Methanesulfonyl chloride → HCID 20184568, compound
Reaction equation
[NH2:1][C:2]1[CH:19]=[CH:18][C:5]2[N:6]=[C:7]([C:9]3[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][C:10]=3[O:16][CH3:17])[NH:8][C:4]=2[CH:3]=1.[CH3:20][S:21](Cl)(=[O:23])=[O:22]>>[CH3:20][S:21]([NH:1][C:2]1[CH:19]=[CH:18][C:5]2[N:6]=[C:7]([C:9]3[CH:14]=[CH:13][C:12]([O:15][S:21]([CH3:20])(=[O:23])=[O:22])=[CH:11][C:10]=3[O:16][CH3:17])[NH:8][C:4]=2[CH:3]=1)(=[O:23])=[O:22]Participants
3
Procedure
Prepared analogously to Example 1 from 5-amino-2-(2'-methoxy-4'-hydroxy-phenyl)-benzimidazole and methanesulfonic acid chloride.
Sources & evidence
- ORD record
- ord-b9d3cdf3fe7e4eaa85b66dc6d0b96281
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04582837
Reaction notes
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