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HRID1358341

反应详情

EQUATION

反应方程式

HRID 1358341 的结构方程式

REACTANTS

反应物

2
结构：COc1ccccc1Oc1c(Cl)nc(C2CC2)nc1Cl
HCID21979562

未命名化合物

结构：CC(C)(C)c1ccc(S(N)(=O)=O)cc1.[K]
HCID66748434

未命名化合物

PRODUCTS

生成物

1
结构：COc1ccccc1Oc1c(Cl)nc(C2CC2)nc1NS(=O)(=O)c1ccc(C(C)(C)C)cc1
HCID18184267

未命名化合物

PROCEDURE

实验过程

According to the procedure described in Example 1g) 3.3 g 4,6-dichloro-2-cyclopropyl-5-(o-methoxyphenoxy)-pyrimidine (prepared according to procedures described in Example 1) was reacted with 4-tert.-butylphenylsulfonamide potassium salt to give 4.22 g 4-tert.-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-cyclopropyl-pyrimidin-4-yl]-benzene-sulfonamide. LC-MS: tR=6.24 min, [M+1]+=488.23.