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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60450생성일: 2026년 10월 23일

4-(Trifluoromethyl)benzaldehyde → 5-(hydroxy(4-(trifluoromethyl)phenyl)methyl)-1-methyl-3-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-6-(3-(trifluoromethyl)phenoxy)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/ko/reaction/60450

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzaldehydeHCID 67996—
반응물Lithium diisopropylamideHCID 2724682—
반응물1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)-6-(3-(trifluoromethyl) phenoxy)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 118875509—
용매TetrahydrofuranHCID 8028—
생성물5-(hydroxy(4-(trifluoromethyl)phenyl)methyl)-1-methyl-3-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-6-(3-(trifluoromethyl)phenoxy)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 11887554169.9%

반응 조건

온도-78 °C

반응 단계

To a solution of 1-methyl-3-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-6-(3-(trifluoromethyl) phenoxy)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione (210 mg, 0.438 mmol) in THF (5 mL) at −78° C. was added LDA (1.8 M in THF, 1.2 mL, 2.16 mmol). The reaction was stirred at −78° C. for 30 min then 4-(trifluoromethyl)benzaldehyde (153 mg, 0.879 mmol) was added. The reaction was stirred for 1 h, quenched with aq. NaHCO3 (5 mL) then diluted with EA (10 mL) and water (10 mL). The organic layer was dried over Na2SO4 and concentrated to a residue which was purified by Prep TLC eluted with PE/EA (4:1) to give 5-(hydroxy(4-(trifluoromethyl)phenyl)methyl)-1-methyl-3-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-6-(3-(trifluoromethyl)phenoxy)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione (200 mg, 69.9% yield) as a clear oil. LCMS: [MH+-THP] 570 and TR=1.933 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440972B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-8eecdcb85c2a4af5b81e90d9a221b889
출처 메모uspto-grants-2016_09