p-Toluenesulfonic acid → HCID 178500761, compound
Reaction equation
[NH2:1][CH:2]=[C:3]([C:8](=[O:18])[C:9]1[CH:14]=[C:13]([F:15])[C:12]([F:16])=[CH:11][C:10]=1[Cl:17])[C:4]([O:6][CH3:7])=[O:5].[F:19][C:20]1[CH:26]=[CH:25][C:23](N)=[CH:22][CH:21]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>O>[Cl:17][C:10]1[CH:11]=[C:12]([F:16])[C:13]([F:15])=[CH:14][C:9]=1[C:8]([C:3](=[CH:2][NH:1][C:23]1[CH:25]=[CH:26][C:20]([F:19])=[CH:21][CH:22]=1)[C:4]([O:6][CH3:7])=[O:5])=[O:18]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The preparation was carried out analogously to Example 10 with 1.0 g of the product from Example 5, 1.01 g of p-fluoroaniline and 0.69 g of p-toluenesulphonic acid.H2O.
Sources & evidence
- ORD record
- ord-726a597480dd46a4a87d0d3bf17e23d4
- Source dataset
- uspto-grants-1991_04
- Patent number
- US05011971
Reaction notes
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