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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898891Generated: October 31, 2026

2-[4-(Aminomethyl)phenyl]benzonitrile → 7-[(2'-Cyanobiphenyl-4-yl)methylamino]-5-ethylpyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1898891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[4-(Aminomethyl)phenyl]benzonitrileHCID 1393341—
Reactant7-Chloro-5-ethylpyrazolo[1,5-a]pyrimidineHCID 10535410—
SolventEthanolHCID 702—
Product7-[(2'-Cyanobiphenyl-4-yl)methylamino]-5-ethylpyrazolo[1,5-a]pyrimidineHCID 10522018—

Reaction Steps

5.5 g (30.3 mmol) of the chloride from Example 1, Step B and 6.3 g (30.3 mmol) of 4-aminomethyl-2'-cyanobiphenyl (prepared according to EP 459 136) were heated in 150 ml dry ethanol for 10 h. After removal of the solvent in vacuo yellow crystals formed. These were purified by suspension in acetone and dissolved in ethyl acetate. The solution was washed with 10% sodium carbonate solution, the organic layer dried over sodium sulfate, and evaporated to dryness to give colorless crystals of the title compound, m.p. 230°-233° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571813
Source datasetuspto-grants-1996_11
ORD IDord-543dcf9616d443eeb84ae19692392c7e
Source noteuspto-grants-1996_11