HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibutylamine → HCID 22914238, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | 7-Chloro-3-(5-chloromethyl-[1,2,4]oxadiazol-3-yl)-5-methyl-4,5-dihydro-imidazo[1,5-a][1,4]benzodiazepin-6-one | HCID 22462191 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22914238 | HCID 22914238 | 61.2% |
Reaction Steps
1.6 g (4.4 mmol) of 7-chloro-3-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one were stirred at room temperature for 48 hours with 3.6 ml (21 mmol) of dibutylamine and 10 ml of N,N-dimethylformamide. By evaporation of the reaction mixture and chromatography of the residue on silica gel while eluting with ethyl acetate there was obtained 1.23 g (61%) of 7-chloro-3-(5-dibutylaminomethyl-1,2,4-oxadiazol-3-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one of m.p. 140°-142°, which was converted into the hydrochloride of m.p. 184°-187°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-b815af6b18b94cba8c8e82e75ff25523 |
| Source note | uspto-grants-1997_09 |