関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phosphorus pentachloride | HCID 24819 | — |
| 反応物 | N-(2-Amino-5-nitro-phenyl)-2-(4-ethoxy-phenyl)-acetamide | HCID 59799754 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 溶媒 | Ammonium Hydroxide | HCID 14923 | — |
| 生成物 | HCID 178466243 | HCID 178466243 | — |
反応手順
N-(2-Amino-5-nitro-phenyl)-2-(4-ethoxy-phenyl)-acetamide 41 (590 mg, 1.871 mmol), Phosphorous pentachloride (390 mg, 1.871 mmol) were dissolved in anhydrous chloroform (20 mL) in a small, argon purged flask fitted with an condenser and magnetic stirbar. The solution was heated to reflux in an oil bath for 4 hours and cooled to room temperature overnight. The mixture was diluted with H2O and chloroform and 2M ammonium hydroxide solution added to adjust pH to 9-10. The mixture was transferred to a separatory funnel and the organic layer collected. The aqueous layer was further extracted with chloroform and the combined organic layers were washed with brine, dried over magnesium sulphate, filtered and concentrated to afford crude. The product was purified using dry silica gel column chromatography eluting with 20 mL portions of solvent system (2.5% 2M NH3 in methanol/95% dichloromethane) to afford a yellow residue 42 2-(4-Ethoxy-benzyl)-5-nitro-1H-benzimidazole. 1H NMR (DMSO) δ: 1.30 (t, 3H, J=6.5), 3.87 (q, 2H, J=7.3), 4.11 (s, 2H), 6.88 (d, 2H, J=8.0), 7.25 (d, 2H, J=7.9), 7.65 (d, 1H, J=8.9), 8.07 (d, 1H, J=9.0), 8.36-8.40 (m, 1H); MS (ESI): 298 (MH+, 100%)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07919510B2 |
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| 出典データセット | uspto-grants-2011_04 |
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| ORD ID | ord-a2b153bcfa3a4c59a9c0c9974527216f |
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| 出典メモ | uspto-grants-2011_04 |
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