Methanesulfonyl chloride → HCID 20184543, compound
Reaction equation
[F:1][C:2]([F:22])([F:21])[C:3]1[CH:20]=[CH:19][C:6]2[N:7]=[C:8]([C:10]3[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][C:11]=3[O:17][CH3:18])[NH:9][C:5]=2[CH:4]=1.[CH3:23][S:24](Cl)(=[O:26])=[O:25]>>[F:22][C:2]([F:1])([F:21])[C:3]1[CH:20]=[CH:19][C:6]2[N:7]=[C:8]([C:10]3[CH:15]=[CH:14][C:13]([O:16][S:24]([CH3:23])(=[O:26])=[O:25])=[CH:12][C:11]=3[O:17][CH3:18])[NH:9][C:5]=2[CH:4]=1Participants
3
Procedure
Prepared analogously to Example 1 from 5-trifluoromethyl-2-(2'-methoxy-4'-hydroxy-phenyl)-benzimidazole and methanesulfonic acid chloride.
Sources & evidence
- ORD record
- ord-344dfdd856834901aa2caa7360ab6166
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04582837
Reaction notes
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