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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803094Generated: November 1, 2026

1,3-Dimethyl-1H-pyrazole-4-carbonyl chloride → N-(3',4',5'-trifluorobiphenyl-2-yl)-1,3-dimethyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1803094

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-1H-pyrazole-4-carbonyl chlorideHCID 3159698—
Reactant3,4,5-Trifluoro-2'-aminobiphenylHCID 44249263—
SolventTolueneHCID 1140—
ProductN-(3',4',5'-trifluorobiphenyl-2-yl)-1,3-dimethyl-1H-pyrazole-4-carboxamideHCID 52932283—

Reaction Conditions

Temperature85 °C

Reaction Steps

79.1 g (0.494 mol, 99% pure) of 1,3-dimethyl-1H-pyrazole-4-carbonyl chloride were dissolved at 25° C. in 257.2 g of toluene. The solution was evacuated to 400 mbar and heated to 85° C. Subsequently, within 3 hours, 483.0 g (0.489 mol, 23% strength) of toluenic 3′,4′,5′-trifluorobiphenyl-2-ylamine solution were metered in and the reaction mixture was stirred for a further 1 hour. After venting and cooling to 70° C., the mixture was cooled to 20° C. with a cooling ramp of 5° C./h and stirred overnight. Subsequently, the mixture was cooled to 0° C., and the solids were filtered off, washed with cold toluene and dried at 80° C. under reduced pressure. The yield (without further processing of the mother liquor) was 155.4 g (92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350046B2
Source datasetuspto-grants-2013_01
ORD IDord-3cb53bd6fc364d6a9c19dba2366665e2
Source noteuspto-grants-2013_01