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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60157생성일: 2026년 10월 24일

3-Methylbutanal → 3-(3-(tert-butyldimethylsilyloxy)propyl)-6-chloro-5-(1-hydroxy-3-methylbutyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/ko/reaction/60157

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참여 물질

역할이름HCID투입량
반응물3-MethylbutanalHCID 11552—
반응물Lithium diisopropylamideHCID 2724682—
반응물3-(3-(tert-butyldimethylsilyloxy)propyl)-6-chloro-5-((4-chlorophenyl) (hydroxy)methyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dioneHCID 131737076—
용매TetrahydrofuranHCID 8028—
생성물3-(3-(tert-butyldimethylsilyloxy)propyl)-6-chloro-5-(1-hydroxy-3-methylbutyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dioneHCID 13173707732.9%

반응 조건

온도-78 °C

반응 단계

To a solution of 3-(3-(tert-butyldimethylsilyloxy)propyl)-6-chloro-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione (See Compound 49, step 3, 1.149 g, 3 mmol) in THF (30 mL) at −78° C. was added LDA (2M in THF, 7.5 mL, 15 mmol) dropwise. The reaction was stirred at −78° C. for 30 min then 3-methylbutanal (516 mg, 6 mmol) in THF (5 mL) was added dropwise. The reaction was stirred at −78° C. for 20 min, quenched with aq. NH4Cl (5 mL) then diluted with EA (15 mL) and water (5 mL). The organic layer was washed with brine (20 mL), dried over Na2SO4 and concentrated to a residue which was purified by chromatography eluted with PE/EA (2:1) to give 3-(3-(tert-butyldimethylsilyloxy)propyl)-6-chloro-5-(1-hydroxy-3-methylbutyl)-1-methylpyrido[3,4-d]pyrimidine-2,4(1H,3H)-dione (464 mg, 30% yield) as a white solid. LCMS: MH+ 470 and TR=2.198 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440973B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-0e41429d939a45ddb02b8777bcd9c56b
출처 메모uspto-grants-2016_09