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HRID 2391803作成日:2026年10月25日

6-(4-Methylpiperazin-1-yl)pyridin-3-amine → 8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid [6-(4-methyl-piperazin-1-yl)-pyridin-3-yl]-amide

https://huagongshe.com/reaction/2391803

反応式

関与物質

役割名称HCID仕込み量
反応物6-(4-Methylpiperazin-1-yl)pyridin-3-amineHCID 2763390—
反応物8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acidHCID 66914636—
溶媒Dichloromethane methanolHCID 21226129—
生成物8-Benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid [6-(4-methyl-piperazin-1-yl)-pyridin-3-yl]-amideHCID 44515978—

反応手順

The title compound was prepared in analogy to the procedure described in Step 14.1 but stirring the reaction mixture for 20 h at rt, using 6-(4-methylpiperazin-1-yl)-pyridin-3-ylamine (prepared as described in Example 33 but using N-methyl-piperazine in Step 33.2) and 8-benzo[b]thiophen-3-yl-quinoxaline-5-carboxylic acid (Example 59). Title compound: ESI-MS: 481.0 [M+H]+; tR=3.81 min (System 1); TLC: Rf=0.40 (DCM/MeOH, 9:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08273882B2
出典データセットuspto-grants-2012_09
ORD IDord-93282a5cbf974232beffa12672538304
出典メモuspto-grants-2012_09