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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887613Generated: October 30, 2026

4-Tert-Butylaniline → N-(4-(Tert-butyl)phenyl)-5-chloro-1-methyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/887613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Tert-ButylanilineHCID 69861—
Reactant5-Chloro-1-methyl-1H-pyrazole-4-carbonyl chlorideHCID 2735773—
SolventDichloromethaneHCID 6344—
ProductN-(4-(Tert-butyl)phenyl)-5-chloro-1-methyl-1H-pyrazole-4-carboxamideHCID 86588705—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Chloro-1-methyl-1H-pyrazole-4-carbonyl chloride (1.0 g, 5.6 mmol) was dissolved in CH2Cl2 (100 mL) under N2 and cooled to 0° C. 4-t-Butylaniline was added and the reaction was stirred with gradual warming to RT overnight. The reaction was quenched with saturated NaHCO3(aq) and extracted 3× with fresh CH2Cl2. The CH2Cl2 extracts were washed with brine, combined, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure giving 5-chloro-1-methyl-1H-pyrazole-4-carboxylic acid (4-tert-butyl-phenyl)-amide as a foamy pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247430B2
Source datasetuspto-grants-2012_08
ORD IDord-51a129c9e3f24786a30dcc5648849b96
Source noteuspto-grants-2012_08