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HRID 3116作成日:2026年10月23日

Water → Dimethyl 7-chloroquinoline-2,3-dicarboxylate

https://huagongshe.com/ja/reaction/3116

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium FormateHCID 2723810—
反応物Dimethyl 4,7-dichloroquinoline-2,3-dicarboxylateHCID 18929951—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物Dimethyl 7-chloroquinoline-2,3-dicarboxylateHCID 18929843134.8%

反応手順

A stirred mixture of dimethyl 4,7-dichloroquinoline-2,3-dicarboxylate (5.00 g, 15.9 mM), sodium formate (1.63 g, 23.9 mM) and tetrakis(triphenylphosphine)palladium(0) (0.92 g, 0.80 mM) in anhydrous dimethylformamide (75 mL) under a nitrogen atmosphere was heated at 90°-95° C. for 7 hr. No reaction occurred so the reaction mixture was degassed and an additional quantity of tetrakis(triphenylphosphine)palladium(0) (0.92 g, 0.80 mM) was added and the reaction mixture again heated at 90°-95° C. for 6 hr. The cooled reaction mixture was poured into water and the resulting mixture extracted with ethyl acetate. The combined extracts were dried (MgSO4), filtered and concentrated to leave an gummy solid (6.0 g). Trituration of this residue with ethyl acetate and subsequent filtration separated a crystalline solid which was shown to be dimethyl 7-chloro-4-hydroxyquinoline-2,3-dicarboxylate. The filtrate was concentrated and the residue was flash chromatographed over silica gel (eluant: hexane/ethyl acetate, 3/2) to provide the title diester (1.13 g, 25.4%) as a light yellow crystalline solid; MS(CI): 280 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733910
出典データセットuspto-grants-1998_03
ORD IDord-e1f559619b474a8e8ddc858df147e65a
出典メモuspto-grants-1998_03