Toluene → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-methylphenyl}-N'-(3-fluorobenzoyl)thiourea
Reaction equation
FC1C=C(C(Cl)=O)C=CC=1.[F:11][C:12]1[CH:13]=[C:14]([C:18]([N:20]=[C:21]=[S:22])=[O:19])[CH:15]=[CH:16][CH:17]=1.[CH3:23][O:24][C:25]1[CH:26]=[C:27]2[C:32](=[CH:33][C:34]=1[O:35][CH3:36])[N:31]=[CH:30][CH:29]=[C:28]2[O:37][C:38]1[CH:44]=[CH:43][C:41]([NH2:42])=[C:40]([CH3:45])[CH:39]=1.C1(C)C=CC=CC=1>C(O)C>[F:11][C:12]1[CH:13]=[C:14]([C:18]([N:20]=[C:21]=[S:22])=[O:19])[CH:15]=[CH:16][CH:17]=1.[CH3:23][O:24][C:25]1[CH:26]=[C:27]2[C:32](=[CH:33][C:34]=1[O:35][CH3:36])[N:31]=[CH:30][CH:29]=[C:28]2[O:37][C:38]1[CH:44]=[CH:43][C:41]([NH:42][C:21]([NH:20][C:18](=[O:19])[C:14]2[CH:15]=[CH:16][CH:17]=[C:12]([F:11])[CH:13]=2)=[S:22])=[C:40]([CH3:45])[CH:39]=1Participants
7
Reactant 4
Product 2
Reagents, catalysts & solvents 1
Procedure
3-Fluoro-1-benzenecarbonyl isothiocyanate was prepared using commercially available 3-fluoro-1-benzenecarbonyl chloride (80 mg) as a starting compound according to the description of the literature. 3-Fluoro-1-benzenecarbonyl isothiocyanate was dissolved in ethanol (1 ml) to prepare a solution. 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-methylaniline (50 mg), toluene (5 ml), and ethanol (1 ml) were added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (64 mg, yield 81%).
Workup
- customto prepare a solution
- concentrationThe reaction solution was concentrated
- customthe residue was purified by chromatography on silica gel
Sources & evidence
- ORD record
- ord-b021ad0c473547e094f0209c78d57e7f
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07135466B2
Reaction notes
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