4-Methylmorpholine → Boc-Leu-Glu-OtBu

HRID 32338

반응식

HRID 32338 반응식
[NH:1]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[C@H:2]([C:7]([O:9]N1C(=O)CCC1=O)=O)[CH2:3][CH:4]([CH3:6])[CH3:5].[NH2:24][C@H:25]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[CH2:26][CH2:27][C:28](=[O:30])[OH:29].CN1CCOCC1>CN(C=O)C.CN(C1C=CN=CC=1)C>[NH:1]([C:17]([O:19][C:20]([CH3:21])([CH3:22])[CH3:23])=[O:18])[C@H:2]([C:7]([NH:24][C@H:25]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[CH2:26][CH2:27][C:28](=[O:29])[OH:30])=[O:9])[CH2:3][CH:4]([CH3:5])[CH3:6]

참가 물질

6

실험 절차

To a solution of Boc-Leu-OSu and Glu-OtBu in DMF was added NMM and DMAP. The solution was stirred at ambient temperatures for 18 hours then the solvent was removed. Crude product was taken up in 100 ml CHCl3, washed 3× with pH 3 water (100 ml), once with water (100 ml) and once with brine (100 ml). Organic layer was dried with MgSO4 and filtered. Solvent was removed and solid was dried over vacuum. Solid was collected as a white powder (8.78 g, quant. yield, ˜80% purity TLC). Product was used directly without further characterization.

후처리

  1. customthe solvent was removed
  2. washwashed 3× with pH 3 water (100 ml)
  3. dry with materialOrganic layer was dried with MgSO4
  4. filtrationfiltered
  5. customSolvent was removed
  6. customsolid was dried over vacuum
  7. customSolid was collected as a white powder (8.78 g, quant. yield, ˜80% purity TLC)

출처 및 근거

ORD 기록
ord-a4465bcbca00476b927678186da410d5
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07427600B2

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