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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802256Generated: October 30, 2026

Diisopropylethylamine → HCID 86666020, compound

https://huagongshe.com/reaction/1802256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2,7-Dibromo[1,2,4]triazolo[1,5-a]pyridineHCID 67774274—
Reactant(2-Fluoroethyl)(methyl)amine hydrochlorideHCID 85799809—
SolventEthanolHCID 702—
ProductHCID 86666020HCID 8666602034.5%

Reaction Conditions

Temperature130 °C

Reaction Steps

To the solution of 2,7-dibromo-[1,2,4]triazolo[1,5-a]pyridine (5 g, 18.05 mmol) and (2-fluoro-ethyl)-methyl-amine hydrochloride (20 g, 180.5 mmol) in ethanol (30 ml) was added di-isopropylethylamine (47 ml, 270.75 mmol) and the reaction mixture was heated at 130° C. in a sealed tube for 84 hours. The reaction mixture was concentrated under reduced pressure, the resulting residue was diluted with dichloromethane (100 ml). The organic layer was washed with water (2×75 ml), dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The crude material was purified by column chromatography over silicagel using 0.5% methanol/dichloromethane as eluent affording (7-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-(2-fluoro-ethyl)-methyl-amine (1.7 g, 34.5%) as an off white solid. MS: m/z=275.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-bfb48cd994424fccbde0b66bcaacd411
Source noteuspto-grants-2013_01