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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280644Generated: October 29, 2026

Cyanoacetamide → HCID 13649665, compound

https://huagongshe.com/reaction/280644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetamideHCID 7898—
ReactantSodiumHCID 5360545—
ReactantHCID 15065217HCID 15065217—
SolventEthanolHCID 702—
ProductHCID 13649665HCID 1364966560.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of sodium (0.147 g, 6.41 mmol) in ethanol (20 ml) under nitrogen atmosphere was added 2-cyanoacetamide (539 mg, 6.41 mmol) and the mixture was refluxed 10 minutes. The mixture was cooled slightly, 3-(4-chlorobenzoyl)-4-chlorobenzyl azide (1.51 g, 4.93 mmol) was added, and the mixture was refluxed 1 hour. The mixture was cooled to 0° C. and filtered. The product was washed with ice cold ethanol (2×5 ml), water (3×5 ml), ice cold ethanol (2×5 ml), and diethyl ether (10 ml), and dried at 50° C. for 3 hours under vacuum to provide 1.16 g (60%) of 5-amino-1-(3-[4-chlorobenzoyl]-4-chlorobenzyl)-1,2,3-triazole-4-carboxamide, m.p. 189°-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590201
Source datasetuspto-grants-1986_05
ORD IDord-70e07a0ce3a3461da0a6d7998eb15692
Source noteuspto-grants-1986_05