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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054243Generated: October 25, 2026

1,3-Butanedione, 1-(4-chloro-3-methylphenyl)-4,4,4-trifluoro- → 5-(4-Chloro-3-methyl-phenyl)-3-pyridin-2-yl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2054243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Butanedione, 1-(4-chloro-3-methylphenyl)-4,4,4-trifluoro-HCID 67000978—
ReactantHCID 178509250HCID 178509250—
Product5-(4-Chloro-3-methyl-phenyl)-3-pyridin-2-yl-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidineHCID 6721330769.4%

Reaction Steps

Reaction of 1-(4-chloro-3-methyl-phenyl)-4,4,4-trifluoro-butane-1,3-dione (265 mg, 1.0 mmol), prepared from commercially available 4-chloro-3-methyl-acetophenone according to general procedure A, and 3-amino-4-(2-pyridinyl)-pyrazole [CAS No. 493038-87-2; prepared from 2-cyanomethyl-pyridine as described in Bioorg. Med. Chem. Lett. 12 (2002) 3537-3541] (160 mg, 1.0 mmol) according to general procedure B yielded the title compound as a yellow solid (270 mg, 69%). MS (ISP) 389.2 [(M+H)+]; mp 183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329662B2
Source datasetuspto-grants-2008_02
ORD IDord-9cdd6b7906434f258069fa5966c9d50e
Source noteuspto-grants-2008_02