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HRID 70865作成日:2026年10月24日

Trifluoroacetic acid → (R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl ester

https://huagongshe.com/ja/reaction/70865

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Succinic anhydrideHCID 7922—
反応物(R)-ethyl 4-(biphenyl-4-yl)-3-(tert-butoxycarbonylamino)butanoateHCID 59607632—
溶媒DichloromethaneHCID 6344—
生成物(R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl esterHCID 4982222350.2%

反応手順

To a solution of (R)-4-biphenyl-4-yl-3-tert-butoxycarbonylamino-butyric acid ethyl ester (400 mg, 1.04 mmol) in DCM (10 mL) at room temperature is added TFA (2.009 mL, 26.1 mmol) and the mixture is stirred at room temperature for 1 hour. The mixture is concentrated under reduced pressure. To the obtained TFA salt in DCM (10 mL) at ice bath temperature is added succinic anhydride (125 mg, 1.25 mmol) and followed by TEA (0.363 mL, 2.61 mmol). The reaction is stirred at room temperature for 16 hours. The mixture is concentrated under reduced pressure. The obtained residue is purified by flash chromatography (silica gel, 2% to 5% EtOH/DCM) give (R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl ester (200 mg). HPLC retention time=1.53 minutes (condition C); MS=384 (m+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822534B2
出典データセットuspto-grants-2014_09
ORD IDord-d1bb9c9294a7440fa0cfad366f1f6fab
出典メモuspto-grants-2014_09