HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Acetyl-1,2-oxazole-3-carboxylic acid → HCID 67172077, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Acetyl-1,2-oxazole-3-carboxylic acid | HCID 17867521 | — |
| Reactant | (S)-4-(1-(1-aminopropan-2-yl)-1H-pyrazol-3-yl)-2-chlorobenzonitrile | HCID 67171193 | — |
| Product | HCID 67172077 | HCID 67172077 | 24.6% |
Reaction Steps
(S)-5-acetyl-N-(2-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propyl)-isoxazole-3-carboxamide was prepared using the method of Example 34(d) starting from (S)-4-(1-(1-aminopropan-2-yl)-1H-pyrazol-3-yl)-2-chlorobenzonitrile (106 mg, 0.408 mmol) and 5-acetylisoxazole-3-carboxylic acid (76 mg, 0.490 mmol). The product was purified by Flash-chromatography. Yield 24.6%. 1H-NMR (400 MHz; CDCl3): δ 1.63 (d, 3H), 2.63 (s, 3H), 3.78-3.88 (m, 1H), 3.91-4.00 (m, 1H), 4.59-4.69 (m, 1H), 6.63 (d, 1H), 7.29 (s, 1H), 7.50 (s, UT), 7.67-7.77 (m, 2H), 7.82 (dd, 1H), 8.05 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08975254B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-c39bb57ca8d445c0b14a9022930ac325 |
| Source note | uspto-grants-2015_03 |