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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645696생성일: 2026년 10월 24일

Chlorotrimethylsilane → 1-(4-(4-(4-(1H-indazol-6-ylamino)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanone

https://huagongshe.com/ko/reaction/645696

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물1-[4-(4-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 736269—
반응물2-Chloro-N-(1H-indazol-6-yl)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 86628037—
용매1-ButanolHCID 263—
생성물1-(4-(4-(4-(1H-indazol-6-ylamino)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanoneHCID 6858017017.7%

반응 조건

온도115 °C

반응 단계

To a mixture of 2-Chloro-N-(1H-indazol-6-yl)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.18 g, 0.4 mmol) and 1-(4-(4-aminophenyl)piperazin-1-yl)ethanone (0.22 g, 1 mmol) in n-butyl alcohol (2 mL) was added trimethylsilyl chloride (TMSCl) (0.026 mL, 0.2 mmol). After heating at 115° C. for 15 h, the mixture was purified by preparative HPLC to give 1-(4-(4-(4-(1H-indazol-6-ylamino)-5-methyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)piperazin-1-yl)ethanone (0.045 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07705004B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-6cc7cd34432a4af0a55f7f2cfa81f0cf
출처 메모uspto-grants-2010_04