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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713388Generated: November 2, 2026

Triethylamine → Pyrazolo[1,5-a]pyridine-3-carboxylic acid [2-methyl-5-(3-trifluoromethyl-benzoylamino) phenyl]-amide

https://huagongshe.com/reaction/1713388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPyrazolo[1,5-a]pyridine-3-carbonyl chlorideHCID 2795463—
ReactantN-(3-amino-4-methylphenyl)-3-(trifluoromethyl)benzamideHCID 11529455—
ProductPyrazolo[1,5-a]pyridine-3-carboxylic acid [2-methyl-5-(3-trifluoromethyl-benzoylamino) phenyl]-amideHCID 16662082—

Reaction Steps

Pyrazolo[1,5-a]pyridine-3-carbonylchloride (100 mg, 0.55 mmol, Maybridge Lot # 291259) and N-(3-amino-4-methyl-phenyl)-3-trifluoromethyl-benzamide (163 mg, 0.55 mmol) are dissolved in 2 ml dry methylenehloride. Triethylamine (93 μl, 0.66 mmol) is added and the reaction mixture is stirred at room temperature. After complete formation of the product, the reaction mixture is quenched with water and the product is extracted with methylenehloride. The solvent is removed under reduced pressure and the crude product is absorbed to Isolute. The product is purified by automated reversed phase column chromatography (column: Interchrom Puriflash 15/35U C18, 70 g cartouche; solvents: water+0.1% trifluoroacetic acid and acetonitrile+0.1% trifluoroacetic acid) and is dried at the high vacuum pump, yielding the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795273B2
Source datasetuspto-grants-2010_09
ORD IDord-1f42dc1794b6405c83e9d4c21a4e9440
Source noteuspto-grants-2010_09