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HRID 223103作成日:2026年10月26日

Trifluoroacetic acid → L-Phenylalanyl-L-alanine

https://huagongshe.com/reaction/223103

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1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-oneHCID 13035214—
触媒PalladiumHCID 23938—
生成物Trifluoroacetic acidHCID 6422—
生成物L-Phenylalanyl-L-alanineHCID 548819694%

反応手順

After 1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-one (300 mg., 0.95 mmol) was stirred in trifluoroacetic acid (2 ml.) at room temperature for 15 hours, the solvent was removed by distillation under reduced pressure. The thus obtained oil (360 mg.) was hydrogenated in 25 ml. of ethanol at 50° C. for 15 hours under ambient pressure using a 10% Pd-C (300 mg.) as a catalyst to give trifluoroacetic acid salt of L-phenylalanyl-L-alanine (311 mg., yield: 94%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04352752
出典データセットuspto-grants-1982_10
ORD IDord-8446506b615d4f04850806817179a906
出典メモuspto-grants-1982_10