic Chemicals

3-Methoxy-4-(benzyloxy)phenethylamine

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Shanghai Run-Biotech Co., Ltd.

Shanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por

2-(3-METHOXY-4-PHENYLMETHOXYPHENYL)ETHANAMINE HYDROCHLORIDE

Cas:1860-57-7

Min.Order:0

Negotiable

Type:Trading Company

inquiry

Synthetic route

3-methoxy-4-benzyloxy-ω-nitrostyrolene
63909-38-6, 1860-56-6

3-methoxy-4-benzyloxy-ω-nitrostyrolene

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Stage #1: 3-methoxy-4-benzyloxy-ω-nitrostyrolene With lithium aluminium tetrahydride In tetrahydrofuran at 0℃; for 2.5h; Reflux;
Stage #2: With water In tetrahydrofuran at 0℃;
Stage #3: With hydrogenchloride In diethyl ether
75%
3-Methoxy-4-benzyloxy-N-tert.-butyloxycarbonyl-phenaethylamin
23428-81-1

3-Methoxy-4-benzyloxy-N-tert.-butyloxycarbonyl-phenaethylamin

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Stage #1: 3-Methoxy-4-benzyloxy-N-tert.-butyloxycarbonyl-phenaethylamin With trifluoroacetic acid In dichloromethane at 0℃; for 0.666667h;
Stage #2: With sodium hydrogencarbonate In dichloromethane; water Cooling with ice;
Stage #3: With hydrogenchloride In diethyl ether
64%
Multi-step reaction with 2 steps
1: trifluoroacetic acid / dichloromethane / 0.67 h / 0 °C
2: hydrogenchloride / diethyl ether
View Scheme
2-(4-(benzyloxy)-3-methoxyphenyl)acetonitrile
1700-29-4

2-(4-(benzyloxy)-3-methoxyphenyl)acetonitrile

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride; sodium tetrahydroborate; cobalt(II) chloride 1.) MeOH, 20 deg C, 1 h; Multistep reaction;
3-methoxy-4-(phenylmethoxy)benzaldehyde
2426-87-1

3-methoxy-4-(phenylmethoxy)benzaldehyde

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 96.6 percent / NaBH4 / methanol / 3 h
2: 93.5 percent / thionyl chloride / diethyl ether / 6 h
3: dimethylformamide / 168 h / Ambient temperature
4: 1.) cobaltous chloride hexahydrate, NaBH4, 2.) 3 N HCl / 1.) MeOH, 20 deg C, 1 h
View Scheme
Multi-step reaction with 2 steps
1.1: ammonium acetate; acetic acid / 4 h / 90 °C
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 0 °C / Reflux
2.2: 0 °C
View Scheme
4-benzyloxy-3-methoxybenzyl alcohol
33693-48-0

4-benzyloxy-3-methoxybenzyl alcohol

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 93.5 percent / thionyl chloride / diethyl ether / 6 h
2: dimethylformamide / 168 h / Ambient temperature
3: 1.) cobaltous chloride hexahydrate, NaBH4, 2.) 3 N HCl / 1.) MeOH, 20 deg C, 1 h
View Scheme
1-(benzyloxy)-4-(chloromethyl)-2-methoxybenzene
33688-50-5

1-(benzyloxy)-4-(chloromethyl)-2-methoxybenzene

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: dimethylformamide / 168 h / Ambient temperature
2: 1.) cobaltous chloride hexahydrate, NaBH4, 2.) 3 N HCl / 1.) MeOH, 20 deg C, 1 h
View Scheme
2-[4-(benzyloxy)-3-methoxyphenyl]ethylamine
22231-61-4

2-[4-(benzyloxy)-3-methoxyphenyl]ethylamine

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In diethyl ether
benzyl bromide
100-39-0

benzyl bromide

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: potassium carbonate / acetone / 2 h / Reflux
2.1: ammonium acetate; acetic acid / 4 h / 90 °C
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 0 °C / Reflux
3.2: 0 °C
View Scheme
vanillin
121-33-5

vanillin

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: potassium carbonate / acetone / 2 h / Reflux
2.1: ammonium acetate; acetic acid / 4 h / 90 °C
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 0 °C / Reflux
3.2: 0 °C
View Scheme
3-Methoxytyramine
554-52-9

3-Methoxytyramine

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / chloroform / 24 h / 20 °C
2: potassium carbonate / acetone / 12 h / Heating / reflux
3: trifluoroacetic acid / dichloromethane / 0.67 h / 0 °C
4: hydrogenchloride / diethyl ether
View Scheme
tert-butyl 4-hydroxy-3-methoxyphenethylcarbamate
23699-77-6

tert-butyl 4-hydroxy-3-methoxyphenethylcarbamate

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: potassium carbonate / acetone / 12 h / Heating / reflux
2: trifluoroacetic acid / dichloromethane / 0.67 h / 0 °C
3: hydrogenchloride / diethyl ether
View Scheme
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

isobutyryl chloride
79-30-1

isobutyryl chloride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]isobutyramide
1032821-89-8

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]isobutyramide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;96%
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

butyryl chloride
141-75-3

butyryl chloride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]butyramide
1032821-85-4

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]butyramide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;94%
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

isopentanoyl chloride
108-12-3

isopentanoyl chloride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-3-methylbutyramide
95290-23-6

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-3-methylbutyramide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;93%
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

propionyl chloride
79-03-8

propionyl chloride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]propionamide
1032821-81-0

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]propionamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;90%
With triethylamine In dichloromethane at 0℃; for 0.5 - 1h;90%
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

propionic acid anhydride
123-62-6

propionic acid anhydride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]propionamide
1032821-81-0

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]propionamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;90%
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

cyclopropanecarboxylic acid chloride
4023-34-1

cyclopropanecarboxylic acid chloride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-cyclopropanecarboxamide
1032821-96-7

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-cyclopropanecarboxamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;88%
m-methoxyphenylacetic acid
1798-09-0

m-methoxyphenylacetic acid

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3-methoxyphenyl)acetamide
67237-64-3

N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3-methoxyphenyl)acetamide

Conditions
ConditionsYield
Stage #1: m-methoxyphenylacetic acid With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 0.5h;
Stage #2: [2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride In dichloromethane at 20℃; for 8h;
87%
bis(2-chloroethyl)(3-phenylpropyl)amine hydrochloride

bis(2-chloroethyl)(3-phenylpropyl)amine hydrochloride

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

1-(4-(benzyloxy)-3-methoxyphenethyl)-4-(3-phenylpropyl)piperazine
925679-52-3

1-(4-(benzyloxy)-3-methoxyphenethyl)-4-(3-phenylpropyl)piperazine

Conditions
ConditionsYield
With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 70℃; for 5h;83%
(3,5-dimethoxyphenyl)acetic acid
4670-10-4

(3,5-dimethoxyphenyl)acetic acid

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide
1398120-89-2

N-(2-(4-(benzyloxy)-3-methoxyphenyl)ethyl)-2-(3,5-dimethoxyphenyl)acetamide

Conditions
ConditionsYield
Stage #1: (3,5-dimethoxyphenyl)acetic acid With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 0.5h;
Stage #2: [2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride In dichloromethane at 20℃; for 8h;
81%
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

Cyclobutanecarbonyl chloride
5006-22-4

Cyclobutanecarbonyl chloride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-cyclobutanecarboxamide
1032821-99-0

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-cyclobutanecarboxamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;79%
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

phenylacetyl chloride
103-80-0

phenylacetyl chloride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-phenylacetylamide
4876-01-1

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-2-phenylacetylamide

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;63%
5-benzyloxy-4-methoxy-2-nitrophenylacetic acid
78792-73-1

5-benzyloxy-4-methoxy-2-nitrophenylacetic acid

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

N-<4-Benzyloxy-4-methoxyphenethyl>-5-benzyloxy-4-methoxy-2-nitrophenylacetamide
99613-09-9

N-<4-Benzyloxy-4-methoxyphenethyl>-5-benzyloxy-4-methoxy-2-nitrophenylacetamide

Conditions
ConditionsYield
With sodium hydroxide In chloroform; water for 4h; Ambient temperature;56%
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

1-<5-benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-3,4-dihydroisoquinoline
99612-79-0

1-<5-benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-3,4-dihydroisoquinoline

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 56 percent / 2 N NaOH / CHCl3; H2O / 4 h / Ambient temperature
2: 72 percent / POCl3 / acetonitrile / 2 h / Heating
View Scheme
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline
99612-81-4

1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 56 percent / 2 N NaOH / CHCl3; H2O / 4 h / Ambient temperature
2: 72 percent / POCl3 / acetonitrile / 2 h / Heating
3: 81 percent / NaBH4 / methanol / 2 h / Ambient temperature
View Scheme
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-1-[2,3-dihydrobenzo[b]furan-7-yl]cyclopropane carboxamide

N-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-1-[2,3-dihydrobenzo[b]furan-7-yl]cyclopropane carboxamide

Conditions
ConditionsYield
With thionyl chloride; triethylamine In water; ethyl acetate
1-(1-naphthyl)cyclopropane carbonyl chloride

1-(1-naphthyl)cyclopropane carbonyl chloride

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

N-[2-(4-benzyloxy-3-methoxyphenyl)-ethyl]-1-(1-naphthyl)cyclopropane carboxamide

N-[2-(4-benzyloxy-3-methoxyphenyl)-ethyl]-1-(1-naphthyl)cyclopropane carboxamide

Conditions
ConditionsYield
With triethylamine In ethyl acetate
C16H14O6S
1233354-44-3

C16H14O6S

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

C32H33NO8S
1233354-57-8

C32H33NO8S

Conditions
ConditionsYield
With triethylamine In methanol for 5h; Reflux;
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

(S)-2-hydroxy-3,11-dimethoxy-5,8,13,13a-tetrahydro-6H-dibenzo[a,g]quinolizine
1398121-01-1

(S)-2-hydroxy-3,11-dimethoxy-5,8,13,13a-tetrahydro-6H-dibenzo[a,g]quinolizine

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C
1.2: 8 h / 20 °C
2.1: trichlorophosphate / acetonitrile / 0.5 h / Reflux
3.1: [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; formic acid; triethylamine / N,N-dimethyl-formamide / 10 h / 20 °C
3.2: 20 °C / pH 8
4.1: formic acid / 2 h / 25 °C
5.1: hydrogenchloride / ethanol; water / Reflux
5.2: 0 °C / pH 9
View Scheme
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

(S)-2-hydroxy-3,9,11-trimethoxy-5,8,13,13a-tetrahydro-6H-dibenzo-[a,g]quinolizine
1398121-03-3

(S)-2-hydroxy-3,9,11-trimethoxy-5,8,13,13a-tetrahydro-6H-dibenzo-[a,g]quinolizine

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C
1.2: 8 h / 20 °C
2.1: trichlorophosphate / acetonitrile / 0.5 h / Reflux
3.1: [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; formic acid; triethylamine / N,N-dimethyl-formamide / 10 h / 20 °C
3.2: 20 °C / pH 8
4.1: formic acid / 2 h / 50 °C
5.1: hydrogenchloride / ethanol; water / Reflux
5.2: 0 °C / pH 9
View Scheme
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

7-(benzyloxy)-1-((3,5-dimethoxyphenyl)methyl)-6-methoxy-3,4-dihydroisoquinoline
1398120-88-1

7-(benzyloxy)-1-((3,5-dimethoxyphenyl)methyl)-6-methoxy-3,4-dihydroisoquinoline

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C
1.2: 8 h / 20 °C
2.1: trichlorophosphate / acetonitrile / 0.5 h / Reflux
View Scheme
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

C25H27NO3
1422431-23-9

C25H27NO3

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C
1.2: 8 h / 20 °C
2.1: trichlorophosphate / acetonitrile / 0.5 h / Reflux
3.1: [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; formic acid; triethylamine / N,N-dimethyl-formamide / 10 h / 20 °C
3.2: 20 °C / pH 8
View Scheme
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

(S)-7-(benzyloxy)-1-((3,5-dimethoxyphenyl)methyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline
1398120-87-0

(S)-7-(benzyloxy)-1-((3,5-dimethoxyphenyl)methyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C
1.2: 8 h / 20 °C
2.1: trichlorophosphate / acetonitrile / 0.5 h / Reflux
3.1: [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; formic acid; triethylamine / N,N-dimethyl-formamide / 10 h / 20 °C
3.2: 20 °C / pH 8
View Scheme
[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride
1860-57-7

[2-(4-benzyloxy-3-methoxyphenyl)ethyl]amine hydrochloride

(S)-2-benzyloxy-3,11-dimethoxy-5,8,13,13a-tetrahydro-6H-dibenzo[a,g]quinolizine
1398120-70-1

(S)-2-benzyloxy-3,11-dimethoxy-5,8,13,13a-tetrahydro-6H-dibenzo[a,g]quinolizine

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 0.5 h / 20 °C
1.2: 8 h / 20 °C
2.1: trichlorophosphate / acetonitrile / 0.5 h / Reflux
3.1: [N-[(1R,2R)-2-(amino-κN)-1,2-diphenylethyl]-4-methylbenzenesulfonamidato-κN]chloro[(1,2, 3,4,5,6-η)-1-methyl-4-(1-methylethyl)benzene]-ruthenium; formic acid; triethylamine / N,N-dimethyl-formamide / 10 h / 20 °C
3.2: 20 °C / pH 8
4.1: formic acid / 2 h / 25 °C
View Scheme

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