Process for producing dihydro-2H-pyran derivatives
Disclosed is a process for preparing dihydro-2H-pyran derivatives of formula I: wherein R 1 and R 2 are defined herein. The process of the invention provides the compound of formula I in concise cascade reactions and in one pot. The compound of formulae I prepared by the process of the invention and its further transformed derivatives are useful for making pharmaceutical composition for the treatment of proliferative diseases.
1. A compound of formula II:
wherein
R1 is alkyl, cycloalkyl, aryl, heterocycloalkyl or heteroaryl, which is optionally substituted with one or more substituent selected from the group consisting of alkyl, alkenyl, alkynyl, alkoxy, nitro, cyano, halogen, hydroxyl, mono- or polyhalo alkyl, mono- or polyhalo alkoxy and phenyl;
R2 is alkyl or benzyl; and
R 4 is hydroxyl or halogen;
or racemate, enantiomer, diastereomer, mixture thereof, or pharmaceutically acceptable salt thereof.
2. The compounds of formula II according to claim 1 ,
wherein
R 1 is C 1 -C 18 -alkyl, C 3 -C 18 -cycloalkyl, phenyl, naphthyl or 5- or 6-membered heteroaryl containing at least one hetero atom selected from nitrogen, oxygen and sulfur, which is optionally substituted with one or more substituents selected from the group consisting of C 1 -C 18 -alkyl, C 2 -C 18 -alkenyl, C 2 -C 18 -alkynyl, C 1 -C 18 -alkoxy nitro, cyano, halogen, hydroxyl, mono- or polyhalo-C 1 -C 18 -alkyl, mono- or polyhalo-C 1 -C 18 -alkoxy and phenyl;
R 2 is C 1 -C 18 -alkyl or benzyl; and
R 4 is hydroxyl or halogen;
or racemate, enantiomer, diastereomer, mixture thereof, or pharmaceutically acceptable salt thereof.
3. A pharmaceutical composition comprising a compound according to claim 1 , and a pharmaceutically acceptable adjuvant.
4. A compound of formula II according to claim 1 , selected from the group consisting of: