4-Fluoro-2-methylaniline → HCID 21476476, compound
Reaction equation
[Cl:1][C:2]1[N:11]=[C:10]([N:12]2[CH2:21][CH:20]([CH3:22])[C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[CH:13]2[CH3:23])[C:9]2[C:4](=[C:5]([O:24][CH3:25])[CH:6]=[CH:7][CH:8]=2)[N:3]=1.[F:26][C:27]1[CH:33]=[CH:32][C:30]([NH2:31])=[C:29](C)[CH:28]=1>CN(C)C=O>[ClH:1].[F:26][C:27]1[CH:33]=[CH:32][C:30]([NH:31][C:2]2[N:11]=[C:10]([N:12]3[CH2:21][CH:20]([CH3:22])[C:19]4[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=4)[CH:13]3[CH3:23])[C:9]3[C:4](=[C:5]([O:24][CH3:25])[CH:6]=[CH:7][CH:8]=3)[N:3]=2)=[CH:29][CH:28]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In accordance with the same procedures as in Example 18, except that to a mixture of 3.00 g of the compound (8.40 mM) prepared in Example 16 and 10 ml of dimethyl-formamide, 1.90 ml of 4-fluoro-2-methylaniline(20 mM) was added, 1.10 g of the title compound was prepared.
Workup
- additionwas added
Sources & evidence
- ORD record
- ord-a97b74d217b4435284f1cd901311d133
- Source dataset
- uspto-grants-1997_11
- Patent number
- US05686458
Reaction notes
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