HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21413360, compound → HCID 21413341, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21413360 | HCID 21413360 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21413341 | HCID 21413341 | — |
Reaction Steps
To a solution of 0.396 g. of 4-acetoxy-8-chloro-6-phenyl-4H-s-triazolo[1,5-a][1,4]benzodiazepine-2-carboxamide in 10 ml. of methanol are added two drops of concentrated sulfuric acid, and the mixture was refluxed for 5 minutes, followed by evaporation of methanol. The residue is neutralized with saturated aqueous sodium bicarbonate solution and the precipitated crystals are collected by filtration, washed with water and dried to obtain 8-chloro-4-methoxy-6-phenyl-4H-s-triazolo[1,5-a][1,4]benzodiazepine-2-carboxamide as crystals. Recrystallization from a mixture of chloroform and methanol yields colorless prisms (1/3 hydrate) melting at 264° to 267° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04046772 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-9146fa2455264461ad9bc1627924b9b7 |
| Source note | uspto-grants-1977_09 |