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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1984701생성일: 2026년 10월 26일

3,5-Dimethylaniline → N-(3,5-Dimethylphenyl)-2-(2-fluoropyridin-4-ylmethylthio)pyridine-3-carboxamide

https://huagongshe.com/reaction/1984701

반응식

참여 물질

역할이름HCID투입량
반응물3,5-DimethylanilineHCID 7949—
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—
반응물2-(2-Fluoropyridin-4-ylmethylthio)pyridine-3-carboxylic acidHCID 23094028—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(3,5-Dimethylphenyl)-2-(2-fluoropyridin-4-ylmethylthio)pyridine-3-carboxamideHCID 1006754344%

반응 단계

O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (3.0 g, 7.9 mmol) was added to a solution of 2-(2-fluoropyridin-4-ylmethylthio)pyridine-3-carboxylic acid (Reference compound No. 2-1, 1.5 g, 5.7 mmol), 3,5-xylidine (0.90 g, 7.4 mmol) and N,N-diisopropylethylamine (2.0 mL, 11 mmol) in N,N-dimethylformamide (20 mL) at room temperature, and the mixture was stirred for 12 hours. Ethyl acetate (30 mL) was added to the reaction mixture, the whole was washed with brine (50 mL), and then the organic layer was dried over anhydrous magnesium sulfate. The organic layer was evaporated under reduced pressure, and the resulting residue was purified by silica gel column chromatography to give 0.91 g of the title reference compound as a colorless solid. (Yield 44%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07544703B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-ea30108da48641dab223eac646c5af13
출처 메모uspto-grants-2009_06