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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382722Generated: November 1, 2026

4-chloro-1-methyl-1H-pyrazole-5-carboxylic acid → HCID 51034816, compound

https://huagongshe.com/reaction/2382722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-1-methyl-1H-pyrazole-5-carboxylic acidHCID 670823—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant2-Phenylimidazo[1,2-a]pyridin-7-amineHCID 56955502—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 51034816HCID 5103481625%

Reaction Steps

Under an atmosphere of nitrogen, N—N-diisopropylethylamine (749 mg, 6 mmol) and 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU, 744 mg, 1.94 mmol) were added to a solution of 4-chloro-2-methyl-2H-pyrazole-3-carboxylic acid (310 mg, 1.94 mmol, Art-Chem B000148) in DMF (5 ml). After 30 min, 2-phenyl-imidazo[1,2-a]pyridin-7-ylamine (404 mg, 1.94 mmol) was added, and the brown solution was stirred over the weekend (r.t.). The reaction mixture was taken up in ethyl acetate and washed with water. After drying (Na2SO4), the solvent was evaporated and the title compound (170 mg, 25%) was isolated by column chromatography (silica gel, heptane:ethyl acetate=100:0-50:50). MS (m/e)=352.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263584B2
Source datasetuspto-grants-2012_09
ORD IDord-5c1c63ac51354932a1091a8f871d5503
Source noteuspto-grants-2012_09