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HRID 271080作成日:2026年10月25日

Ethyl 4,6-dichloropyridazine-3-carboxylate → (4,6-Dichloro-pyridazin-3-yl)-(2-methoxy-phenyl)-methanone

https://huagongshe.com/reaction/271080

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4,6-dichloropyridazine-3-carboxylateHCID 53428795—
反応物HCID 178489560HCID 178489560—
溶媒TetrahydrofuranHCID 8028—
生成物(4,6-Dichloro-pyridazin-3-yl)-(2-methoxy-phenyl)-methanoneHCID 5983430378.2%

反応条件

温度-78 °C

反応手順

4,6-Dichloro-pyridazine-3-carboxylic acid ethyl ester (1.032 g, 4.67 mmol, prepared as described by Xie et al., WO 2004031174) was dissolved in 25 ml dry THF, and the reaction mixture was cooled in a dry ice/acetone bath for 15 minutes. 2-Methoxyphenyl magnesium bromide (7 mL of 1M solution in THF, 7.00 mmol) was added, and the reaction mixture was stirred for 8 hours under nitrogen at −78° C. Silica gel (11.0 g) was added, and the reaction mixture was allowed to warm to room temperature. Solvent was removed under reduced pressure, and the residue was purified by flash chromatography (0% to 20% EtOAc/Hexanes) to yield 1.029 g (3.65 mmol, 78%) of (4,6-dichloro-pyridazin-3-yl)-(2-methoxy-phenyl)-methanone as a yellow solid. Mass Spec. M+H=283.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452880B2
出典データセットuspto-grants-2008_11
ORD IDord-253eb133e26945d5a80a0781a1b56b86
出典メモuspto-grants-2008_11