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HRID 28893作成日:2026年10月24日

Triethylamine → N-[4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)phenyl]-1-pyrrolidinecarboxamide

https://huagongshe.com/ja/reaction/28893

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物PyrrolidineHCID 31268—
反応物Isopropenyl chloroformateHCID 93846—
反応物4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)anilineHCID 68998168—
溶媒TetrahydrofuranHCID 8028—
生成物N-[4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)phenyl]-1-pyrrolidinecarboxamideHCID 5898002237%

反応条件

温度50 °C

反応手順

A solution of [4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)phenyl]amine (0.204 mmol) in tetrahydrofuran (1 mL) was treated with triethylamine (0.8 mmol) and isopropenyl chloroformate (0.3 mmol). The reaction was stirred for 3 h then pyrrolidine (2 mmol) was added and the reaction heated at 50° C. for 18 h. The reaction was concentrated in vacuo and redissolved in methylene chloride (20 mL) and washed with water (2×10 mL). The methylene chloride was evaporated to give the crude produce which was purified using a Gilson reverse phase HPLC to provide the title product (37%). ESMS [M+H]+: 576.2

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419988B2
出典データセットuspto-grants-2008_09
ORD IDord-c52e79243172441e981407178261ad9f
出典メモuspto-grants-2008_09