Hydrochloric Acid → 2-{2-[4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl]ethoxy}ethanol

To a solution of 2-{2-[4-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl]ethoxy}ethyl benzoate (760 mg) in tetrahydrofuran (7.0 mL) was added 1N aqueous sodium hydroxide solution (7.0 mL), and the mixture was stirred at room temperature for 14 hrs. 1N Hydrochloric acid (7.0 mL) was added to the reaction mixture, and the mixture was stirred at room temperature for 10 min. and extracted with a mixed solvent (100 mL×3) of ethyl acetate/tetrahydrofuran (1/1). The organic layer washed successively with 5% aqueous sodium hydrogen carbonate and saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to basic silica gel column chromatography (eluent:ethyl acetate/methanol=100/0→90/10). The object fraction was concentrated under reduced pressure. A mixed solvent of ethanol/isopropyl ether (1/4) was added to the residue, and the mixture was heated to 80° C. and then allowed to cool to room temperature. The resultant precipitate was collected by filtration and dried under reduced pressure to give the title compound (431 mg) as white powder crystals.

1. stirringthe mixture was stirred at room temperature for 10 min.
2. extractionextracted with a mixed solvent (100 mL×3) of ethyl acetate/tetrahydrofuran (1/1)
3. washThe organic layer washed successively with 5% aqueous sodium hydrogen carbonate and saturated brine
4. dry with materialdried over anhydrous magnesium sulfate
5. customThe solvent was evaporated under reduced pressure
6. concentrationThe object fraction was concentrated under reduced pressure
7. additionA mixed solvent of ethanol/isopropyl ether (1/4) was added to the residue
8. temperaturethe mixture was heated to 80° C.
9. temperatureto cool to room temperature
10. filtrationThe resultant precipitate was collected by filtration
11. customdried under reduced pressure

ORD 기록

ord-5dd3a233d0b0418da20a7b2725f97734

출처 데이터셋

uspto-grants-2009_03

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07507740B2