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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285285Generated: October 30, 2026

Chloroform → Deacetyldiltiazem

https://huagongshe.com/reaction/1285285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant3-Hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one, (2S,3S)-HCID 2733673—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
ReactantBarium hydroxide, octahydrateHCID 17749109—
SolventWaterHCID 962—
ProductDeacetyldiltiazemHCID 9163897.9%

Reaction Steps

3 g of cis-(+)-2-(4'-methoxyphenyl)-3-hydroxy-2,3-dihydro-1,5-benzothiazepine-4(5H)-one and 6.4 g of barium hydroxide octahydrate were added with vigorous stirring to 60 ml of chloroform and 10 ml of water. A solution of 3.2 g of 2-(dimethylamino)-ethyl chloride-hydrochloride in 5 ml of water was added dropwise to the above mixture in the course of 5 minutes. Stirring was continued for 24 hours at room temperature and then for 8 hours at 40°. After cooling to room temperature the aqueous phase was separated and discarded and the chloroform was removed under vacuum. Petroleum-ether (40°-60°) was added to the viscous residue which induced crystallisation. The precipitated crystals were filtered off and dried under vacuum to yield 3.63 g of cis-(+)-2-(4'-methoxyphenyl)-3-hydroxy-5-(2'-dimethylaminoethyl)-2,3-dihydro-1,5-benzothiazepine-4(5H)-one; m.p. 88°; [α]D22 +169 (C=0.25 CH 3 OH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04566995
Source datasetuspto-grants-1986_01
ORD IDord-75368457e20e499f92aad95fd435870d
Source noteuspto-grants-1986_01