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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802142Generated: October 29, 2026

Azetidine → HCID 57378955, compound

https://huagongshe.com/reaction/1802142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzetidineHCID 10422—
ReactantPropylphosphoric anhydrideHCID 16167369—
Reactant1-methyl-5-(2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1H-pyrazole-4-carboxylic acidHCID 57378954—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57378955HCID 57378955100.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 1-methyl-5-(2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamoyl)-1H-pyrazole-4-carboxylic acid (4.5 g, 12.4 mmol), azetidine (2.53 ml, 37.3 mmole), N-diisopropylethylamine (6.51 ml, 37.3 mmol) and propylphosphonic anhydride (50% in ethyl acetate, 18.3 ml, 31 mmol) in tetrahydrofurane (220 ml) is stirred for 2 hours at 70° C. The turbid solution is concentrated to about 100 ml, cooled, poured on cooled sat. aqueous sodium bicarbonate solution (1000 ml) and the suspension is stirred for 20 minutes. The solid is collected by filtration, washed with little water and dried affording 4-(azetidine-1-carbonyl)-2-methyl-2H-pyrazole-3-carboxylic acid (2-phenyl-[1,2,4]triazolo[1,5-a]pyridin-7-yl)-amide (5 g, 100%) as a white solid. mp.: 243-5° C. MS: m/z=402.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349824B2
Source datasetuspto-grants-2013_01
ORD IDord-51fd1d1a030042f48c14a9536549251d
Source noteuspto-grants-2013_01