HCID 21511148, compound → HCID 86734001, compound

HRID 1576535Notes

Reaction equation

HRID 1576535 reaction equation
[NH2:1][C:2]1[NH:3][C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[C:12]=3[CH2:19][CH3:20])=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[Br:21][CH2:22][S:23][C:24]1[CH:29]=[CH:28][C:27]([CH2:30][CH2:31][CH3:32])=[C:26]([CH3:33])[CH:25]=1>>[Br-:21].[NH2:1][C:2]1[N:6]([CH2:22][S:23][C:24]2[CH:29]=[CH:28][C:27]([CH2:30][CH2:31][CH3:32])=[C:26]([CH3:33])[CH:25]=2)[C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[C:12]=3[CH2:19][CH3:20])[C:4]=2[N+:3]=1[CH2:22][S:23][C:24]1[CH:29]=[CH:28][C:27]([CH2:30][CH2:31][CH3:32])=[C:26]([CH3:33])[CH:25]=1

Participants

3

Reactant 2

HCID 21511148HCID 21511148, compoundHCID 178437264HCID 178437264, compound

Product 1

HCID 86734001HCID 86734001, compound

Procedure

Following the procedure of Example 2 and replacing 2-aminobenzimidazole with 2-amino-4-(2-ethyl-3-methoxyphenyl)benzimidazole and replacing 2-bromo-4-chlorophenyl chloromethyl ether with 3-methyl-4-propylphenyl bromomethyl sulfide, the title compound is obtained.

Sources & evidence

ORD record
ord-678f122ef90a4f6092ef29d0addb4a52
Source dataset
uspto-grants-1976_09
Patent number
US03981886

Reaction notes

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