CAS No.30341-92-5,ERGOLINE-8-CARBOXYLIC ACID METHYL ESTER Suppliers

Shanghai Upbio Tech Co.,Ltd

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Ergoline-8-carboxylicacid, methyl ester, (8b)- (9CI)

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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

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TAIZHOU ZHENYU BIOTECHNOLOGY CO., LTD

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ERGOLINE-8-CARBOXYLIC ACID METHYL ESTER

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KAISA GROUP INC

1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer

30341-92-5 CAS NO.30341-92-5

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Hunan chemfish Pharmaceutical co.,Ltd

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ERGOLINE-8-CARBOXYLIC ACID METHYL ESTER

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Henan Tianfu Chemical Co., Ltd.

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Ergoline-8-carboxylicacid, methyl ester, (8b)- (9CI)

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Antimex Chemical Limied

Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali

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Changchun Artel lmport and Export trade company

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Zibo Hangyu Biotechnology Development Co., Ltd

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ERGOLINE-8-CARBOXYLIC ACID METHYL ESTER

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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

ERGOLINE-8-CARBOXYLIC ACID METHYL ESTER

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Jilin haofei import and export trade Co.,Ltd

Price, service, company and transport advantage: 1. Best service, place of origin China, high quality, and reasonable price. 2. It's customers' right to choose the package (EMS, DHL, FEDEX, UPS). 3. It's customers' right

30341-92-5 CAS NO.30341-92-5

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Shanghai united Scientific Co.,Ltd.

United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat

Ergoline-8-carboxylicacid, methyl ester, (8b)- (9CI)

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Finetech Industry Limited

FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the ERGOLINE-8-CARBOXYLIC ACID METHYL ESTER, CAS:30341-92-5 with the most competitive pri

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Nanjing Raymon Biotech Co., Ltd.

Ergoline-8-carboxylicacid, methyl ester, (8b)- (9CI)Appearance:Off white to slight yellow solid Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transport

Ergoline-8-carboxylicacid, methyl ester, (8b)- (9CI)

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Chemical Co.Ltd

Ergoline-8-carboxylicacid, methyl ester, (8b)- (9CI)Appearance:Off white to slight yellow solid Storage:Stored in shaded, cool and dry places Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:Handle with cares to avoid damag

Ergoline-8-carboxylicacid, methyl ester, (8b)- (9CI)

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Synthetic route

: 80993-64-2
9-methyl 7-(2,2,2-trichloroethyl) (6aR,9R,10aR)-6,6a,8,9,10,10a-hexahydroindolo[4,3-fg]quinoline-7,9(4H)-dicarboxylate

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

Conditions

Conditions	Yield
With acetic acid; zinc for 60h; Heating;	72%
With zinc In methanol; acetic acid at 20℃; for 1.08333h;	71%

: 51260-62-9
D-6-cyano-8β-methoxycarbonylergoline

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

Conditions

Conditions	Yield
With hydrogen; W-7 Raney Ni In N,N-dimethyl-formamide
aluminum nickel In N,N-dimethyl-formamide

: 5878-43-3
9,10-dihydrolysergic acid

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: H2SO4 2: CH2Cl2 3: H2 / W-7 Raney Ni / dimethylformamide View Scheme
Multi-step reaction with 3 steps 1: sulfuric acid / 15 h / 20 °C 2: dmap / dichloromethane / 16 h / Reflux; Inert atmosphere 3: zinc / methanol; acetic acid / 1.08 h / 20 °C View Scheme

: 3006-19-7, 5143-94-2, 35470-53-2, 77842-02-5, 87247-99-2, 96648-31-6, 96648-32-7
9,10-dihydrolysergic acid methyl ester

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: CH2Cl2 2: H2 / W-7 Raney Ni / dimethylformamide View Scheme
Multi-step reaction with 2 steps 1: 90 percent / CH2Cl2 / 48 h / Heating 2: 72 percent / Zn, AcOH / 60 h / Heating View Scheme
Multi-step reaction with 2 steps 1: dmap / dichloromethane / 16 h / Reflux; Inert atmosphere 2: zinc / methanol; acetic acid / 1.08 h / 20 °C View Scheme

: 67-56-1
methanol

: ergoline-8-carboxylic acid

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

Conditions

Conditions	Yield
With sulfuric acid

: 25447-66-9
Dihydroergocryptine

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: sodium hydroxide; sodium dithionite / water / 4 h / Reflux 2: sulfuric acid / 15 h / 20 °C 3: dmap / dichloromethane / 16 h / Reflux; Inert atmosphere 4: zinc / methanol; acetic acid / 1.08 h / 20 °C View Scheme

: 24424-99-5
di-tert-butyl dicarbonate

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 1,6-di(tert-butoxycarbonyl)-ergoline-8β-carboxylic acid methyl ester

Conditions

Conditions	Yield
With triethylamine; dmap In dichloromethane at 40℃; for 5h;	95.2%

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 106-95-6
allyl bromide

: 72821-79-5
methyl (6aR,9R,10aR)-7-allyl-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 35℃; for 2.5h;	94%
With potassium carbonate In N,N-dimethyl-formamide	80%

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 103-71-9
phenyl isocyanate

: 1624289-33-3
(4aR,8R,9aR)-methyl 6-(phenylcarbamoyl)-1,4,4a,6,7,8,9,9a-octahydroindolo[1,14-fg]quinoline-8-carboxylate

Conditions

Conditions	Yield
In dichloromethane at 20℃;	90%

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 75-03-6
ethyl iodide

: 30341-94-7
6-nor-6-n-ethyl-9,10-dihydrolysergic acid methyl ester

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 24h;	75%
With potassium carbonate In N,N-dimethyl-formamide

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 106-94-5
propyl bromide

: 63719-09-5
6-nor-6-n-propyl-9,10-dihydrolysergic acid methyl ester

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide	73%

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 107-08-4
1-iodo-propane

: 63719-09-5
6-nor-6-n-propyl-9,10-dihydrolysergic acid methyl ester

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 24h;	47%
With potassium carbonate In N,N-dimethyl-formamide
With potassium carbonate In methanol; chloroform; N,N-dimethyl-formamide

: 74-96-4
ethyl bromide

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 30341-94-7
6-nor-6-n-ethyl-9,10-dihydrolysergic acid methyl ester

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide

: 513-38-2
Isobutyl iodide

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: (6aR,9R,10aR)-7-Isobutyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinoline-9-carboxylic acid methyl ester

: 3282-30-2
pivaloyl chloride

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: (6aR,9R,10aR)-7-(2,2-Dimethyl-propionyl)-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinoline-9-carboxylic acid methyl ester

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 86891-09-0
(5R,8S,10R)-8-methoxycarbonylergoline

Conditions

Conditions	Yield
With lithium diisopropyl amide In tetrahydrofuran at 0℃; for 2h; Product distribution; other time;	16.6 % Chromat.

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 4023-34-1
cyclopropanecarboxylic acid chloride

: 82842-05-5
(6aR,9R,10aR)-7-Cyclopropanecarbonyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinoline-9-carboxylic acid methyl ester

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 63719-20-0
(6-ethyl-ergolin-8-yl)-methanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: K2CO3 / dimethylformamide 2: 94 percent / LiAlH4 / tetrahydrofuran / 0.5 h View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 63719-21-1
D-6-propyl-8β-hydroxymethylergoline

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: K2CO3 / dimethylformamide 2: 96 percent / LiAlH4 / tetrahydrofuran / 0.5 h View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: (6aR,9R,10aR)-9-Imidazol-1-ylmethyl-7-propyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinoline

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: K2CO3 / dimethylformamide 2: 96 percent / LiAlH4 / tetrahydrofuran / 0.5 h 3: 85 percent / pyridine / 3 h / Ambient temperature 4: 1.) NaH / 1.) DMF, 2.) DMF, 90 deg C, 2 h View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: (5R,8R,10R)-6-propyl-8-(1,2,4-triazol-4-ylmethyl)ergoline

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: K2CO3 / dimethylformamide 2: 96 percent / LiAlH4 / tetrahydrofuran / 0.5 h 3: 85 percent / pyridine / 3 h / Ambient temperature 4: 1.) NaH / 1.) DMF, 2.) DMF, 80 deg C, 2 h View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 74627-23-9
Toluene-4-sulfonic acid (6aR,9R,10aR)-7-ethyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinolin-9-ylmethyl ester

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: K2CO3 / dimethylformamide 2: 94 percent / LiAlH4 / tetrahydrofuran / 0.5 h 3: 81 percent / pyridine / 3 h / Ambient temperature View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 79675-18-6
Toluene-4-sulfonic acid (6aR,9R,10aR)-7-propyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinolin-9-ylmethyl ester

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: K2CO3 / dimethylformamide 2: 96 percent / LiAlH4 / tetrahydrofuran / 0.5 h 3: 85 percent / pyridine / 3 h / Ambient temperature View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: (6aR,9R,10aR)-7-Ethyl-9-[1,2,4]triazol-1-ylmethyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinoline

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: K2CO3 / dimethylformamide 2: 94 percent / LiAlH4 / tetrahydrofuran / 0.5 h 3: 81 percent / pyridine / 3 h / Ambient temperature 4: 1.) NaH / 1.) DMF, 2.) DMF, 90 deg C, 2 h View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: (5R,8R,10R)-6-propyl-8-(1,2,4-triazol-1-ylmethyl)ergoline

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: K2CO3 / dimethylformamide 2: 96 percent / LiAlH4 / tetrahydrofuran / 0.5 h 3: 85 percent / pyridine / 3 h / Ambient temperature 4: 1.) NaH / 1.) DMF, 2.) DMF, 80 deg C, 2 h View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: ((6aR,9R,10aR)-7-Isobutyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinolin-9-yl)-methanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 2: NaBH4 View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 72821-88-6
[(6aR,9R,10aR)-7-allyl-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-yl]methanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 2: NaBH4 View Scheme
Multi-step reaction with 2 steps 1: potassium carbonate / N,N-dimethyl-formamide / 2.5 h / 35 °C 2: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 0.75 h / Inert atmosphere; Cooling with ice View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 82842-03-3
6-cyclopropyl-methylergoline-8β-methanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 2: LiAlH4 View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 88133-33-9
6-neopentylergoline-8β-methanol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 2: LiAlH4 View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 2-Cyano-3-((6aR,9S,10aR)-7-isobutyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinolin-9-yl)-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 2: NaBH4 5: NH3 View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 3-((6aR,9S,10aR)-7-Allyl-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinolin-9-yl)-2-cyano-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 2: NaBH4 5: NH3 View Scheme

: 30341-92-5
methyl (6aR,9R,10aR)-4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline-9-carboxylate

: 2-Cyano-3-[(6aR,9S,10aR)-7-(2,2-dimethyl-propyl)-4,6,6a,7,8,9,10,10a-octahydro-indolo[4,3-fg]quinolin-9-yl]-propionamide

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 2: LiAlH4 5: NH3 View Scheme

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Antimex Chemical Limied

Changchun Artel lmport and Export trade company

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