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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903700Generated: November 1, 2026

Potassium Hydroxide → (2S-cis)-5-(2-(Dimethylamino)ethyl)-2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one monohydrochloride

https://huagongshe.com/reaction/1903700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium SulfateHCID 24436—
Reactant3-Hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one, (2S,3S)-HCID 2733673—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
ReactantEthanol hydrochlorideHCID 21887872—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
Product(2S-cis)-5-(2-(Dimethylamino)ethyl)-2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one monohydrochlorideHCID 1244942886.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 30.1 g of cis-(+)-2-(4-methoxyphenyl)-3-hydroxy-2,3-dihydro-1,5-benzothiazepine-4(5H)-one, 17.8 g of 2-(dimethylamino)ethyl chloride hydrochloride, 13.7 g of 96% potassium hydroxide, 60 g of sodium sulfate and 300 ml of acetone is stirred at 50° C. for 7 hours. After the reaction is completed, the mixture is filtered to remove inorganic materials and the filtrate is condensed. The residue is dissolved in ethanol. After cooling the solution, 10% HCl/ethanol is added thereto. The crystalline precipitates are collected by filtration and then dried. 35.1 g of cis-(+)-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-1,5-benzothiazepine-4(5H)-one hydrochloride are thereby obtained. Yield: 86.2%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04438035
Source datasetuspto-grants-1984_03
ORD IDord-75d2890cfa964a9c89e8ea377c8a8d0c
Source noteuspto-grants-1984_03