4-Chloro-2,6-dimethylaniline → HCID 67041118, compound
Reaction equation
[Cl:1][C:2]([Cl:28])([Cl:27])[CH2:3][O:4][C:5](=[O:26])[NH:6][C:7]1[CH:12]=[CH:11][C:10]([S:13][C:14]2[CH:19]=[CH:18][C:17]([C:20](Cl)=[O:21])=[CH:16][C:15]=2[N+:23]([O-:25])=[O:24])=[CH:9][CH:8]=1.[Cl:29][C:30]1[CH:35]=[C:34]([CH3:36])[C:33]([NH2:37])=[C:32]([CH3:38])[CH:31]=1>C1(C)C=CC=CC=1>[Cl:1][C:2]([Cl:28])([Cl:27])[CH2:3][O:4][C:5](=[O:26])[NH:6][C:7]1[CH:12]=[CH:11][C:10]([S:13][C:14]2[CH:19]=[CH:18][C:17]([C:20](=[O:21])[NH:37][C:33]3[C:34]([CH3:36])=[CH:35][C:30]([Cl:29])=[CH:31][C:32]=3[CH3:38])=[CH:16][C:15]=2[N+:23]([O-:25])=[O:24])=[CH:9][CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product of Example 162b (300 mg, 0.6197 mmol) and 4-Chloro-2,6-dimethyl-phenylamine (119 mg, 0.6197 mmol) were combined in toluene (10 mL) and reacted as in Example 162c to give the title compound that was used without further manipulation.
Workup
- customreacted as in Example 162c
Sources & evidence
- ORD record
- ord-ef83e27515d543b0a8c69a291769f1be
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910595B2
Reaction notes
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