Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 178507493 | HCID 178507493 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178514067 | HCID 178514067 | 104.7% |
Reaction Steps
To a suspension of 3-[2-(2-aminophenyl)ethyl]-5-phenyl-1H-pyrazolo[4,3-c][1,8]naphthyridin-4 (5H)-one (38 mg, 0.09 mmol, prepared in Example 36) in a mixture solvent of acetic acid (1 mL) and water (1 mL) was added potassium cyanate (12 mg, 0.15 mmol, 1.7 eq) at room temperature. The mixture was stirred overnight at 35° C., and filtered to give precipitates which were washed with water and then dried to afford 5-phenyl-3-[2-(2-ureidophenyl)ethyl]-1H-pyrazolo[4,3-c][1,8]naphthyridin-4 (5H)-one (40 mg, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608716B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-b39c6090d2eb4b0b937d988ef345b1bc |
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| Source note | uspto-grants-2009_10 |
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