関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Methyl 1-methyl-1H-benzo[d]imidazole-5-carboxylate | HCID 965319 | — |
| 反応物 | Methyl 1-methyl-1H-benzo[d]imidazole-6-carboxylate | HCID 10583823 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-(1-methyl-1H-benzo[d]imidazol-6-yl)-3-oxopropanenitrile | HCID 86729302 | — |
| 生成物 | 3-(1-methyl-1H-benzo[d]imidazol-5-yl)-3-oxopropanenitrile | HCID 86729303 | 38% |
反応手順
A mixture of CH3CN (0.62 mL, 11.84 mmol), DMSO (2 mL) and NaH (410 mg, 10.26 mmol) was stirred for 45 minutes at room temperature before a solution of methyl 1-methyl-1H-benzo[d]imidazole-6-carboxylate and methyl 1-methyl-1H-benzo[d]imidazole-5-carboxylate (1.5 g, 7.89 mmol) in CH3CN (5 mL) was added dropwise. The resulting mixture was stirred at room temperature for 2 h before quenching by the addition of saturated NH4Cl and extraction with DCM (3×30 ml). The combined organic layers were concentrated to give the desired products 3-(1-methyl-1H-benzo[d]imidazol-6-yl)-3-oxopropanenitrile and 3-(1-methyl-1H-benzo[d]imidazol-5-yl)-3-oxopropanenitrile (600 mg, 38%) and used in the next step without further purification. LCMS (m/z): 200.07 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08906900B2 |
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| 出典データセット | uspto-grants-2014_12 |
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| ORD ID | ord-061694533e4f4f89912683ed3ee68ff0 |
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| 出典メモ | uspto-grants-2014_12 |
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