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HRID 18647作成日:2026年10月26日

Methyl vinyl ketone → 1-{4-[2-(2,4-Dichloro-phenyl)-5-methyl-pyrrol-1-yl]-benzenesulfonyl}-piperidine

https://huagongshe.com/reaction/18647

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl vinyl ketoneHCID 6570—
反応物2,4-DichlorobenzaldehydeHCID 13404—
反応物4-(Piperidine-1-sulfonyl)anilineHCID 236648—
生成物1-{4-[2-(2,4-Dichloro-phenyl)-5-methyl-pyrrol-1-yl]-benzenesulfonyl}-piperidineHCID 68486248—

反応手順

2,4-Dichlorobenzaldehyde and but-3-en-2-one were treated according to the procedure outlined in General Procedure C followed by subjecting the resulting product to conditions outlined in General Procedure D along with p-piperidinylsulfonyl phenylamine to obtain the titled compound. 1H NMR (CDCl3) δ ppm 1.50 (6H), 2.10 (3H), 2.80 (4H), 6.08 (1H), 6.35 (1H), 7.33-7.90 (7H); MS (ESI) m/z 449/451 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741364B2
出典データセットuspto-grants-2010_06
ORD IDord-36737fdcfcb24e1d99dd19a0931e567f
出典メモuspto-grants-2010_06