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HRID 1511583생성일: 2026년 10월 25일

(2S)-2-amino-3-(tert-butoxy)propanoic acid → O-(tert-Butyl)-N-{[(2,2-dimethylhex-5-en-1-yl)oxy]carbonyl}-L-serine

https://huagongshe.com/reaction/1511583

반응식

참여 물질

역할이름HCID투입량
반응물(2S)-2-amino-3-(tert-butoxy)propanoic acidHCID 7004940—
반응물2,2-Dimethylhex-5-en-1-olHCID 10240821—
반응물3-Methyl-N-{[(pent-4-en-1-yl)oxy]carbonyl}-L-valineHCID 45379928—
생성물O-(tert-Butyl)-N-{[(2,2-dimethylhex-5-en-1-yl)oxy]carbonyl}-L-serineHCID 45379614—

반응 단계

O-(tert-Butyl)-N-{[(2,2-dimethylhex-5-en-1-yl)oxy]carbonyl}-L-serine was prepared according to the procedure for 3-methyl-N-[(pent-4-enyloxy)carbonyl]-L-valine using O-(tert-butyl)-L-serine and 2,2-dimethylhex-5-en-1-ol. 1H NMR (500 MHz, CDCl3, ppm) δ 5.75-5.86 (m, 1H), 4.90-5.04 (m, 2H), 4.02 (m, 1H), 3.57-3.90 (m, 4H), 1.98-2.05 (m, 2H), 1.27-1.36 (m, 2H), 1.14 (s, 9H), 1.01 (d, J=6.5 Hz, 1H), and 6.09 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08216999B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-929d101e350f4956a8cebb479ca48c55
출처 메모uspto-grants-2012_07