4-Fluoro-2-methylaniline → HCID 70197304, compound

HRID 2293145Notes

Reaction equation

HRID 2293145 reaction equation
[Cl:1][C:2]1[N:11]=[C:10]([N:12]2[CH2:21][CH2:20][C:19]3[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=3)[CH:13]2[CH3:22])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[F:23][C:24]1[CH:30]=[CH:29][C:27]([NH2:28])=[C:26]([CH3:31])[CH:25]=1>CN(C)C=O>[ClH:1].[F:23][C:24]1[CH:30]=[CH:29][C:27]([NH:28][C:2]2[N:11]=[C:10]([N:12]3[CH2:21][CH2:20][C:19]4[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=4)[CH:13]3[CH3:22])[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)=[C:26]([CH3:31])[CH:25]=1

Participants

4

Reactant 2

HCID 679824-Fluoro-2-methylanilineHCID 21476447HCID 21476447, compound

Product 1

HCID 70197304HCID 70197304, compoundYield 78%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

In accordance with the same procedures as in Example 14, except that to a mixture of 1.61 g of the compound (5.20 mM) prepared in Example 2 and 15 ml of dimethyl-formamide, 0.89 ml of 4-fluoro-2-methylaniline(10.9 mM) was added, 1.76 g of the title compound was prepared.

Workup

  1. additionwas added

Sources & evidence

ORD record
ord-e9e6a32a13384ae39912a80babbc33d8
Source dataset
uspto-grants-1997_11
Patent number
US05686458

Reaction notes

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