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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 645704생성일: 2026년 10월 26일

Tetravinylstannane → 2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/645704

반응식

참여 물질

역할이름HCID투입량
반응물TetravinylstannaneHCID 66189—
반응물2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 86628040—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
생성물2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 8662804129.6%

반응 조건

온도60 °C

반응 단계

To a solution of 2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.45 g, 0.8 mmol) in dimethylformamide (2.0 mL) was added tetravinyltin (0.29 mL, 1.6 mmol) and tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)4) (0.092 g, 0.08 mmol). After degassing, the mixture was heated at 60° C. for 15 h. before it was diluted with EtOAc, and washed sequentially with Sat. NaHCO3 and brine. The organic extract was dried over Na2SO4 and concentrated to give a crude residue. Purification by flash column chromatography (Hexane/EtOAc=1:1) gave 2-chloro-N-(1H-indazol-6-yl)-5-vinyl-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (0.11 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07705004B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-f5ee33c6b49a4a03a14cc86261f53e97
출처 메모uspto-grants-2010_04