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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 921536생성일: 2026년 10월 26일

4-(Pyrrolidin-1-ylcarbonyl)aniline → 4-{3-Isopropyl-4-(quinolin-3-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl}-2-{4-(pyrrolidine-1-carbonyl)phenylamino}benzamide

https://huagongshe.com/reaction/921536

반응식

참여 물질

역할이름HCID투입량
반응물4-(Pyrrolidin-1-ylcarbonyl)anilineHCID 577800—
반응물4-{3-isopropyl-4-(quinolin-3-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl}-2-{4-(pyrrolidine-1-carbonyl)phenylamino}benzonitrileHCID 67500765—
생성물4-{3-Isopropyl-4-(quinolin-3-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl}-2-{4-(pyrrolidine-1-carbonyl)phenylamino}benzamideHCID 4987208259%

반응 단계

According to Example 1(6), 4-{3-isopropyl-4-(quinolin-3-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl}-2-{4-(pyrrolidine-1-carbonyl)phenylamino}benzonitrile was prepared using compound (6d) instead of compound (1e) and using (4-aminophenyl)(pyrrolidin-1-yl)methanone instead of trans-aminocyclohexanol and was used in the subsequent reaction without being purified. According to Example 1(7), compound (34) (the second stage yield: 59%) was prepared as a white solid using 4-{3-isopropyl-4-(quinolin-3-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl}-2-{4-(pyrrolidine-1-carbonyl)phenylamino}benzonitrile instead of compound (1f).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273045B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-2dacc2b4d3cd487aa40a363c3ed7bda2
출처 메모uspto-grants-2016_03