Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 10762413 | HCID 10762413 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53746288 | HCID 53746288 | 46.1% |
Reaction Steps
1.5 g (3.9 mmol) of (S)-N-(α-ethylbenzyl)-3-amino-2-phenylquinoline-4-carboxamide (compound of Description 2) were dissolved in 30 ml of dry CH2Cl2, 10 ml of dry THF and 10 ml of dry CH3CN. 0.47 ml (4.3 mmol) of phenylisocyanate dissolved in 10 ml of CH2Cl2 were added and the reaction mixture heated to 40° C. for 4 hours. After cooling of the reaction mixture, the precipitate was collected by filtration and washed with CH2Cl2 to yield 0.9 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06277862B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-939f6365ab1a45bf9bb72a6f98debf20 |
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| Source note | uspto-grants-2001_08 |
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