関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tributylphosphine | HCID 13831 | — |
| 反応物 | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| 反応物 | N-ethyl-2-bromo-5-nitro-N-phenyl-benzamide | HCID 22288552 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 触媒 | HCID 178418647 | HCID 178418647 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-ethyl-8-nitro-5H-phenanthridin-6-one | HCID 22288545 | — |
反応手順
Palladium acetate (129 mg, 0.57 mmol) was added to a suspension of silver carbonate (1.6 g, 5.72 mmol), 1,3-bis(diphenylphosphino)propane (236 mg, 0.57 mmol), tributylphosphine (0.713 ml, 579 mg, 2.86 mmol) and N-ethyl-2-bromo-5-nitro-N-phenyl-benzamide (1.0 g, 2.86 mmol) in DMF (15 ml). The reaction mixture was heated to reflux for 30 minutes and cooled to 23° C. The mixture was filtered through a plug of celite, and the filter cake was washed with ethyl acetate (50 ml). The combined filtrates were washed with saturated sodium chloride (3-30 ml portion), dried over anhydrous sodium sulfate, and were concentrated. The residue was purified by flash column chromatography (10% ethyl acetate in dichloromethane) afforded 5-ethyl-8-nitro-5H-phenanthridin-6-one I-16b (111 mg, 14%) as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06958347B2 |
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| 出典データセット | uspto-grants-2005_10 |
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| ORD ID | ord-6589a8992bb5451d94025660954e41c7 |
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| 出典メモ | uspto-grants-2005_10 |
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