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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558554Generated: October 28, 2026

Ammonium Chloride → 5-(4-Chloro-phenyl)-7-cyclopropyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/558554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Chloro-5-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidineHCID 21035702—
ReactantHCID 178420628HCID 178420628—
ReactantHCID 178420684HCID 178420684—
Catalystzinc chloride THFHCID 66790640—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product5-(4-Chloro-phenyl)-7-cyclopropyl-pyrazolo[1,5-a]pyrimidineHCID 6700093969%

Reaction Steps

To a solution of 7-chloro-5-(4-chloro-phenyl)-pyrazolo[1,5-a]pyrimidine (2.1 g, 8.0 mmol) and tetrakis(triphenylphosphine)palladium (0.92 g, 0.8 mmol) in THF (14 mL) was added at 20° C. 0.25 M cyclopropylzinc chloride/THF suspension (ca. 128 mL, 32 mmol; freshly prepared by stirring a mixture of 64 mL of 0.5 M cyclopropylmagnesium bromide/THF and 64 mL of 0.5 M zinc chloride/THF for 1 h at 0° C., followed by 1 h at 20° C.) and the mixture was refluxed in an atmosphere of argon for 1.5 h. After the slow addition at 0° C. of saturated aqueous NH4Cl solution (20 mL), the mixture was partitioned between EtOAc and 10% sodium chloride solution. The organic layer was dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed on silica gel using EtOAc/hexane (1:5 v/v) as eluent to give 5-(4-chloro-phenyl)-7-cyclopropyl-pyrazolo[1,5-a]pyrimidine (1.50 g, 69%) as an off-white solid. MS (ISP) 270.4 [(M+H)+]; mp 137-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063048B2
Source datasetuspto-grants-2011_11
ORD IDord-f163d6108885443baaf127a88bfa5764
Source noteuspto-grants-2011_11