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HRID 242016作成日:2026年10月24日

Water → Ethyl 8-chloro-1-[(6-methylpyridin-3-yl)methyl]-4-oxo-1,4-dihydrocinnoline-3-carboxylate

https://huagongshe.com/ja/reaction/242016

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl 1-[(6-bromopyridin-3-yl)methyl]-8-chloro-4-oxo-1,4-dihydrocinnoline-3-carboxylateHCID 86659998—
反応物HCID 178477797HCID 178477797—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 8-chloro-1-[(6-methylpyridin-3-yl)methyl]-4-oxo-1,4-dihydrocinnoline-3-carboxylateHCID 86660002—

反応手順

Ethyl 1-[(6-bromopyridin-3-yl)methyl]-8-chloro-4-oxo-1,4-dihydrocinnoline-3-carboxylate [(Example 69, Step 1), 0.11 g, 0.25 mmol] was dissolved in tetrahydrofuran (1.5 mL), sparged under nitrogen and treated with methylzinc chloride (0.18 mL, 2.0 M tetrahydrofuran solution, 0.35 mmol, 1.4 equiv) and 1,1′bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (10 mg, 0.013 mmol, 0.05 equiv). After stirring for 15 minutes, tetrakis(triphenylphosphine)palladium(0) (58 mg, 0.050 mmol, 0.2 equiv) were added and the mixture was stirred at ambient temperature for an additional 2 hours. The mixture was poured into water, extracted twice with ethyl acetate and the combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel gradient chromatography (100:0 to 0:100; hexanes:ethyl acetate), providing the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653079B2
出典データセットuspto-grants-2014_02
ORD IDord-547ee74b171543ceae2c8d5a3225ab07
出典メモuspto-grants-2014_02