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HRID 34413作成日:2026年10月24日

3-Bromo-1-propanol → 3-bromopropyl Methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

https://huagongshe.com/ja/reaction/34413

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromo-1-propanolHCID 12308—
反応物Thionyl ChlorideHCID 24386—
反応物2,6-Dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid monomethyl esterHCID 173322—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物3-bromopropyl Methyl 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylateHCID 3274278—

反応手順

A solution of 2,6-dimethyl-3-carbomethoxy-4-(3-nitrophenyl)-5-carboxy-1,4-dihydropyridine (107 g, 0.32 mol) in CH2Cl2 (520 mL) and DMF (100 mL) was cooled to 0° C. and thionyl chloride (28 mL, 0.39 mol) slowly added. The mixture was stirred at room temperature for 1 hour, then cooled to 5° C. Distilled 3-bromopropanol (35 mL, 3.9 mol) was slowly added, and the solution stirred for 1 hour at room temperature. The solution was then washed with water and the organic layer dried over sodium sulfate and evaporated under reduced pressure. The product was recrystallized from ethyl acetate to yield 2,6-dimethyl-3-carbomethoxy-4-(3-nitrophenyl)-5-(3-bromopropoxycarbonyl)-1,4-dihydropyridine (12, mp=146° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04761420
出典データセットuspto-grants-1988_08
ORD IDord-456b9033347340a1acbd3539a4ba158d
出典メモuspto-grants-1988_08