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HRID 387425作成日:2026年10月27日

Methanol → 4-Chloro-N-methylpicolinamide

https://huagongshe.com/reaction/387425

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物MethylamineHCID 6329—
反応物Methyl 4-chloropyridine-2-carboxylate--hydrogen chloride (1/1)HCID 16655470—
溶媒TetrahydrofuranHCID 8028—
生成物4-Chloro-N-methylpicolinamideHCID 147681480.5%

反応条件

温度0 °C

反応手順

A suspension of 17.8 g (0.103 mol, 1 eq) of 4-chloro-pyridine-2-carboxylic acid methyl ester hydrochloride in 15 mL, of methanol was cooled to 0° C. and slowly treated with a 2.0 M solution of methylamine in tetrahydrofuran at a rate that kept internal temperature below 5° C. The reaction mixture was stirred at 0° C. for 2 hours, then slowly allowed to warm up to ambient temperature and stirred for 18 hours. Solvent was removed in vacuum, approx. 200 mL of ethyl acetate was added and the resulting suspension was filtered. The precipitate was washed with 100 mL of ethyl acetate. The combined ethyl acetate solutions were washed three times with 100 mL of brine and dried over sodium sulfate. Solvent was removed in vacuum to yield 14.16 g of the product as orange oil. Yield: 80.5%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08372971B2
出典データセットuspto-grants-2013_02
ORD IDord-a4e4c8b5a6254c1f8b5c73c2e6f29149
出典メモuspto-grants-2013_02