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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978341Generated: October 29, 2026

Acetic Anhydride → HCID 70430585, compound

https://huagongshe.com/reaction/978341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 67941806HCID 67941806—
CatalystPyridineHCID 1049—
ProductHCID 70430585HCID 7043058585.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2.84 g of (+)-cis-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(dimethylamino)ethyl]-9-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one, 30 ml of acetic anhydride and 30 drops of pyridine is stirred at 100° C. for 4 hours. After the reaction is completed, the reaction mixture is evaporated under reduced pressure to remove solvent. Toluene is added to the residue, and the mixture is evaporated under reduced pressure to remove solvent. The residue is converted to its hydrochloride and recrystallized from a mixture of ethanol and ether. 3.02 g of (+)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(dimethylamino)ethyl]-9-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride hydrate are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04665068
Source datasetuspto-grants-1987_05
ORD IDord-99a3299b1e6548519ee63bf00270373e
Source noteuspto-grants-1987_05