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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285343Generated: November 1, 2026

Acetic Anhydride → HCID 70453272, compound

https://huagongshe.com/reaction/1285343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 11004065HCID 11004065—
SolventPyridineHCID 1049—
ProductHCID 70453272HCID 70453272—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 6.4 g of (+)-cis-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(dimethylamino)ethyl]-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one, 65 ml of acetic anhydride and 0.7 ml of pyridine is stirred at 110° C. for 3 hours. After the reaction is completed, the reaction mixture is evaporated to remove solvent. The residue is converted to its hydrochloride and recrystallized from a mixture of acetone and ethanol. 4.7 g of (+)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(dimethylamino)ethyl]-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride are thereby obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567175
Source datasetuspto-grants-1986_01
ORD IDord-c2a11b1b1d9548609b674a6fcea168c1
Source noteuspto-grants-1986_01