p-Toluenesulfonic acid → HCID 12110021, compound

HRID 2084773Notes

Reaction equation

HRID 2084773 reaction equation
C1(C)C=CC(S(O)(=O)=O)=CC=1.[Cl:12][C:13]1[CH:14]=[N:15][CH:16]=[C:17]([Cl:35])[C:18]=1[CH2:19][CH:20]([C:22]1[C:27]2[CH2:28][C:29]([CH3:32])([CH3:31])[O:30][C:26]=2[C:25]([O:33][CH3:34])=[CH:24][CH:23]=1)O.C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[Cl:12][C:13]1[CH:14]=[N:15][CH:16]=[C:17]([Cl:35])[C:18]=1/[CH:19]=[CH:20]/[C:22]1[C:27]2[CH2:28][C:29]([CH3:32])([CH3:31])[O:30][C:26]=2[C:25]([O:33][CH3:34])=[CH:24][CH:23]=1

Participants

5

Procedure

p-Toluenesulfonic acid (0.8 g) was added to a suspension of Compound 45a (1.0 g) obtained in Step A of Example 45 in toluene (27 ml), followed by heating under reflux for 30 minutes. After being allowed to stand for cooling, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution for neutralization, followed by extraction with ether. The organic layer was washed with a saturated saline and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by silica gel column chromatography (chloroform/methanol=20/1) to give Compound 67 (0.59 g, 62.2%) as yellow crystals.

Workup

  1. temperatureby heating
  2. temperatureunder reflux for 30 minutes
  3. temperaturefor cooling
  4. extractionfollowed by extraction with ether
  5. washThe organic layer was washed with a saturated saline
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure
  8. customThe resultant residue was purified by silica gel column chromatography (chloroform/methanol=20/1)

Sources & evidence

ORD record
ord-1bcaba57e6274753ae8dab949827dd33
Source dataset
uspto-grants-2004_04
Patent number
US06716987B1

Reaction notes

Loading…