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HRID 428502作成日:2026年10月26日

4-(1H-Indol-3-YL)cyclohexanone → 3-(4-oxocyclohexyl)-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/428502

反応式

関与物質

役割名称HCID仕込み量
反応物4-(1H-Indol-3-YL)cyclohexanoneHCID 10846264—
反応物3-(1,4-Dioxa-spiro[4,5]dec-8-yl)-5-cyano-1H-indoleHCID 15521973—
生成物3-(4-oxocyclohexyl)-1H-indole-5-carbonitrileHCID 1124188681%

反応手順

This compound was prepared in the manner described above for intermediate 3a by replacing 3-(1,4-dioxa-spiro[4,5]dec-8-yl)-1H-indole with 3-(1,4-dioxa-spiro[4,5]dec-8-yl)-5-cyano-1H-indole (6 g) to afford 4.03 g (81%) of the title compound as a white solid: mp 162.5-164° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313126B1
出典データセットuspto-grants-2001_11
ORD IDord-363ced524074411ea8c2145efb9a10ce
出典メモuspto-grants-2001_11