Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoamylamine | HCID 7894 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178512268 | HCID 178512268 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11197309 | HCID 11197309 | 54.6% |
Reaction Steps
To N-(3,5-Dichlorophenyl)-N'-cyano-O-phenylisourea (0.98 mmol, 300 mg) in dry acetonitrile (2 ml), 3-methylbutylamine (2.16 mmol, 0.255 ml) and triethylamine (1.08 mmol, 0.150 ml) were added. The reaction mixture was stirred for 16 h at 85° C. under nitrogen. The precipitated material was filtered off and recrystallized from ethyl acetate to give the title compound (160 mg, 54%) as white crystals. Mp 146.5-1451.5° C.; 1H-NMR (CDCl3): δ 0.94 (d, 6H), 1.43 (q, 2H), 1.6 (m, 1H), 3.31 (q, 2H), 4.9 (br, 1H), 7.18 (br s, 2H), 7.29 (br s, 1H), 7.5 ppm (br, 1H); MA calc for C13H16Cl2N4 : C, 52.19%; H, 5.39%; N, 18.73%. Found: C, 52.23%; H, 5.51%; N, 18.60%.
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-e2876621ba3044ad899581ad34d74af3 |
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| Source note | uspto-grants-2000_11 |
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