HCID 53863510, compound → HCID 178484219, compound

HRID 431638Notes

Reaction equation

HRID 431638 reaction equation
[CH3:1][N:2]([S:18]([C:21]1[CH:26]=[C:25]([Cl:27])[C:24]([Cl:28])=[CH:23][C:22]=1[Cl:29])(=[O:20])=[O:19])[CH2:3][CH2:4]OS(C1C=C(Cl)C(Cl)=CC=1Cl)(=O)=O.[F:30][C:31]1[CH:45]=[CH:44][C:34]2[NH:35][C:36]([N:38]3[CH2:43][CH2:42][NH:41][CH2:40][CH2:39]3)=[N:37][C:33]=2[CH:32]=1>>[Cl:29][C:22]1[CH:23]=[C:24]([Cl:28])[C:25]([Cl:27])=[CH:26][C:21]=1[S:18]([N:2]([CH2:3][CH2:4][N:41]1[CH2:42][CH2:43][N:38]([C:36]2[NH:35][C:34]3[CH:44]=[CH:45][C:31]([F:30])=[CH:32][C:33]=3[N:37]=2)[CH2:39][CH2:40]1)[CH3:1])(=[O:19])=[O:20]

Participants

3

Procedure

The title compound was prepared using the procedure described in Example 1 using 2,4,5-Trichlorobenzenesulfonic acid 2-(methyl-(2,4,5-trichlorobenzenesulfonyl)-amino)-ethyl ester (D4) and 1-(5-fluoro-1H benzimidazol-2-yl) piperazine. MH+ 520/522/524/526.

Sources & evidence

ORD record
ord-8992b5b1e2f94bc69735d91e507c5f1e
Source dataset
uspto-grants-2003_12
Patent number
US06660751B1

Reaction notes

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