Sodium Carbonate → (3R,4S)-4-[4-(2-Methoxypyridin-3-yl)phenoxy]-1-pyridin-3-yl-pentan-3-ol

HRID 1856700노트

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HRID 1856700 반응식
C(=O)([O-])[O-].[Na+].[Na+].[OH:7][C@H:8]([CH2:21][CH2:22][C:23]1[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=1)[C@H:9]([CH3:20])[O:10][C:11]1[CH:16]=[CH:15][C:14](B(O)O)=[CH:13][CH:12]=1.I[C:30]1[C:31]([O:36][CH3:37])=[N:32][CH:33]=[CH:34][CH:35]=1>C(O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:37][O:36][C:31]1[C:30]([C:14]2[CH:15]=[CH:16][C:11]([O:10][C@@H:9]([CH3:20])[C@H:8]([OH:7])[CH2:21][CH2:22][C:23]3[CH:24]=[N:25][CH:26]=[CH:27][CH:28]=3)=[CH:12][CH:13]=2)=[CH:35][CH:34]=[CH:33][N:32]=1

참가 물질

6

실험 절차

Prepared according to the method described in Example 21b) from 2M aqueous sodium carbonate (2.0 ml), (1S,2R)-4-(2-hydroxy-1-methyl-4-pyridin-3-ylbutoxy)benzeneboronic acid (Example 21a), 0.508 g), 3-iodo-2-methoxypyridine (0.730 g, J. Org. Chem., 1988 53(12), 2740), and tetrakis(triphenylphosphine)palladium(0) (0.216 g) in ethanol (10 ml). The mixture was heated at reflux for 6 hours. After cooling to room temperature the mixture was concentrated under reduced pressure. The residue was purified by column chromatography over silica eluting with ethyl acetate to give an oil, which was further purified by normal phase HPLC eluting with 2-propanol:dichloromethane (3:97) to give the title compound as an oil.

후처리

  1. customPrepared
  2. temperatureThe mixture was heated
  3. temperatureat reflux for 6 hours
  4. concentrationwas concentrated under reduced pressure
  5. customThe residue was purified by column chromatography over silica eluting with ethyl acetate
  6. customto give an oil, which
  7. customwas further purified by normal phase HPLC
  8. washeluting with 2-propanol:dichloromethane (3:97)

출처 및 근거

ORD 기록
ord-13ac3cea18514ce4bbe87e682f2d81c3
출처 데이터셋
uspto-grants-2000_11
특허 번호
US06143751

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