HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-chloro-2-methylmercapto-5-phenyl-3H-1,4-benzodiazepine → 1-(fluoromethyl)-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-chloro-2-methylmercapto-5-phenyl-3H-1,4-benzodiazepine | HCID 12570858 | — |
| Reactant | 2-Fluoroacetic acid hydrazide | HCID 19789195 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 1-(fluoromethyl)-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine | HCID 20473074 | — |
Reaction Steps
A solution of 8 g of 2-(methylthio)-5-phenyl-7-chloro-3H-1,4-benzodiazepine and 3.68 g of 2-fluoroacetic acid hydrazide [cp. M. A. Phillips, Agr.Vet.Chem. 2, 86-87 (1961), C. A. 57, 12314 (1962)] in 80 ml of hexamethylphosphoric acid triamide is heated for 8 hours at 140° The solvent is then distilled off in vacuo, and the residue distributed between methylene chloride and water. The organic phase is separated, washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate, and concentrated by evaporation. The residue is recrystallized from ethyl acetate/petroleum ether to obtain 1-(fluoromethyl)-6-phenyl-8-chloro-4H-s-triazolo[4,3-a][1,4]benzodiazepine, M.P. 153°-154°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04427590 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-fcadbb4a5da643d1a1ed9bbde3d48d36 |
| Source note | uspto-grants-1984_01 |