HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881595Generated: November 2, 2026
5-Methoxycarbonyl-2-thiophenecarboxylic acid hydrazide → methyl 5-[(2-{1-[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethylidene}hydrazino)carbonyl]-2-thiophenecarboxylate
https://huagongshe.com/reaction/1881595
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Methoxycarbonyl-2-thiophenecarboxylic acid hydrazide | HCID 14871961 | — |
| Reactant | 1-[5-(4-t-Butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethanone | HCID 67050084 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 5-[(2-{1-[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethylidene}hydrazino)carbonyl]-2-thiophenecarboxylate | HCID 72359930 | 31.4% |
Reaction Steps
1-[5-(4-t-Butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethanone (38.0 mg, 0.14 mmol) and methyl 5-hydrazinocarbonyl-2-thiophenecarboxylate (27.9 mg, 0.14 mmol) were dissolved in dimethylformamide (2.0 mL) and stirred at 110° C. for 12 hours. After cooling, the solvent was evaporated, and ethyl acetate was added to the resulting crude product. The precipitated solid was recovered by filtration to give 20.0 mg of the desired product as a pale yellow solid (yield 31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318796B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-dfc95d35cc1f4433b69cbe0f622a95fb |
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| Source note | uspto-grants-2012_11 |
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