HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 135838222, compound → HCID 135838114, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 135838222 | HCID 135838222 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | HCID 135838114 | HCID 135838114 | — |
Reaction Steps
A mixture of 3-amino-5,6-dihydro-7,9-dimethylbenzo[f]quinazolin-1(2H)one (0.25 g, 1.04 mmole) and 10% palladium on carbon (0.5 g) in diglyme (25 ml) was vigorously stirred and refluxed under a nitrogen atmosphere for 2.5 hours, and then filtered while still hot through a bed of celite. Diglyme was removed from the filtrate under reduced pressure, and the residue was triturated with hot methanol, filtered, washed with methanol and ether, and dried to give 3-amino-7,9-dimethylbenzo[f]quinazolin-1(2H)-one as an off-white solid. (0.14 g, 55%) 1H NMR(DMSO-d6, 200 MHz) δ: 2.43(s, 3H, CH3); 2.60(s, 3H, CH3); 6.48(s, 2H, NH2); 7.14(s, 1H, Ar); 7.25(d, J=9.2 Hz, 1H, Ar); 8.11(d, J=9.1 Hz, 1H, Ar); 9.38(s, 1H, Ar); 11.07(s, 1H, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05405851 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-944e446bdc294e39a705e32c45792fd1 |
| Source note | uspto-grants-1995_04 |