5,6-Dimethylbenzimidazol-2-ylamine → HCID 86734005, compound

HRID 1576538Notes

Reaction equation

HRID 1576538 reaction equation
[NH2:1][C:2]1[NH:3][C:4]2[CH:10]=[C:9]([CH3:11])[C:8]([CH3:12])=[CH:7][C:5]=2[N:6]=1.[Cl:13][CH2:14][S:15][C:16]1[CH:21]=[C:20]([Br:22])[CH:19]=[C:18]([Br:23])[CH:17]=1>>[Cl-:13].[NH2:1][C:2]1[N:3]([CH2:14][S:15][C:16]2[CH:21]=[C:20]([Br:22])[CH:19]=[C:18]([Br:23])[CH:17]=2)[C:4]2[CH:10]=[C:9]([CH3:11])[C:8]([CH3:12])=[CH:7][C:5]=2[N+:6]=1[CH2:14][S:15][C:16]1[CH:21]=[C:20]([Br:22])[CH:19]=[C:18]([Br:23])[CH:17]=1

Participants

3

Reactant 2

HCID 931255,6-Dimethylbenzimidazol-2-ylamineHCID 21511106HCID 21511106, compound

Product 1

HCID 86734005HCID 86734005, compound

Procedure

Following the procedure of Example 2 and replacing 2-aminobenzimidazole with 2-amino-5,6-dimethylbenzimidazole and replacing 2-bromo-4-chlorophenyl chloromethyl ether with 3,5-dibromophenyl chloromethyl sulfide, the title compound is obtained.

Sources & evidence

ORD record
ord-a9dd2fecce884009b921161cdae6d70c
Source dataset
uspto-grants-1976_09
Patent number
US03981886

Reaction notes

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