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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487351Generated: October 29, 2026

Sodium Thiosulfate → 6-(4-Acetoxypiperidino)-5-bromo-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/487351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
Reactant6-(4-Acetoxypiperidino)-3,4-dihydrocarbostyrilHCID 19094724—
SolventChloroformHCID 6212—
Product6-(4-Acetoxypiperidino)-5-bromo-3,4-dihydrocarbostyrilHCID 19094718—
Product6-(4-Acetoxypiperidino)-7-bromo-3,4-dihydrocarbostyrilHCID 19094725—

Reaction Steps

To a solution of 300 mg of 6-(4-acetoxypiperidino)-3,4-dihydrocarbostyril in 7 ml of chloroform was added 370 mg of N-bromosuccinimide, and the mixture was stirred at room temperature for 1 hr. Then, an aqueous sodium thiosulfate was added to the reaction mixture, and the mixture was extracted with chloroform. The extract was washed with brine, dried and evaporated under a reduced pressure. The crude mixture was purified by a silica gel column chromatography to give 87 mg of 6-(4-acetoxypiperidino)-7-bromo-3,4-dihydrocarbostyril and 41 mg of 6-(4-acetoxypiperidino)-5-bromo-3,4-dihydrocarbostyril.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05294718
Source datasetuspto-grants-1994_03
ORD IDord-6a4c00ab4b6745099a9539b782c4dfc4
Source noteuspto-grants-1994_03