HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-5-cyanobenzoic acid → 2-Chloro-5-cyano-N-(2-(2-(4-fluorophenyl)oxazol-4-yl)-2-methylpropyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-5-cyanobenzoic acid | HCID 14203095 | — |
| Reactant | 2-(2-(4-Fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amine | HCID 67323086 | — |
| Product | 2-Chloro-5-cyano-N-(2-(2-(4-fluorophenyl)oxazol-4-yl)-2-methylpropyl)benzamide | HCID 69950217 | 44% |
Reaction Steps
This compound was synthesized from 2-(2-(4-fluorophenyl)oxazol-4-yl)-2-methylpropan-1-amine and 2-chloro-5-cyanobenzoic acid as described in example 8 step 6 (300 mg, yield 44%). 1H NMR (400 MHz, CDCl3) δ 8.02 (d, J=2.0 Hz, 1H), 7.98-7.95 (m, 2H), 7.66-7.63 (m, 1H), 7.56-7.54 (d, J=8.3 Hz, 1H), 7.48 (s, 1H), 7.39 (m, 1H), 7.17-7.13 (t, J=8.8 Hz, 2H), 3.68-3.66 (d, J=5.8 Hz, 2H), 1.41 (s, 6H). MS (ESI) m/z: Calculated for C21H17ClFN3O2: 397.10. found: 396.4 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901156B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-a6579794480340c097ecf0c9a64fa15b |
| Source note | uspto-grants-2014_12 |