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HRID 2170306作成日:2026年10月26日

Methanamine, N-methoxy-, hydrochloride (1:1) → 6-acetamido-3-bromo-N-methoxy-N-methylpicolinamide

https://huagongshe.com/reaction/2170306

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Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物3-Bromo-6-acetamidopyridine-2-carboxylic acidHCID 25306988—
溶媒DichloromethaneHCID 6344—
生成物6-acetamido-3-bromo-N-methoxy-N-methylpicolinamideHCID 90280477—

反応手順

HATU (1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate) (4.56 g, 12.0 mmol) was added to a solution of 6-acetamido-3-bromopicolinic acid (2.6 g, 10.0 mmol) and DIPEA (N,N-diisopropylethylamine)(5.2 ml, 30 mmol) in DCM (dichloromethane)(10 ml). After 10 minutes, N,O-dimethylhydroxylamine hydrochloride (1.5 g, 15.0 mmol) was added to the reaction. The reaction was stirred at room temperature for 5 min. The reaction mixture was partitioned between EtOAc (ethyl acetate) and saturated NH4Cl solution. The organic phase was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude material was used in the next step without further purification. MS (m/z) 302.1 [M+H]+. 1H NMR (400 MHz, cd3cl) δ 8.14 (s, 1H), 8.13 (d, J=8.4 Hz, 1H), 7.85 (d, J=8.4 Hz, 1H), 3.56 (s, 3H), 3.37 (s, 3H), 2.20 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09050344B2
出典データセットuspto-grants-2015_06
ORD IDord-09ae41a2569b4559a9b8ed40f4786d39
出典メモuspto-grants-2015_06