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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558656Generated: October 28, 2026

5-Bromo-2-cyclopropylpyridine → 3-(2-Cyclopropyl-pyridin-5-ylethynyl)-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/558656

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-cyclopropylpyridineHCID 22317722—
Reactant3-Ethynyl-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidineHCID 71539732—
Product3-(2-Cyclopropyl-pyridin-5-ylethynyl)-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidineHCID 11852131—

Reaction Steps

The title compound was prepared from 3-ethynyl-7-trifluoromethyl-5-(4-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine (example C.1) (355 mg, 1.0 mmol) and 5-bromo-2-cyclopropyl-pyridine (Example B.11) (257 mg, 1.3 mmol) according to general procedure II. Obtained as an orange solid (110 mg, 23%). MS (ISP) 473.0 [(M+H)+]; mp 138-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063048B2
Source datasetuspto-grants-2011_11
ORD IDord-5ce452c662344e89be0c7414835055db
Source noteuspto-grants-2011_11