HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21442717, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 21442729 | HCID 21442729 | — |
| Product | HCID 21442717 | HCID 21442717 | — |
Reaction Steps
A mixture of 1.2 g. of 6--(2-chlorophenyl)-8-ethyl-4H-thieno[3,2-f]-s-triazolo[1,5-a][1,4]diazepine-2-carboxamide-5-oxide and 20 ml. of acetic anhydride is heated at 90° to 95° C. for 50 minutes, and then the solvent is evaporated. The residue is washed with ether to give 4-acetoxy-6-(2-chlorophenyl)-8-ethyl-4H-thieno[3,2-f]-s-triazolo[1,5-a][1,4]diazepine-2-carboxamide as crystals. Recrystallization from ethyl acetate gives colorless prisms melting at 168° to 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017620 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-cc0da7effdcc4d2f90ddec6abc358b1a |
| Source note | uspto-grants-1977_04 |