Methanesulfonyl chloride → HCID 20184560, compound
Reaction equation
[CH3:1][O:2][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.[CH3:21][S:22](Cl)(=[O:24])=[O:23]>>[CH3:1][O:2][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:22]([CH3:21])(=[O:24])=[O:23])=[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-methoxy-2-(2'-methoxy-4'-hydroxy-phenyl)-benzimidazole and methanesulfonic acid chloride.
Sources & evidence
- ORD record
- ord-0fd8107dfa454c26bfa1cf8e20215f2c
- Source dataset
- uspto-grants-1987_09
- Patent number
- US04696931
Reaction notes
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