Ethanol → (S)-2-hydroxy-1-(piperazin-1-yl)propan-1-one oxalate

HRID 341318노트

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HRID 341318 반응식
C(O)C.C([N:11]1[CH2:16][CH2:15][N:14]([C:17](=[O:21])[C@@H:18]([OH:20])[CH3:19])[CH2:13][CH2:12]1)C1C=CC=CC=1.C1CCCCC=1.O.O.[C:30]([OH:35])(=[O:34])[C:31]([OH:33])=[O:32]>O1CCCC1.[Pd]>[C:30]([OH:35])(=[O:34])[C:31]([OH:33])=[O:32].[OH:20][C@@H:18]([CH3:19])[C:17]([N:14]1[CH2:13][CH2:12][NH:11][CH2:16][CH2:15]1)=[O:21]

참가 물질

7

실험 절차

Ethanol (350 kg), Palladium (10% on activated carbon) (8.40 kg, 7.89 mol) and (S)-1-(4-benzylpiperazin-1-yl)-2-hydroxypropan-1-one 5 (70.0 kg, 282 mol) were charged to a reactor and the mixture was purged with nitrogen and heated to reflux. Cyclohexene (70.0 kg, 852 mol) was slowly added. The reaction mixture was heated to reflux and stirred for 24 h. After cooling to ambient temperature, the mixture was filtered through a pad of CELITE® and the cake was washed with ethanol (20 kg). The filtrate was cooled to 10-15° C. and a solution of oxalic acid dihydrate (36.0 kg, 286 mol) in tetrahydrofuran (156 kg) was slowly added at a rate to maintain the reaction temperature at 10-20° C. After aging for 2 h, the solid was collected by filtration, washed with ethanol (100 kg) and dried under reduced pressure at 50-55° C. to afford (S)-2-hydroxy-1-(piperazin-1-yl)propan-1-one oxalate salt V (58.2 kg, 83%). 1H NMR (300 MHz, D2O) δ 4.73-4.51 (m, 1H), 3.93-3.59 (m, 4H), 3.26 (dd, J=8.8, 4.0 Hz, 4H), 1.27 (d, J=6.7 Hz, 3H).

후처리

  1. customthe mixture was purged with nitrogen
  2. temperatureheated to reflux
  3. temperatureThe reaction mixture was heated
  4. temperatureto reflux
  5. filtrationthe mixture was filtered through a pad of CELITE®
  6. washthe cake was washed with ethanol (20 kg)
  7. temperatureThe filtrate was cooled to 10-15° C.
  8. temperatureto maintain the reaction temperature at 10-20° C
  9. waitAfter aging for 2 h
  10. filtrationthe solid was collected by filtration
  11. washwashed with ethanol (100 kg)
  12. customdried under reduced pressure at 50-55° C.

출처 및 근거

ORD 기록
ord-523f24f22b6840bfb40c109c6cdf7ac9
출처 데이터셋
uspto-grants-2014_11
특허 번호
US08895729B2

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