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HRID 460561作成日:2026年10月26日

4-(Naphthalen-2-yl)piperidine → ethyl (S)-7-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)benzo(b)furan-2-carboxylate

https://huagongshe.com/reaction/460561

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Naphthalen-2-yl)piperidineHCID 22029264—
反応物ethyl (S)-7-(glycidyloxy)benzo(b)furan-2-carboxylateHCID 86585640—
生成物ethyl (S)-7-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)benzo(b)furan-2-carboxylateHCID 6007790877.3%

反応手順

By the reactions in the same manner as in Starting Material Synthesis Example 11 using ethyl (S)-7-(glycidyloxy)benzo(b)furan-2-carboxylate (5.3 g) and 4-(naphthalen-2-yl)piperidine (3.0 g), the title compound (5.2 g) was obtained as a brown oil.

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-21b098ff6bb2424684f71519495d1967
出典メモuspto-grants-2007_03