HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 3-methyl-3H-benzo[d][1,2]diazepin-4(5H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Ortho-formylphenylacetic acid | HCID 5289058 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-methyl-3H-benzo[d][1,2]diazepin-4(5H)-one | HCID 22243679 | 50% |
Reaction Steps
To a solution of o-formylphenylacetic acid (10 g, 61 mmol) (Bleasdale et al., J. Chem. Soc. Perkin Trans. I 1991, 1683) in 60 mL of EtOH was added N-methylhydrazine (4.2 g, 91 mmol) and refluxed for 1 h. The reaction mixture cooled, solvent removed and transferred the crude reaction mixture to a vaccum sublimation apparatus. The imine was heated at 140° C. under high vaccum for 1 h and collected the cyclized product by extracting with hot 20% ethyl acetate in hexane (Nagarajan et al., J. Med. Chem., 1972, 15(10), 1091). The product was crystallized from 20% ethyl acetate in hexane. 4,5-dihydro-3-methyl-3H-2,3-benzodiazepin-4-one was obtained in 50% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07001901B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-708b156744614d6f9d75633070ab9979 |
| Source note | uspto-grants-2006_02 |