Methanesulfonyl chloride → HCID 20184509, compound

HRID 2309892Notes

Reaction equation

HRID 2309892 reaction equation
[NH:1]([C:5]1[CH:22]=[CH:21][C:8]2[N:9]=[C:10]([C:12]3[CH:17]=[CH:16][C:15]([OH:18])=[CH:14][C:13]=3[O:19][CH3:20])[NH:11][C:7]=2[CH:6]=1)[C:2]([CH3:4])=[O:3].[CH3:23][S:24](Cl)(=[O:26])=[O:25]>>[NH:1]([C:5]1[CH:22]=[CH:21][C:8]2[N:9]=[C:10]([C:12]3[CH:17]=[CH:16][C:15]([O:18][S:24]([CH3:23])(=[O:26])=[O:25])=[CH:14][C:13]=3[O:19][CH3:20])[NH:11][C:7]=2[CH:6]=1)[C:2]([CH3:4])=[O:3]

Participants

3

Reactant 2

HCID 31297Methanesulfonyl chlorideHCID 136113980HCID 136113980, compound

Product 1

HCID 20184509HCID 20184509, compound

Procedure

Prepared analogously to Example 1 from 5-acetamino-2-(2'-methoxy-4'-hydroxy-phenyl)-benzimidazole and methanesulfonic acid chloride.

Sources & evidence

ORD record
ord-9dd4fcbbd9ab498e80cc587344792007
Source dataset
uspto-grants-1987_09
Patent number
US04696931

Reaction notes

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