HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 70453360, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Oxalate | HCID 71081 | — |
| Reactant | HCID 70453286 | HCID 70453286 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Product | HCID 70453360 | HCID 70453360 | — |
Reaction Steps
A mixture of 0.67 g of (+)-cis-2-(4-methoxyphenyl)-3-hydroxy-5-[2-(diethylamino)ethyl]-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one, 7 ml of acetic anhydride and 2 drops of pyridine is treated in the same manner as described in Example 16. The crude product is converted into its oxalate and recrystallized from ethanol. 0.634 g of (+)-cis-2-(4-methoxyphenyl)-3-acetoxy-5-[2-(diethylamino)ethyl]-8-chloro-2,3-dihydro-1,5-benzothiazepin-4(5H)-one oxalate is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04567175 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-eba8ffe574614e4ea5e780ca0de4e1be |
| Source note | uspto-grants-1986_01 |