HCID 13879179, compound → HCID 178436266, compound

HRID 1576533Notes

Reaction equation

HRID 1576533 reaction equation
[NH2:1][C:2]1[NH:3][C:4]2[CH:10]=[C:9]([CH2:11][C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)[CH:8]=[CH:7][C:5]=2[N:6]=1.[I:18][CH2:19][S:20][C:21]1[CH:26]=[C:25]([CH2:27][CH3:28])[CH:24]=[C:23]([CH2:29][CH3:30])[CH:22]=1>>[I-:18].[NH2:1][C:2]1[N:6]([CH2:19][S:20][C:21]2[CH:26]=[C:25]([CH2:27][CH3:28])[CH:24]=[C:23]([CH2:29][CH3:30])[CH:22]=2)[C:5]2[CH:7]=[CH:8][C:9]([CH2:11][C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)=[CH:10][C:4]=2[N+:3]=1[CH2:19][S:20][C:21]1[CH:26]=[C:25]([CH2:27][CH3:28])[CH:24]=[C:23]([CH2:29][CH3:30])[CH:22]=1

Participants

3

Reactant 2

HCID 13879179HCID 13879179, compoundHCID 21511218HCID 21511218, compound

Product 1

HCID 178436266HCID 178436266, compound

Procedure

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

Sources & evidence

ORD record
ord-ba20d92e691b4381aaed46af7a8f95f7
Source dataset
uspto-grants-1976_09
Patent number
US03981886

Reaction notes

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