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HRID 430802作成日:2026年10月26日

Tert-Butylamine → (S)-[2-[(1,1-dimethylethyl)amino]-2-oxo-1-(phenylmethyl)ethyl]-carbamic acid 1,1-dimethylethyl ester

https://huagongshe.com/reaction/430802

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-ButylamineHCID 6385—
反応物DiisopropylethylamineHCID 81531—
反応物O-benzyl-N-((tert-butoxy)carbonyl)-L-tyrosineHCID 98763—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物(S)-[2-[(1,1-dimethylethyl)amino]-2-oxo-1-(phenylmethyl)ethyl]-carbamic acid 1,1-dimethylethyl esterHCID 11809380153.7%

反応条件

温度0 °C

反応手順

A solution of N-(tert-Butyloxycarbonyl)-O-benzyl-L-tyrosine (Bachem, 2.00 g, 5.38 mmol) in 20 mL of DMF was cooled to 0° C. and treated with i-Pr2NEt (1.5 mL, Aldrich, Milwaukee, Wis.) followed by O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluoro-phosphate (2.04 g, 5.38 mmol, Novabiochem, La Jolla, Calif.). The resulting suspension was stirred for 30 minutes at 0° C. and then treated with tert-butylamine (0.48 g, 6.56 mmol, Aldrich, Milwaukee, Wis.). The reaction mixture was stirred for 1 hour at 0° C. and warmed to room temperature. The reaction mixture was then poured into Et2O, and washed sequentially with saturated aqueous NaHCO3 solution and saturated aqueous NaCl solution. The organic phase was dried over MgSO4, filtered, and concentrated. The crude residue was purified by chromatography (silica gel, 3:1 heptane/ethyl acetate) to give (S)-[2-[(1,1-dimethylethyl)amino]-2-oxo-1-(phenylmethyl)ethyl]-carbamic acid 1,1-dimethylethyl ester (2.65 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06323243B1
出典データセットuspto-grants-2001_11
ORD IDord-ffb257c994604a6284a9c938c8f41e60
出典メモuspto-grants-2001_11