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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194718Generated: November 1, 2026

Cyanoacetamide → 5-Amino-1-(4-chloro-3-cyanobenzyl)-1,2,3-triazole-4-carboxamide

https://huagongshe.com/reaction/1194718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetamideHCID 7898—
ReactantSodium MethoxideHCID 10942334—
Reactant4-Chloro-3-cyanobenzyl azideHCID 23036238—
SolventEthanolHCID 702—
Product5-Amino-1-(4-chloro-3-cyanobenzyl)-1,2,3-triazole-4-carboxamideHCID 1403303232.7%

Reaction Steps

A stirred suspension of 2-cyanoacetamide (790 mg, 9.40 mmol) in absolute ethanol (40 ml) was treated with sodium methoxide (495 mg, 9.16 mmol) and refluxed 10 minutes. The mixture was cooled slightly, a solution of 4-chloro-3-cyanobenzyl azide (1.35 g, 7.01 mmol) in absolute ethanol (10 ml) was added in one portion, and the mixture was refluxed 2.5 hours. The mixture was filtered hot, the solid was washed with absolute ethanol, and the combined filtrate and wash were evaporated to dryness under vacuum. The residue was triturated with diethyl ether, filtered, and washed twice with diethyl ether. The solid was recrystallized from methanol (6 ml) and dried at 65° C. under vacuum to provide 635 mg (24%) 5-amino-1-(4-chloro-3-cyanobenzyl)-1,2,3-triazole-4-carboxamide, m.p. 172°-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04816469
Source datasetuspto-grants-1989_03
ORD IDord-30eebdbcba7545109cb966db5fac197d
Source noteuspto-grants-1989_03