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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237861Generated: November 2, 2026

Iodine chloride → 3-Iodo-7-trifluoromethyl-5-(3-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/2237861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
ReactantSodium AcetateHCID 517045—
Reactant5-(3-Trifluoromethyl-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidineHCID 86607997—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product3-Iodo-7-trifluoromethyl-5-(3-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidineHCID 8660799894%

Reaction Steps

To a stirred solution of 5-(3-trifluoromethyl-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine (5.0 g, 15.1 mmol) in acetic acid (25 mL) was added at room temperature sodium acetate (1.40 g, 17.1 mmol) and drop wise a solution of iodine monochloride (2.77 g, 17.1 mmol) in acetic acid (10 mLl). The reaction mixture was stirred at room temperature for 16 h, diluted slowly with water (up to 100 mL), stirred at room temperature for 30 min, the precipitate was filtered off, washed with water and dried to give 3-iodo-7-trifluoromethyl-5-(3-trifluoromethyl-phenyl)-pyrazolo[1,5-a]pyrimidine (6.49 g, 94%) as a yellow solid. MS (EI) 457.0[(M)+]; mp 142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718661B2
Source datasetuspto-grants-2010_05
ORD IDord-cadcf9b4cdd94d3d837223c0f3bf518c
Source noteuspto-grants-2010_05