2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel-

2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel- Basic information
Product Name:2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel-
Synonyms:2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel-;2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, 6,6,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, exo-;Glycolic acid, di-2-thienyl-, 6,6,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, exo-;(8,8,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl) 2-hydroxy-2,2-dithiophen -2-yl-acetate hydrochloride
CAS:38738-59-9
MF:C21H28ClNO3S2
MW:0
EINECS:
Product Categories:
Mol File:38738-59-9.mol
2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel- Structure
2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel- Chemical Properties
Safety Information
MSDS Information
2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel- Usage And Synthesis
OriginatorPentona, Tanabe ,Japan ,1978
Manufacturing ProcessA 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 FunctionAntiparkinsonian
2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel- Preparation Products And Raw materials
Tag:2-Thiopheneacetic acid, alpha-hydroxy-alpha-2-thienyl-, (1R,3R,5R)-6,6 ,9-trimethyl-9-azabicyclo(3.3.1)non-3-yl ester, hydrochloride, rel-(38738-59-9) Related Product Information