Aniline → HCID 57671024, compound

HRID 1892863Notes

Reaction equation

HRID 1892863 reaction equation
[CH2:1]([CH:8]1[CH2:14][N:13]([CH2:15][C:16]([NH:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[O:17])[C:12](=[O:25])[CH2:11][N:10]([S:26]([C:29]2[CH:34]=[CH:33][C:32]([Cl:35])=[CH:31][CH:30]=2)(=[O:28])=[O:27])[C:9]1=[O:36])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.N[C:38]1C=CC=CC=1.CNC1C=CC=CC=1>>[CH2:1]([CH:8]1[CH2:14][N:13]([CH2:15][C:16]([N:18]([CH3:38])[C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[O:17])[C:12](=[O:25])[CH2:11][N:10]([S:26]([C:29]2[CH:30]=[CH:31][C:32]([Cl:35])=[CH:33][CH:34]=2)(=[O:28])=[O:27])[C:9]1=[O:36])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Reactant 3

HCID 6115AnilineHCID 7515N-MethylanilineHCID 57671023HCID 57671023, compound

Product 1

HCID 57671024HCID 57671024, compound

Procedure

Instead of the starting material compound of Example 270, that is, aniline, N-methylaniline was used for the similar procedure as in Example 270 to obtain the title compound.

Sources & evidence

ORD record
ord-1a7a2a3af84c44878e0c813b667cbde3
Source dataset
uspto-grants-2013_08
Patent number
US08507714B2

Reaction notes

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