amesergide

amesergide Suppliers list
Company Name: Hangzhou MolCore BioPharmatech Co.,Ltd.
Tel: +86-057181025280; +8617767106207
Email: sales@molcore.com
Products Intro: Product Name:LY 237733
CAS:121588-75-8
Purity:NLT 98% Remarks:MC512135
Company Name: Nantong QuanYi Biotechnology Co., Ltd  
Tel: 0513-66337626 18051384581
Email: sales@chemhifuture.com
Products Intro: Product Name:amesergide
CAS:121588-75-8
Purity:98%+ HPLC Package:10mg,500mg,1g,2g,5g,10g,More
amesergide Basic information
Product Name:amesergide
Synonyms:1-Isopropyl-6-methyl-N-cyclohexylergoline-8β-carboxamide;LY-237733;amesergide;Ergoline-8-carboxamide, N-cyclohexyl-6-methyl-1-(1-methylethyl)-, (8β)-
CAS:121588-75-8
MF:C25H35N3O
MW:393.56
EINECS:
Product Categories:
Mol File:121588-75-8.mol
amesergide Structure
amesergide Chemical Properties
Safety Information
MSDS Information
amesergide Usage And Synthesis
OriginatorAmesergide,Onbio Inc.
UsesSerotonin antagonist.
Manufacturing ProcessTo a 250 ml three-neck round bottom flask was added 10.0 g (32.01 mmol) of (8β)-1-isopropyl-6-methylergoline-8-carboxylie acid, 4.43 g (32.1 mmol) of potassium carbonate and 200 ml of N,N-dimethylformamide. The mixture was refluxed and 25 ml of a distillate was collected. The remaining solution was cooled in an ice bath, and then with an acetonitrile/carbon dioxide bath which lowered the temperature of the reaction mixture to about -45°C this mixture was added 4.59 g (33.62 mmol) of isobutyl chloroformate dropwise. The resulting mixture was stirred for approximately 5 min and 3.49 g (35.21 mmol) of cyclohexylamine was added. The reaction mixture was allowed to warm to room temperature and stirred for approximately 19 h. To the mixture was added 500 ml of ice water containing 25 ml of concentrated ammonium hydroxide. The mixture was cooled and the precipitated solid was collected by vacuum filtration. The resulting solid was washed with water and dried in vacuo to provide 10.13 g (yield 76.8%) of the (8β)-N-cyclohexyl-1-isopropyl- 6-methylergoline-8-carboxamide having a purity of 92.3%.
The resulting solid was combined with three other lots of the desired compound previously synthesized to provide a total weight of 33.6 g. This material was dissolved in 1200 ml of hot methanol and the resulting solution was filtered. The filtrate was allowed to cool to room temperature and 600 ml of water was added dropwise. The mixture was cooled in the freezer and the precipitated crystals were collected by vacuum filtration. The crystals were washed with methanol and dried in vacuo to provide 26.95 g of the desired compound having a purity of 96.5% as determined by HPLC. The dried solid was dissolved in 1100 ml of hot methanol, and the resulting solution was filtered hot and allowed to cool. To this mixture was added 600 ml of water and again the precipitated solid was collected by vacuum filtration. The solid was washed with water and dried in vacuo to provide 25.82 g of the (8β)-Ncyclohexyl- 1-isopropyl-6-methylergoline-8-carboxamide, melting point 250°C. The assayed material indicated 98.7% purity.
Therapeutic FunctionSerotonin antagonist
amesergide Preparation Products And Raw materials
Raw materialsCyclohexylamine-->Isobutyl chloroformate-->Potassium carbonate-->Ammonium hydroxide
Tag:amesergide(121588-75-8) Related Product Information
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