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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230647생성일: 2026년 10월 26일

Methanamine, N-methoxy-, hydrochloride (1:1) → N-methoxy-N,1-dimethyl-1H-imidazole-2-carboxamide

https://huagongshe.com/reaction/230647

반응식

참여 물질

역할이름HCID투입량
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물DiisopropylethylamineHCID 81531—
반응물1-methyl-1H-imidazole-2-carboxylic acidHCID 557678—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DimethylformamideHCID 6228—
생성물N-methoxy-N,1-dimethyl-1H-imidazole-2-carboxamideHCID 57762806212.1%

반응 단계

HATU (O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate) (1.75 g; 4.60 mmol) was added in on portion to a stirring solution of 1-methyl-1H-imidazole-2-carboxylic acid (509 mg; 4.04 mmol), N,O-dimethylhydroxylamine hydrochloride (391 mg; 4.01 mmol), and diisopropylethylamine (2.0 mL; 11.9 mmol) in anhydrous DMF (14 mL). The mixture was stirred at room temperature for 17 hours and partitioned between ethyl acetate (100 mL) and water (100 mL). The organic phase was dried (MgSO4) and concentrated in vacuo, giving a colourless oil (1.45 g). This was purified by column chromatography, giving the title compound as a colourless oil (494 mg; 73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566735B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-1b057176fc3b4694a4209927e8cc5045
출처 메모uspto-grants-2009_07