HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 21413360, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 21413348 | HCID 21413348 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21413360 | HCID 21413360 | — |
Reaction Steps
To a solution of 0.38 g. of 8-chloro-4-hydroxy-6-phenyl-4H-s-triazolo[1,5-a][1,4]benzodiazepine-2-carboxamide (3/2 hydrate) in 5 ml. of pyridine is added 0.2 ml. of acetic anhydride and the mixture is left to stand at room temperature for 2 hours, followed by addition of water. The precipitated crystals are collected by filtration to yield 4-acetoxy-8-chloro-6-phenyl-4H-s-triazolo[1,5-a][1,4]-benzodiazepine-2-carboxamide as crystals. This product is identical with the product in Example 1 with respect to melting point and infrared absorption spectrum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04046772 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-6d7c930d0edf41c1a2a953ae65fd1181 |
| Source note | uspto-grants-1977_09 |