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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2281454생성일: 2026년 10월 26일

Chlorotrimethylsilane → N-(4-(4-(3-aminosulfonyl-phenylamino)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)-N-methylacetamide

https://huagongshe.com/reaction/2281454

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참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물N-(4-Aminophenyl)-N-methylacetamideHCID 67068—
반응물2-chloro-N-(3-aminosulfonyl-phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 57990423—
용매1-ButanolHCID 263—
용매1,4-DioxaneHCID 31275—
생성물N-(4-(4-(3-aminosulfonyl-phenylamino)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)-N-methylacetamideHCID 6687806515.7%

반응 조건

온도110 °C

반응 단계

A mixture of 2-chloro-N-(3-aminosulfonyl-phenyl)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (100 mg, 0.21 mmol), N-(4-aminophenyl)-N-methylacetamide (100 mg, 0.61 mmol) and trimethylsilyl chloride (0.050 mL, 0.40 mmol) in nBuOH (2 mL) and dioxane (2 mL) was heated at 110° C. for 4 h. More trimethylsilyl chloride (0.100 mL, 0.79 mmol) was added. The mixture was stirred at 110° C. for another 72 h. It was then purified by HPLC to give N-(4-(4-(3-aminosulfonyl-phenylamino)-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)phenyl)-N-methylacetamide as a solid (20 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09139581B2
출처 데이터셋uspto-grants-2015_09
ORD IDord-a9b3002f638442569eebc0da317a2c70
출처 메모uspto-grants-2015_09