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HRID 460637作成日:2026年10月25日

Ethyl Acetate → (S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-3-methylbenzo(b)furan-2-yl methyl ketone maleate

https://huagongshe.com/reaction/460637

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Maleic AcidHCID 444266—
反応物Ethanone, 1-(3-methyl-2-benzofuranyl)-HCID 2507689—
反応物4-(Naphthalen-2-yl)piperidineHCID 22029264—
生成物(S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-3-methylbenzo(b)furan-2-yl methyl ketone maleateHCID 69497936—

反応手順

By the reactions in the same manner as in Example 3 using (S)-4-glycidyloxy-3-methylbenzo(b)furan-2-yl methyl ketone (0.60 g) obtained in Starting Material Synthesis Example 72 and 4-(naphthalen-2-yl)piperidine (0.51 g), (S)-4-(2-hydroxy-3-(4-naphthalen-2-yl)piperidino)propyloxy)-3-methylbenzo(b)furan-2-yl methyl ketone (1.1 g) was obtained as a brown oil. This was dissolved in ethyl acetate and maleic acid (0.25 g) was added. The precipitated crystals were recrystallized from a mixed solvent of isopropanol-ethyl acetate to give the title compound (0.82 g) as pale-yellow crystals, melting point 163–164° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196199B2
出典データセットuspto-grants-2007_03
ORD IDord-888c58cf896f4edeb77d3319628a93b9
出典メモuspto-grants-2007_03