4-Fluoro-2-methylaniline → HCID 21476483, compound

HRID 2293160Notes

Reaction equation

HRID 2293160 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[CH2:22][F: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]([CH3:34])[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][CH2:20][C:19]4[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=4)[CH:13]3[CH2:22][F:23])[C:9]3[C:4](=[C:5]([O:24][CH3:25])[CH:6]=[CH:7][CH:8]=3)[N:3]=2)=[C:29]([CH3:34])[CH:28]=1

Participants

4

Reactant 2

HCID 679824-Fluoro-2-methylanilineHCID 54493425HCID 54493425, compound

Product 1

HCID 21476483HCID 21476483, compoundYield 15%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

In accordance with the same procedures as in Example 18, except that to a mixture of 3.3 g of the compound (9.0 mM) prepared in Example 9 and 15 ml of dimethylform-amide, 2.2 ml of 4-fluoro-2-methylaniline(20 mM) was added, 0.65 g of the title compound was prepared.

Workup

  1. additionwas added

Sources & evidence

ORD record
ord-8ba28fe8aaab460485b3f541b5084bf1
Source dataset
uspto-grants-1997_11
Patent number
US05686458

Reaction notes

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