Ethyl Acetoacetate → HCID 66746856, compound

To a solution of 2-amino-6-isobutoxybenzonitrile (Example 41b, 16.4 g, 86.32 mmol) and ethyl acetoacetate (10.9 mL, 86.32 mmol) in anhydrous toluene (200 mL) was added SnCl4 (19.9 mL, 172.63 mmol) over a period of 15 minutes at room temperature under nitrogen. The stirred reaction mixture was then refluxed for 3.5 h under nitrogen. After it was cooled down to room temperature, the reaction solution was concentrated to remove most of the solvent under reduced pressure. The residue was re-dissolved in EtOAc (3 L) and carefully neutralized to pH 8 with aqueous NaOH solution (6.0 N, ˜110 mL) at 0° C. The resultant mixture was stirred at room temperature overnight. The precipitate was filtered off, and the organic layer was separated and washed with brine (400 mL), dried over Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel eluting with 50% EtOAc in hexanes to give the title compound as a white solid (18.0 g, 69%). MS 303 (MH+).

1. customThe stirred reaction mixture
2. temperaturewas then refluxed for 3.5 h under nitrogen
3. concentrationthe reaction solution was concentrated
4. customto remove most of the solvent under reduced pressure
5. dissolutionThe residue was re-dissolved in EtOAc (3 L)
6. customcarefully neutralized to pH 8 with aqueous NaOH solution (6.0 N, ˜110 mL) at 0° C
7. filtrationThe precipitate was filtered off
8. customthe organic layer was separated
9. washwashed with brine (400 mL)
10. dry with materialdried over Na2SO4
11. concentrationconcentrated under reduced pressure
12. customThe residue was purified by column chromatography on silica gel eluting with 50% EtOAc in hexanes

ORD record

ord-acd5e52fc43e421b978cfd3998ec87d1

Source dataset

uspto-grants-2015_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09000054B2