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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588429Generated: October 31, 2026

Diisopropylethylamine → 6-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine

https://huagongshe.com/reaction/588429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantEthyl [(5-bromopyridin-2-yl)carbamothioyl]carbamateHCID 59286274—
SolventEthanolHCID 702—
Product6-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 2521594085.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of hydroxylamine hydrochloride (40.0 g, 575 mmol) and N-ethyldiisopropylamine (44.6 g, 60.3 ml, 345 mmol) in ethanol (734 ml) was stirred for a few minutes at 25° C., then the mixture was added to 1-ethoxycarbonyl-3-(5-bromo-pyridin-2-yl)-thiourea (35 g, 115 mmol) and the resulting mixture was refluxed for 1 day. The solvent was evaporated under reduced pressure and the white solid was treated with 400 ml water. The suspension was stirred for 1 hour, the solid was filtered off, washed with water 3 times and dried under reduced pressure, affording 6-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (21 g, 85%) as white solid. Mp.: 185° C. MS: m/z=213.0/215.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227970B2
Source datasetuspto-grants-2016_01
ORD IDord-38c989441e964fc685b2b681346a94b9
Source noteuspto-grants-2016_01