Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 117696310 | HCID 117696310 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178421970 | HCID 178421970 | 99.2% |
Reaction Steps
Ammonium acetate (10.0 g, 130 mmol) followed by 4-methyl-3-(2-oxo-propyl)-pyridine-2-carboxylic acid tert-butylamide (1.61 g, 6.48 mmol) are added to acetic acid (20 mL) and the reaction mixture is heated at 110° C. for 3 h. The reaction mixture is cooled to RT and 20% NaOH is added until pH 6-7. The aqueous layer is extracted with DCM (3 times) and the combined organic layers are washed with brine, dried and evaporated under reduce pressure to furnish 4,6-dimethyl-[1,7]naphthyridin-8-ol (1.12 g, 99%) that is used as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09371282B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-4db65f4c0b22495da64c0d2cf0dbb05a |
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| Source note | uspto-grants-2016_06 |
|---|