Nomenclature
CAS number: 262352-17-0
(2
R,4
S)-4-[[[3,5-Bis(trifluoromethyl)phenyl]methyl](methoxycarbonyl)amino]-2-ethyl-3,4-dihydro-6-(trifluoromethyl)-1(2
H)-quinolinecarboxylic acid ethyl ester; (2
R,4
S)-4-[(3,5-bis-trifluoromethylbenzyl)methoxycarbonylamino]-2-ethyl-6-trifluoromethyl-3,4-dihydro-2
H-quinoline-1-carboxylic acid ethyl ester; CP-529414.
C
26H
25F
9N
2O
4; mol wt 600.47.
C 52.01%, H 4.20%, F 28.48%, N 4.67%, O 10.66%.
Description and references
Cholesteryl ester transfer protein (CETP) inhibitor.
Prepn: M. P. DeNinno et al., WO 0017164; eidem, US 6197786 (2000, 2001 both to Pfizer); of crystalline forms: D. J.
M. Allen et al., WO 0140190 (2001 to Pfizer). Mechanism of
action study: R. W. Clark et al., J. Lipid Res. 47, 537 (2006). Clinical evaluation
of effects on HDL cholesterol levels: R. W. Clark et al., Arterioscler. Thromb. Vasc. Biol. 24, 490 (2004); M. E. Brousseau et al., N. Engl. J. Med. 350, 1505 (2004).
Review of clinical development in combination with atorvastatin:
J. R. Burnett, Curr. Opin. Investig. Drugs 6, 944-950 (2005).
Properties
Anhydrous, non-hygroscopic crystals, mp 89-90°. d 1.406.Derivative
Ethanolate.
Nomenclature
CAS number: 343798-00-5
C
26H
25F
9N
2O
4.C
2H
6O; mol wt 646.54.
C 52.02%, H 4.83%, F 26.45%, N 4.33%, O 12.37%.
Properties
White crystalline powder, mp 54-58°. [α]D 93.3° (c = 1.08 in methanol). d 1.402. Non-hygroscopic.
Higher aqueous soly than anhydrous form.Therapeutic Category
Antilipemic; antiatherosclerotic.
Keywords
Antilipemic; CETP Inhibitor; Antiatherosclerotic