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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2170306생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/2170306

반응식

참여 물질

역할이름HCID투입량
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물3-Bromo-6-acetamidopyridine-2-carboxylic acidHCID 25306988—
용매DichloromethaneHCID 6344—
생성물6-acetamido-3-bromo-N-methoxy-N-methylpicolinamideHCID 90280477—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09050344B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-09ae41a2569b4559a9b8ed40f4786d39
출처 메모uspto-grants-2015_06