4-Fluoro-2-methylaniline → HCID 21476504, compound

HRID 2293168Notes

Reaction equation

HRID 2293168 reaction equation
[Cl:1][C:2]1[N:11]=[C:10]([N:12]2[CH2:21][CH2:20][C:19]3[C:14](=[C:15]([CH3:22])[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]([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](=[C:15]([CH3:22])[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)=[C:29]([CH3:34])[CH:28]=1

Participants

4

Reactant 2

HCID 679824-Fluoro-2-methylanilineHCID 21476465HCID 21476465, compound

Product 1

HCID 21476504HCID 21476504, compoundYield 21%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

In accordance with the same procedures as in Example 18, except that to a mixture of 2.50 g of the compound (7.06 mM) prepared in Example 14 and 15 ml of dimethyl-formamide, 1.21 ml of 4-fluoro-2-methylaniline(14.9 mM) was added, 0.70 g of the title compound was prepared.

Workup

  1. additionwas added

Sources & evidence

ORD record
ord-e9f136876f7f4d3c9be0e9dd17959c7d
Source dataset
uspto-grants-1997_11
Patent number
US05686458

Reaction notes

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