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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429125생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/429125

반응식

참여 물질

역할이름HCID투입량
반응물Tert-ButylamineHCID 6385—
반응물O-benzyl-N-((tert-butoxy)carbonyl)-L-tyrosineHCID 98763—
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 iPr NEt (1.5 mL) followed by O-benzotriazol-1-yl-N,N,N′,N′-bis(tetramethylene)-uronium 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). The reaction mixture was stirred for 1 hour at 0° C. and warmed to room temperature. The reaction mixture was poured into Et O and washed sequentially with saturated aqueous NaHCO3 solution, and saturated aqueous NaCl solution. The organic phase was dried (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 번호US06316440B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-98330b56fc844dfb816bef8d687b4095
출처 메모uspto-grants-2001_11