HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-amino-4-methylbenzoate → Methyl 3-[(1-chloro-9-fluorobenzo[c]-2,6-naphthyridin-5-yl)amino]-4-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-amino-4-methylbenzoate | HCID 337778 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 1,5-Dichloro-9-fluorobenzo[c]-2,6-naphthyridine | HCID 59436118 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-[(1-chloro-9-fluorobenzo[c]-2,6-naphthyridin-5-yl)amino]-4-methylbenzoate | HCID 59436117 | — |
Reaction Steps
To a solution of 1,5-dichloro-9-fluorobenzo[c]-2,6-naphthytidine (Example 1, Step 5) (500 mg, 1.87 mmol) and methyl 3-amino-4-methylbenzoate (340 mg, 2.06 mmol) in THF (9.3 mL) was added sodium tert-butoxide (396 mg, 4.12 mmol). The reaction stirred at room temperature for ten minutes and was then quenched by the addition of sat. aq. NaHCO3 solution. The mixture was extracted with EtOAc and the extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification by silica gel column chromatography (0-30% EtOAc/heptane) afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349865B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-13067376039147abb3299da62522dbba |
| Source note | uspto-grants-2013_01 |