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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 639489생성일: 2026년 10월 26일

2-Furancarboxylic acid, hydrazide → N'-(2-Amino-7-(2-(4-(2,4-difluorophenyl)piperazin-1-yl)ethyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)furan-2-carbohydrazide

https://huagongshe.com/reaction/639489

반응식

참여 물질

역할이름HCID투입량
반응물2-Furancarboxylic acid, hydrazideHCID 18731—
반응물4-chloro-7-(2-(4-(2,4-difluorophenyl)piperazin-1-yl)ethyl)-7H-pyrrolo[2,3-d]pyrimidin-2-amineHCID 86623469—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N'-(2-Amino-7-(2-(4-(2,4-difluorophenyl)piperazin-1-yl)ethyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl)furan-2-carbohydrazideHCID 68414926—

반응 단계

A solution of the title A compound, 4-chloro-7-(2-(4-(2,4-difluorophenyl)piperazin-1-yl)ethyl)-7H-pyrrolo[2,3-d]pyrimidin-2-amine (75 mg, 0.19 mmol) and 2-furoic acid hydrazide (49 mg, 0.39 mmol) in 1 mL of NMP is heated at 150° C. for 3 h. After cooling to RT, the crude reaction is purified by column chromatography on silica gel, eluting with a gradient of 5% to 10% of MeOH in EtOAc. Fractions containing the product are combined and evaporated to dryness to 4-yl)furan-2-carbohydrazide as a yellow solid: LC/MS (M+1=483.2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07691869B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-6f6ccccfbe3c436ca1b922553e0ee16d
출처 메모uspto-grants-2010_04