関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | P-Xylene | HCID 7809 | — |
| 反応物 | 3-Methoxy-5-nitroaniline | HCID 2759598 | — |
| 反応物 | N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide | HCID 5007601 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(3-(3-methoxy-5-nitrophenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide | HCID 56601996 | 42% |
反応手順
N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide (700 mg, 1.92 mmol), 3-methoxy-5-nitroaniline (645 mg, 3.84 mmol) and p-xylene (7 mL) were combined and heated to 140° C., then stirred for 16 hours at 130° C. The reaction was allowed to cool, placed in a sep. funnel, diluted with DCM, and washed with 2M HCl and brine and concentrated in vacuo. The resulting solid was washed with Et2O to give N-(3-(3-methoxy-5-nitro-phenylamino)quinoxalin-2-yl)-3-nitrobenzenesulfonamide (400 mg, 42%). MS (EI) m/z for C21H16N6O7S: 496.94 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08889664B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-6c8076cdb86d43ccbf6e3a0bad6e4e4d |
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| 出典メモ | uspto-grants-2014_11 |
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