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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802198Generated: October 31, 2026

Diisopropylethylamine → ethyl 5-(2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/1802198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphoric anhydrideHCID 16167369—
Reactant4-(Ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acidHCID 25247567—
Reactant2-Isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-amineHCID 67776349—
SolventTetrahydrofuranHCID 8028—
Productethyl 5-(2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylateHCID 67775033103.3%

Reaction Steps

A mixture of 2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-amine (159 mg, 902 μmol), 4-(ethoxycarbonyl)-1-methyl-1H-pyrazole-5-carboxylic acid (215 mg, 1.08 mmol), propylphosphonic anhydride (50% in ethyl acetate, 1.33 ml, 2.26 mmol) and diisopropylethylamine (473 μl, 2.71 mmol) in tetrahydrofurane (7 ml) is refluxed for 18 hours. The solvent is evaporated and the residue stirred for 1 hr with sat. aqueous sodium hydrogencarbonate solution. The precipitated solid is collected by filtration, washed with water and dried affording ethyl 5-(2-isopropyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1-methyl-1H-pyrazole-4-carboxylate (332 mg, 103%) as a white solid. Mp.: 175-7° C. MS: m/z=357.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-7ccb1ee00c214cdebb0c8606c743b66d
Source noteuspto-grants-2013_01