関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 3-Isopropoxy-4-nitrobenzoic acid | HCID 602928 | — |
| 反応物 | 4-Amino-1-methylpiperidine | HCID 2737531 | — |
| 反応物 | HCID 178484289 | HCID 178484289 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Sodium Carbonate | HCID 10340 | — |
| 生成物 | 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide | HCID 67076401 | 95.7% |
反応手順
To a mixture of 0.88 g (3.9 mmole) of 3-isopropoxy-4-nitro-benzoic acid, 2.8 mL (16 mmole) of ethyldiisopropyl amine, 0.54 g (4.7 mmole) of 4-amino-1-methyl-piperidine and 18 mL of dimethylformamide was added 1.63 g (4.3 mmole) of 1-[bis(dimethylamino)methylene)-1H-benzotriazolium 3-oxide hexafluorophosphate. The mixture was stirred at room temperature for 2 hours, then diluted with ice water and saturated sodium carbonate. The mixture was extracted with ethyl acetate 3 times. The combined organic layers were washed three times with sodium carbonate, three times with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel chromatography, eluting with dichloromethane-methanol (gradient, 100:0-40:60) gave 1.2 g of 3-isopropoxy-N-(1-methyl-piperidin-4-yl)-4-nitro-benzamide 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 | US08003785B2 |
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| 出典データセット | uspto-grants-2011_08 |
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| ORD ID | ord-9a8a08cb7178483b9f4aea6a46c0219a |
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| 出典メモ | uspto-grants-2011_08 |
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