Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- → 1,1-Dimethylethyl N-((1S)-2-(methoxymethylamino)-2-oxo-1-(phenylmethyl)ethyl)carbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- | HCID 77857 | — |
| 반응물 | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| 생성물 | 1,1-Dimethylethyl N-((1S)-2-(methoxymethylamino)-2-oxo-1-(phenylmethyl)ethyl)carbamate | HCID 11055945 | 8,042.2% |
반응 단계
The title compound was synthesized from tert-butyloxycarbonyl-L-phenylalanine (2.65 g, 0.1 mmol) and N,O-dimethylhydroxylamine hydrochloride (1.07 g, 11 mmol) according to the procedure given for 1. The synthesis yielded compound 5 as an oil (2.48 g, 81%): Rf 0.40 (ethyl acetate/hexane, 1:1), Rf 0.78 (chloroform/methanol/acetic acid, 85:10:5); 1H-NMR (CDCl3, 17° C.)δ 1.38 (9H, s, C(CH3)3, 3.05 (2H, m, CH2), 3.18 (3H, s, N--CH3),3.66 (3 H, s, O--CH3), 4.97 (1H, m, CH), 5.18 (1H, d (br.),NH), 7.17-7.28 (5H, m, C6H5).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05616605 |
| 출처 데이터셋 | uspto-grants-1997_04 |
| ORD ID | ord-c99631c59dbc425dab03627caac5bade |
| 출처 메모 | uspto-grants-1997_04 |