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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750341Generated: October 31, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1750341

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxylic acidHCID 53422598—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamideHCID 8672117988%

Reaction Steps

A solution of the compound (16.87 g, 64.32 mmol) obtained in step 2, WSC (16.03 g, 83.62 mmol), HOBt (11.30 g, 83.62 mmol), TEA (11.65 mL, 83.62 mmol) and ammonium chloride (4.47 g, 83.62 mmol) in DMF (200 mL) was stirred at room temperature for 2 days. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 5→85% ethyl acetate/hexane) to give 1-tert-butyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamide (14.72 g, 56.3 mmol, 88%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156837B2
Source datasetuspto-grants-2015_10
ORD IDord-5c402c2ac0b7421f88cfbd185ffaa0e4
Source noteuspto-grants-2015_10