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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802302Generated: October 27, 2026

4-(Ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acid → 5-[2-(6-fluoro-pyridin-2-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl]-1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1802302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acidHCID 25247567—
Reactant2-(6-Fluoropyridin-2-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-amineHCID 67774407—
Product5-[2-(6-fluoro-pyridin-2-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl]-1-methyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 6777578440.5%

Reaction Steps

The product was prepared in the same manner as described in example 44d using 2-(6-fluoropyridin-2-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-amine (350 mg, 1.53 mmol) and 4-(ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acid (363 mg, 1.83 mmol) as starting materials. The reaction affords 5-[2-(6-fluoro-pyridin-2-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl]-1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester (253.1 mg, 40.5%) as white solid. mp.: 290° C., MS: m/z=410.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-33d54fedac264d2ea6a6585e7096aa4b
Source noteuspto-grants-2013_01