反应详情
EQUATION
反应方程式
REACTANTS
反应物
Hydrogen Bromide
BrH
4-Methylmorpholine
C5H11NO
2-Methoxypyridin-4-amine
C6H8N2O
4,5-dichloro-2-fluorobenzoic acid
C7H3Cl2FO2
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 95 °C
PROCEDURE
实验过程
A solution of 2-methoxypyridin-4-amine (186.2 mg, 1.5 mmol), 4,5-dichloro-2-fluoro-benzoic acid (285.1 mg, 1.36 mmol), HATU (622.4 mg, 1.64 mmol) and n-methylmorpholine (299.9 μL, 2.73 mmol) in DMF (3 mL) was stirred at room temperature for 16 hours. The reaction mixture was poured into water and extracted with ethyl acetate (3×). The organics were combined, washed with water (3×), brine and dried over Na2SO4, filtered through a short plug of silica and evaporated to dryness. The material was taken up in HBr (in acetic acid) (6.689 mL of 33% w/v, 27.28 mmol) and stirred at 95° C. for 16 h. The solution was cooled to room temperature, filtered and solid product washed with water (2×) and then ether (2×) and dried under vacuum to give 4,5-dichloro-2-fluoro-N-(2-oxo-1H-pyridin-4-yl)benzamide (250 mg, 61%) as an off white solid. ESI-MS m/z calc. 299.99. found 301.3 (M+1)+; Retention time: 1.16 minutes (3 minutes run).
WORKUP
后处理
- extractionextracted with ethyl acetate (3×)
- washwashed with water (3×), brine
- dry with materialdried over Na2SO4
- filtrationfiltered through a short plug of silica
- customevaporated to dryness
- temperatureThe solution was cooled to room temperature
- filtrationfiltered
- washsolid product washed with water (2×)
- dry with materialether (2×) and dried under vacuum