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HRID 35608作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Butyric AcidHCID 264—
反応物Hydrochloric AcidHCID 313—
反応物Ethyl 3,4-DiaminobenzoateHCID 458855—
反応物4-[3-(1-Piperidinylmethyl)phenoxy]butanoic acidHCID 14221805—
溶媒WaterHCID 962—
生成物5-Ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04767769
出典データセットuspto-grants-1988_08
ORD IDord-6ca45163fe16494d994857b3c6d78a42
出典メモuspto-grants-1988_08