HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183263Generated: October 29, 2026
3,5-Dimethylpyrazole → HCID 178509134, compound
https://huagongshe.com/reaction/2183263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dimethylpyrazole | HCID 6210 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22479863 | HCID 22479863 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178509134 | HCID 178509134 | 4.7% |
Reaction Steps
To a solution of N-amino[3-(4-fluorophenyl)(1H-indazol-5-yl)]carboxamide (440 mg, 1.6 mmol) and 3,5-dimethylpyrazole (321 mg, 1.6 mmol) in water (˜15 mL) was added triethylamine (0.21 mL, 1.6 mmol). The reaction was heated to reflux overnight. The solvent was removed and the crude reaction mixture was taken up in butanol with molecular sieves. The reaction was heated to reflux overnight. The molecular sieves were removed and the solution concentrated. The crude mixture was purified by preparative HPLC. The material was taken up in ethyl acetate and washed with aqueous sodium bicarbonate. The organic layer was dried with magnesium sulfate, filtered and concentrated to yield the title compound (0.022 g, 4.6% yield). 1H NMR (DMSO-d6) δ 13.5 (s, 1H), 12.0 (s, 1H), 8.5 (s, 1H), 8.0 (m, 3H), 7.7 (d, 1H), 7.4 (m, 2H), 6.1 (s, 2H), ES-MS (m/z) 295 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897231B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-866d53fbe0164c0495ba731fde2bd4ba |
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| Source note | uspto-grants-2005_05 |
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