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HRID 2382905作成日:2026年10月27日

Pyridine → N-[5-(cyclopropylamino)-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]-4-[(dimethylamino)methyl]benzamide

https://huagongshe.com/reaction/2382905

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-(N,N-dimethylaminomethyl) benzoyl chlorideHCID 13748965—
反応物N5-cyclopropyl-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridine-2,5-diamineHCID 59437445—
溶媒DichloromethaneHCID 6344—
生成物N-[5-(cyclopropylamino)-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]-4-[(dimethylamino)methyl]benzamideHCID 5943747252%

反応手順

To a reaction vessel containing N5-cyclopropyl-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridine-2,5-diamine ((A18), 77 mg, 0.3 mmol, 1 eq.) and pyridine (0.063 mL, 1.2 mmol, 4 eq.) in dichloromethane (1 mL) was added 4-dimethylaminomethyl-benzoyl chloride (118 mg, 0.6 mmol, 2 eq.) as a solution in dichloromethane (2 mL), dropwise. The vessel was capped and heated to reflux for approximately 16 hours. The reaction mixture was cooled and the solvent removed in vacuo. The residue dissolved in DMSO (1.5 mL) and purified by reverse phase preparatory HPLC to give the title compound as a white solid (65.1 mg, 52%). HPLC, Rt: 2.59 min (purity: 100%). LC/MS M+(ESI): 419.2, M−(ESI) 417.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08263595B2
出典データセットuspto-grants-2012_09
ORD IDord-21e668023a2d44a6ae77f996b98c7ab0
出典メモuspto-grants-2012_09