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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558557Generated: October 29, 2026

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

https://huagongshe.com/reaction/558557

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 numberUS08063048B2
Source datasetuspto-grants-2011_11
ORD IDord-e526dbd0a5cc4a40bc67b11cb4ddb542
Source noteuspto-grants-2011_11