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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046695Generated: October 27, 2026

4'-(Aminomethyl)-biphenyl-2-carboxylic acid 1,1-dimethylethyl ester → 4'-[3-(t-Butoxycarbonylaminomethyl)-5-propyl-[1,2,4]-triazol-4-ylmethyl]biphenyl-2-carboxylic acid t-butyl ester

https://huagongshe.com/reaction/1046695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-(Aminomethyl)-biphenyl-2-carboxylic acid 1,1-dimethylethyl esterHCID 9971073—
Reactant[1-Ethoxy-but-(e)-ylidene-hydrazinocarbonylmethyl]carbamic acid t-butyl esterHCID 131728639—
SolventEthanolHCID 702—
Product4'-[3-(t-Butoxycarbonylaminomethyl)-5-propyl-[1,2,4]-triazol-4-ylmethyl]biphenyl-2-carboxylic acid t-butyl esterHCID 5754975430,366.199%

Reaction Conditions

Temperature50 °C

Reaction Steps

4′-Aminomethylbiphenyl-2-carboxylic acid t-butyl ester (1.5 g, 5.2 mmol) and [1-ethoxy-but-(E)-ylidene-hydrazinocarbonylmethyl]carbamic acid t-butyl ester (1.0 g, 3.5 mmol) were combined and dissolved in ethanol (50 mL). The mixture was heated at 50° C. for 2 hours and then 70° C. overnight. The mixture was then cooled and concentrated. The product was purified by silica gel chromatography (0-20% MeOH:DCM) to obtain intermediate (23a) (400 g). MS m/z: [M+H+] calcd for C29H38N4O4, 507.6. found 507.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569351B2
Source datasetuspto-grants-2013_10
ORD IDord-a36a900c146b441f8b0d2b687c513395
Source noteuspto-grants-2013_10