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HRID 254254作成日:2026年10月27日

Methanol → Methyl 6-chloropyridazine-3-carboxylate

https://huagongshe.com/reaction/254254

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Oxalyl chlorideHCID 65578—
反応物Sodium BicarbonateHCID 516892—
反応物6-chloropyridazine-3-carboxylic AcidHCID 6415762—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Methyl 6-chloropyridazine-3-carboxylateHCID 1237980165%

反応手順

Oxalyl chloride (1.14 mL, 13.09 mmol), was added dropwise to an ice-cold suspension of 6-chloro-pyridazine-3-carboxylic acid [(1.9 g, 11.9 mmol), J. Het. Chem. 29(6), 1583-92; 1992] in a mixture of dichloromethane (50 mL) and N,N-dimethylformamide (1 drop) and the mixture was stirred for 1 hour at room temperature. The reaction mixture was then evaporated under reduced pressure and the residue was diluted with dichloromethane (30 mL) and cooled to 0° C. Methanol (485 μL, 11.9 mmol) was added and the mixture was stirred at 0° C. for 1 hour. Sodium hydrogen carbonate solution was then added to the reaction mixture and the aqueous layer was separated and extracted with dichloromethane (×2). The combined organic solutions were washed with brine, dried over sodium sulfate and concentrated in vacuo to afford the title compound as a white solid in 65% yield, 1.33 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07875615B2
出典データセットuspto-grants-2011_01
ORD IDord-dda68b37c44b4ec6986e2b8cd03b57be
出典メモuspto-grants-2011_01