HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2-Cyclohexylphenyl)-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Cyclohexylbenzenamine | HCID 407899 | — |
| Reactant | 1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carbonyl chloride | HCID 2794581 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-Cyclohexylphenyl)-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide | HCID 19754740 | 111.3% |
Reaction Steps
To 1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid chloride (1.6 g) in CH2Cl12 (25 mL) at 0° C. was added dropwise a solution of 2-cyclohexylaniline (1.3 g) and triethylamine (1.0 mL) in CH2Cl2 (25 mL). The contents were stirred overnight, coming to RT. The contents were washed with water, 2N HCl (2×100 mL), dried (MgSO4) and concentrated in vacuo leaving an amber foam (2.9 g). Crystallization from EtOAc/hexane gave the desired amide as white crystals (1.2 g). Most of the compounds of the present invention were made via this coupling procedure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05223526 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-11d9c13f5ebf4b6a92dc2e9a0a23d981 |
| Source note | uspto-grants-1993_06 |