HCID 21484165, compound → HCID 178509026, compound

HRID 1576534Notes

Reaction equation

HRID 1576534 reaction equation
[NH2:1][C:2]1[NH:3][C:4]2[CH:10]=[C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[Br:17])[CH:8]=[CH:7][C:5]=2[N:6]=1.[Cl:18][CH2:19][S:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=1[C:27]([F:30])([F:29])[F:28]>>[Cl-:18].[NH2:1][C:2]1[N:6]([CH2:19][S:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=2[C:27]([F:30])([F:29])[F:28])[C:5]2[CH:7]=[CH:8][C:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=3[Br:17])=[CH:10][C:4]=2[N+:3]=1[CH2:19][S:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=1[C:27]([F:28])([F:29])[F:30]

Participants

3

Reactant 2

HCID 21484165HCID 21484165, compoundHCID 21511074HCID 21511074, compound

Product 1

HCID 178509026HCID 178509026, compound

Procedure

Following the procedure of Example 2 and replacing 2-aminobenzimidazole with 2-amino-5-(2-bromophenyl)benzimidazole and replacing 2-bromo-4-chlorophenyl chloromethyl ether with 2-trifluoromethylphenyl chloromethyl sulfide, the title compound is obtained.

Sources & evidence

ORD record
ord-7cced4a676714a82a07e0f8abd24e186
Source dataset
uspto-grants-1976_09
Patent number
US03981886

Reaction notes

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