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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280515Generated: October 29, 2026

Acetic Anhydride → HCID 86740803, compound

https://huagongshe.com/reaction/280515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 86740804HCID 86740804—
SolventAcetic AcidHCID 176—
ProductHCID 86740803HCID 8674080378%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1 g of (±)-cis-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(dimethylamino)ethyl]-7-methoxy-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride, 1.5 ml of acetic anhydride and 1.5 ml of acetic acid is stirred at 110° C. for 4 hours. After the reaction is completed, the mixture is evaporated under reduced pressure to remove acetic anhydride and acetic acid. Benzene is added to the residue, and the mixture is evaporated under reduced pressure to remove acetic anhydride and acetic acid. The residue thus obtained is recrystallized from a mixture of ethanol and ether. 0.87 g of (±)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(dimethylamino)ethyl]-7-methoxy-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride 1/2 hydrate is obtained. Yield: 78%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590188
Source datasetuspto-grants-1986_05
ORD IDord-d63d8a8bd09243d1ae4a36045e09d10d
Source noteuspto-grants-1986_05