関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Lithium amide | HCID 24532 | — |
| 反応物 | Lithium | HCID 3028194 | — |
| 反応物 | methyl 5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxylate | HCID 13840803 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-Methoxy-3-(1-methylethoxy)-1H-indole-2-carboxamide | HCID 10753063 | 76% |
反応手順
Lithium amide in liquid ammonia is prepared as described by Unangst PC and Carethers ME, J. Heterocyclic Chem. 1984;21:709, from lithium metal ribbon (0.059 g, 8.5 mmol). A solution of methyl 5-methoxy-3-(1-methylethoxy)-1H-indole-2-carboxylate (0.15 g, 0.57 mmol; Unangst PC, et al., J, Heterocyclic Chem. 1987;24:811) in 4.0 mL of tetrahydrofuran is added dropwise. The mixture is stirred for 1 hour and the excess ammonia is allowed to evaporate. The residue is diluted with ethyl acetate, and the organic layer is washed with 1.0N HCl brine, saturated sodium bicarbonate solution, and brine again. The solution is dried (anhydrous magnesium sulfate) and evaporated. Recrystallization of the residue from ethyl acetatehexane gives 0.11 g (76%) of product; mp 138.5°-140° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05424329 |
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| 出典データセット | uspto-grants-1995_06 |
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| ORD ID | ord-0e93488b29b740aba879b81f4633c0a3 |
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| 出典メモ | uspto-grants-1995_06 |
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