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HRID 30095作成日:2026年10月25日

Methanamine, N-methoxy-, hydrochloride (1:1) → 2,6-Dichloro-N-methoxy-N-methylpyridine-3-carboxamide

https://huagongshe.com/reaction/30095

反応式

関与物質

役割名称HCID仕込み量
反応物Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
反応物DiisopropylethylamineHCID 81531—
反応物2,6-Dichloronicotinic acidHCID 854047—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2,6-Dichloro-N-methoxy-N-methylpyridine-3-carboxamideHCID 5340341150%

反応手順

To a solution of 2,6-dichloronicotinic acid (500 mg, 2.63 mmol, Aldrich 90%) in anhydrous N,N-dimethylformamide (5 mL) were added O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate (1.28 g, 3.37 mmol, Aldrich), 1-hydroxybenzotriazole hydrate (456 mg, 3.37 mmol, Aldrich) followed by N,N-diisopropylethylamine (1.3 g, 10.0 mmol) and N,O-dimethylhydroxylamine hydrochloride (306 mg, 3.15 mmol, Aldrich) at 0° C. The reaction was stirred for 1-2 hrs, treated with water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried and concentrated. The crude product was purified on silica gel with hexanes/ethyl acetate to give 2,6-Dichloro-N-methoxy-N-methyl-nicotinamide as a white solid (304.5 mg, 50% yield). HRMS, observed: 233.9968, Calcd for M+: 233.9963

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423051B2
出典データセットuspto-grants-2008_09
ORD IDord-1b00b34e51a549dc9e5341edcc4b3b6e
出典メモuspto-grants-2008_09