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HRID 1399122作成日:2026年10月27日

Methyl Ethyl Ketone → 1-(2,4-Dichlorophenyl)-N-(1-methylpropyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-amine

https://huagongshe.com/reaction/1399122

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl Ethyl KetoneHCID 6569—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物1-(2,4-Dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-amineHCID 57786170—
溶媒MethanolHCID 887—
溶媒Sodium BicarbonateHCID 516892—
生成物1-(2,4-Dichlorophenyl)-N-(1-methylpropyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-amineHCID 5778598740%

反応手順

Sodium triacetoxyborohydride (171 mg, 0.807 mmol) was added to a stirred solution of 1-(2,4-dichlorophenyl)-1,2,3,4-tetrahydropyrimido[1,2-a]benzimidazol-6-amine (183 mg, 0.549 mmol) and butan-2-one (1.0 mL) in methanol (1.0 ml) at 0° C., and the mixture was stirred at room temperature for 8 hr. The mixture was diluted with saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 5-50% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the solid, which was recrystallized from ethyl acetate/n-hexane to give the title compound as a colorless crystal (86.4 mg, 0.222 mmol, 40%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08901141B2
出典データセットuspto-grants-2014_12
ORD IDord-d5f5c40d49f945038d54c469baba06c5
出典メモuspto-grants-2014_12