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HRID 3719作成日:2026年10月24日

4-Fluoroaniline → N-(4-fluorophenyl)-2-[[2-[(4-fluorophenyl)carbamoyl]phenyl]disulfanyl]benzamide

https://huagongshe.com/ja/reaction/3719

反応式

関与物質

役割名称HCID仕込み量
反応物4-FluoroanilineHCID 9731—
反応物2,2'-Dithiodibenzoyl chlorideHCID 88164—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物N-(4-fluorophenyl)-2-[[2-[(4-fluorophenyl)carbamoyl]phenyl]disulfanyl]benzamideHCID 4653379.7%

反応手順

This compound was prepared according to the general method of Example 77 using 2,2'-dithiobisbenzoyl chloride (1.00 g, 2.92 mmol) in 20 mL of dichloromethane and 4-fluoroaniline (0.657 g, 5.91 mmol) in 5 mL of pyridine. The crude product was triturated with hot ethanol-ethyl acetate mixture, filtered, and recrystallized from ethanol-DMF to yield 0.14 g of the title compound, mp 242°-244° 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-1e404142def44ea88cbeeff7e6caace1
出典メモuspto-grants-1998_03