HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22648055, compound → 5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-7-nitro-3,4-dihydroquinazolin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22648055 | HCID 22648055 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-7-nitro-3,4-dihydroquinazolin-2(1H)-one | HCID 22648156 | — |
Reaction Steps
A solution of 5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-3-(4-methoxybenzyl)-7-nitro-3,4-dihydroquinazolin-2(1H)-one (32 mg, 0.56 mmol) in 1 mL trifluoroacetic acid was stirred at 95° C. for 1.25 h. The solvent was removed under reduced pressure and the product was purified by preparative thin-layer chromatography, eluting with 93:7 CH2Cl2-methanol to yield 5-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-7-nitro-3,4-dihydroquinazolin-2(1H)-one. Mass spectrum (ESI) 448 (M+1). 1H NMR (500 MHz, CDCl3): δ 3.35 (½ ABq, J=15.5 Hz, 1H); 3.52 (½ ABq, J=15.5 Hz. 1H); 7.00 (s, 1H); 7.32 (d, J=2.1 Hz, 1H); 7.46 (m, 3H); 7.58 (m, 3H); 7.81 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809199B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-b7962b7f6e3f4a629a1907e8e8e57ffc |
| Source note | uspto-grants-2004_10 |