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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16462생성일: 2026년 10월 24일

Vertellus → 4-Pyrimidinebutanol,2-amino-6-[[3-fluoro-4-(1h-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]amino]-

https://huagongshe.com/ko/reaction/16462

반응식

참여 물질

역할이름HCID투입량
반응물VertellusHCID 22959485—
반응물4-Pyrimidinebutanoic acid,2-amino-6-[[3-fluoro-4-(1h-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]amino]-,ethyl esterHCID 58733394—
용매EthanolHCID 702—
생성물4-Pyrimidinebutanol,2-amino-6-[[3-fluoro-4-(1h-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]amino]-HCID 17979272—

반응 단계

300 mg (0.67 mmol) of 4-(2-amino-6-{[3-fluoro-4-(1H-pyrrolo[2,3-b]pyridin-4-yloxy)phenyl]amino}pyrimidin-4-yl)butan-1-ol (from example 132) are suspended in 15 ml of ethanol, and 253 mg (6.66 mmol) of sodium borohydrate are added a little at a time at RT. The mixture is stirred at RT for 24 hours and then concentrated, and ethyl acetate and water are added. The organic phase is dried over sodium sulfate. The product is purified by column chromatography (silica gel 60; gradient column, mobile phase: DCM:methanol=9:1 to 3:1). 133 mg (27%) of the starting material are recovered. The product fraction is re-purified by preparative HPLC. This gives the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737153B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9bdc979f3ea34dbe87830441684289c4
출처 메모uspto-grants-2010_06