HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dihexylamine → HCID 54093883, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dihexylamine | HCID 8920 | — |
| Reactant | (S)-8-chloro-1-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]-imidazo[1,5-a][1,4]benzodiazepin-9-one | HCID 53954665 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54093883 | HCID 54093883 | 56.5% |
Reaction Steps
1.13 g (3 mmol) of (S)-8-chloro-1-(5-chloromethyl-1,2,4-oxadiazol-3-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one were stirred at room temperature overnight with 1.7 g (9 mmol) of dihexylamine and 15 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 0.89 g (56%) of (S)-8-chloro-1-(5-dihexylaminomethyl-1,2,4-oxadiazol-3-yl)-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one, which was converted into the hydrochloride (amorphous).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665718 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-0e10f4e1e71e42f5a574c35cd9bb6e72 |
| Source note | uspto-grants-1997_09 |