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HRID 621534作成日:2026年10月27日

Methyl iodide → FK 664

https://huagongshe.com/reaction/621534

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物2,4,6-TrimethylanilineHCID 6913—
反応物3,4-dihydro-6-(3,4-dimethoxyphenyl)-1-ethyl-3-methyl-4-thioxo-2(1H)-pyrimidinoneHCID 21243227—
溶媒TetrahydrofuranHCID 8028—
生成物FK 664HCID 14686837%

反応手順

To a solution of 3,4-dihydro-6-(3,4-dimethoxyphenyl)-1-ethyl-3-methyl-4-thioxo-2(1H)-pyrimidinone (0.59 g) in tetrahydrofuran (50 ml) was added methyl iodide (10 ml) and the mixture was refluxed for 90 minutes. The precipitate was added to 2,4,6-trimethylaniline (2 g) and the mixture was heated to 110°-120° C. for 3 hours. The reaction mixture was washed with a mixture of hexane and diisopropyl ether to remove excess 2,4,6-trimethylaniline. The resulting precipitate was collected by filtration and then dissolved in chloroform. The solution was washed with an aqueous solution of sodium bicarbonate, dried over magnesium sulfate and evaporated under reduced pressure to give crude product, which was purified by silica gel column chromatography to give 3,4-dihydro-6-(3,4-dimethoxyphenyl)-1-ethyl-3-methyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinone (0.29 g); mp 57°-61° C. Thus obtained compound was recrystallised from a mixture of ethanol and water (3:1) to give the desired compound as crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04824851
出典データセットuspto-grants-1989_04
ORD IDord-a74ae822fc4c47c995631f1c20378478
出典メモuspto-grants-1989_04