US2006106228A1PendingUtilityA1
Process for preparing 5-(4-fluorophenyl)-1-[2-((2R,4R)-4-hydroxy-6-oxo-tetrahydro-pyran-2-yl) ethyl]-2-isopropyl-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide
Individually held — no corporate assignee on recordPriority: Aug 6, 2002Filed: Jan 11, 2006Published: May 18, 2006
Est. expiryAug 6, 2022(expired)· nominal 20-yr term from priority
C07D 405/06A61P 3/06
56
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Abstract
A method for preparing 5-(4-fluorophenyl)-1-[2-((2R,4R)-4-hydroxy-6-oxo-tetrahydro-pyran-2-yl)-ethyl]-2-isopropyl-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide (I), a key intermediate in the synthesis of atorvastatin calcium, is described.
Claims
exact text as granted — not AI-modified1 - 8 . (canceled)
9 A transition metal catalyst, wherein the transition metal catalyst is prepared from a transition metal catalyst precursor and a chiral, non racemic ligand which is a chiral diamine ligand or a chiral alcohol amine ligand.
10 . The transition metal catalyst of claim 9 , wherein the transition metal catalyst precursor is selected from [dichloro-(1,5-cycloocta-diene)]ruthenium (II) oligomer, [RuCl 2 benzene] 2 , [RuCl 2 p-cymene] 2 , [RuCl 2 mesitylene] 2 , [dibromo-(1,5-cyclooctadiene)]ruthenium (II) dimer, [bis-(2-methallyl)cycloocta-1,5-diene]ruthenium (II) complex, pentamethylcyclopentadienyl iridium (III)chloride dimer, and pentamethylcyclopentadienyl rhodium (III)chloride dimer.
11 . The transition metal catalyst of claim 9 , wherein the non racemic ligand is a chiral diamine ligand or a chiral alcohol amine ligand selected from norephedrine or compounds 7 or 8:
12 - 59 . (canceled)Join the waitlist — get patent alerts
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