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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1898894Generated: October 26, 2026

Propylamine → 7-[N-(2'-Cyanobiphenyl-4-yl)methyl-N-propylamino]-5-methylpyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1898894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylamineHCID 7852—
Reactant4'-(Bromomethyl)-2-cyanobiphenylHCID 1501912—
Reactant7-Chloro-5-methylpyrazolo[1,5-a]pyrimidineHCID 10487287—
ReactantN-(2'-cyanobiphenyl-4-ylmethyl)-N-propyl-amineHCID 15338355—
SolventEthanolHCID 702—
Product7-[N-(2'-Cyanobiphenyl-4-yl)methyl-N-propylamino]-5-methylpyrazolo[1,5-a]pyrimidineHCID 19975933—

Reaction Steps

2.5 g (10.0 mmol) of N-(2'-cyanobiphenyl-4-yl)methyl-N-propyl amine (prepared from n-propylamine and 4-bromomethyl-2'-cyanobiphenyl by the method described in EP 490 820) and 1.8 g (10.7 mmol) 7-chloro-5-methylpyrazolo[1,5-a]pyrimidine (prepared according to Y. Makisumi, Chem. Pharm. Bull. 1962, 10, 620) were heated with reflux in 20 ml dry ethanol for 4 h. The mixture was concentrated to halve of the volume in vacuo and cooled with ice, while the remaining starting amine crystallized. It was filtered with suction, and the rest of the solvent was removed. The title compound was obtained from the residue after column chromatography (silica gel, acetone/hexane 1:9 and 2:3) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571813
Source datasetuspto-grants-1996_11
ORD IDord-b9ba051b8e2647168e11a860c3b59d39
Source noteuspto-grants-1996_11