HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 5-{1-[4-Hydroxy-1-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazol-3-yl]ethylidenehydrazinocarbonyl}thiophene-2-carboxylic Acid Diethylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | N,N-Diethyl-5-(hydrazinecarbonyl)thiophene-2-carboxamide | HCID 57688164 | — |
| Reactant | 1-[4-hydroxy-1-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazol-3-yl]ethanone | HCID 60206790 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 5-{1-[4-Hydroxy-1-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazol-3-yl]ethylidenehydrazinocarbonyl}thiophene-2-carboxylic Acid Diethylamide | HCID 73175129 | 53.2% |
Reaction Steps
1-[4-Hydroxy-1-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazol-3-yl]ethanone (28 mg, 0.10 mmol, synthesized in accordance with WO2004/108683), 5-hydrazinocarbonylthiophene-2-carboxylic acid diethylamide (24 mg, 0.10 mmol) prepared in Reference Synthetic Example 1 and p-toluenesulfonic acid (6 mg) were heated with 2-propanol (4 mL) for 14 hours with reflux. After cooling, the solvent was evaporated, and the resulting solid was recrystallized from 2-propanol-diethyl ether-n-hexane to give 27 mg of the desired product (yield 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960425B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-39ccdd806be14e8a84624b231308dd0b |
| Source note | uspto-grants-2011_06 |