戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1359729作成日:2026年10月25日

Piperidine → 5-(2,6-Dichloro-phenylmethanesulfonyl)-3-[1-[4-(4-hydroxy-piperidin-1-ylmethyl)-3,5-dimethyl-1h-pyrrol-2-yl]-meth-(z)-ylidene]-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1359729

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物5-(2,6-Dichloro-phenylmethanesulfonyl)-1,3-dihydro-indol-2-oneHCID 18179768—
反応物4-(4-hydroxy-piperidin-1-ylmethyl)-3,5-dimethyl-1H-pyrrole-2-carbaldehydeHCID 22561861—
溶媒EthanolHCID 702—
生成物5-(2,6-Dichloro-phenylmethanesulfonyl)-3-[1-[4-(4-hydroxy-piperidin-1-ylmethyl)-3,5-dimethyl-1h-pyrrol-2-yl]-meth-(z)-ylidene]-1,3-dihydro-indol-2-oneHCID 59077531—

反応手順

A mixture of 5-(2,6-dichloro-phenylmethanesulfonyl)-1,3-dihydro-indol-2-one (150 mg, 0.42 mmol), 4-(4-hydroxy-piperidin-1-ylmethyl)-3,5-dimethyl-1H-pyrrole-2-carbaldehyde (99 mg, 1 eq.) and piperidine (0.5 eq.) in ethanol (2 mL) was stirred at rt for days. The reaction was concentrated and the residue was purified on a silica gel column to give the titled compound as a pale greenish-brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06599902B2
出典データセットuspto-grants-2003_07
ORD IDord-b83c59ac88594a708124421528d83636
出典メモuspto-grants-2003_07