HRID419208

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID16414246

6-Fluoropyridine-3-carbaldehyde

C6H4FNO

结构：COCN(c1cc(Cl)cnc1Br)S(=O)(=O)c1ccc(C(C)(C)C)cc1

HCID57942088

未命名化合物

PRODUCTS

生成物

结构：COCN(c1cc(Cl)cnc1C(=O)c1ccc(F)nc1)S(=O)(=O)c1ccc(C(C)(C)C)cc1

HCID57942563

未命名化合物

收率 38%

PROCEDURE

实验过程

4-tert-Butyl —N-[5-chloro-2-(6-fluoro-pyridine-3-carbonyl)-pyridin-3-yl]-N-methoxymethyl-benzenesulfonamide was prepared from N-(2-bromo-5-chloro-pyridin-3-yl)-4-tert-butyl-N-methoxymethyl-benzenesulfonamide and 6-fluoro-pyridine-3-carbaldehyde using the procedure described in examples 35 and 36.