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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293667Generated: October 30, 2026

Triethylamine → 5-(4-Chloro-phenyl)-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1293667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant7-Chloro-5-(4-chlorophenyl)pyrazolo[1,5-a]pyrimidineHCID 21035702—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-(4-Chloro-phenyl)-pyrazolo[1,5-a]pyrimidineHCID 6700083767.5%

Reaction Steps

A mixture of 7-chloro-5-(4-chloro-phenyl)-pyrazolo[1,5-a]pyrimidine (example C.5, step 2) (1.06 g, 4.0 mmol), triethylamine (0.84 mL), and 5% Pd—C (0.1 g) in EtOH (40 mL) was stirred in an atmosphere of hydrogen for 1.5 h. The catalyst was filtered off, the solution was evaporated in vacuo and the residue was crystallized from EtOAc/cyclohexane to give 5-(4-chloro-phenyl)-pyrazolo[1,5-a]pyrimidine (0.62 g, 67%) as a pale-yellow solid. MS (ISP) 230.4 [(M+H)+]; mp 178–180° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238808B2
Source datasetuspto-grants-2007_07
ORD IDord-196d8b8cc81448a9beecb4b959901386
Source noteuspto-grants-2007_07