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HRID 12678作成日:2026年10月26日

3-Benzoyl-1-(4-chloro-butyl)-5-(2-methyl-pyridin-4-yl)-1H-pyrimidine-2,4-dione → 1-(4-Chloro-butyl)-5-(2-methyl-pyridin-4-yl)-1H-pyrimidine-2,4-dione

https://huagongshe.com/reaction/12678

反応式

関与物質

役割名称HCID仕込み量
反応物3-Benzoyl-1-(4-chloro-butyl)-5-(2-methyl-pyridin-4-yl)-1H-pyrimidine-2,4-dioneHCID 58994184—
溶媒AmmoniaHCID 222—
溶媒MethanolHCID 887—
生成物1-(4-Chloro-butyl)-5-(2-methyl-pyridin-4-yl)-1H-pyrimidine-2,4-dioneHCID 58994179—

反応手順

3-Benzoyl-1-(4-chloro-butyl)-5-(2-methyl-pyridin-4-yl)-1H-pyrimidine-2,4-dione (Prep 45, 100 mg, 0.25 mmol) was dissolved in a solution of 3% NH3 in MeOH (5 mL). The mixture was stirred at room temperature for 3 hours, the solvent was then evaporated under vacuum to give the title compound that was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727988B2
出典データセットuspto-grants-2010_06
ORD IDord-67e7e7cac166413a9063e2eaf416ec76
出典メモuspto-grants-2010_06