Phosphorus oxychloride → 5-(3-(9-(4-methoxybenzyl)-9H-purin-6-yl)pyridin-2-yloxy)-1-chloro-6-methylisoquinoline

A mixture of 5-(3-(9-(4-methoxybenzyl)-9H-purin-6-yl)pyridin-2-yloxy)-6-methylisoquinolin-1(2H)-one (0.76 g, 1.5 mmol) in phosphorous oxychloride (10 mL, 107 mmol) was stirred in a 100° C. oil bath for 1.0 h. The reaction mixture was allowed to cool to RT, diluted with toluene (100 mL) and concentrated in vacuo. The residue was partitioned between DCM (100 mL) and satd NaHCO3 (70 mL). The aqueous layer was extracted with DCM (50 mL). The combined organic layers were washed with satd NaHCO3 (50 mL), water (50 mL) brine (50 mL), dried over Na2SO4, filtered, and concentrated in vacuo to give 960 mg as a dark red solid. The crude product was adsorbed onto a plug of silica gel and chromatographed through a Redi-Sep® pre-packed silica gel column (80 g), eluting with a gradient of 50% to 80% EtOAc in CH2Cl2, to provide 5-(3-(9-(4-methoxybenzyl)-9H-purin-6-yl)pyridin-2-yloxy)-1-chloro-6-methylisoquinoline as a clear viscous oil that solidified to a white solid upon standing. MS (ESI, pos. ion) m/z: 509.2 [M+H]+.

1. temperatureto cool to RT
2. concentrationconcentrated in vacuo
3. customThe residue was partitioned between DCM (100 mL) and satd NaHCO3 (70 mL)
4. extractionThe aqueous layer was extracted with DCM (50 mL)
5. washThe combined organic layers were washed with satd NaHCO3 (50 mL), water (50 mL) brine (50 mL)
6. dry with materialdried over Na2SO4
7. filtrationfiltered
8. concentrationconcentrated in vacuo
9. customto give 960 mg as a dark red solid
10. customchromatographed through a Redi-Sep® pre-packed silica gel column (80 g)
11. washeluting with a gradient of 50% to 80% EtOAc in CH2Cl2

ORD record

ord-0770cd8221114a9197da6dccfb86fa5b

Source dataset

uspto-grants-2013_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08557830B2