(+/-)-tert-butyl (1R,5S,6S)-6-ethoxy-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enylcarbamate → Carbamate
反応式
[CH2:1]([O:3][C@@H:4]1[C@H:9]([NH:10][C:11](=[O:17])[O:12][C:13]([CH3:16])([CH3:15])[CH3:14])[CH:8]=[C:7]([C:18]2[CH:23]=[CH:22][N:21]=[CH:20][C:19]=2[N+:24]([O-])=O)[CH2:6][C@@H:5]1[CH3:27])[CH3:2]>CCCCCCC.CCO>[C:11](=[O:12])([O-:17])[NH2:10].[NH2:24][C:19]1[CH:20]=[N:21][CH:22]=[CH:23][C:18]=1[C@H:7]1[CH2:8][C@@H:9]([NH:10][C:11](=[O:17])[O:12][C:13]([CH3:14])([CH3:15])[CH3:16])[C@@H:4]([O:3][CH2:1][CH3:2])[C@@H:5]([CH3:27])[CH2:6]1参加物
4
実験手順
Method 6 was followed using (+/−)-tert-butyl (1R,5S,6S)-6-ethoxy-5-methyl-3-(3-nitropyridin-4-yl)cyclohex-2-enylcarbamate with Chiral HPLC (Heptane/EtOH=90/10, 20 mL/min, IC column) to yield tert-butyl a 1S,2R,3R,5S)-5-(3-aminopyridin-4-yl)-2-ethoxy-3-methylcyclohexyl)carbamate (33% yield, 99% ee) and tert-butyl ((1R,2S,3S,5R)-5-(3-aminopyridin-4-yl)-2-ethoxy-3-methylcyclohexyl)carbamate (28% yield, 99% ee). LC/MS (m/z)=350.2 (MH+), Rt=0.72 min.
出典と根拠
- ORDレコード
- ord-a957c749a95e4938be968835861bda11
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09173883B2
反応ノート
読み込み中…