HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylamine → HCID 22914316, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylamine | HCID 8085 | — |
| Reactant | HCID 22914481 | HCID 22914481 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22914316 | HCID 22914316 | 86.8% |
Reaction Steps
1.09 g (3 mmol) of 7-chloro-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 0.97 g (7.5 mmol) of diisobutylamine and 15 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 1.19 g (86%) of 7-chloro-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. 181°-182°, which was converted into the hydrochloride of m.p. 161°-163°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-d0fcf71601f44e0389aeee108c2d9483 |
| Source note | uspto-grants-1997_09 |