Potassium Carbonate → (+)-2-(4-Cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-(2-methylquinolin-7-yl)phenyl)acetamide

温度

100 °C

A solution of 2-(4-bromo-2-fluorophenyl)-2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)acetamide (0.341 mmol) in dry 1,4-dioxane (1.5 mL) was treated with bis(pinacolato)diboron (0.409 mmol), potassium acetate (0.499 mmol) and PdCl2(dppf)-CH2Cl2 adduct (0.017 mmol). The solution was degassed with a stream of nitrogen for three minutes, at which point the reaction vessel was purged with nitrogen and sealed, and the mixture stirred in an oil bath at 100° C. overnight. At this point the reaction was cooled to room temperature and 7-bromo-2-methylquinoline (0.341 mmol), PdCl2(dppf)-CH2Cl2 adduct (0.017 mmol), and 2M aq potassium carbonate (1.022 mmol) were added. The reaction vessel was purged with nitrogen and sealed, and the mixture irradiated in a Biotage Initiator Microwave at 120° C. for 15 min. The resulting black mixture was diluted with water (100 mL) and brine (30 mL) and was extracted with ethyl acetate three times. The combined organic layers were treated with Silicycle Si-thiol (20 mg), dried over sodium sulfate, filtered and concentrated in vacuo. Purification of the residue by silica gel chromatography (0-9% methanol/dichloromethane) followed by chiral HPLC (Chromegachiral CC4, methanol) and lyophilization from water (w/25% acetonitrile) afforded the title compound as a white solid in >98% ee (38 mg, 21% yield). MS(ES)+ m/e 503.0 [M+H]+. αD=+48 deg (c=0.04, methanol).

1. customThe solution was degassed with a stream of nitrogen for three minutes, at which
2. customwas purged with nitrogen
3. customsealed
4. temperatureAt this point the reaction was cooled to room temperature
5. customThe reaction vessel was purged with nitrogen
6. customsealed
7. customthe mixture irradiated in a Biotage Initiator Microwave at 120° C. for 15 min
8. additionThe resulting black mixture was diluted with water (100 mL) and brine (30 mL)
9. extractionwas extracted with ethyl acetate three times
10. additionThe combined organic layers were treated with Silicycle Si-thiol (20 mg)
11. dry with materialdried over sodium sulfate
12. filtrationfiltered
13. concentrationconcentrated in vacuo
14. customPurification of the residue by silica gel chromatography (0-9% methanol/dichloromethane)

ORDレコード

ord-5e604e0feb454ae390f13163c6bcd6bb

出典データセット

uspto-grants-2015_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09084794B2