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HRID 42701作成日:2026年10月24日

Triethylamine → 6-[Allyl(methyl)amino]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde

https://huagongshe.com/ja/reaction/42701

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N-MethylallylamineHCID 69391—
反応物6-Chloro-5-formyl-1,3-dimethyluracilHCID 319971—
溶媒EthanolHCID 702—
生成物6-[Allyl(methyl)amino]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehydeHCID 86658689—

反応手順

To a stirred solution of 6-chloro-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde (0.500 g, 2.47 mmol) and triethyl-amine (0.52 ml, 3.71 mmol) in dry ethanol (10 ml), N-methylprop-2-en-1-amine (0.36 ml, 3.71 mmol) was added under argon. The resulting mixture was stirred at room temperature under argon overnight. After evaporation of the solvent in vacuo, water (15 ml) was added to the yellow oily residue, and the mixture was extracted with dichloromethane (4×15 ml). The combined organic phases were dried over anhydrous MgSO4. The solvent was evaporated in vacuo, and the crude product was purified by crystallization from a mixture of cyclohexane:isopropyl alcohol (4:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536210B2
出典データセットuspto-grants-2013_09
ORD IDord-cc7929173e2d446b981067cd1f9e794d
出典メモuspto-grants-2013_09