Cesium carbonate → 1-(tert-Butyl) 2-methyl (2S,4R)-4-((3-chloro-7-methoxyquinoxalin-2-yl)oxy)pyrrolidine-1,2-dicarboxylate

HRID 659826노트

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HRID 659826 반응식
[Cl:1][C:2]1[C:3](O)=[N:4][C:5]2[C:10]([N:11]=1)=[CH:9][C:8](OC)=[CH:7][CH:6]=2.[C:15]([O-:18])([O-])=O.[Cs+].[Cs+].BrC1C=CC(S([O:31][C@@H:32]2[CH2:36][N:35]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])[C@H:34]([C:44]([O:46][CH3:47])=[O:45])[CH2:33]2)(=O)=O)=CC=1>CN1C(=O)CCC1.O.CCOC(C)=O>[Cl:1][C:2]1[C:3]([O:31][C@H:32]2[CH2:36][N:35]([C:37]([O:39][C:40]([CH3:41])([CH3:42])[CH3:43])=[O:38])[C@H:34]([C:44]([O:46][CH3:47])=[O:45])[CH2:33]2)=[N:4][C:5]2[C:10]([N:11]=1)=[CH:9][CH:8]=[C:7]([O:18][CH3:15])[CH:6]=2

참가 물질

7

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온도
50 °C

실험 절차

A solution (0.35 M) of 3-chloro-6-methoxyquinoxalin-2-ol in NMP was treated with Cs2CO3 (1.5 eq) and 1-tert-butyl 2-methyl (2S,4S)-4-{[(4-bromophenyl)sulfonyl]oxy}pyrrolidine-1,2-dicarboxylate (1.1 eq). The resulting mixture was stirred at 50° C. for 18 h, then a further portion (0.1 eq) of 1-tert-butyl 2-methyl (25,45)-4-{[(4-bromophenyl)sulfonyl]oxy}pyrrolidine-1,2-dicarboxylate was added. After stirring for 2 h, the mixture was cooled and diluted with H2O and EtOAc. The organic phases were washed with aqueous HCl (1 N), saturated aqueous NaHCO3 and brine. The dried organic phase was concentrated to a residue that was purified by flash-chromatography (0-60% EtOAc/petroleum ether) to give the title compound (35% for two steps) as a solid. MS (ES+) m/z 438 (M+H)+

후처리

  1. stirringAfter stirring for 2 h
  2. temperaturethe mixture was cooled
  3. washThe organic phases were washed with aqueous HCl (1 N), saturated aqueous NaHCO3 and brine
  4. concentrationThe dried organic phase was concentrated to a residue that
  5. customwas purified by flash-chromatography (0-60% EtOAc/petroleum ether)

출처 및 근거

ORD 기록
ord-a987acc13f214100b871d93ff6a1ebed
출처 데이터셋
uspto-grants-2011_12
특허 번호
US08080654B2

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