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HRID 3743作成日:2026年10月24日

Benzoic acid, 2-mercapto-, methyl ester → Methyl 2-[[2-[(4-sulfamoylphenyl)carbamoyl]phenyl]disulfanyl]benzoate

https://huagongshe.com/ja/reaction/3743

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoic acid, 2-mercapto-, methyl esterHCID 21009—
反応物4-(3-Oxo-1,2-benzothiazol-2-yl)benzenesulfonamideHCID 462938—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-[[2-[(4-sulfamoylphenyl)carbamoyl]phenyl]disulfanyl]benzoateHCID 648356092.7%

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 0.27 g (1.6 mmol) of methyl thiosalicylate. The product was triturated with ether, filtered, washed with ether and dried in vacuo to give 0.66 g of the title compound, mp 288°-290° 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-52d9d3961073476a8fa59d53b9462e89
出典メモuspto-grants-1998_03