Gabapentin → Boc-Tyr Gabapentin

HRID 28766

반응식

HRID 28766 반응식
[NH:1]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[C@H:2]([C:11]([OH:13])=[O:12])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.ONC(=O)CCC(N)=O.[CH2:30]1[CH2:35][CH2:34][C:33]([CH2:40][NH2:41])([CH2:36][C:37]([OH:39])=[O:38])[CH2:32][CH2:31]1.[OH-].[Na+]>C(#N)C>[NH:1]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[C@H:2]([C:11]([OH:13])=[O:12])[CH2:3][C:4]1[CH:5]=[CH:6][C:7]([OH:10])=[CH:8][CH:9]=1.[CH2:30]1[CH2:31][CH2:32][C:33]([CH2:40][NH2:41])([CH2:36][C:37]([OH:39])=[O:38])[CH2:34][CH2:35]1

참가 물질

6

실험 절차

To a solution of Boc-Tyr-OH (4.2 g, 15 mmol) in acetonitrile (100 mL) was added N-hydroxysuccinamide (1.84 g, 16 mmol) and N,N-dicyclohexylcarbodiimide (3.3 g, 16 mmol). The reaction was stirred at ambient temperature for 2 h. The reaction mixture was filtered directly into an aqueous solution (100 mL) of gabapentin (2.7 g, 16 mmol) and sodium hydroxide (640 mg, 16 mmol), and the resulting mixture stirred at ambient temperature for 16 h. The reaction was concentrated under reduced pressure, the residue was dissolved in ethyl acetate/diethyl ether (1/1, 200 mL) and washed with 0.1M aqueous potassium hydrogensulfate (2×200 mL). The organic phase was separated, dried over Na2SO4, filtered, and concentrated to dryness under reduced pressure to afford Boc-Tyr-Gabapentin as a white solid (7.4 g, 16 mmol).

후처리

  1. stirringthe resulting mixture stirred at ambient temperature for 16 h
  2. concentrationThe reaction was concentrated under reduced pressure
  3. dissolutionthe residue was dissolved in ethyl acetate/diethyl ether (1/1, 200 mL)
  4. washwashed with 0.1M aqueous potassium hydrogensulfate (2×200 mL)
  5. customThe organic phase was separated
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-d195102459e34c60aa3bc9d223c309ab
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07420002B2

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