Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | HCID 178512266 | HCID 178512266 | — |
| Product | HCID 9841980 | HCID 9841980 | 82% |
Reaction Steps
To a suspension of N-(3,5-bis(trifluoromethyl)phenyl)-N'-cyano-O-phenylisourea (0.400 g, 1.1 mmol) in dry acetonitrile (2.5 ml) triethylamine (0.164 ml, 1.2 mmol) and cyclopentylamine (0.116 ml, 1.2 mmol) was added. The homogenous solution was stirred at 85° C. under N2 for 3.5 h. The solvent was evaporated, and the residue was dissolved in ethyl acetate and washed with water twice. The organic layer was dried (Na2SO4) and concentrated. The crude product was purified by flash chromatography using ethyl acetate/heptane 1:2 to give the title compound. Yield 82% (0.320 g). mp 156-159° C.
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-cbd2b2c12d38440eb3b1030934e91455 |
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| Source note | uspto-grants-2000_11 |
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