(4-Aminophenoxy)benzene → HCID 69527863, compound

HRID 1743320Notes

Reaction equation

HRID 1743320 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1Cl)=[CH:13][CH:12]=[CH:11][C:10]=2[N+:17]([O-])=O)=[O:5])[CH3:2].[O:20]([C:27]1[CH:33]=[CH:32][C:30]([NH2:31])=[CH:29][CH:28]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:31][C:30]1[CH:29]=[CH:28][C:27]([O:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[CH:33][CH:32]=1)=[CH:13][CH:12]=[CH:11][C:10]=2[NH2:17])=[O:5])[CH3:2]

Participants

3

Reactant 2

HCID 8764(4-Aminophenoxy)benzeneHCID 11196760Ethyl 4-chloro-8-nitroquinoline-3-carboxylate

Product 1

HCID 69527863HCID 69527863, compound

Procedure

The compound prepared in Example 3 was reacted with 4-phenoxyaniline according to the method as described in Example 4 and the obtained compound was treated as described in Example 14 to prepare the title compound.

Workup

  1. additionthe obtained compound was treated

Sources & evidence

ORD record
ord-6435aad03fc14fa6ad65e4f92b1341ac
Source dataset
uspto-grants-2006_03
Patent number
US07009053B2

Reaction notes

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