Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
(2S)-2-amino-3-(tert-butoxy)propanoic acid → O-(tert-Butyl)-N-{[(2,2-dimethylhex-5-en-1-yl)oxy]carbonyl}-L-serine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | (2S)-2-amino-3-(tert-butoxy)propanoic acid | HCID 7004940 | — |
| 반응물 | 2,2-Dimethylhex-5-en-1-ol | HCID 10240821 | — |
| 반응물 | 3-Methyl-N-{[(pent-4-en-1-yl)oxy]carbonyl}-L-valine | HCID 45379928 | — |
| 생성물 | O-(tert-Butyl)-N-{[(2,2-dimethylhex-5-en-1-yl)oxy]carbonyl}-L-serine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08216999B2 |
| 출처 데이터셋 | uspto-grants-2012_07 |
| ORD ID | ord-929d101e350f4956a8cebb479ca48c55 |
| 출처 메모 | uspto-grants-2012_07 |