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HRID 975145作成日:2026年10月24日

5-(3-Hydroxy-1-but-1-enyl)-3-(N-methyl-4-piperidyl)-1H-indole → 5-(3-Hydroxy-1-butyl)-3-(N-methyl-4-piperidyl)-1H-indole

https://huagongshe.com/ja/reaction/975145

反応式

関与物質

役割名称HCID仕込み量
反応物5-(3-Hydroxy-1-but-1-enyl)-3-(N-methyl-4-piperidyl)-1H-indoleHCID 54086563—
触媒PalladiumHCID 23938—
溶媒DichloromethaneHCID 6344—
生成物5-(3-Hydroxy-1-butyl)-3-(N-methyl-4-piperidyl)-1H-indoleHCID 19970945—

反応手順

Obtained from the title compound of Example 42 by a procedure similar to that described in Example 2, but using 10% palladium on charcoal as catalyst, as a foam. Rf 0.50 (SS 4). C,73.39; H,8.77; N,9.06. C18H26N2O; 0.125 CH2Cl2 requires C,73.28; H,8.91; N,9.43%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05607960
出典データセットuspto-grants-1997_03
ORD IDord-631587a7f2de4c9a86ff6b175d215833
出典メモuspto-grants-1997_03