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HRID 867026作成日:2026年10月26日

Diethyl Ether → 4-Benzoyl-1-(5,6-dimethoxy-2-methylindol-3-ylglyoxyloyl)piperidine

https://huagongshe.com/reaction/867026

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Potassium CarbonateHCID 11430—
反応物Phenyl(piperidin-4-yl)methanoneHCID 226102—
反応物5,6-Dimethoxy-2-methyl-3-indoleglyoxylyl chlorideHCID 13195539—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物4-Benzoyl-1-(5,6-dimethoxy-2-methylindol-3-ylglyoxyloyl)piperidineHCID 13195540—

反応手順

The above ether suspension of 5,6-dimethoxy-2-methyl-3-indoleglyoxylyl chloride is added portionwise to a cooled stirring mixture of 4-benzoylpiperidine [Example 9(a)], 150 ml of water, 150 ml of chloroform and 25 g of potassium carbonate. The mixture is stirred for 16 hours at ambient temperature, the organic layer is separated and the solvent is removed, leaving a brown oil which is triturated with cyclohexane and then stirred for 16 hours with ether. A white solid results which is collected, dried and recrystallized thrice from methanol to give the compound, mp 188°-190° C., 4-benzoyl-1-(5,6-dimethoxy-2-methylindol-3-ylglyoxyloyl)piperidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04101663
出典データセットuspto-grants-1978_07
ORD IDord-b08f444901ae49b4bd339ed9754cb66e
出典メモuspto-grants-1978_07