関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Oxobutanoic acid | HCID 1112 | — |
| 反応物 | 1-Hydroxybenzotriazole | HCID 75771 | — |
| 反応物 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | HCID 178478721 | HCID 178478721 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | HCID 178522093 | HCID 178522093 | — |
反応手順
Trans-3-(4-aminocyclohexylcarbonylamino)-N-(5-chloropyridin-2-yl)benzofuran-2-carboxamide dihydrochloride (150 mg) obtained in Example 219 is suspended in dichloromethane (5 ml), and thereto is added triethylamine (129 μl) under ice-cooling, and the mixture is stirred for several minutes. Then, 15% aqueous succinic semialdehyde solution (290 μl) and sodium triacetoxy borohydride (131 mg) are successively added thereto, and under ice-cooling, the mixture is stirred for 0.5 hour. Then, 1-hydroxybenzotriazole (63 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (118 mg) and N,N-dimethylformamide (3 ml) are successively added thereto, and the mixture is stirred at room temperature for 15 hours. The reaction solution is concentrated under reduced pressure, and thereto is poured chloroform. The mixture is washed successively with a saturated aqueous sodium hydrogen carbonate solution, water, and a saturated brine, dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The resulting residue is purified by NH-silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1, then ethyl acetate), and the resulting residue is suspended in n-hexane, and collected by filtration to give the title compound (29 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07531537B2 |
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| 出典データセット | uspto-grants-2009_05 |
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| ORD ID | ord-5ad8afeebb6c42709fa960d21496a0c1 |
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| 出典メモ | uspto-grants-2009_05 |
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