Ozone → 6-methoxy-piperazine-1,2,4-tricarboxylic Acid 4-benzyl Ester 1-tert-butyl Ester 2-methyl Ester
반응식
[CH3:1][O:2][C:3](=[O:28])[C@@H:4]([NH:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:5][N:6]([CH2:17][CH:18]=C)[C:7]([O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:8].O=[O+][O-].C(Cl)Cl.[CH3:35][OH:36]>CO>[CH3:1][O:2][C:3]([CH:4]1[CH2:5][N:6]([C:7]([O:9][CH2:10][C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)=[O:8])[CH2:17][CH:18]([O:36][CH3:35])[N:20]1[C:21]([O:23][C:24]([CH3:27])([CH3:25])[CH3:26])=[O:22])=[O:28]참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
A solution containing 3-(allylbenzyloxycarbonylamino)-2-(S)-tert-butoxycarbonylamino propionic acid methyl ester (5.2 g, 12.8 mmol) in 550 mL of 10:1 CH2Cl2/MeOH is cooled to −78° C. Ozone gas is passed through the solution until a blue color persists. The solution is purged with N2 to remove excess ozone and is then treated with excess dimethylsulfide. The solution is allowed to warm to rt overnight and the next morning concentrated in vacuo. The crude residue obtained is re-dissolved in MeOH and treated with Dowex50x-200. After stirring for 4 h, the solution was filtered, concentrated and immediately purified by flash chromatography on silica gel (EtOAc/hexane) to afford 2.75 g (53% yield) of the desired product. 1H NMR (CDCl3) δ 7.40 (m, 5H), 5.60–3.40 (series of m, 6H), 5.19 (br s, 2H), 3.74 (s, 3H), 3.40 (series of s, 3H), 1.50 (series of s, 9H); MS 409 (M+H)+.
후처리
- customThe solution is purged with N2
- customto remove excess ozone
- additionis then treated with excess dimethylsulfide
- temperatureto warm to rt overnight
- concentrationthe next morning concentrated in vacuo
- customThe crude residue obtained
- additiontreated with Dowex50x-200
- filtrationthe solution was filtered
- concentrationconcentrated
- customimmediately purified by flash chromatography on silica gel (EtOAc/hexane)
출처 및 근거
- ORD 기록
- ord-3d97566faee64db5a5edfc000fb2d3d9
- 출처 데이터셋
- uspto-grants-2006_11
- 특허 번호
- US07138395B2
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