HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Quinazolinamine, N,2-dimethyl-N-(4-nitrophenyl)- → N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Quinazolinamine, N,2-dimethyl-N-(4-nitrophenyl)- | HCID 11150552 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-methyl-N-(2-methylquinazolin-4-yl)benzene-1,4-diamine | HCID 11311597 | 78% |
Reaction Steps
A mixture of (2-methyl-quinazolin-4-yl)-(4-nitro-phenyl)-methylamine (200 mg, 0.68 mmol) in 25 mL of ethyl acetate was hydrogenated over Palladium on carbon (70 mg) at 50 psi for 4 h, and the reaction mixture was filtered through a pad of celite and concentrated. The resulting crude product was purified by chromatography (50% ethyl acetate/hexane) to obtain the title compound (140 mg, 78%). 1H NMR (CDCl3): 7.71 (m, 1H), 7.51 (ddd, J=8.4, 6.9, 1.5, 1H), 7.09 (m, 1H), 6.93-7.05 (m, 3H), 6.68 (m, 2H), 3.74 (s, broad, 2H), 3.56 (s, 3H), 2.71 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309562B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-9d2aadaba35d4049b6e68c56b52b4689 |
| Source note | uspto-grants-2012_11 |