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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940928Generated: October 30, 2026

Ethanol → 2-Amino-5-chloro-8-methoxy[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1940928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantN-(6-Chloro-3-methoxy-2-pyridinyl)-N'-carboethoxythioureaHCID 21464341—
SolventWaterHCID 962—
Product2-Amino-5-chloro-8-methoxy[1,2,4]triazolo[1,5-a]pyridineHCID 1836619558.6%

Reaction Steps

Hydroxylamine hydrochloride (9.6 g, 138 mmol) and diisopropylethylamine (14.4 mL, 10.7 g, 83 mmol) were mixed with ethanol (300 mL) for a few minutes and then N-(6-chloro-3-methoxy-2-pyridinyl)-N'-carboethoxythiourea (7.6 g, 27.5 mmol) was added with stirring. The resulting mixture was stirred at room temperature for 20 min and then heated to reflux for 3 hours. The volatile components were removed by evaporation and the residue obtained was mixed with water. The resulting slurry was filtered and the solids collected were washed with ether, a small amount of methanol, and finally hexane and were then dried. The title compound (3.2 g) was obtained as a tan powder melting at 207°-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05700940
Source datasetuspto-grants-1997_12
ORD IDord-2e93278c6de64f08ad22b94276dcdead
Source noteuspto-grants-1997_12