p-Toluenesulfonic acid → HCID 12110021, compound
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]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- temperatureby heating
- temperatureunder reflux for 30 minutes
- temperaturefor cooling
- extractionfollowed by extraction with ether
- washThe organic layer was washed with a saturated saline
- dry with materialdried over anhydrous magnesium sulfate
- distillationthe solvent was distilled off under reduced pressure
- 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
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