関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 3-Ethylpentanoic acid | HCID 134460 | — |
| 反応物 | 2,6-Dimethyl-4-morpholin-4-yl-phenylamine | HCID 23009414 | — |
| 反応物 | Sodium bicarbonate brine water | HCID 131727349 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-Ethyl-pentanoic acid (2,6-dimethyl-4-morpholin-4-yl-phenyl)-amide | HCID 11666873 | 30.5% |
反応手順
3-Ethylpentanoic acid (0.79 g) and thionyl chloride (0.44 mL) were mixed-in acetonitrile (10 mL) and heated to 110° C. for 5 minutes in a sealed microwave process vial. 2,6-Dimethyl-4-morpholin-4-yl-phenylamine (1:25 g) dissolved in acetonitrile (10 mL) was added to the reaction mixture and heated to 150° C. for 15 minutes in a sealed microwave process vial. Saturated aqueous sodium bicarbonate/brine/water (1:1:1, 50 mL) was added to the crude mixture and it was extracted with ethyl acetate (3×50 mL). The combined organic phases were dried over magnesium sulfate and concentrated in vacuo. The crude product was recrystallized from hot toluene, and the product was collected by filtration, washed with cold toluene and dried in vacuo to furnish 0.59 g (30% yield) of the title compound as an off-white solid. LC-MS (m/z) 319 (MH+); tR=2.04, (UV, ELSD) 98%, 99%. 1H NMR (500 MHz, DMSO-d6): 0.87 (t, 6H), 1.35 (qui, 4H), 1.76 (m, 1H), 2.07 (s, 6H), 2.20 (d, 2H), 3.05 (t, 4H), 3.71 (t, 4H), 6.62 (s, 2H), 8.94 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07501414B2 |
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| 出典データセット | uspto-grants-2009_03 |
|---|
| ORD ID | ord-5211cc71422745739d3aa7d204c09c02 |
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| 出典メモ | uspto-grants-2009_03 |
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