Ozone → 6-methoxy-piperazine-1,2,4-tricarboxylic Acid 4-benzyl Ester 1-tert-butyl Ester 2-methyl Ester

HRID 722719노트

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HRID 722719 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

5

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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

  1. customThe solution is purged with N2
  2. customto remove excess ozone
  3. additionis then treated with excess dimethylsulfide
  4. temperatureto warm to rt overnight
  5. concentrationthe next morning concentrated in vacuo
  6. customThe crude residue obtained
  7. additiontreated with Dowex50x-200
  8. filtrationthe solution was filtered
  9. concentrationconcentrated
  10. 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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