HRID1064450
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
N-(5-fluoro-2-nitrophenyl)benzenesulfonamide (2×0.50 g, 1.688 mmol) was treated with N-methyl-piperazine (2×4.65 g, 45.6 mmol) and put in two pyrex tubes and sealed. Each tube was put in a LabWell MW-10 microwave oven for 2 min at 50 W. The reaction mixtures were combined and poured into 0.5 M NaOH (aq) and extracted with CH2Cl2, dried (MgSO4) and concentrated to give 0.99 g, (2.63 mmol) in 78% yield as a yellow solid. Anal (C17 H20 N4 O4 S) C, H, N, S; MS (posES-FIA) m/z=found: 377.4. Calcd: 376.12.
WORKUP
后处理
- customsealed
- customThe reaction mixtures
- extractionextracted with CH2Cl2
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customto give 0.99 g, (2.63 mmol) in 78% yield as a yellow solid