돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2382905생성일: 2026년 10월 27일

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

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-(N,N-dimethylaminomethyl) benzoyl chlorideHCID 13748965—
반응물N5-cyclopropyl-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridine-2,5-diamineHCID 59437445—
용매DichloromethaneHCID 6344—
생성물N-[5-(cyclopropylamino)-7-(trifluoromethyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]-4-[(dimethylamino)methyl]benzamideHCID 5943747252%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08263595B2
출처 데이터셋uspto-grants-2012_09
ORD IDord-21e668023a2d44a6ae77f996b98c7ab0
출처 메모uspto-grants-2012_09