1,3-Thiazole-2-carbaldehyde → HCID 178484461, compound

HRID 13239Notes

Reaction equation

HRID 13239 reaction equation
[CH3:1][N:2]([CH3:38])[C:3]([C:5]1[CH:37]=[CH:36][C:8]([O:9][C:10]2[C:24]([O:25][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=3[S:32]([CH3:35])(=[O:34])=[O:33])=[CH:23][C:13]3[NH:14][C:15]([C:17]4C=C[CH:20]=[CH:19][N:18]=4)=[N:16][C:12]=3[CH:11]=2)=[CH:7][CH:6]=1)=[O:4].[S:39]1C=CN=C1C=O>>[CH3:1][N:2]([CH3:38])[C:3]([C:5]1[CH:37]=[CH:36][C:8]([O:9][C:10]2[C:24]([O:25][C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=3[S:32]([CH3:35])(=[O:34])=[O:33])=[CH:23][C:13]3[NH:14][C:15]([C:17]4[S:39][CH:20]=[CH:19][N:18]=4)=[N:16][C:12]=3[CH:11]=2)=[CH:7][CH:6]=1)=[O:4]

Participants

3

Procedure

The entitled compound was obtained in the same method as in Example 1 (step 4) or in accordance with the method or by combining it with an ordinary method but using 4-(4-dimethylcarbamoyl-phenoxy)-5-(2-methanesulfonyl-phenoxy)-benzene-1,2-diamine obtained in Example 20 and thiazol-2-carboxaldehyde.

Workup

  1. customThe entitled compound was obtained in the same method as in Example 1 (step 4) or in accordance with the method

Sources & evidence

ORD record
ord-a703f6b1d4324e8d8b438d132506ebda
Source dataset
uspto-grants-2010_06
Patent number
US07728025B2

Reaction notes

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