PG 501

PG 501 구조식 이미지
카스 번호:
32891-29-5
상품명:
PG 501
동의어(영문):
PG 501;Pentona;KAO 264;mazaticol hydrochloride;9-Azabicyclo[3.3.1]nonane, 2-thiopheneacetic acid deriv.;6,6,9-Trimethyl-9-azabicyclo[3.3.1]non-3b-yl a,a-di(2-thienyl)glycolate hydrochloride;6,6,9-Trimethyl-9-azabicyclo[3.3.1]nonan-3b-ol a,a-di-2-thienylglycolate (ester) hydrochloride;Glycolic acid, di-2-thienyl-, 6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester hydrochloride, exo- (8CI);2-Thiopheneacetic acid, a-hydroxy-a-2-thienyl-, 6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester, hydrochloride, exo-;2-Thiopheneacetic acid, a-hydroxy-a-2-thienyl-, (1R,3R,5R)-6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester, hydrochloride, rel- (9CI)
CBNumber:
CB61269985
분자식:
C21H27NO3S2.HCl
포뮬러 무게:
0
MOL 파일:
32891-29-5.mol

PG 501 속성

안전

PG 501 C화학적 특성, 용도, 생산

Originator

Pentona, Tanabe ,Japan ,1978

Manufacturing Process

A mixture of 1.0 g of 6,6,9-trimethyl-9-azabicyclo[3.3.1]nonan-3β-ol, methyl α,α-di-(2-thienyl)-glycolate and 30 mg of metallic sodium is heated at 80°C to 90°C for about 2 hours under reduced pressure. After cooling, ether is added to the reaction mixture. The mixture is extracted with 10% hydrochloric acid. The aqueous layer is alkalified with sodium carbonate and reextracted with ethyl acetate. The extract is washed with water, dried and concentrated to dryness. The residue thus obtained is treated with hydrogen chloride by conventional manner. 2.0 g of the α,α-di-(2-thienyl)glycolate of 6,6,9- trimethyl-9-azabicyclo[3.3.1]nonan-3β-ol hydrochloride are obtained. Yield 83%.

Therapeutic Function

Antiparkinsonian

PG 501 준비 용품 및 원자재

원자재

준비 용품


PG 501 공급 업체

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