Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Chlorophenethylamine | HCID 139381 | — |
| Reactant | N-(1H-benzo[d]imidazol-2-yl)-1H-imidazole-1-carbothioamide | HCID 19704123 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54247213 | HCID 54247213 | 14.5% |
Reaction Steps
A solution of 1-[(2-benzimidazolyl)thiocarbamoyl]imidazole (1.22 g, 5.0 mmol) and 2-(3-chlorophenyl)ethylamine (0.79 g, 5.0 mmol) in N,N-dimethylformamide (20 mL) was stirred at 90° C. for 2 h. The reaction was cooled to room temperature, poured into ethyl acetate, washed with water, 1N aqueous HCl, water, saturated sodium bicarbonate, and brine. The organic layer was concentrated and the resultant solid was crystallized from EtOAc to provide 0.24 g (14%) of the titled product as a white solid: mp 171°-177° C.; IR (KBr, cm-1) 3387, 1574, 1539, 1461, 1426, 1237, 1175, 734, 699, 477; 1H NMR (300 MHz, DMSO-d6) δ 11.18 (m, 2H), 7.28 (m, 8H), 7.06 (m, 1H), 3.83 (m, 2H), 2.94 (t, J=7 Hz, 2H); MS (FD) m/e 330 (M+); UV (EtOH) 293 nm (ε=17219), 266 nm (ε=9969), 260 nm (ε=9196), 240 nm (ε=8196), 203 nm (ε=27483).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05658907 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-45f3e893fc414c48903f158a5db012d2 |
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| Source note | uspto-grants-1997_08 |
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