Pyridinium chloride → HCID 11042902, compound
Reaction equation
C[O:2][C:3]1[C:18]([O:19]C)=[CH:17][C:6]2[C:7](=[O:16])[CH2:8][C:9]3[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=3[O:11][C:5]=2[CH:4]=1.Cl.N1C=CC=CC=1>O>[OH:2][C:3]1[C:18]([OH:19])=[CH:17][C:6]2[C:7](=[O:16])[CH2:8][C:9]3[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=3[O:11][C:5]=2[CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 190 °C
Procedure
A mixture of 7,8-dimethoxy-10,11-dihydrodibenz[b,f]oxepin-10-one (5 mg) and pyridine hydrochloride (20 mg) was heated at 190° C. for two hours. Water was added to the reaction mixture followed by extracting with ethyl acetate. This was washed with water and dried over magnesium sulfate and the solvent was evaporated to give the title compound (Compound 13) (3 mg, 60%) as brown plates.
Workup
- extractionby extracting with ethyl acetate
- washThis was washed with water
- dry with materialdried over magnesium sulfate
- customthe solvent was evaporated
Sources & evidence
- ORD record
- ord-1314476f631b40ef8e6b59f0441cc039
- Source dataset
- uspto-grants-2001_01
- Patent number
- US06180659B2
Reaction notes
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