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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231654Generated: November 4, 2026

Glycine ethyl ester → Ethyl N-(2-amino-3-methyl-5-[1,2,4-triazol-1-yl]benzyl)glycinate

https://huagongshe.com/reaction/2231654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycine ethyl esterHCID 12176—
Reactant1-(4-Amino-3-formyl-5-methylphenyl)-1,2,4-triazoleHCID 21285533—
SolventChloroformHCID 6212—
ProductEthyl N-(2-amino-3-methyl-5-[1,2,4-triazol-1-yl]benzyl)glycinateHCID 2128553551.7%

Reaction Steps

A mixture of ethyl glycinate (0.38 g), 1-(4-amino-3-formyl-5-methylphenyl)-1,2,4-triazole (0.5 g) and 3Å molecular sieves (1.0 g; "Fluka" [Trade Mark] article No. 69828) was stirred and heated under reflux in chloroform (10 cm3) for 4 hours. The cooled mixture was filtered, evaporated in vacuo, and the residue taken into ethanol (30 cm3). The solution was then hydrogenated at 60 p.s.i. (4.13×105Pa) pressure and room temperature (20°) over 10% palladised charcoal (0.2 g) for 16 hours. The catalyst was then removed by filtration through "Solkafloc" (Trade Mark) and the solution was evaporated in vacuo to give an oil which was chromatographed on silica (Merck "MK 60.9385" [Trade Mark]) eluting with chloroform. Combination and evaporation of the appropriate fractions afforded the title compound as an oil (0.37 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04783467
Source datasetuspto-grants-1988_11
ORD IDord-5e2319d83dd4442793c8033c90c3376d
Source noteuspto-grants-1988_11