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HRID 460636作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/460636

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2-AcetylbenzofuranHCID 15435—
反応物Maleic AcidHCID 444266—
反応物4-(Naphthalen-2-yl)piperidineHCID 22029264—
生成物(S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)-propyloxy)benzo(b)furan-2-yl methyl ketone maleateHCID 69497711—

反応手順

By the reactions in the same manner as in Example 3 using (S)-4-glycidyloxybenzo(b)furan-2-yl methyl ketone (0.52 g) obtained in Starting Material Synthesis Example 71 and 4-(naphthalen-2-yl)piperidine (0.47 g), (S)-4-(2-hydroxy-3-(4-naphthalen-2-yl)piperidino)propyloxy)benzo(b)furan-2-yl methyl ketone (0.87 g) was obtained as a brown oil. This was dissolved in ethyl acetate and maleic acid (0.22 g) was added. The precipitated crystals were recrystallized from a mixed solvent of isopropanol-ethyl acetate to give the title compound (0.76 g) as pale-yellow crystals, melting point 153–155° 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-0fc6302ec1ee4ea392d094007397ede9
出典メモuspto-grants-2007_03