Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-(2-Chlorophenyl)ethylamine | HCID 83117 | — |
| Reactant | N-(1H-benzo[d]imidazol-2-yl)-1H-imidazole-1-carbothioamide | HCID 19704123 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54093329 | HCID 54093329 | 40.5% |
Reaction Steps
A solution of 1-[(2-benzimidazolyl)thiocarbamoyl]imidazole (1.22 g, 5.0 mmol) and 2-(2-chlorophenyl)ethylamine (0.81 g, 5.0 mmol) in 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 0.67 g (40%) of the titled product as a white solid: mp 166°-169° C.; IR (KBr, cm-1) 3235, 1656, 1554, 1459, 1248, 1224, 1192, 754, 737, 629; 1H NMR (300 MHz, DMSO-d6) δ 11.95 (br s, 1H), 10.82 (br s, 1H), 7.42 (m, 5H), 7.25 (m, 2H), 7.12 (m, 2H), 3.83 (m, 2H), 3.05 (t, J=7 Hz, 2H); MS (FD) m/e 330 (M+); UV (EtOH) 301 nm (ε=18044), 293 nm (ε=18559), 266 nm (ε=11113), 260 nm (ε=10441), 239 nm (ε=8428), 206 nm (ε=27620).
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-cabe090722d542339de00a04076830b9 |
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| Source note | uspto-grants-1997_08 |
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