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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474367Generated: October 29, 2026

Diisopropylethylamine → 5-chloro-N-(1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

https://huagongshe.com/reaction/474367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(3-Trifluoromethylphenyl)-2H-pyrazol-3-ylamineHCID 43316770—
Reactant5-Chloropyrazolo[1,5-a]pyrimidine-3-carbonyl chlorideHCID 58063136—
SolventDichloromethaneHCID 6344—
Product5-chloro-N-(1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamideHCID 5806311058.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-5-amine (200 mg, 0.88 mmol) in dichloromethane (30 mL) was added 5-chloropyrazolo[1,5-a]pyrimidine-3-carbonyl chloride (215 mg, 1.0 mmol) and diisopropylethylamine (130 mg, 1.0 mmol). The mixture was heated to 50° C. overnight. After cooling to room temperature, the mixture was concentrated to afford crude 5-chloro-N-(1-(3-(trifluoromethyl)phenyl)-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide (210 mg, yield 58%), which was used for the next step without further purification. MS (ESI) m/z: 407.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637526B2
Source datasetuspto-grants-2014_01
ORD IDord-af9af61c59c34225bfe8c47e59d73f36
Source noteuspto-grants-2014_01