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HRID 4327作成日:2026年10月25日

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/reaction/4327

反応式

関与物質

役割名称HCID仕込み量
反応物N-MethylbenzylamineHCID 7669—
反応物2-Chloro-3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-4-(2,4,6-trimethylphenylimino)pyrimidineHCID 20152293—
溶媒EthanolHCID 702—
溶媒ChloroformHCID 6212—
生成物3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-2-(N-methyl-N-benzylamino)-4-(2,4,6-trimethylphenylimino)pyrimidineHCID 20152273—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725600
出典データセットuspto-grants-1988_02
ORD IDord-1bd4c3ba7a204a948c9a3d8d4191dea3
出典メモuspto-grants-1988_02