HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978341Generated: October 29, 2026
Acetic Anhydride → HCID 70430585, compound
https://huagongshe.com/reaction/978341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 67941806 | HCID 67941806 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Product | HCID 70430585 | HCID 70430585 | 85.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04665068 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-99a3299b1e6548519ee63bf00270373e |
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| Source note | uspto-grants-1987_05 |
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