戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 28894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]-4-thiomorpholinecarboxamide 1,1-dioxide

https://huagongshe.com/ja/reaction/28894

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Isopropenyl chloroformateHCID 93846—
反応物Thiomorpholine 1,1-dioxideHCID 6484228—
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]-4-thiomorpholinecarboxamide 1,1-dioxideHCID 5898000330%

反応手順

To a solution of 4-(1-ethyl-4-{2-[4-(4-morpholinylmethyl)phenyl]-1H-pyrrolo[2,3-b]pyridin-4-yl}-1H-pyrazol-3-yl)aniline (0.25 mmol) in anhydrous THF (2 mL) cooled to 5° C., was added triethylamine (4 mmol) and isopropenyl chloroformate (0.5 mmol). The reaction mixture was stirred overnight at room temperature. Thiomorpholine 1,1-dioxide (2.5 mmol) was added and the reaction heated at 50° C. for three days. The crude reaction was purified by reverse phase chromatography to give the title product (30%). ESMS [M+H]+: 640.0.

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-abf75457714741d6972343e0af14de02
出典メモuspto-grants-2008_09