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3-(1-cyano-1-methylethyl)-N-{4-cyano-3-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide → N-{3-[(5-aminopyridin-2-yl)oxy]-4-cyanophenyl}-3-(1-cyano-1-methylethyl)benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-(1-cyano-1-methylethyl)-N-{4-cyano-3-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide | HCID 68417908 | — |
| 触媒 | HCID 178418390 | HCID 178418390 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | N-{3-[(5-aminopyridin-2-yl)oxy]-4-cyanophenyl}-3-(1-cyano-1-methylethyl)benzamide | HCID 68418578 | 90.2% |
反応手順
To a solution of 3-(1-cyano-1-methylethyl)-N-{4-cyano-3-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide (0.65 g, 1.59 mmol) in methanol (20 mL) was added 10% palladium-carbon (130 mg), and the mixture was stirred at room temperature for 20 hr under a hydrogen atmosphere (2.8 atm). The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (0.57 g, 90%) as a pale-yellow oil. This was used for the next reaction without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08344135B2 |
| 出典データセット | uspto-grants-2013_01 |
| ORD ID | ord-b3d1a42008d94805b3ea5f5b8f5f5d6d |
| 出典メモ | uspto-grants-2013_01 |