HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498922Generated: October 25, 2026
Dimethylformamide → 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (3-tert-butyl-2-vinylphenyl)amide
https://huagongshe.com/reaction/498922
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid | HCID 2775665 | — |
| Reactant | 3-Tert-butyl-2-ethenylaniline | HCID 68463211 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (3-tert-butyl-2-vinylphenyl)amide | HCID 11617265 | — |
Reaction Steps
197 mg (1,01 mmol) 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid and 135 mg (1,07 mmol) oxalylic acid chloride are dissolved in 8 ml methylenechloride. The solution is stirred for 3 hours at room temperature in the presence of a catalytic amount of dimethylformamide (DMF). After this the solution is slowly added to a solution consisting of 180 mg (1,01 mmol) 3-tert-butyl-2-vinyl-phenylamine, 155 mg (1,52 mmol) triethylamine and 7 ml methylenechloride. The resulting reaction mixture is then stirred at room temperature for 16 hours. After removal of the solvent in a water jet vacuum, the residue is purified by flash chromatography over silicagel (eluent: hexane/ethylacetate 2:1). This gives 0,27 g 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (3-tert-butyl-2-vinylphenyl)amide in the form of a colourless solid (m.p. 118-119° C.; 76% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767625B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-2ef4725139d742d496e09cfb23d1adca |
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| Source note | uspto-grants-2010_08 |
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