HCID 21484168, compound → HCID 178509027, compound

HRID 1576539Notes

Reaction equation

HRID 1576539 reaction equation
[NH2:1][C:2]1[NH:3][C:4]2[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[C:7]([C:15]([F:18])([F:17])[F:16])[C:5]=2[N:6]=1.[Cl:19][CH2:20][S:21][C:22]1[CH:27]=[CH:26][C:25]([F:28])=[CH:24][C:23]=1[Br:29]>>[Cl-:19].[NH2:1][C:2]1[N:6]([CH2:20][S:21][C:22]2[CH:27]=[CH:26][C:25]([F:28])=[CH:24][C:23]=2[Br:29])[C:5]2[C:7]([C:15]([F:18])([F:16])[F:17])=[CH:8][C:9]([C:11]([F:12])([F:13])[F:14])=[CH:10][C:4]=2[N+:3]=1[CH2:20][S:21][C:22]1[CH:27]=[CH:26][C:25]([F:28])=[CH:24][C:23]=1[Br:29]

Participants

3

Reactant 2

HCID 21484168HCID 21484168, compoundHCID 21511208HCID 21511208, compound

Product 1

HCID 178509027HCID 178509027, compound

Procedure

Following the procedure of Example 2 and replacing 2-aminobenzimidazole with 2-amino-5,7-bis-trifluoromethylbenzimidazole and replacing 2-bromo-4-chlorophenyl chloromethyl ether with 2-bromo-4-fluorophenyl chloromethyl sulfide, the title compound is obtained.

Sources & evidence

ORD record
ord-f3fffd86c9834448b0194597870b624f
Source dataset
uspto-grants-1976_09
Patent number
US03981886

Reaction notes

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