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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 334437생성일: 2026년 10월 24일

Trifluoroacetic acid → HCID 89465782, 화합물

https://huagongshe.com/ko/reaction/334437

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물4-(4-Methylpiperazin-1-yl)benzaldehydeHCID 736533—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물HCID 178509236HCID 178509236—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물HCID 89465782HCID 89465782—

반응 단계

41.5 μl of trifluoroacetic acid (0.539 mmol) and, in small fractions, 129 mg (0.611 mmol) of sodium triacetoxyborohydride are added to a solution of 100 mg (0.35 mmol) of 5-(3,5-difluorophenylthio)-1H-pyrazolo[3,4-b]pyridin-3-amine and 81 mg (0.395 mmol) of 4-(4-methylpiperazin-1-yl)benzaldehyde in 20 ml of a 1:1 mixture of dichloromethane and tetrahydrofuran. The reaction medium is stirred for 16 hours at room temperature. An additional fraction of 125 μl of trifluoroacetic acid and 388 mg of sodium triacetoxyborohydride are added and the reaction medium is stirred for an additional 24 hours. The solvent is then concentrated and the reaction medium extracted with ethyl acetate and washed using saturated sodium bicarbonate solution. The organic phases are combined, dried on magnesium sulfate and then concentrated to yield a yellow oil. A trituration of this oil in methanol leads to the isolation of 135 mg of a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883821B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-989af7569fa646248dd773bdda084e66
출처 메모uspto-grants-2014_11