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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645686생성일: 2026년 10월 24일

Water → N4-(1H-indazol-6-yl)-N2-(4-(methylthio)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine

https://huagongshe.com/ko/reaction/645686

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ChlorotrimethylsilaneHCID 6397—
반응물4-(Methylthio)anilineHCID 66038—
반응물2-chloro-N-(1H-indazol-6-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 86628035—
용매1-ButanolHCID 263—
용매Ethyl AcetateHCID 8857—
생성물N4-(1H-indazol-6-yl)-N2-(4-(methylthio)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamineHCID 5758578245.5%

반응 조건

온도116 °C

반응 단계

A mixture of 2-chloro-N-(1H-indazol-6-yl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (400 mg, 0.912 mmol), 4-(methylthio)aniline (0.227 mL, 1.83 mmol) and trimethylsilyl chloride (TMSCl) (0.231 mL, 1.83 mmol) in n-butyl alcohol (8 mL) was heated at 116° C. for 72 h. Water and ethyl acetate were then added. The organic phase was separated, washed with 5% NaHCO3, dried over Na2SO4, and concentrated in vacuo. The residue was dissolved in CH3CN (20 mL), and water was added to induced precipitation. The solid was collected by filtration to give N4-(1H-indazol-6-yl)-N2-(4-(methylthio)phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamine (225 mg). The filtrate was also purified by HPLC to give another portion of the desired product (127 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07705004B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-8a6b4e6e18b543378769ec5d14376460
출처 메모uspto-grants-2010_04