Method for the preparation of atorvastatin and intermediates used therein
The present invention relates to a novel method for preparing atorvastatin. According to the present invention, provided are a novel intermediate of the preparation of atorvastatin and a method of preparing large amounts of atorvastatin in a safe manner using the intermediate.
1. A compound of the following formula 7a:
wherein A 1 and A 2 are oxygen;
A 3 is CH 2 ;
W is
wherein R 1 and R 2 are each independently hydrogen, OH, a straight or branched chain alkyl having 1-8 carbon atoms, or phenyl, or R 1 and R 2 together form oxygen (═O) or —(CH 2 ) n —, wherein n is 4 or 5, R 3 is oxygen or sulfur, R 4 is Cl, Br, F, I, a straight or branched chain having 1-8 carbon atoms, phenyl, trityl, OH, an alkoxy having 1-8 carbon atoms, or phenoxy, and R 5 is oxygen (═O), a straight or branched chain alkyl having 1-8 carbon atoms, an alkoxy having 1-8 carbon atoms, an aryl or aryloxy, wherein an aryl or aryloxy is unsubstituted or substituted with an alkyl having 1-4 carbon atoms, an alkoxy having 1-4 carbon atoms, nitro or halogen, or a C 6 -C 10 heteroaryl comprising one or two heteroatoms selected from a group consisting of N, O and S; and
Z is —CH 2 COR 8 , wherein R 8 is
R 9 is hydrogen, a straight or branched chain alkyl having 1-8 carbon atoms, a cycloalkyl group having 3-6 carbon atoms, phenyl, benzyl or α,α-dimethylbenzyl, and R 10 and R 11 are each independently hydrogen, a straight or branched chain alkyl having 1-8 carbon atoms, a cycloalkyl group having 3-6 carbon atoms, benzyl or phenyl, or R 10 and R 11 together form —(CH 2 ) 4 —, —(CH 2 ) 5 —, —(CH(R 12 )CH 2 ) 3 —, —(CH(R 12 )CH 2 ) 4 —, —(CH(R 12 )(CH 2 ) 2 CH(R 12 ))—, —(CH(R 12 )(CH 2 ) 3 CH(R 12 ))—, —CH 2 CH 2 —O—CH 2 CH 2 —, —CH(R 12 )CH 2 —O—CH 2 CH 2 — or —CH(R 12 )CH 2 —O—CH 2 CH(R 12 )—, wherein R 12 is an alkyl having 1-4 carbon atoms.
2. The compound of claim 1 , which is a compound of the following formula 7a:
wherein A 1 and A 2 are oxygen;
A 3 is CH 2 ;
W is
wherein R 1 and R 2 are each independently hydrogen, OH, methyl, ethyl, t-butyl, isopropyl or phenyl, or R 1 and R 2 together form oxygen (═O) or —(CH 2 ) n —, wherein n is 4 or 5, R 3 is oxygen or sulfur, R 4 is Cl, Br, F, I, methyl, ethyl, t-butyl, isopropyl, trityl, phenyl, OH, methoxy, ethoxy or phenoxy, and R 5 is oxygen (═O), methyl, ethyl, t-butyl, isopropyl, methoxy, ethoxy, phenoxy, t-butoxy, phenyl, naphthalenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl, difluorophenyl or quinolinyl; and
Z is —CH 2 COR 8 , wherein R 8 is
R 9 is hydrogen, methyl, ethyl, isopropyl, t-butyl, cyclohexyl, phenyl, benzyl or α,α-dimethylbenzyl, and R 10 and R 11 are each independently hydrogen, methyl, ethyl, t-butyl, isopropyl, cyclohexyl, benzyl or phenyl, or R 10 and R 11 , together form —(CH 2 ) 4 —, —(CH 2 ) 5 —, —(CH(R 12 )CH 2 ) 3 —, —(CH(R 12 )CH 2 ) 4 —, —(CH(R 12 )(CH 2 ) 2 CH(R 12 ))—, —(CH(R 12 )(CH 2 ) 3 CH(R 12 ))—, —CH 2 CH 2 —O—CH 2 CH 2 —, —CH(R 12 )CH 2 —O—CH 2 CH 2 — or —CH(R 12 )CH 2 —O—CH 2 CH(R 12 )—, wherein R 12 is an alkyl having 1-4 carbon atoms.
3. The compound of claim 2 , which is a compound of the following formula 7b: