2-Chloromethylbenzimidazole → N-(2-Dimethylaminoethyl)-N'-[2-(2-benzimidazolylmethylamino)-ethyl]thiourea

HRID 903281

Reaction equation

HRID 903281 reaction equation
[N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[NH:3][C:2]=1[CH2:10][NH:11][CH2:12][CH2:13][NH2:14].ClCC1NC2C=CC=CC=2N=1.[CH3:26][N:27]([CH3:33])[CH2:28][CH2:29][N:30]=[C:31]=[S:32]>>[CH3:26][N:27]([CH3:33])[CH2:28][CH2:29][NH:30][C:31]([NH:14][CH2:13][CH2:12][NH:11][CH2:10][C:2]1[NH:1][C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=1)=[S:32]

Participants

4

Procedure

N-(2-Benzimidazolylmethyl)ethylenediamine, prepared by reacting ethylenediamino with 2-chloromethylbenzimidazole by the procedure of Example 40, is reacted with 2-dimethylaminoethyl isothiocyanate by the procedure of Example 40 to give the title compound.

Sources & evidence

ORD record
ord-dec2ef44db6e4988a424bbfae68a9d10
Source dataset
uspto-grants-1980_10
Patent number
US04226874

Linked notes

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