HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280515Generated: October 29, 2026
Acetic Anhydride → HCID 86740803, compound
https://huagongshe.com/reaction/280515
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 86740804 | HCID 86740804 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86740803 | HCID 86740803 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04590188 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-d63d8a8bd09243d1ae4a36045e09d10d |
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| Source note | uspto-grants-1986_05 |
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