HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-(2-Fluoro-4-(pyridin-4-yl)phenyl)benzo[d]oxazole-7-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methyl 2-(2-fluoro-4-(pyridin-4-yl)phenyl)benzo[d]oxazole-7-carboxylate | HCID 66620942 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2-Fluoro-4-(pyridin-4-yl)phenyl)benzo[d]oxazole-7-carboxamide | HCID 44181674 | 62% |
Reaction Steps
Methyl 2-(2-fluoro-4-(pyridin-4-yl)phenyl)benzo[d]oxazole-7-carboxylate (500 mg, 1.43 mmol) was added to ammonia in methanol (30 mL) and the mixture was stirred at room temperature for 3 days. Then the solid was filtered, washed with methanol and dried in vacuum to obtain 2-(2-fluoro-4-(pyridin-4-yl)phenyl)benzo[d]oxazole-7-carboxamide as white solid (300 mg, yield 62%). 1H-NMR (400 MHz, DMSO-d6) δ (ppm): 7.52-7.56 (t, J=7.6 Hz, 1H), 7.85-7.89 (m, 5H), 7.95-7.97 (d, J=8.4 Hz, 1H), 8.03-8.05 (m, 2H), 8.45-8.49 (t, J=7.6 Hz, 1H); 8.72-8.73 (d, J=4.4 Hz, 2H); LC-MS (ESI) m/z: 334 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088760B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-2d0d7543c50445148607bc7d9764c50f |
| Source note | uspto-grants-2012_01 |