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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898890Generated: November 1, 2026

Triethylamine → 7-[N-(2'-Cyanobiphenyl-4-yl)methyl-N-methylamino]-5-ethylpyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1898890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant7-Chloro-5-ethylpyrazolo[1,5-a]pyrimidineHCID 10535410—
ReactantN-(2'-Cyanobiphenyl-4-yl)methyl-N-methyl amineHCID 15337416—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product7-[N-(2'-Cyanobiphenyl-4-yl)methyl-N-methylamino]-5-ethylpyrazolo[1,5-a]pyrimidineHCID 15337417—

Reaction Steps

1.8 g (10 mmol) of the chloro compound of Step B and 2.2 g (10 mmol) of the amine of Step C were dissolved in 60 ml ethanol and heated with reflux for 4 h. After addition of 3 ml triethylamine the heating was continued for an additional hour. The mixture was diluted with water and extracted twice with dichloromethane. The combined organic layers were dried over sodium sulfate, evaporated in vacuo, and the title compound obtained as an oil after purification by column chromatography on silica gel using ethyl acetate/hexane 9:1 as eluent,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571813
Source datasetuspto-grants-1996_11
ORD IDord-308976575b8c480b857eb099169e8c1b
Source noteuspto-grants-1996_11