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

Reactant 2

HCID 31297Methanesulfonyl chloride

HCID 136140188HCID 136140188, compound

Product 1

HCID 20184568HCID 20184568, compound

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-e7fb9f331a48459ab695ef71bc5637b4
Source dataset: uspto-grants-1987_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04696931

Reaction notes

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