Phosphate → HCID 19352637, compound

HRID 725678Notes

Reaction equation

HRID 725678 reaction equation
[CH2:1]([O:9][C:10]1[CH:11]=[N:12][C:13]([C:16]2[CH:21]=[CH:20][C:19](/[CH:22]=[CH:23]/[CH2:24][CH2:25][CH2:26][CH:27]([O:29][C:30](=[O:32])[CH3:31])[CH3:28])=[CH:18][CH:17]=2)=[N:14][CH:15]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].P([O-])([O-])([O-])=O>C(Cl)(Cl)Cl>[CH2:1]([O:9][C:10]1[CH:15]=[N:14][C:13]([C:16]2[CH:17]=[CH:18][C:19](/[CH:22]=[CH:23]/[CH2:24][CH2:25][CH2:26][CH:27]([OH:29])[CH3:28])=[CH:20][CH:21]=2)=[N:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH2:1]([O:9][C:10]1[CH:15]=[N:14][C:13]([C:16]2[CH:21]=[CH:20][C:19](/[CH:22]=[CH:23]/[CH2:24][CH2:25][CH2:26][CH:27]([O:29][C:30](=[O:32])[CH3:31])[CH3:28])=[CH:18][CH:17]=2)=[N:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

Participants

5

Procedure

A mixture of 4.5 g (10 mmol) of the 5-octyloxy-2-{4-(6-acetoxy-1-trans-heptenyl)-phenyl}-pyrimidine, 140 ml of 0.3M phosphate buffer solution (pH 7.0), 2 ml of chloroform and 0.5 g of Genus Pseudomonas lipase was stirred at 30°-35° C. for 40 hours. The mixture was then extracted with 100 ml of toluene, and the organic layer was washed with water and concentrated under reduced pressure. Separation of the residue thus obtained by silica gel column chromatography gave 1.8 g (yield 46%) of (-)-5-octyloxy-2-{4-(6-hydroxy-1-trans-heptenyl)phenyl}-pyrimidine ([α]D20 =-1.2 (c=1.0, CHCl3)) and 2.3 g (yield 53%) of (-)-5-octyloxy-2-{4-(6-acetoxy-1-trans-heptenyl)-phenyl}-pyrimidine.

Workup

  1. extractionThe mixture was then extracted with 100 ml of toluene
  2. washthe organic layer was washed with water
  3. concentrationconcentrated under reduced pressure
  4. customSeparation of the residue
  5. customthus obtained by silica gel column chromatography

Sources & evidence

ORD record
ord-c8de85db6d954ebfbb4a9d401917eb00
Source dataset
uspto-grants-1998_01
Patent number
US05707547

Reaction notes

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