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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 621534생성일: 2026년 10월 26일

Methyl iodide → FK 664

https://huagongshe.com/reaction/621534

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물2,4,6-TrimethylanilineHCID 6913—
반응물3,4-dihydro-6-(3,4-dimethoxyphenyl)-1-ethyl-3-methyl-4-thioxo-2(1H)-pyrimidinoneHCID 21243227—
용매TetrahydrofuranHCID 8028—
생성물FK 664HCID 14686837%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04824851
출처 데이터셋uspto-grants-1989_04
ORD IDord-a74ae822fc4c47c995631f1c20378478
출처 메모uspto-grants-1989_04