Ethanol → 6-(4-Fluorophenyl)picolinic acid

Temperatur

100 °C

A solution of 2-bromo-picolinic acid (Aldrich, 2.02 g, 10 mmol) in DME containing 4 mL of 10% aq Na2CO3 was purged with Ar gas. To this mixture was added Pd(PPh3)4 followed by 2-(4-fluorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane (Aldrich, 2.40 g, 11.5 mmol) and EtOH (20 mL), and the mixture was purged with Ar gas. The reaction mixture was heated at 100° C. for 2.5 h in a sealed tube. Additional 2-bromo-picolinic acid (900 mg) and Pd(PPh3)4 was added, and after purging with Ar gas it was heated at 100° C. for 4.5 h. Trifluoroacetic acid (20 mL) was added to the reaction and the mixture was concentrated in vacuo. MeOH (150 mL) was added to the residue and the insoluble material was filtered, and the filtrate solution was concentrated in vacuo. Purification of the resulting residue by flash column chromatography on silica gel eluting with EtOAc/MeOH/900:100 followed by EtOAc/MeOH/HOAc/700:1500:50 provided the desired product (1.0 g, 40% based on borinane starting material) as a white solid. 1H NMR (CD3OD) δ 8.01 (d, 1H, J=7.7 Hz), 7.94-7.87 (m, 3H), 7.73 (d, 1H, J=7.7 Hz), 7.13 (t, 2H, J=8.8 Hz); MS (ESI+) m/z 234 (M+H)+.

1. customthe mixture was purged with Ar gas
2. additionAdditional 2-bromo-picolinic acid (900 mg) and Pd(PPh3)4 was added
3. customafter purging with Ar gas it
4. temperaturewas heated at 100° C. for 4.5 h
5. additionTrifluoroacetic acid (20 mL) was added to the reaction
6. concentrationthe mixture was concentrated in vacuo
7. additionMeOH (150 mL) was added to the residue
8. filtrationthe insoluble material was filtered
9. concentrationthe filtrate solution was concentrated in vacuo
10. customPurification of the resulting residue by flash column chromatography on silica gel eluting with EtOAc/MeOH/900:100

ORD-Eintrag

ord-422d22036de5476b9a2d0adf925c4803

Quelldatensatz

uspto-grants-2011_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07989477B2