3,4-dihydro-2H-pyran → HCID 20081831, compound

HRID 1681258Notes

Reaction equation

HRID 1681258 reaction equation
[O:1]1[CH:6]=[CH:5][CH2:4][CH2:3][CH2:2]1.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.[CH:24]([C:27]1[C:32]([C:33]([O:35][CH2:36][CH3:37])=[O:34])=[C:31]([C:38]2[CH:43]=[CH:42][C:41]([F:44])=[CH:40][CH:39]=2)[C:30]([CH2:45][OH:46])=[C:29]([CH:47]([CH3:49])[CH3:48])[N:28]=1)([CH3:26])[CH3:25]>ClCCl>[CH:24]([C:27]1[C:32]([C:33]([O:35][CH2:36][CH3:37])=[O:34])=[C:31]([C:38]2[CH:39]=[CH:40][C:41]([F:44])=[CH:42][CH:43]=2)[C:30]([CH2:45][O:46][CH:6]2[CH2:5][CH2:4][CH2:3][CH2:2][O:1]2)=[C:29]([CH:47]([CH3:48])[CH3:49])[N:28]=1)([CH3:26])[CH3:25]

Participants

5

Procedure

1.88 g (22.4 mmol) of dihydropyran and 0.525 g (1.49 mmol) of pyridinium p-toluene-sulphonate are added to a solution of 5.36 g (14.9 mmol) of the compound from Example 4 in 100 ml of dry dichloromethane and the mixture is heated to reflux for 48 hours. After cooling to room temperature, the mixture is diluted using dichloromethane and extracted several times using water. The organic phase is dried over magnesium sulphate and concentrated in vacuo, and the residue is chromatographed on a column (silica gel 70-230 mesh, using dichloromethane).

Workup

  1. temperaturethe mixture is heated
  2. temperatureto reflux for 48 hours
  3. additionthe mixture is diluted
  4. extractionextracted several times
  5. dry with materialThe organic phase is dried over magnesium sulphate
  6. concentrationconcentrated in vacuo
  7. customthe residue is chromatographed on a column (silica gel 70-230 mesh, using dichloromethane)

Sources & evidence

ORD record
ord-26d2a4ae37364e9ba2ca44e85e622bd4
Source dataset
uspto-grants-1992_12
Patent number
US05169857

Reaction notes

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