HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521631Generated: October 30, 2026
Dichloromethane → N-(3-(4-chloro-1-methyl-1H-pyrazol-5-yl)-4-hydroxyphenyl)-5-methylisoxazole-3-carboxamide
https://huagongshe.com/reaction/521631
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3-Methyl-5-isoxazolecarboxylic acid | HCID 76947 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 4-amino-2-(1-methyl-1H-pyrazol-5-yl)phenol | HCID 135582024 | — |
| Product | N-(3-(4-chloro-1-methyl-1H-pyrazol-5-yl)-4-hydroxyphenyl)-5-methylisoxazole-3-carboxamide | HCID 136388020 | 59% |
Reaction Steps
To a solution of 5-methylisoxazole-3-carboxylic acid (284.0 mg, 2236.0 μmol) dissolved in DCM(10.0 mL) was added HATU (1020.0 mg, 2683.0 μmol) followed by DIEA (58411, 3353 μmol). The solution was stirred at room temperature for 5 minutes. 4-amino-2-(1-methyl-1H-pyrazol-5-yl)phenol (500.00 mg, 2236 μmol) was added and the reaction mixture was stirred at 25° C. for 15 hours. The reaction mixture was subjected to purification by column chromatography (ethyl acetate:hexane 50:50) to afford the title compound as an off-white solid in 59.0% yield. LCMS m/z=333.2 (M+H), 1H NMR (400 MHz, DMSO-d6) δ ppm 2.69 (s, 3H), 3.66 (s, 3H), 6.64 (s, 1H), 7.00 (d, J=8.84 Hz, 1H), 7.61 (s, 1H), 7.64 (d, J=2.53 Hz, 1H), 7.73 (dd, J=8.84, 2.53 Hz, 1H), 10.04 (s, 1H), 10.60 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328107B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-7dd01965aa104ab58bcf7cfc2857aca4 |
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| Source note | uspto-grants-2016_05 |
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