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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338700생성일: 2026년 10월 25일

Aniline → 4-Bromo-pyridine-2-carboxylic acid phenylamide

https://huagongshe.com/reaction/338700

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물4-MethylmorpholineHCID 7972—
반응물4-Bromopyridine-2-carboxylic acidHCID 735150—
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—
생성물4-Bromo-pyridine-2-carboxylic acid phenylamideHCID 8669582671.2%

반응 단계

To a suspension of 4-bromo-pyridine-2-carboxylic acid (1.00 g, 5.00 mmol) in dimethylformamide (10 mL) was added 1-methylmorpholine (1.1 mL, 10 mmol) and O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyl-uronium hexafluorophosphate (HATU) (2.37 g, 6.23 mmol). The mixture became an orange solution after 10 minutes. Aniline (0.5 mL, 5.5 mmol) was added and the solution was stirred at room temperature for 66 hours. The dimethylformamide was evaporated in vacuo and the residue was partitioned between water and ethyl acetate. The separated water layer was extracted with ethyl acetate. The combined ethyl acetate extract was washed with water and saturated sodium bicarbonate. The organic layer was dried (MgSO4), filtered and evaporated to crude 2. Chromatography on silica gel (40 g) applied in dichloromethane and eluted with hexanes:ethyl acetate (1:1) gave the title compound (0.986 g, 71%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889870B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-5ff8ad58779c434bace6846b494b7950
출처 메모uspto-grants-2014_11