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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1515880생성일: 2026년 10월 26일

Hexane → (1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-(4-methylsulfanyl-phenyl)-methanol

https://huagongshe.com/reaction/1515880

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물4-(Methylthio)benzaldehydeHCID 76985—
반응물1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 852078—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-(4-methylsulfanyl-phenyl)-methanolHCID 67229059107.9%

반응 조건

온도-78 °C

반응 단계

To a suspension of 1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridine (6.0 g, 23.3 mmol) in dry tetrahydrofuran (300 mL) at −78° C. was added n-butyllithium in n-hexane (1.6 M, 10 mL, 16 mmol). The mixture was stirred at −78° C. for 5 min and then treated with 4-methylsulfanylbenzaldehyde (2.4 g, 15.8 mmol) dropwise. The resulting mixture was stirred at −78° C. for 1 h and quenched with brine. The mixture was extracted with ethyl acetate (2×500 mL), washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was washed with dichloromethane (2×5 mL) and dried in vacuo to afford (1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-(4-methylsulfanyl-phenyl)-methanol (7.0 g, 73%) as a white solid: LC/MS m/e calcd for C21H18N2O3S2 [M+H]+ 411.52, observed 411.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08222416B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-d0f27f5ca9de4bc793bff7b07a1fd0f1
출처 메모uspto-grants-2012_07