HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280519Generated: October 29, 2026
Acetic Anhydride → HCID 86740807, compound
https://huagongshe.com/reaction/280519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 70483404 | HCID 70483404 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 86740807 | HCID 86740807 | — |
Reaction Steps
A mixture of 0.618 g of (±)-cis-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(dimethylamino)ethyl]-6,7-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride, 6 ml of acetic anhydride and 6 ml of acetic acid is heated at 105° C. for 18 hours. After the reaction is completed, the mixture is evaporated under reduced pressure to remove solvent. Benzene is added to the residue, and the mixture is evaporated under reduced pressure to remove solvent. The residue is recystallized from a mixture of ethanol and ether. 0.44 g of (±)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(dimethylamino)ethyl]-6,7-dimethyl-2,3-dihydro-1,5-benzothiazepin-4(5H)-one hydrochloride 3/2 H2O is obtained.
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-38fd644dc1c4490d851bd0a413646e43 |
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| Source note | uspto-grants-1986_05 |
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