HCID 178523908, compound → HCID 178512144, compound
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][S:11][CH2:12][CH2:13][NH:14][C:15]([NH:25]C(=O)C1C=CC=CC=1)=[N:16][CH2:17][CH2:18][CH2:19][C:20]1[N:21]=[CH:22][NH:23][CH:24]=1>Cl>[N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[NH:3][C:2]=1[CH2:10][S:11][CH2:12][CH2:13][NH:14][C:15]([NH:16][CH2:17][CH2:18][CH2:19][C:20]1[N:21]=[CH:22][NH:23][CH:24]=1)=[NH:25]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
0.65 g (1.4 mmol) of N-[2-[(benzimidazol-2-yl) methylthio]ethyl]-N'-benzoyl-N"-[3-(imidazol-4-yl)propyl]-guanidine are heated under reflux in 45 ml of 18% hydrochloric acid for 6 hours and worked up by a method analogous to that of Example 109.
Sources & evidence
- ORD record
- ord-ec316d178bc644f782b02be2ae4ce3f8
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05021431
Reaction notes
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