反应 #3838

ord-40ccfc0f214f4effb36ca78515638c20

反应方程式

NS(=O)(=O)c1ccc(-n2sc3ccccc3c2=O)cc1
4-(3-oxo-3H-benzo[d]isothiazol-2-yl)benzene sulfonamide
O=C(O)c1ccccc1S
thiosalicylic acid
NS(=O)(=O)c1ccc(NC(=O)c2ccccc2SSc2ccccc2C(=O)O)cc1
title compound
收率 95.5%
NS(=O)(=O)c1ccc(NC(=O)c2ccccc2SSc2ccccc2C(=O)O)cc1
2-[2-(4-Sulfamoylphenylcarbamoyl)phenyldisulfanyl]benzoic acid
收率 95.5%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他This compound was prepared
  2. 2
    洗涤The product was washed with ether
  3. 3
    其他dried in vacuo

实验过程

This compound was prepared according to the method of Example 132 using a suspension of 0.46 g (1.5 mmol) of 4-(3-oxo-3H-benzo[d]isothiazol-2-yl)benzene sulfonamide in a mixture of 15 mL of methanol and 15 mL of tetrahydrofuran, and 0.23 g (1.5 mmol) of thiosalicylic acid. The product was washed with ether and dried in vacuo to give 0.66 g of the title compound, mp 276°-278° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05734081uspto-grants-1998_03