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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4327생성일: 2026년 10월 24일

N-Methylbenzylamine → 3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-2-(N-methyl-N-benzylamino)-4-(2,4,6-trimethylphenylimino)pyrimidine

https://huagongshe.com/ko/reaction/4327

반응식

참여 물질

역할이름HCID투입량
반응물N-MethylbenzylamineHCID 7669—
반응물2-Chloro-3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-4-(2,4,6-trimethylphenylimino)pyrimidineHCID 20152293—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
생성물3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-2-(N-methyl-N-benzylamino)-4-(2,4,6-trimethylphenylimino)pyrimidineHCID 20152273—

반응 단계

To a suspension of 2-chloro-3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-4-(2,4,6-trimethylphenylimino)pyrimidine (1.5 g) in ethanol (15 ml) was added N-methylbenzylamine (1.47 ml). The mixture was refluxed for 5 hours. The resulting suspension was dissolved in chloroform, washed with brine, dried over magnesium sulfate and evaporated in vacuo. The obtained syrup was triturated in diisopropyl ether and filtered to afford 3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-2-(N-methyl-N-benzylamino)-4-(2,4,6-trimethylphenylimino)pyrimidine (1.18 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04725600
출처 데이터셋uspto-grants-1988_02
ORD IDord-1bd4c3ba7a204a948c9a3d8d4191dea3
출처 메모uspto-grants-1988_02