HRID2414317

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(C)NS(=O)(=O)c1ccc(Cl)c([N+](=O)[O-])c1

HCID66780

Benzenesulfonamide, 4-chloro-N-(1-methylethyl)-3-nitro-

C9H11ClN2O4S

HCID22063089

1-(Piperidin-4-yl)-1,4-dihydro-2H-3,1-benzoxazin-2-one--hydrogen chloride (1/1)

C13H17ClN2O2

PRODUCTS

生成物

结构：CC(C)NS(=O)(=O)c1ccc(N2CCC(N3C(=O)OCc4ccccc43)CC2)c([N+](=O)[O-])c1

HCID22644650

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from the product of step (i) (0.14 g) and 1-piperidin-4-yl-1,4-dihydro-2H-3,1-benzoxazin-2-one hydrochloride (0.1 g) using the method of example 115 step (ii). Yield 0.037 g.