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HRID 921536作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Pyrrolidin-1-ylcarbonyl)anilineHCID 577800—
反応物4-{3-isopropyl-4-(quinolin-3-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl}-2-{4-(pyrrolidine-1-carbonyl)phenylamino}benzonitrileHCID 67500765—
生成物4-{3-Isopropyl-4-(quinolin-3-yl)-1H-pyrazolo[3,4-b]pyridin-1-yl}-2-{4-(pyrrolidine-1-carbonyl)phenylamino}benzamideHCID 4987208259%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09273045B2
出典データセットuspto-grants-2016_03
ORD IDord-2dacc2b4d3cd487aa40a363c3ed7bda2
出典メモuspto-grants-2016_03