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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268995Generated: October 27, 2026

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

https://huagongshe.com/reaction/268995

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 numberUS07446113B2
Source datasetuspto-grants-2008_11
ORD IDord-b100907883954291834e788b580d3cf5
Source noteuspto-grants-2008_11