1H-indole-3-glyoxylamide sPLA2 inhibitors

Details 1H-indole-3-glyoxylamide sPLA2 inhibitors 1H-indole-3-glyoxylamide sPLA2 inhibitors

1999-02-26

2001-01-16

McKane, Joseph K. (Department: 1626)

Organic compounds -- part of the class 532-570 series

Organic compounds

Heterocyclic carbon compounds containing a hetero ring...

C548S495000

Reexamination Certificate

active

06175021

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to novel 1H-indole-3-glyoxylamides useful for inhibiting sPLA
2
mediated release of fatty acids for conditions such as septic shock.
2. Background Information
The structure and physical properties of human non-pancreatic secretory phospholipase A
2
(hereinafter called, “sPLA
2
”) has been thoroughly described in two articles, namely, “Cloning and Recombinant Expression of Phospholipase A
2
Present in Rheumatoid Arthritic Synovial Fluid” by Seilhamer, Jeffrey J.; Pruzanski, Waldemar; Vadas Peter; Plant, Shelley; Miller, Judy A.; Kloss, Jean; and Johnson, Lorin K.;
The Journal of Biological Chemistry
, Vol. 264, No. 10, Issue of April 5, pp. 5335-5338, 1989; and “Structure and Properties of a Human Non-pancreatic Phospholipase A
2
” by Kramer, Ruth M.; Hession, Catherine; Johansen, Berit; Hayes, Gretchen; McGray, Paula; Chow, E. Pingchang; Tizard, Richard; and Pepinsky, R. Blake;
The Journal of Biological Chemistry
, Vol. 264, No. 10, Issue of April 5, pp. 5768-5775, 1989; the disclosures of which are incorporated herein by reference.
It is believed that sPLA
2
is a rate limiting enzyme in the arachidonic acid cascade which hydrolyzes membrane phospholipids. Thus, it is important to develop compounds which inhibit sPLA
2
mediated release of fatty acids (e.g., arachidonic acid). Such compounds would be of value in general treatment of conditions induced and/or maintained by overproduction of sPLA
2;
such as septic shock, adult respiratory distress syndrome, pancreatitis, trauma, bronchial asthma, allergic rhinitis, rheumatoid arthritis, and etc.
The article, “Recherches en serie indolique. VI sur tryptamines substituees”, by Marc Julia, Jean Igolen and Hanne Igolen,
Bull. Soc. Chim. France,
1962, pp. 1060-1068, describes certain indole-3-glyoxylamides and their conversion to tryptamine derivatives.
The article, “2-Aryl-3-Indoleglyoxylamides (FGIN-1): A New Class of Potent and Specific Ligands for the Mitochondrial DBI Receptor (MDR)” by E. Romeo, et al.,
The Journal of Pharmacoloy and Experimental Therapeutics
, Vol. 262, No. 3, (pp. 971-978) describes certain 2-aryl-3-indolglyoxylamides having research applications in mammalian central nervous systems.
The abstract, “Fragmentation of N-benzylindoles in Mass Spectrometry”; Chemical Abstracts, Vol. 67, 1967, 73028h, reports various benzyl substituted phenols including those having glyoxylamide groups at the 3 position of the indole nucleus.
European Patent 490263 discloses oxoacetamide derivatives of indoles having serotonin receptor activity.
U.S. Pat. No. 3,449,363 describes trifluoromethylindoles having glyoxylamide groups at the 3 position of the indole nucleus. These compounds are stated to be analgesics in antagonizing phenyl-p-quinone “writhing syndrome.”
U.S. Pat. No. 3,351,630 describes alpha-substituted 3-indolyl acetic acid compounds and their preparation inclusive of glyoxylamide intermediates.
U.S. Patent No. 2,825,734 describes the preparation of 3-(2-amino-1-hydroxyethyl) indoles using 3-indole glyoxylamide intermediates such as 1-phenethyl-2-ethyl-6-carboxy-N-propyl-3-indoleglyoxylamide (see, Example 30).
U.S. Pat. No. 4,397,850 prepares isoxazolyl indolamines using glyoxylamide indoles as intermediates.
U.S. Pat. No. 3,801,594 describes analgesics prepared using 3-indole glyoxylamide intermediates.
The article, “No. 565.—Inhibiteurs d'enzymes. XII.—Preparation de (propargyamino-2 ethyl)-3 indoles” by A. Alemanhy, E. Fernandez Alvarez, O. Nieto Lopey and M. E. Rubio Herraez;
Bulletin Do La Societe Chimiqque De France,
1974, No. 12, pgs. 2883-2888 describes various indolyl-3 glyoxamides which are hydrogen substituted on the 6 membered ring of the indole nucleus.
The article “Indol-Umlagerung von 1-Diphenylamino-2,3-dihydro-2,3-pyrroldionen” by Gert Kollenz and Christa Labes;
Liebigs Ann. Chem.,
1975, pgs. 1979-1983 describes phenyl substituted 3-glyoxylamides.
It is desirable to develop new compounds and treatments for sPLA
2
induced diseases.
SUMMARY OF THE INVENTION
This invention is a novel use of the class of compounds known as 1H-indole-3-glyoxylamides to inhibit human sPLA
2
mediated release of fatty acids.
This invention is also novel classes of 1H-indole-3-glyoxylamides having potent and selective effectiveness as inhibitors of human sPLA
2
.
This invention is also pharmaceutical compositions containing the 1H-indole-3-glyoxylamides of the invention.
This invention is also a method of preventing and treating septic shock, adult respiratory distress syndrome, panceatitus, trauma, bronchial asthma, allergic rhinitis, rheumatoid arthritis, and related diseases by contact with a therapeutically effective amount of the 1H-indole-3-glyoxylamides of the invention.
DETAILED DESCRIPTION OF THE INVENTION
Definitions
The 1H-indole-3-acetamides of the invention employ certain defining terms as follows:
The term, “alkyl” by itself or as part of another substituent means, unless otherwise defined, a straight or branched chain monovalent hydrocarbon radical such as methyl, ethyl, n-propyl, isopropyl, n-butyl, tertiary butyl, isobutyl, sec-butyl, n-pentyl, and n-hexyl.
The term, “alkenyl” employed alone or in combination with other terms means a straight chain or branched monovalent hydrocarbon group having the stated number range of carbon atoms, and typified by groups such as vinyl, propenyl, crotonyl, isopentenyl, and various butenyl isomers.
The term, “hydrocarbyl” means an organic group containing only carbon and hydrogen.
The term, “halo” means fluoro, chloro, bromo, or iodo.
The term, “heterocyclic radical”, refers to radicals derived from monocyclic or polycyclic, saturated or unsaturated, substituted or unsubstituted heterocyclic nuclei having 5 to 14 ring atoms and containing from 1 to 3 hetero atoms selected from the group consisting of nitrogen, oxygen or sulfur. Typical heterocyclic radicals are pyrrolyl, furanyl, thiophenyl, pyrazolyl, imidazolyl, phenylimidazolyl, triazolyl, isoxazolyl, oxazolyl, thiazolyl, thiadiazolyl, indolyl, carbazolyl, norharmanyl, azaindolyl, benzofuranyl, dibenzofuranyl, thianaphtheneyl, dibenzothiophenyl, indazolyl, imidazo(1.2-A)pyridinyl, benzotriazolyl anthranilyl, 1,2-benzisoxazolyl, benzoxazolyl, benzothiazolyl, purinyl, pryidinyl, dipyridylyl. phenylpyridinyl, benzylpyridinyl, pyrimidinyl, phenylpyrimidinyl, pyrazinyl, 1,3,5-triazinyl, quinolinyl, phthalazinyl, quinazolinyl, and quinoxalinyl.
The term, “carbocyclic radical” refers to radicals derived from a saturated or unsaturated, substituted or unsubstituted 5 to 14 membered organic nucleus whose ring forming atoms (other than hydrogen) are solely carbon atoms. Typical carbocyclic radicals are cycloalkyl, cycloalkenyl, phenyl, naphthyl, norbornanyl, bicycloheptadienyl, tolulyl, xylenyl, indenyl, stilbenyl, terphenylyl, diphenylethylenyl, phenyl-cyclohexenly, acenaphthylenyl, and anthracenyl, biphenyl, bibenzylyl and related bibenzylyl homologues represented by the formula (bb),
where n is a number from 1 to 8.
The term, “non-interfering substituent”, refers to radicals suitable for substitution at positions 4, 5, 6, and/or 7 on the indole nucleus (as hereinafter depicted in Formula I) and radical(s) suitable for substitution on the heterocyclic radical and carbocyclic radical as defined above. Illustrative non-interfering radicals are C
1
-C
6
alkyl, C
1
-C
6
alkenyl, C
1
-C
6
alkynyl, C
7
-C
12
aralkyl, C
7
-C
12
alkaryl, C
3
-C
8
cycloalkyl, C
3
-C
8
cycloalkenyl, phenyl, tolulyl, xylenyl, biphenyl, C
1
-C
6
alkoxy, C
1
-C
6
alkenyloxy, C
1
-C
6
alkynyloxy, C
2
-C
12
alkoxyalkyl, C
2
-C
12
alkoxyalkyloxy, C
2
-C
12
alkylcarbonyl, C
2
-C
12
alkylcarbonylamino, C
2
-C
12
alkoxyamino, C
2
-C
12
alkoxyaminocarbonyl, C
2
-C
12
alkylamino, C
1
-C
6
alkylthio, C
2
-C
12
alkylthiocarbonyl, C
1
-C
6
alkylsulfinyl, C
1
-C
6
alkylsulfonyl, C
2
-C
6
haloalkoxy, C
1
-C
6
haloalkylsulfonyl, C
2
-C
6
haloalkyl, C
1
-C
6
hydroxyalkyl, —C(O)O(C
1
-C
6
alkyl), —(CH
2
)
n
—O—(C
1
-C
6
alkyl), benzyloxy, phenoxy, phe

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