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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Pyrazolo[1,5-a]pyridine-3-carbonyl chloride | HCID 2795463 | — |
| Reactant | N-(3-amino-4-methylphenyl)-3-(trifluoromethyl)benzamide | HCID 11529455 | — |
| Product | Pyrazolo[1,5-a]pyridine-3-carboxylic acid [2-methyl-5-(3-trifluoromethyl-benzoylamino) phenyl]-amide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795273B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-1f42dc1794b6405c83e9d4c21a4e9440 |
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| Source note | uspto-grants-2010_09 |
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