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Amafolone

CAS No.
50588-47-1
Chemical Name:
Amafolone
Synonyms
Amafolone;3α-Amino-2β-hydroxy-5α-androstan-17-one;Androstan-17-one, 3-amino-2-hydroxy-, (2β,3α,5α)-
CBNumber:
CB31116893
Molecular Formula:
C19H31NO2
Molecular Weight:
305.459
MDL Number:
MFCD00864749
MOL File:
50588-47-1.mol
Last updated:2022-12-21 16:56:50

Amafolone Properties

FDA UNII N8Y78OKP8D

Amafolone Chemical Properties,Uses,Production

Originator

Amafolone hydrochloride,ZYF Pharm Chemical

Manufacturing Process

A solution of 70% perchloric acid (60 ml) in water (280 ml) was added to a stirred solution of 5α-androst-2-en-17-one (200.0 g) in ether (1.15 l) at 15°C followed by portionwise addition of N-bromacetamide (112.0 g) over 10 min. After stirring for 1 h the precipitated white crystalline solid was filtered off, washed neutral with ether and water and crystallised to give 2β-hydroxy-3α- bromo-5α-androstan-17-one (172.0 g). The ether layer of the filtrate was washed neutral, dried (Na2SO4) and concentrated to give a second crop (28.0 g). The two crops (200.0 g) were suspended in methanol (1 L), 10 N aqueous potassium hydroxide solution (100 ml) added and the mixture slowly distilled over 45 min. Addition of water precipitated the product as a white solid which was filtered off, washed with water, dried and 88.0 g of 2β,3β-epoxy-5α- androstan-17-one were obtained (crystallisation from ether:light petrol).
A solution of the 2β,3β-epoxy-5α-androstan-17-one (30.0 g) in ethanol (130 ml), water (15 ml) and liquid ammonia was heated in an autoclave at 150°C for 6 h and the resultant crystalline suspension evaporated to dryness. Water (35 ml) and acetic acid (36 ml) were added and the solution kept at 90°C for 1 h, cooled and excess water added. The precipitated material was filtered off and the filtrate made alkaline with aqueous 10 N potassium hydroxide solution to precipitate a white solid which was filtered off, washed neutral with water, dissolved in methylene chloride, the solution dried (Na2SO4) concentrated and ether added to give 2β-hydroxy-3α-amino-5α-androstan-17-one (14.3 g), melting point l92°-195°C.
In practice it is usually used as hydrochloride.

Therapeutic Function

Antiarrhythmic

Amafolone Preparation Products And Raw materials

Amafolone Suppliers

Global( 5)Suppliers
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TargetMol Chemicals Inc.
support@targetmol.com United States 38632 58
Supplier Advantage
TargetMol Chemicals Inc.
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50588-47-1(Amafolone)Related Search:

3α-Amino-2β-hydroxy-5α-androstan-17-one Amafolone Androstan-17-one, 3-amino-2-hydroxy-, (2β,3α,5α)- 50588-47-1