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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079331Generated: October 25, 2026

Hydrochloric Acid → 6-Chloro-4-methylsulphinyl-2,3,4,5-tetrahydro-1,4-benzothiazepine

https://huagongshe.com/reaction/1079331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfinyl chlorideHCID 548463—
Reactant6-Chloro-2,3,4,5-tetrahydro-1,4-benzothiazepineHCID 10198105—
SolventDichloromethaneHCID 6344—
Product6-Chloro-4-methylsulphinyl-2,3,4,5-tetrahydro-1,4-benzothiazepineHCID 9881666—

Reaction Steps

A solution of methanesulphinyl chloride (0.98 g) in dichloromethane (10 ml) was added dropwise at room temperature to a stirred solution of 6-chloro-2,3,4,5-tetrahydro-1,4-benzothiazepine (1.99 g, prepared in a similar manner to its hydrochloride, Example 1 above) and triethylamine (1.01 g) in dichloromethane (50 ml). The reaction mixture was stirred at room temperature for one hour, washed with water, dried and the solvent was removed by evaporation. Purification of the residue by flash chromatography using dichloromethane/ethanol (98:2) as eluent gave 6-chloro-4-methylsulphinyl-2,3,4,5-tetrahydro-1,4-benzothiazepine, which was recrystallised from ethylacetate/hexane. Yield 2.1 g (m.p. 82°-84° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580866
Source datasetuspto-grants-1996_12
ORD IDord-a4b39ac55d1746fba3b43ffd23dfb566
Source noteuspto-grants-1996_12