![155206-00-1](/CAS/GIF/155206-00-1.gif)
Bimatoprost synthesis
- Product Name:Bimatoprost
- CAS Number:155206-00-1
- Molecular formula:C25H37NO4
- Molecular Weight:415.57
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1240483-19-5
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![Bimatoprost](/CAS/GIF/155206-00-1.gif)
155206-00-1
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$45.00/5mg
Yield:155206-00-1 91%
Reaction Conditions:
Stage #1: (Z)-7-((1R,2R,3R,5S)-3-(tert-butyldimethylsilyloxy)-2-((S,E)-3-(tert-butyldimethylsilyloxy)-5-phenylpent-1-enyl)-5-hydroxycyclopentyl)-N-ethylhept-5-enamidewith hydrogenchloride;water in tetrahydrofuran at 20; for 18 h;
Stage #2: in tetrahydrofuran; pH=6.8;Aqueous phosphate buffer;
Steps:
3
Preparation of the compound X (Bimatoprost)HCl 1.2 N (2 mL) is added at room temperature to a solution of the compound IX (950 mg, 1.5 mmoles) in a tetrahydrofuran/water 1:1 (50 mL) mixture, the reaction is performed under vigorous stirring and is complete after approximately 18 hours. It is quenched by adding phosphate buffer (pH = 6.8, 150 mL), then the organic phase is diluted with AcOEt, the two phases are separated, the aqueous phase is extracted with AcOEt, the re-combined organic phases are dried on magnesium sulphate and filtered, and lastly the solvent is removed at reduced pressure. The product is purified by means of column chromatography (AcOEt-methanol 95:5 v/v) . The Bimatoprost is obtained pure as a colourless oil with a yield of 91%.
References:
WO2010/97672,2010,A1 Location in patent:Page/Page column 20
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![Bimatoprost](/CAS/GIF/155206-00-1.gif)
155206-00-1
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![Bimatoprost](/CAS/GIF/155206-00-1.gif)
155206-00-1
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![Bimatoprost](/CAS/GIF/155206-00-1.gif)
155206-00-1
534 suppliers
$45.00/5mg
![Ethylamine](/CAS/GIF/75-04-7.gif)
75-04-7
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$10.00/20mg
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38315-47-8
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$64.00/1mg
![Bimatoprost](/CAS/GIF/155206-00-1.gif)
155206-00-1
534 suppliers
$45.00/5mg