HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Nitro-1,2,4,5-tetrahydro-benzo(e)(1,3)diazepin-3-one → 7-Amino-1,2,4,5-tetrahydro-(2,4)-benzodiazepin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Nitro-1,2,4,5-tetrahydro-benzo(e)(1,3)diazepin-3-one | HCID 10512508 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Amino-1,2,4,5-tetrahydro-(2,4)-benzodiazepin-3-one | HCID 57853868 | 70.2% |
Reaction Steps
Compound 7-nitro-1,2,4,5-tetrahydro-benzo(e)(1,3)diazepin-3-one (2.00 g, 9.65 mmol) was dissolved in methanol (60 mL) and the solution was carefully added to a Parr shaker vessel containing 10% Palladium/Carbon (200 mg) under nitrogen. The reaction was then shaken under 50 psi of hydrogen until uptake of hydrogen had ceased (3 hours). Catalyst was then removed via filtration through a Celite pad. The filter cake was rinsed with methanol (3×50 mL) and the filtrate was reduced en vacuo to afford 1.20 g of 7-amino-1,2,4,5-tetrahydro-(2,4)-benzodiazepin-3-one as a white solid. LC/MS (ESI)=178.32 (M+H). Rf: (10% MeOH/DCM)=0.31.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08148391B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-220d03f07ae1497396c1b8193e5350b3 |
| Source note | uspto-grants-2012_04 |