Prenderol → HCID 53986985, compound

HRID 1170635Notes

Reaction equation

HRID 1170635 reaction equation
[CH2:1]([C:3]([CH2:8][OH:9])([CH2:6][CH3:7])[CH2:4][OH:5])[CH3:2].[CH2:10]([O:17][C:18]([NH:20][C@H:21]([C:25](O)=[O:26])[CH:22]([CH3:24])[CH3:23])=[O:19])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C1(N=C=NC2CCCCC2)CCCCC1>CN(C)C1C=CN=CC=1.ClCCl>[CH2:10]([O:17][C:18]([NH:20][C@H:21]([C:25]([O:5][CH2:4][C:3]([CH2:6][CH3:7])([CH2:1][CH3:2])[CH2:8][OH:9])=[O:26])[CH:22]([CH3:24])[CH3:23])=[O:19])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

6

Procedure

To a cooled solution of 2-ethyl-2-hydroxymethyl-butan-1-ol (33.1 g, 250 mmole), 4-dimethylaminopyridine (1.22 g, 10 mmole) and N-benzyloxycarbonyl-L-valine (12.6 g, 50 mmole) in 350 ml dichloromethane was added dropwise a solution of dicyclohexyl-carbodiimide (12.4 g, 60 mmole) in 50 ml dichloromethane. The mixture was stirred 2 days at room temperature and cooled. The urethane was filtered and the solution evaporated under reduced pressure. 350 ml ethyl acetate was added and the organic phase was washed twice with 5% acetic acid, 5% sodium-hydrogencarbonate and water. The organic phase was dried with sodium sulfat and evaporated under reduced pressure. The product was isolated by silica gel column chromatography with dichloromethane/methanol. Yield: 16.4 g=90%.

Workup

  1. temperaturecooled
  2. filtrationThe urethane was filtered
  3. customthe solution evaporated under reduced pressure
  4. addition350 ml ethyl acetate was added
  5. washthe organic phase was washed twice with 5% acetic acid, 5% sodium-hydrogencarbonate and water
  6. dry with materialThe organic phase was dried with sodium sulfat
  7. customevaporated under reduced pressure
  8. customThe product was isolated by silica gel column chromatography with dichloromethane/methanol

Sources & evidence

ORD record
ord-e99f1d53252e43c5b253f654e0facafb
Source dataset
uspto-grants-2010_11
Patent number
US07825238B2

Reaction notes

Loading…