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HRID 3742作成日:2026年10月25日

2-Mercaptobenzoic Acid → 2-[2-(4-Sulfamoylphenylcarbamoyl)phenyldisulfanyl]benzoic acid

https://huagongshe.com/reaction/3742

反応式

関与物質

役割名称HCID仕込み量
反応物2-Mercaptobenzoic AcidHCID 5443—
反応物4-(3-Oxo-1,2-benzothiazol-2-yl)benzenesulfonamideHCID 462938—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物2-[2-(4-Sulfamoylphenylcarbamoyl)phenyldisulfanyl]benzoic acidHCID 1076639595.5%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05734081
出典データセットuspto-grants-1998_03
ORD IDord-40ccfc0f214f4effb36ca78515638c20
出典メモuspto-grants-1998_03