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HRID 2114982作成日:2026年10月27日

5-Amino-2-oxindole → 2-Oxo-N-(2-oxo-2,3-dihydro-1H-indol-5-yl)-2-(4-p-tolyloxy-piperidin-1-yl)-acetamide

https://huagongshe.com/reaction/2114982

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-2-oxindoleHCID 2773213—
反応物Oxo-(4-p-tolyloxy-piperidin-1-yl)-acetic acidHCID 69100252—
生成物2-Oxo-N-(2-oxo-2,3-dihydro-1H-indol-5-yl)-2-(4-p-tolyloxy-piperidin-1-yl)-acetamideHCID 69100718—

反応手順

The title compound is prepared from oxo-(4-p-tolyloxy-piperidin-1-yl)-acetic acid and 5-amino-1,3-dihydro-indol-2-one according to the method described in Example 2. The filtered crystals are purified by column chromatography using Kieselgel 60 (Merck) as adsorbent and toluene:methanol=4:1 as eluent. Melting Point: 176-178° C. (diethyl ether)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07435744B2
出典データセットuspto-grants-2008_10
ORD IDord-52765ca6e0a44ddea76137d35145b8fb
出典メモuspto-grants-2008_10