HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Pyrroline → HCID 22914484, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Pyrroline | HCID 66059 | — |
| Reactant | 3-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one | HCID 22914314 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22914484 | HCID 22914484 | 12.3% |
Reaction Steps
1.5 g (4.5 mmol) of 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 80° for 20 hours in 1 ml (14 mmol) 3-pyrroline and 30 ml of N,N-dimethylformamide. By evaporation of the reaction mixture and chromatography of the residue on silica gel while eluting with methylene chloride/methanol 19/1 there was obtained 0.2 g (12%) of 5-methyl-3-[5-(3-pyrrolin-1-yl)methyl-1,2,4-oxadiazol-3-yl]-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one, which was converted into the hydrochloride of m.p. 215°-220°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-699052591de645f4b22104b0aab71742 |
| Source note | uspto-grants-1997_09 |