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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450393Generated: November 2, 2026

7-Chloro-5-methylpyrazolo[1,5-a]pyrimidine → 7-[(3-Bromo-2-(2-cyanophenyl)benzofuran-5-yl)methylamino]-5-methylpyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1450393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-5-methylpyrazolo[1,5-a]pyrimidineHCID 10487287—
Reactant5-(Aminomethyl)-3-bromo-2-(2-cyanophenyl)benzofuranHCID 19975970—
SolventEthanolHCID 702—
Product7-[(3-Bromo-2-(2-cyanophenyl)benzofuran-5-yl)methylamino]-5-methylpyrazolo[1,5-a]pyrimidineHCID 19975961—

Reaction Steps

A solution of 1.7 g (10.1 mmol) 7-chloro-5-methylpyrazolo[1,5-a]pyrimidine (prepared according to Y. Makisumi, Chem. Pharm. Bull. 1962, 10, 620) and 3.27 g (10.0 mmol) 5-(aminomethyl)-3-bromo-2-(2-cyanophenyl)benzofuran (prepared according to WO 92/09600) in 50 ml dry ethanol was heated with reflux for 5 h. The title compound precipitated upon cooling to room temperature, was filtered with suction, and recrystallized from ethanol to give colorless crystals. yield: 3.5 g (76%), m.p. 210°-215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602137
Source datasetuspto-grants-1997_02
ORD IDord-7b9c4cce776d47f8a7ce17c3a898c3b9
Source noteuspto-grants-1997_02