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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802297Generated: October 31, 2026

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

https://huagongshe.com/reaction/1802297

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acidHCID 25247567—
ReactantHCID 67774127HCID 67774127—
Product5-[2-(2-fluoro-pyridin-4-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl]-1-methyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 6777573865.6%

Reaction Steps

The product was prepared in the same manner as described in example 44d using 2-(2-fluoropyridin-4-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-amine (0.5 g, 2.18 mmol) and 4-(ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acid (519 mg, 2.62 mmol) as starting materials. The reaction affords 5-[2-(2-fluoro-pyridin-4-yl)-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl]-1-methyl-1H-pyrazole-4-carboxylic acid ethyl ester (585 mg, 65.5%) as white solid. mp.: 220-230° 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-da5e017a139a4f1fbfe6db863b9ee1f4
Source noteuspto-grants-2013_01