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HRID 2374719作成日:2026年10月27日

Hydrochloric Acid → 4-[2-(2-Chlorobenzoylamino)benzoylamino]butanoic acid

https://huagongshe.com/reaction/2374719

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物ChlorotrimethylsilaneHCID 6397—
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物2-Chlorobenzoyl chlorideHCID 69110—
反応物4-(2-Aminobenzamido)butanoic acidHCID 13442375—
溶媒DichloromethaneHCID 6344—
生成物4-[2-(2-Chlorobenzoylamino)benzoylamino]butanoic acidHCID 23118564—

反応手順

To a suspension of 2.00 g (9.01 mmol) of 4-(2-aminobenzoylamino)butanoic acid in 20 mL of dry methylene chloride, add 8.36 g (77.00 mmol) of trimethylsilyl chloride and allow the reaction to reflux for 5 hours. Then place the flask in an ice bath and add 1.17 g (11.55 mmol) of triethylamine and a solution of 1.35 g (7.70 mmol) of 2-chlorobenzoyl chloride dissolved in 5 mL of dry methylene chloride. Allow the reaction to stir for 30 minutes in an ice bath and 24 hours at room temperature. Eliminate the solvent at low pressure, add 30 ml of 10% NaOH to the crude product and continue stirring the mixture until the oil has completely disappeared. Immediately acidify with concentrated HCl and extract several times with ethyl acetate. Dry the organic phase with MgSO4 anhydrous and eliminate at low pressure. Wash the crude product several times with ether and finally, purify by recrystallization (EtOH/H2O). This yields 1.27 g (36%) of 4-[2-(2-chlorobenzoylamino)benzoylamino]butanoic acid as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07462735B2
出典データセットuspto-grants-2008_12
ORD IDord-deb66748c80c4cb08482d6a424814c9e
出典メモuspto-grants-2008_12