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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1426539생성일: 2026년 10월 24일

Ethanol → 5-(Methylthio)-3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]pentanenitrile

https://huagongshe.com/ko/reaction/1426539

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물TetrahydrofuranHCID 8028—
반응물Ammonium HydroxideHCID 14923—
반응물5-(Methylthio)-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanenitrileHCID 57477648—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물5-(Methylthio)-3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]pentanenitrileHCID 1775490550.7%

반응 단계

A solution of 5-(methylthio)-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]-pyrimidin-4-yl)-1H-pyrazol-1-yl]pentanenitrile (0.35 g, 0.00079 mol) in THF (4 mL, 0.05 mol) and 3.0 M HCl (HCl) in water (4 mL) was heated to reflux overnight. The solvent was removed by rotary evaporation to give a pale orange oil. The oil was stirred in ethanol (3 mL, 0.05 mol) and 8.0 M ammonium hydroxide in water (1 mL) overnight. The reaction was concentrated and purified by prep LCMS (C18 column eluting with a gradient of ACN/H2O containing 0.15% NH4OH) to give 125 mg of a white foam. The white foam was triturated with MTBE (˜1.5 mL). The resulting solid was filtered, washed and dried to give 80 mg of the product (32% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08933086B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-34b5ce40b54a4e4db10f4877935f1a92
출처 메모uspto-grants-2015_01