関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Butyric Acid | HCID 264 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Ethyl 3,4-Diaminobenzoate | HCID 458855 | — |
| 反応物 | 4-[3-(1-Piperidinylmethyl)phenoxy]butanoic acid | HCID 14221805 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 5-Ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazole | HCID 21294573 | — |
反応手順
A mixture of ethyl 3,4-diaminobenzoate (0.9 g), 4-(3-piperidinomethylphenoxy)butyric acid (2.1 g) prepared as described in Example 42 and 4N hydrochloric acid (6 ml) was heated and stirred under reflux for 90 minutes. A further portion of the butyric acid (2.1 g) and of 4N hydrochloric acid (6 ml) was added and the mixture heated under reflux for 90 minutes. The reaction mixture was cooled and poured into water (10 volumes). Aqueous ammonia (S.G. 0.880) was added until the solution was alkaline and the mixture was extracted with ethyl acetate. The extracts were washed with water, dried and on removal of the solvent gave a residue which was purified by preparative layer chromatography on silica gel plates using a 1:1 mixture of dichloromethane and methanol to give 5-ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazole as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04767769 |
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| 出典データセット | uspto-grants-1988_08 |
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| ORD ID | ord-6ca45163fe16494d994857b3c6d78a42 |
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| 出典メモ | uspto-grants-1988_08 |
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