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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802199Generated: October 26, 2026

Lithium hydroxide, monohydrate → 5-(2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1802199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactantethyl 5-(2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylateHCID 67775033—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-(2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylic acidHCID 6777671193.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of ethyl 5-(2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylate (330 mg, 926 μmol) and lithium hydroxide monohydrate (155 mg, 3.7 mmol) in methanol (6 ml) and water (2 ml) is stirred for 18 hours at 25° C. The solvents are evaporated, the white residue is dissolved in water and acidified with 37% aqueous hydrochloric acid. The precipitated white solid is collected by filtration, washed with water and dried affording 5-(2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylic acid (285 mg, 93.7%) as a white solid. Mp.: >250° C. MS: m/z=327.3 (M−H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-a653c65f8da54a0780090efa765a3eb6
Source noteuspto-grants-2013_01