HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepin-6-one | HCID 12359340 | — |
| Reactant | Diborane dimethylsulfide | HCID 22038413 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepine | HCID 12359341 | 99.9% |
Reaction Steps
To a solution of 0.070 g of 6,7-dihydro-5H-pyrrolo[1,2-a][1,5]benzodiazepin-6-one in 2 ml of tetrahydrofuran is added 0.45 ml of a 2.0 M solution of diborane-dimethylsulfide in tetrahydrofuran. The mixture is refluxed for 3 hours, poured into water and make basic with 2 N NaOH. The tetrahydrofuran is removed under vacuum and the residual aqueous mixture extracted with diethyl ether. The extract is washed with brine, dried (Na2SO4) and the solvent removed to give 0.065 g of a colorless oil; one spot by thin layer chromatography (silica gel) with ethyl acetate-hexane (1:2) as solvent (Rf 0.81).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05968937 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-94a9cf06ea2749e6a6b6cbb0b3d45d3a |
| Source note | uspto-grants-1999_10 |