Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | HCID 21948152 | HCID 21948152 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 11596751 | HCID 11596751 | 92% |
Reaction Steps
A mixture of 7-chloro-5-methyl-1-phenyl-2-phenylamino-1H-[1,8]naphthyridin-4-one (68.3 mg, 0.189 mmol) and morpholine (0.05 mL, 0.48 mmol) in dioxane (3 mL) was heated to 80° C. for 2 d. The reaction was cooled, concentrated in vacuo, diluted with water and extracted with EtOAc (3×). The combined organic extracts were washed with brine, dried over Na2SO4, and concentrated in vacuo to give 5-methyl-7-morpholin-4-yl-1-phenyl-2-phenylamino-1H-[1,8]naphthyridin-4-one (67 mg, 92%) as yellow solid: LCMS RT: 2.33 min, MH+: 413.4, Rf=0.49 (EtOAc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109196B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-a0f2b1f792614b6d804bec7b816ff28f |
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| Source note | uspto-grants-2006_09 |
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