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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430802생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/430802

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참여 물질

역할이름HCID투입량
반응물Tert-ButylamineHCID 6385—
반응물DiisopropylethylamineHCID 81531—
반응물O-benzyl-N-((tert-butoxy)carbonyl)-L-tyrosineHCID 98763—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물(S)-[2-[(1,1-dimethylethyl)amino]-2-oxo-1-(phenylmethyl)ethyl]-carbamic acid 1,1-dimethylethyl esterHCID 11809380153.7%

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06323243B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-ffb257c994604a6284a9c938c8f41e60
출처 메모uspto-grants-2001_11