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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1160005생성일: 2026년 10월 24일

Lithium Hydroxide → N-[5-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]-2-(methyloxy)phenyl]-2,6-difluorobenzamide

https://huagongshe.com/ko/reaction/1160005

반응식

참여 물질

역할이름HCID투입량
반응물Lithium HydroxideHCID 3939—
반응물Tris(hydroxymethyl)aminomethaneHCID 6503—
반응물2,6-Difluorobenzoyl chlorideHCID 87438—
반응물N-[5-[3-(2-Chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]-2-(methyloxy)phenyl]-2,2,2-trifluoroacetamideHCID 59511425—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물N-[5-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]-2-(methyloxy)phenyl]-2,6-difluorobenzamideHCID 59513745100.4%

반응 단계

A solution of N-[5-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]-2-(methyloxy)phenyl]-2,2,2-trifluoroacetamide (370 mg, 0.83 mmol) and 1M LiOH (4.97 ml, 4.97 mmol) in 10:1 THF:H2O (10 mL) was heated at 50° C. overnight. The reaction was washed with brine (25 mL), aqueous layer extracted with EtOAc (25 mL), organic layers combined, filtered through a cotton plug, and solvent removed by rotary evaporation. After high vacuum removal of residual solvent, the crude mixture was dissolved in THF (25 mL) and to this was added 2,6-difluorobenzoyl chloride (920 mg, 5.25 mmol). After stirring 3 h at rt, DMF (25 mL) was added to dissolve any suspended solids followed by the addition of excess polymer-bound trisamine resin. Upon overnight stirring, the amine resin was removed by vacuum filtration, rinsed with MeOH (50 mL), and filtrate concentrated under reduced pressure to afford the desired amide (410 mg, 79%) as an off-white solid. ESIMS (M+H)+=492.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07812022B2
출처 데이터셋uspto-grants-2010_10
ORD IDord-f84c06e5a2754956b89943333b077a40
출처 메모uspto-grants-2010_10