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HRID 1878157作成日:2026年10月25日

N-(2-Cyanophenyl)piperazine → 1-[(2-Methoxy-6-methylquinoxalin-3-yl)aminocarbonyl]-4-(2-cyanophenyl)piperazine

https://huagongshe.com/reaction/1878157

反応式

関与物質

役割名称HCID仕込み量
反応物N-(2-Cyanophenyl)piperazineHCID 2735875—
反応物Ethyl N-(2-methoxy-6-methylquinoxalin-3-yl)carbamateHCID 66917958—
生成物1-[(2-Methoxy-6-methylquinoxalin-3-yl)aminocarbonyl]-4-(2-cyanophenyl)piperazineHCID 6691824591%

反応手順

Ethyl N-(2-methoxy-6-methylquinoxalin-3-yl)carbamate and 1-(2-cyanophenyl)piperazine were reacted by the same way with the example 43 to obtain the titled compound (yield, 91%). 1H NMR (300 MHz, CDCl3): δ 2.46 (s, 3H), 3.28 (s, 4H), 3.86 (s, 3H), 4.08-4.19 (m, 4H), 7.01-7.08 (m, 3H), 7.17-7.37 (m, 1H), 7.49-7.61 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08314100B2
出典データセットuspto-grants-2012_11
ORD IDord-8904e34f177d49fba80899dd7bbc6d66
出典メモuspto-grants-2012_11