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HRID 1907634作成日:2026年10月25日

1-(3-Chlorophenyl)piperazine → 1-[(6,7-Dichloro-2-methoxyquinoxalin-3-yl)aminocarbonyl]-4-(3-chlorophenyl)piperazine

https://huagongshe.com/reaction/1907634

反応式

関与物質

役割名称HCID仕込み量
反応物1-(3-Chlorophenyl)piperazineHCID 1355—
反応物Ethyl N-(6,7-dichloro-2-methoxyquinoxalin-3-yl)carbamateHCID 69243293—
生成物1-[(6,7-Dichloro-2-methoxyquinoxalin-3-yl)aminocarbonyl]-4-(3-chlorophenyl)piperazineHCID 6924440961%

反応手順

Ethyl N-(6,7-dichloro-2-methoxyquinoxalin-3-yl)carbamate and 1-(3-chlorophenyl)piperazine were reacted by the same way with the example 176 to obtain the titled compound (yield, 61%). 1H NMR (300 MHz, CDCl3) δ 3.31-3.30 (m, 4H), 3.75-3.76 (m, 4H), 4.15 (s, 3H), 6.80-6.82 (m, 1H), 6.90-6.91 (m, 2H), 7.18-7.23 (m, 1H), 7.32 (br s, 1H), 7.85 (s, 1H), 7.91 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08598173B2
出典データセットuspto-grants-2013_12
ORD IDord-2ce6299cd91847eba359cf84616a50a5
出典メモuspto-grants-2013_12