関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pentanoic Acid | HCID 7991 | — |
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2,6-Dimethyl-4-morpholin-4-yl-phenylamine | HCID 23009414 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Pentanoic acid(2,6-dimethyl-4-morpholin-4-yl-phenyl)-amide | HCID 11630683 | 40% |
反応手順
Pentanoic acid (0.37 g), N,N-diisopropyl-ethylamine (1.51 mL) and N-[(dimethylamino)-1H-1,2,3-triazolo-[4,5-b]pyridin-1-yl-methylene]-N-methyl-methanaminium hexafluoro-phosphate N-oxide (1.66 g) were mixed in dry N,N-dimethylformamide (3 mL) and stirred under argon for 2 minutes. 2,6-Dimethyl-4-morpholin-4-yl-phenylamine (0.50 g) dissolved in dry N,N-dimethylformamide (2 mL) was added to the reaction mixture, which was stirred at 25° C. under argon for 16 hours. Ethyl acetate (20 mL) was added and the organic phase was washed with saturated aqueous ammonium chloride/water (1:1, 20 mL), water (20 mL), brine/water (1:1, 20 mL), dried over magnesium sulfate, concentrated in vacuo and purified by flash chromatography to furnish 0.28 g (40% yield) of the title compound as a white solid. LC-MS (m/z) 291 (MH+); tR=1.61, (UV, ELSD) 99%, 99%. 1H NMR (500 MHz, DMSO-d6): 0.91 (t, 3H), 1.34 (m, 2H), 1.58 (qui, 2H), 2.06 (s, 6H), 2.27 (t, 2H), 3.04 (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 |
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| ORD ID | ord-70b7f9e8e896453db39b8050c826a880 |
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| 出典メモ | uspto-grants-2009_03 |
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