참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Butyric Acid | HCID 264 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethyl 3,4-Diaminobenzoate | HCID 458855 | — |
| 반응물 | 4-[3-(1-Piperidinylmethyl)phenoxy]butanoic acid | HCID 14221805 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-Ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazole | HCID 21294573 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04767769 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-6ca45163fe16494d994857b3c6d78a42 |
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| 출처 메모 | uspto-grants-1988_08 |
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