3-Methoxypyridine → 5-Chloro-3-hydroxy-3-(3-methoxy-pyridin-2-yl)-1,3-dihydro-indol-2-one

온도

-78 °C

A 1.7 M solution of tert-butyllithium in pentane (57.8 mL) was added to THF (200 ml) at −78° C. 2-Bromomesitylene (3.6 mL) was added dropwise, keeping the temperature below −60° C., and the mixture stirred at −78° C. for 1 h. 3-Methoxypyridine (3.6 mL) was added dropwise at −78° C. and then the mixture was stirred between −30° C. and −20° C. The reaction mixture was re-cooled to −78° C. and a slurry of 5-chloroisatin (3.26 g) in THF (100 mL) was added portionwise, keeping the temperature below −60° C. The reaction mixture was stirred at −78° C. for 1 h. The cooling bath was removed and the reaction mixture was stirred for 30 min. The reaction mixture was quenched with 10% aqueous ammonium chloride solution and extracted several times with ethyl acetate. The combined organic layers were washed with water, dried over magnesium sulfate and evaporated to low volume. Upon standing, 1.05 g of a cream-colored solid separated which was filtered off, washed with ethyl acetate and dried in vacuo.

1. customthe temperature below −60° C.
2. stirringthe mixture was stirred between −30° C. and −20° C
3. temperatureThe reaction mixture was re-cooled to −78° C.
4. customthe temperature below −60° C
5. stirringThe reaction mixture was stirred at −78° C. for 1 h
6. customThe cooling bath was removed
7. stirringthe reaction mixture was stirred for 30 min
8. customThe reaction mixture was quenched with 10% aqueous ammonium chloride solution
9. extractionextracted several times with ethyl acetate
10. washThe combined organic layers were washed with water
11. dry with materialdried over magnesium sulfate
12. customevaporated to low volume
13. custom1.05 g of a cream-colored solid separated which
14. filtrationwas filtered off
15. washwashed with ethyl acetate
16. customdried in vacuo

ORD 기록

ord-147a4bc83edf47938af5cb28e064f44c

출처 데이터셋

uspto-grants-2011_03

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07902379B2