HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)aniline → 1-(4-Phenylthiazol-2-yl)-N-(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl)pyrrolidine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl)aniline | HCID 20297549 | — |
| Reactant | 1-(4-Phenylthiazol-2-yl)pyrrolidine-3-carboxylic acid | HCID 63031329 | — |
| Product | 1-(4-Phenylthiazol-2-yl)-N-(3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenyl)pyrrolidine-3-carboxamide | HCID 53327810 | 28% |
Reaction Steps
This compound was synthesized from 3-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)aniline and 1-(4-phenylthiazol-2-yl)pyrrolidine-3-carboxylic acid as described for example 37 step 3 (20 mg, yield 28%). 1H NMR (400 MHz, MeOD) δ 8.47 (t, J=1.8 Hz, 1H), 7.88-7.81 (m, 3H), 7.57-7.53 (t, J=7.9 Hz, 1H), 7.39-7.35 (m, 2H), 7.30-7.25 (m, 2H), 6.90 (s, 1H), 3.90-3.86 (m, 1H), 3.82-3.78 (m, 1H), 3.76-3.71 (m, 1H), 3.64-3.58 (m, 1H), 3.47-3.39 (m, 1H), 2.46-2.40 (m, 2H). MS (ESI) m/z: Calculated for C23H18F3N5O2S: 485.11. found: 486.0 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08981084B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-03433d47371b4226872a629676bf4164 |
| Source note | uspto-grants-2015_03 |