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HRID 3708作成日:2026年10月23日

Dichloromethane → (2-{2-[(Carboxy-phenyl-methyl)-carbamoyl]phenyldisulfanyl}-benzoylamino)-phenyl-acetic acid

https://huagongshe.com/ja/reaction/3708

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Trifluoroacetic acidHCID 6422—
反応物(2-{2-[(tert-Butoxycarbonyl-phenyl-methyl)carbamoyl]-phenyldisulfanyl}-benzoylamino)phenyl-acetic acid tert-butyl esterHCID 76120819—
溶媒Diethylether hexaneHCID 21584099—
生成物(2-{2-[(Carboxy-phenyl-methyl)-carbamoyl]phenyldisulfanyl}-benzoylamino)-phenyl-acetic acidHCID 46536542.5%

反応手順

This compound was prepared according to the procedure described in Example 50 using [R-(R*,R*)] (2-{2-[(tert-butoxycarbonyl-phenyl-methyl)-carbamoyl]-phenyldisulfanyl}-benzoylamino)-phenyl-acetic acid tert-butyl ester (0.2 g, 0.3 mmol) from Example 38, 10 mL dichloromethane, and 10 mL trifluoroacetic acid. The crude product was stirred with ether/hexane and filtered to afford 73.0 mg of the title compound, mp 231°-232° 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-90c1ac43b2814299a03384dc402e2956
出典メモuspto-grants-1998_03