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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298019Generated: October 29, 2026

Guanidine Hydrochloride → HCID 178433869, compound

https://huagongshe.com/reaction/2298019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantDimethylformamideHCID 6228—
ReactantMethyl 5-methyl-2-phenyl-2H-1,2,3-triazole-4-carboxylateHCID 2774347—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178433869HCID 17843386947%

Reaction Conditions

Temperature70 °C

Reaction Steps

Guanidine hydrochloride (2.42 g, 25.32 mmol) was dissolved in 20 ml of anhydrous methanol and then treated with sodium methoxide (1.50 g, 27.83 mmol), added in one portion at room temperature. The reaction mixture was stirred under nitrogen for 1 hour, then filtered under a nitrogen atmosphere. The solids were washed with anhydrous methanol (3×10 ml) and the filtrate concentrated under reduced pressure. Anhydrous benzene (60 ml) was added to the residue, the mixture reconcentrated in vacuo and the residue was dried under high vacuum. Anhydrous dimethylformamide (10 ml), anhydrous tetrahydrofuran (20 ml) and methyl 4-methyl-2-phenyl-2H-1,2,3-triazole-5-carboxylate (1.00 g, 4.60 mmol) were added to the solid residue and the resulting mixture was heated at 70° C. under nitrogen for 7 h, then stirred at ambient temperature overnight. The reddish colored solution was then diluted with water (90 ml) to give the free base corresponding to the title compound as a tan solid (0.53 g, 47% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492401B1
Source datasetuspto-grants-2002_12
ORD IDord-a4696c1e38c44b4da380132238b94530
Source noteuspto-grants-2002_12