Hydrochloric Acid → (αR)-6-Methoxy-α-[[4-[[(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)methyl]amino]-1-piperidinyl]methyl]-4-quinolinemethanol

To a stirred solution of the mono hydrochloride salt of (R)-2-(4-aminopiperidin-1-yl)-1-(6-methoxyquinolin-4-yl) ethanol (1d) (0.34 g, 1.0 mmole) in CH2Cl2 (25 mL) and dry ethanol (10 mL) at RT was added 5,6,7,8-tetrahydro[1,8]naphthyridine-2-carboxaldehyde (prepared according to the procedure of WO 98/08840, 0.17 g, 1.0 mmole), triethylamine (0.10 g, 1.0 mmole), and granular Na2SO4 (approximately 200 mg). After 36 h, the reaction was filtered through a sintered-glass funnel and the filtrate was concentrated. The remaining residue was dissolved in dry ethanol and reacted with NaBH4 (0.04 g, 1.0 mmole). After 12 h at RT, the reaction was concentrated under vacuum and the residue was dissolved in a mixture of H2O (2 mL) and saturated aqueous NaHCO3 (10 mL). The aqueous solution was extracted with EtOAc (2×50 mL) and the combined organic phases were washed with brine then were dried over Na2SO4. Flash chromatography on silica gel (9:1 CHCl3/MeOH containing 5% NH4OH) afforded the title compound (0.31 g, 69%) as a white solid:

1. customprepared
2. filtrationthe reaction was filtered through a sintered-glass funnel
3. concentrationthe filtrate was concentrated
4. dissolutionThe remaining residue was dissolved in dry ethanol
5. waitAfter 12 h at RT
6. concentrationthe reaction was concentrated under vacuum
7. dissolutionthe residue was dissolved in a mixture of H2O (2 mL) and saturated aqueous NaHCO3 (10 mL)
8. extractionThe aqueous solution was extracted with EtOAc (2×50 mL)
9. washthe combined organic phases were washed with brine
10. dry with materialthen were dried over Na2SO4

ORDレコード

ord-0dd36d99dfe24c749b11b4b2e4998759

出典データセット

uspto-grants-2007_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07205408B2