HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoroaniline → HCID 178523230, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | HCID 178498466 | HCID 178498466 | — |
| Reactant | HCID 178498467 | HCID 178498467 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 178523230 | HCID 178523230 | — |
Reaction Steps
Methyl 2-(4-fluorophenyl)amino-4-hydroxy-6-nitroquinazoline-8-carboxylate. A solution of methyl 2-chloro-4-hydroxy-6-nitroquinazoline-8-carboxylate (1.50 g) and 4-fluoroaniline (1.76 g) in N-methylpyrrolidone (30 mL) was heated to 100° C. for 1 h. After cooling to room temperature, the reaction was cooled to 0° C. and a precipitate formed. The precipitate was isolated by filtration and washed with water (100 mL), 1M HCl (100 mL), and water (100 mL). The resulting material was dried to afford the title compound as a yellow solid (1.89 g). 1H NMR (300 MHz, DMSO-d6 (w/TFA (50 uL)): 8.80 (d, J=2.6 Hz, 1H), 8.69 (d, J=2.2 Hz, 1H), 7.85 (dd, J=8.4, 5.3 Hz, 2H), 7.24 (t, J=8.7 Hz, 2H), 3.97 (s, 3H). HPLC (Method F): 6.71 min. MS (APCI+): m/z 359.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399603B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-ca9380845599447984b0a66b9b291f28 |
| Source note | uspto-grants-2002_06 |