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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382774Generated: November 1, 2026

Cyclopropylamine → N5-cyclopropyl-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridine-2,5-diamine

https://huagongshe.com/reaction/2382774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropylamineHCID 69828—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chloro-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25216184—
Solvent1-ButanolHCID 263—
ProductN5-cyclopropyl-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridine-2,5-diamineHCID 5943744551.1%

Reaction Steps

A suspension of 5-chloro-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridin-2-amine ((A7), 3.60 g; 15.22 mmol; 1.0 eq.), cyclopropylamine (5.27 mL; 76.1 mmol; 5.0 eq.), and N-ethyldiisopropylamine (26.22 mL; 152.2 mmol; 10.0 eq.) was heated at 80° C. in 1-butanol (36.0 mL) for 23 h., then 15 h. at 100° C. The reaction mixture was then concentrated under vacuum till dryness. Diethyl ether was added and the solid was filtered, washed with water and dried. The product was then purified by chromatography on silicagel (from 5% to 95% EtOAc in c-Hex), to give the title compound as a white solid (2.0 g; 51.1%). HPLC, Rt: 2.54 min. (purity 100%). LC/MS, M+(ESI): 258.0, M−(ESI): 256.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263595B2
Source datasetuspto-grants-2012_09
ORD IDord-c01dd4be239145a3acb93bf64da15100
Source noteuspto-grants-2012_09