Water → HCID 22086866, compound

HRID 1062601Notes

Reaction equation

HRID 1062601 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:11](=[O:12])[N:10]2[C:13]([CH2:23][N:24]([CH3:32])[CH2:25][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)=[C:14]([C:16]3[CH:21]=[CH:20][C:19]([NH2:22])=[CH:18][CH:17]=3)[N:15]=[C:9]2[N:8]([CH2:33][C:34]2[C:39]([F:40])=[CH:38][CH:37]=[CH:36][C:35]=2[F:41])[CH:7]=1)=[O:5])[CH3:2].O.[CH:43](Cl)(Cl)Cl>CC(O)C.CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-]>[CH:1]([O:3][C:4]([C:6]1[C:11](=[O:12])[N:10]2[C:13]([CH2:23][N:24]([CH3:32])[CH2:25][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)=[C:14]([C:16]3[CH:17]=[CH:18][C:19]([NH2:22])=[CH:20][CH:21]=3)[N:15]=[C:9]2[N:8]([CH2:33][C:34]2[C:35]([F:41])=[CH:36][CH:37]=[CH:38][C:39]=2[F:40])[CH:7]=1)=[O:5])([CH3:43])[CH3:2]

Participants

6

Conditions

Temperature
80 °C

Procedure

To a solution of the compound obtained in Example 12 (0.10 g, 0.18 mmol) in chloroform (5 ml) is added a solution of titanium(IV) isopropoxide (0.3 ml, 1.0 mmol) in 2-propanol (10 ml). Then the mixture is refluxed at 80° C. for 8 hours, successively is stirred at room temperature for 150 minutes. To this mixture is added a mixture of chloroform (50 ml) and water (50 ml). The aqueous layer is extracted with chloroform (20 ml). The combined organic extract is dried over Na2SO4 and concentrated under reduced pressure to give the residue, which is chromatographed on silica gel to afford white-brown crystalline solid, which is recrystallized from chloroform-n-hexane to afford pale brown crystals (0.58 g, 94%).

Workup

  1. additionTo this mixture is added
  2. extractionThe aqueous layer is extracted with chloroform (20 ml)
  3. extractionThe combined organic extract
  4. dry with materialis dried over Na2SO4
  5. concentrationconcentrated under reduced pressure
  6. customto give the residue, which
  7. customis chromatographed on silica gel
  8. customto afford white-brown crystalline solid, which
  9. customis recrystallized from chloroform-n-hexane

Sources & evidence

ORD record
ord-835506f0ce4e44ea9c72a67d79f71475
Source dataset
uspto-grants-2005_11
Patent number
US06962919B2

Reaction notes

Loading…