Toluene → (3S,5R,6S)-3-Allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((S)-1-methoxy-2-methylpent-1-en-3-yl)-3-methylpiperidin-2-one

温度

0 °C

(Methoxymethyl)triphenylphosphonium chloride was dried at 80° C. under vacuum for 2 h. To a solution of the dried (methoxymethyl)triphenylphosphonium chloride (673 mg, 1.96 mmol) in THF (3.5 mL) was added 0.5 M KHMDS in toluene (3.49 mL, 1.75 mmol) at −78° C. The solution resulted in a blood red color. After addition, the reaction was stirred at 0° C. for 30 min and a solution of (3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-1-((S)-2-oxopentan-3-yl)piperidin-2-one prepared above in Step B (200 mg, 0.436 mmol) in THF (3.5 mL) was added dropwisely at 0° C. The reaction was allowed to warm to rt and stirred for 1.5 h. Then the reaction was quenched (sat NH4Cl solution), extracted (2×EtOAc), and washed (brine). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. Purification by combi flash (SiO2, 24 g, 15% and 20% EtOAc/Hexanes) provided the title compound as a colorless film.

1. dry with material(Methoxymethyl)triphenylphosphonium chloride was dried at 80° C. under vacuum for 2 h
2. customThe solution resulted in a blood red color
3. additionAfter addition
4. additionwas added dropwisely at 0° C
5. temperatureto warm to rt
6. stirringstirred for 1.5 h
7. customThen the reaction was quenched (sat NH4Cl solution)
8. extractionextracted (2×EtOAc)
9. washwashed (brine)
10. dry with materialThe combined organic layers were dried (Na2SO4)
11. concentrationconcentrated under reduced pressure
12. customPurification by combi flash (SiO2, 24 g, 15% and 20% EtOAc/Hexanes)

ORDレコード

ord-a05ab6e618034f0bb36f760a3caeae66

出典データセット

uspto-grants-2013_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08569341B2