Water → 2-{2-[5-{[5-(Methylsulfonyl)pyridin-2-yl]oxy}-7-(tetrahydro-2H-pyran-4-yloxy)-1H-indol-2-yl]-4,5-dihydro-1,3-thiazol-5-yl}ethanol

Ethyl{2-[5-{[5-(methylsulfonyl)pyridin-2-yl]oxy}-7-(tetrahydro-2H-pyran-4-yloxy)-1H-indol-2-yl]-4,5-dihydro-1,3-thiazol-5-yl}acetate (207 mg) was dissolved in tetrahydrofuran (5 mL)-methanol (2 mL), lithium tetrahydroborate (22 mg) was added under ice-cooling, and the mixture was stirred at room temperature for 50 min. To the reaction solution were added lithium tetrahydroborate (32 mg) and methanol (1 mL), and the mixture was stirred at room temperature for 1 hr. Furthermore, lithium tetrahydroborate (15 mg) was added, and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The obtained crude product was subjected to silica gel column chromatography (methanol:ethyl acetate:hexane=0:50:50 to 20:80:0, volume ratio) to give the title compound as a yellow amorphous solid (99 mg, yield 52%). The obtained amorphous solid was crystallized from diethyl ether, and the obtained crystals were recrystallized from ethyl acetate-diethyl ether to give the title compound as colorless crystals.

1. additionwas added under ice-
2. temperaturecooling
3. stirringthe mixture was stirred at room temperature for 1 hr
4. stirringthe mixture was stirred at room temperature for 1 hr
5. extractionthe mixture was extracted with ethyl acetate
6. washThe organic layer was washed with saturated brine
7. dry with materialdried over magnesium sulfate
8. filtrationfiltered
9. concentrationconcentrated under reduced pressure
10. customThe obtained crude product

ORDレコード

ord-2fb44e6d1bec4822ad9e1cd89486af94

出典データセット

uspto-grants-2013_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08557805B2