Potassium Phosphate, Tribasic → 5,7-difluoro-N-(2'-methoxy-5-morpholino-2,4'-bipyridin-3-yl)-3-methyl-2-(pyridin-2-yl)quinolin-4-amine

温度

90 °C

N-(2-chloro-5-morpholinopyridin-3-yl)-5,7-difluoro-3-methyl-2-(pyridin-2-yl)-quinolin-4-amine (42.8 mg, 0.091 mmol), 2-methoxypyridin-4-ylboronic acid (28.7 mg, 0.19 mmol), tricyclohexylphosphine (5.1 mg, 0.018 mmol), and tris(dibenzylideneacetone)dipalladium (0) (5.7 mg, 6.2 μmol) were added to a flask then degassed and backfilled with argon. To the flask, 1,4-dioxane (1.0 mL) and aq. 1.3M potassium phosphate tribasic (0.22 mL, 0.29 mmol) were added by syringe. The resulting reaction was heated to 90° C. and monitored with TLC and LC-MS. After 19 h, the reaction was cooled to rt then poured into water. After extracting twice with EtOAc and twice with DCM, the combined organic extractions were dried over anhydrous magnesium sulfate. After filtration and concentration, the residue was purified on basic alumina (0-100% EtOAc in hexanes) to afford an impure yellow residue. The light yellow film was further purified with HPLC (10-90% of 0.1% TFA acetonitrile solution in 0.1% TFA water solution). The desired fractions were cond then diluted with EtOAc. After washing twice with satd aq. sodium bicarbonate solution and once with brine, the solvent was removed under reduced pressure to yield a light yellow solid as 5,7-difluoro-N-(2′-methoxy-5-morpholino-2,4′-bipyridin-3-yl)-3-methyl-2-(pyridin-2-yl)quinolin-4-amine. 1H NMR (400 MHz, CDCl3) δ ppm 8.69 (1H, dt, J=4.8, 1.4 Hz), 8.35 (1H, m), 8.10 (1H, m), 7.98 (2H, m), 7.70 (1H, m), 7.47 (1H, m), 7.37 (1H, m), 7.21 (1H, s), 7.00 (2H, ddd, J=13.5, 8.6, 2.5 Hz), 6.55 (1H, d, J=2.3 Hz), 4.05 (3H, m), 3.89 (4H, m), 3.28 (4H, m), 2.31 (3H, m). Mass Spectrum (pos.) m/e: 541.2 (M+1).

1. customthen degassed
2. customThe resulting reaction
3. temperaturethe reaction was cooled to rt
4. extractionAfter extracting twice with EtOAc and twice with DCM
5. extractionthe combined organic extractions
6. dry with materialwere dried over anhydrous magnesium sulfate
7. filtrationAfter filtration and concentration
8. customthe residue was purified on basic alumina (0-100% EtOAc in hexanes)
9. customto afford an impure yellow residue
10. customThe light yellow film was further purified with HPLC (10-90% of 0.1% TFA acetonitrile solution in 0.1% TFA water solution)
11. additionThe desired fractions were cond then diluted with EtOAc
12. washAfter washing twice with satd aq. sodium bicarbonate solution and once with brine
13. customthe solvent was removed under reduced pressure

ORDレコード

ord-ba0496d150d048fbb8d4861a31930b93

出典データセット

uspto-grants-2015_01

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08940724B2