Water → HCID 68997756, compound

HRID 750078Notes

Reaction equation

HRID 750078 reaction equation
[C:1]([N:8]1[CH2:14][CH2:13][CH2:12][C@H:9]1[CH2:10][OH:11])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[H-].[Na+].CCO[C:20]([CH3:22])=[O:21].O.[CH3:24][N:25]([CH:27]=O)C>>[C:4]([O:3][C:1]([N:8]1[CH2:14][CH2:13][CH2:12][C@H:9]1[CH2:10][O:11][C:24]1[CH:6]=[CH:4][C:5]([C:20](=[O:21])[C:22]2[CH:14]=[CH:13][CH:12]=[CH:9][CH:10]=2)=[CH:27][N:25]=1)=[O:2])([CH3:7])([CH3:6])[CH3:5]

Participants

6

Procedure

To a solution of N—BOC-L-prolinol (500 mg, 3.25 mmol) in anhydrous DMF (7 ml) was added NaH (124 mg, 60% dispersion in oil, 3.1 mmol) and stirred for 15 min at rt. A solution of product from Example 140, step 2 (364 mg, 1.68 mmol) in anhy.DMF (5 ml) was added dropwise over 5 min. The mixture was stirred at rt for 48 h. The mixture was poured into EtOAc and water, the organic layer dried over MgSO4, and concentrated. Silica gel flash chromatography using EtOAc/hexanes gave the title compound (185 mg, 29%).

Workup

  1. stirringThe mixture was stirred at rt for 48 h
  2. dry with materialthe organic layer dried over MgSO4
  3. concentrationconcentrated

Sources & evidence

ORD record
ord-02aff264080f4a049e190ea5c3d7b4ad
Source dataset
uspto-grants-2008_07
Patent number
US07402684B2

Reaction notes

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