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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 510110생성일: 2026년 10월 26일

2-Chloro-7H-pyrrolo[2,3-d]pyrimidine → 5-Fluoro-1-(2-fluorobenzyl)-3-(7H-pyrrolo[2,3-d]pyrimidin-2-yl)-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/510110

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5706774—
반응물5-Fluoro-1-(2-fluorobenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridineHCID 58065602—
반응물HCID 178448238HCID 178448238—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물5-Fluoro-1-(2-fluorobenzyl)-3-(7H-pyrrolo[2,3-d]pyrimidin-2-yl)-1H-pyrazolo[3,4-b]pyridineHCID 66614193—

반응 단계

Under an argon atmosphere, 2.000 g (5.389 mmol) of the compound from example 24A were dissolved in 200 ml of 1,4-dioxane, and 9.378 g (16.167 mmol) of hexabutyldistannane were added. Added to the mixture were 2.000 g (1.731 mmol) of tetrakis(triphenylphosphine)palladium(0) and 0.910 g (5.928 mmol) of 2-chloro-7H-pyrrolo[2,3-d]pyrimidine (described in Bioorg. Med. Chem. 17(19), 6926-6936; 2009). The mixture was heated to reflux for 60 h. After cooling, the reaction mixture was filtered through Celite and the filtrate was concentrated on a rotary evaporator. The residue was stirred successively with ethyl acetate, acetonitrile and dimethyl sulfoxide. Subsequently, the residue was dissolved in trifluoroacetic acid, and acetonitrile and water were added until slight turbidity. The mixture was filtered and the filtrate was concentrated on a rotary evaporator and the residue was dried under high vacuum. 161 mg (8% of theory) of the title compound were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096592B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-764991be8e434bd8a4cf8f0ea7c7308d
출처 메모uspto-grants-2015_08