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HRID 35608생성일: 2026년 10월 23일

Ammonia → 5-Ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazole

https://huagongshe.com/ko/reaction/35608

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Butyric AcidHCID 264—
반응물Hydrochloric AcidHCID 313—
반응물Ethyl 3,4-DiaminobenzoateHCID 458855—
반응물4-[3-(1-Piperidinylmethyl)phenoxy]butanoic acidHCID 14221805—
용매WaterHCID 962—
생성물5-Ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04767769
출처 데이터셋uspto-grants-1988_08
ORD IDord-6ca45163fe16494d994857b3c6d78a42
출처 메모uspto-grants-1988_08