HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2-Fluoroethyl)-N,1-dimethyl-1H-pyrazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methyl-1H-pyrazole-4-carboxylic acid | HCID 643160 | — |
| Reactant | (2-Fluoro-ethyl)-methyl-amine hydrochloride | HCID 85799809 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-Fluoroethyl)-N,1-dimethyl-1H-pyrazole-4-carboxamide | HCID 58446960 | — |
Reaction Steps
Methyl-1H-pyrazole-4-carboxylic acid (1.0 g, 7.93 mmol) was combined with DMF (10.0 ml) to give a colorless solution. Et3N (3.3 ml, 23.8 mmol) and 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium tetrafluoroborate (TBTU, 2.8 g, 8.72 mmol) were added and the reaction mixture was stirred at RT for 1 h. 2-Fluoroethyl-methylamine hydrochloride (991 mg, 8.72 mmol) was added and stirring was continued overnight. DMF was removed under HV and the crude product (5.93 g brown oil) was purified by chromatography with a 50 g SiO2—NH2 cartridge (CH2Cl2/MeOH 95:5). The resulting product was dried under HV at RT for 48 h. Yellow oil (1.40 g, 92%); MS: m/z=186.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349824B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-d58d93c2119c4c649809a446e768894d |
| Source note | uspto-grants-2013_01 |