HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylamine → HCID 22914304, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylamine | HCID 8085 | — |
| Reactant | HCID 22914464 | HCID 22914464 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22914304 | HCID 22914304 | 77.2% |
Reaction Steps
1.64 g (5 mmol) of 3-(5-chloromethyl-1,3,4-oxadiazol-2-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one were stirred at room temperature overnight with 1.62 g (12.5 mmol) of diisobutylamine and 20 ml of N,N-dimethylformamide. After evaporation of the reaction mixture and chromatography of the residue on silica gel while eluting with ethyl acetate there were obtained 1.63 g (77%) of 3-(5-diisobutylaminomethyl-1,3,4-oxadiazol-2-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one of m.p. 138°-140°, which was converted into the hydrochloride of m.p. 177°-180°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-482a245537b5443c9abbdbb81a3add3b |
| Source note | uspto-grants-1997_09 |