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HRID 275722作成日:2026年10月25日

5-Chloro-1-[1-[2-(indan-2-yl)ethyl]-1,2,3,6-tetrahydropyridin-4-yl]-1H-indole → 5-Chloro-1-[1-[2-(indan-2-yl)ethyl]piperidin-4-yl]-1H-indole

https://huagongshe.com/reaction/275722

反応式

関与物質

役割名称HCID仕込み量
反応物5-Chloro-1-[1-[2-(indan-2-yl)ethyl]-1,2,3,6-tetrahydropyridin-4-yl]-1H-indoleHCID 18545836—
反応物HCID 178418361HCID 178418361—
触媒Platinum oxide (PtO)HCID 82844—
溶媒Acetic AcidHCID 176—
生成物5-Chloro-1-[1-[2-(indan-2-yl)ethyl]piperidin-4-yl]-1H-indoleHCID 18545841—

反応手順

A mixture of 5-Chloro-1-[1-[2-(indan-2-yl)ethyl]-1,2,3,6-tetrahydropyridin-4yl]-1H-indol. 28a. (1.9 g), acetic acid (50 ml), and platinum oxide (0.1 g) was shaken for 3 h under 3 atm. hydrogen pressure. The mixture was filtered and evaporated in vacuo. The residue was dissolved in ethyl acetate and the organic phase was shaken with dilute ammonium hydroxide and then worked up in a conventional manner. Further purification was done on silica gel eluted with ethyl acetate-heptane (1:1) to give 2.0 g of crude product. The crude product was crystallized (ethyl acetate), and the title compound was collected by filtration (1.1 g, 58%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06352988B2
出典データセットuspto-grants-2002_03
ORD IDord-54697a72aafd4e599ffd898a88433804
出典メモuspto-grants-2002_03