Aniline → HCID 57670984, compound

HRID 1892864Notes

Reaction equation

HRID 1892864 reaction equation
[CH2:1]([CH:8]1[CH2:14][N:13]([CH2:15][C:16]([NH:18]C2C=CC=CC=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.NC1C=CC=CC=1.[CH2:44](N)[C:45]1[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=1>>[CH2:44]([NH:18][C:16](=[O:17])[CH2:15][N:13]1[CH2:14][CH:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:9](=[O:36])[N:10]([S:26]([C:29]2[CH:34]=[CH:33][C:32]([Cl:35])=[CH:31][CH:30]=2)(=[O:28])=[O:27])[CH2:11][C:12]1=[O:25])[C:45]1[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=1

Participants

4

Reactant 3

HCID 6115AnilineHCID 7504BenzylamineHCID 57671023HCID 57671023, compound

Product 1

HCID 57670984HCID 57670984, compound

Procedure

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

Sources & evidence

ORD record
ord-dc5b7609e56c416b8f9117ec887d4453
Source dataset
uspto-grants-2013_08
Patent number
US08507714B2

Reaction notes

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