Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chlorobenzylamine | HCID 66648 | — |
| Reactant | HCID 178512268 | HCID 178512268 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54533324 | HCID 54533324 | 73.5% |
Reaction Steps
To a solution of N-(3,5-dichlorophenyl)-N'-cyano-O-phenylisourea (0.8 mmol, 250 mg) in dry acetonitrile (2 ml), 2-chlorobenzylamine (0.9 mmol, 0.108 ml) and triethylamine (0.125 ml) were added. The mixture was stirred for 21/2 h at 82° C. under nitrogen. After concentration the residue was recrystallized from ethyl acetate to give the title compound (208 mg, 72%). Mp 186-187.5° C.; 1H-NMR (CDCl3): δ 4.54 (d, 2H), 5.53 (br, 1H), 7.15 (m, 2H), 7.3 (m, 3H), 7.4 (m, 2H), 7.75 ppm (br, 1H); EI SP/MS: 394 (M+). MA calc for C15H11C13N4 : C, 50.95%; H, 3.14%; N, 15.84%. Found: C, 50.68%; H, 3.10%; N, 15.49%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06147098 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-707e4ff12aa04cfb92f331738385a5de |
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| Source note | uspto-grants-2000_11 |
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