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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988861Generated: November 3, 2026

2-Chlorophenyl-(6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl)acetamide → (S)-2-(2-chloro-phenyl)(4,5,6,7-tetrahydrothieno[3,2-c]pyrid-5-yl)acetamide (+)-camphor sulfonic acid salt

https://huagongshe.com/reaction/988861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chlorophenyl-(6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl)acetamideHCID 11312824—
Reactant[(1S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-YL]methanesulfonic acid hydrateHCID 87205896—
SolventAcetoneHCID 180—
Product(S)-2-(2-chloro-phenyl)(4,5,6,7-tetrahydrothieno[3,2-c]pyrid-5-yl)acetamide (+)-camphor sulfonic acid saltHCID 13172410470%

Reaction Steps

A solution of 5 g (16.31 mmol) of (±)-(2-chloro-phenyl)-(6,7-dihydro-4H-thieno[3,2-c]pyrid-5-yl) acetamide (prepared as given in Examples 10-15) and 4.15 g (16.2 mmol) (1S)-(+)-camphor-10-sulphonic acid monohydrate in 100 mL acetone was kept warm for 20 hrs followed by storing it in temperature below 10° C. A few crystals appeared, the mother liquor was concentrated further and repeated recrystallization, followed by storage in cold condition for few days gave 3.1 g (70% yield) of (S)-2-(2-chloro-phenyl)-(4,5,6,7-tetrahydrothieno[3,2-c]pyrid-5-yl)acetamide (+)-camphor sulfonic acid salt. The salt was further purified by recrystallization in acetone, until constant specific optical rotation was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06635763B2
Source datasetuspto-grants-2003_10
ORD IDord-5d84c9d99f4e45b3847fdd244a7c7e9b
Source noteuspto-grants-2003_10