U.S. patent application number 12/959849 was filed with the patent office on 2011-07-21 for novel carboxylic acid derivatives, their preparation and use.
This patent application is currently assigned to Abbott GmbH & Co. KG. Invention is credited to Wilhelm Amberg, Ernst Baumann, Andrea Hager-Wernet, Andreas Kling, Dagmar Klinge, Stefan Muller, Manfred Raschack, Joachim Rheinheimer, Hartmut Riechers, Liliane Unger, Uwe Vogelbacher, Wolfgang Wernet.
Application Number | 20110178294 12/959849 |
Document ID | / |
Family ID | 6530833 |
Filed Date | 2011-07-21 |
United States Patent
Application |
20110178294 |
Kind Code |
A1 |
Riechers; Hartmut ; et
al. |
July 21, 2011 |
NOVEL CARBOXYLIC ACID DERIVATIVES, THEIR PREPARATION AND USE
Abstract
Carboxylic acid derivatives ##STR00001## where R--R.sup.6, X, Y
and Z have the meanings stated in the description, and the
preparation thereof, are described. The novel compounds are
suitable for controlling diseases.
Inventors: |
Riechers; Hartmut;
(Neustadt, DE) ; Klinge; Dagmar; (Schriesheim,
DE) ; Amberg; Wilhelm; (Mannheim, DE) ; Kling;
Andreas; (Mannheim, DE) ; Muller; Stefan;
(Speyer, DE) ; Baumann; Ernst; (Speyer, DE)
; Rheinheimer; Joachim; (Ludwigshafen, DE) ;
Vogelbacher; Uwe; (Ludwigshafen, DE) ; Wernet;
Wolfgang; (Neustadt, DE) ; Hager-Wernet; Andrea;
(Neustadt, DE) ; Unger; Liliane; (Ludwigshafen,
DE) ; Raschack; Manfred; (Weisenheim, DE) |
Assignee: |
Abbott GmbH & Co. KG
Wiesbaden
DE
|
Family ID: |
6530833 |
Appl. No.: |
12/959849 |
Filed: |
December 3, 2010 |
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09309770 |
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6197958 |
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5969134 |
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09309770 |
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Current U.S.
Class: |
544/219 ;
544/253; 544/278; 544/279; 544/300; 544/302; 544/310; 544/311;
544/316 |
Current CPC
Class: |
C07D 403/06 20130101;
C07D 405/12 20130101; A61P 15/00 20180101; C07D 251/26 20130101;
C07D 239/60 20130101; C07D 491/048 20130101; A61P 13/12 20180101;
C07D 251/52 20130101; A61P 43/00 20180101; C07D 239/48 20130101;
C07D 239/52 20130101; A61P 11/08 20180101; C07D 239/96 20130101;
C07D 405/14 20130101; A61P 7/02 20180101; A61P 11/06 20180101; A61P
25/04 20180101; A61P 25/06 20180101; A61P 13/02 20180101; C07D
417/12 20130101; A61P 9/00 20180101; C07D 251/20 20130101; C07D
413/12 20130101; A61P 9/08 20180101; C07D 487/04 20130101; A61P
9/10 20180101; C07D 495/04 20130101; A61P 13/08 20180101; C07D
239/70 20130101; C07D 491/04 20130101; C07D 403/12 20130101; A61P
25/08 20180101; C07D 239/34 20130101; A61P 9/12 20180101 |
Class at
Publication: |
544/219 ;
544/302; 544/311; 544/278; 544/279; 544/316; 544/253; 544/310;
544/300 |
International
Class: |
C07D 239/60 20060101
C07D239/60; C07D 239/52 20060101 C07D239/52; C07D 491/08 20060101
C07D491/08; C07D 487/04 20060101 C07D487/04; C07D 239/34 20060101
C07D239/34; C07D 239/70 20060101 C07D239/70; C07D 251/30 20060101
C07D251/30; C07D 251/20 20060101 C07D251/20; C07D 417/12 20060101
C07D417/12 |
Foreign Application Data
Date |
Code |
Application Number |
Oct 14, 1994 |
DE |
P 44 36 851.8 |
Sep 7, 1995 |
DE |
195 33 023.4 |
Claims
1. A carboxylic acid derivative of the formula I ##STR00016## where
R is formyl, tetrazole [sic], nitrile [sic], a COOH group or a
radical which can be hydrolyzed to COOH, and the other substituents
have the following meanings: R.sup.2 hydrogen, hydroxyl, NH2,
NH(C.sub.1-C.sub.4alkyl), N(C.sub.1-C.sub.4-alkyl).sub.2 halogen,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-fialoalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy or
C.sub.1-C.sub.4-alkylthio; X nitrogen or CR.sup.14 where R.sup.14
is hydrogen or C.sub.1-5-alkyl, or CR.sup.14 forms together with
CR.sup.3 a 5- or 6-membered alkylene or alkenylene ring which can
be substituted by one or two C.sub.1-4-alkyl groups and in-which in
each case a methylene group can be replaced by oxygen, sulfur, --NH
or --NC.sub.1-4-alkyl; hydrogen, hydroxyl, NH2,
NH(C.sub.1-C.sub.4-Alkyl), N(C.sub.1-C.sub.4-alkyl).sub.2, halogen,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy,
--NH--O--C.sub.1-4-alkyl, C.sub.1-C.sub.4-alkylthio or CR.sup.3 is
linked to CR.sup.14 as indicated above to give a 5- or 6-membered
ring; R.sup.4 and R.sup.5 (which can be identical or different):
phenyl or naphthyl, which can be substituted by one or more of the
following radicals: halogen, nitro, cyano, hydroxyl,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy, phenoxy,
C.sub.1-C.sub.4-alkylthio, amino, C.sub.1-C.sub.4-alkylamino or
C.sub.1-C.sub.4-dialkylamino; or phenyl or naphthyl, which are
connected together in the ortho positions via a direct linkage, a
methylene, ethylene or ethenylene group, an oxygen or sulfur atom
or an SO.sub.2, NH or N-alkyl group or C.sub.3-C.sub.7-cycloalkyl;
R.sup.6 hydrogen, C.sub.1-C.sub.8-alkyl, C.sub.3-C.sub.6-alkenyl,
C.sub.3-C.sub.8-alkynyl or C.sub.3-C.sub.8-cycloalkyl, where each
of these radicals can be substituted one or more times by: halogen,
nitro, cyano, C.sub.1-C.sub.4-alkoxy, C.sub.3-C.sub.6-alkenyloxy,
C.sub.3-C.sub.6-alkynyloxy, C.sub.1-C.sub.4-alkylthio,
C.sub.1-C.sub.4-haloalkoxy, C.sub.1-C.sub.4-alkylcarbonyl,
C.sub.1-C.sub.4-alkoxycarbonyl, C.sub.3-8-alkylcarbonylalkyl,
C.sub.1-C.sub.4-alkylamino, di-C.sub.1-C.sub.4-alkylamino, phenyl
or phenyl or phenoxy which is substituted one or more times, eg.
one to three times, by halogen, nitro, cyano,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy or C.sub.1-C.sub.4-alkylthio; phenyl or
naphthyl, each of which can be substituted by one or more of the
following radicals: halogen, nitro, cyano, hydroxyl, amino,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxyl C.sub.1-C.sub.4-haloalkoxy, phenoxy,
C.sub.1-C.sub.4-alkylthio, C.sub.1-C.sub.4-alkylamino,
C.sub.1-C.sub.4-dialkylamino or dioxomethylene [sic] or
dioxoethylene [sic]; a five- or six-membered heteroaromatic moiety
containing one to three nitrogen atoms and/or one sulfur or oxygen
atom, which can carry one to four halogen atoms and/or one or two
of the following radicals: C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy, C.sub.1-C.sub.4-alkylthio, phenyl,
phenoxy or phenylcarbonyl, it being possible for the phenyl
radicals in turn to carry one to five halogen atoms and/or one to
three of the following radicals: C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy and/or C.sub.1-C.sub.4-alkylthio; with
the proviso that R.sup.6 can be hydrogen only when Z is not a
single bond; Y sulfur or oxygen or a single bond; z sulfur, oxygen,
--SO--, --SO2- or a single bond. Novel carboxylic acid derivatives,
their preparation and use
Description
[0001] The present invention relates to novel carboxylic acid
derivatives, their preparation and use.
[0002] Endothelin is a peptide which is composed of 21 amino acids
and is synthesized and released by the vascular endothelium.
Endothelin exists in three isoforms, ET-1, ET-2 and ET-3. In the
following text, "endothelin" or "ET" signifies one or all isoforms
of endothelin. Endothelin is a potent vasoconstrictor and has a
potent effect on vessel tone. It is known that this
vasoconstriction is caused by binding of endothelin to its receptor
(Nature, 332, (1988) 411-415; FEBS Letters, 231, (1988) 440-444 and
Biochem. Biophys. Res. Commun., 154, (1988) 868-875).
[0003] Increased or abnormal release of endothelin causes
persistent vasoconstruction in the peripheral, renal and cerebral
blood vessels, which may lead to illnesses. It has been reported in
the literature that elevated plasma levels of endothelin were found
in patients with hypertension, acute myocardial infarct, pulmonary
hypertension, Raynaud's syndrome, atherosclerosis and in the
airways of asthmatics (Japan J. Hypertension, 12, (1989) 79, J.
Vascular Med. Biology 2, (1990) 207, J. Am. Med. Association 264,
(1990) 2868).
[0004] Accordingly, substances which specifically inhibit the
binding of endothelin to the receptor ought also to antagonize the
various abovementioned physiological effects of endothelin and
therefore be valuable drugs.
[0005] We have found that certain carboxylic acid derivatives are
good inhibitors of endothelin receptors.
[0006] The invention relates to carboxylic acid derivatives of the
formula I.
##STR00002##
where R is formyl, tetrazole [sic], nitrile [sic], a COOH group or
a radical which can be hydrolyzed to COOH, and the other
substituents have the following meanings: [0007] R.sup.2 hydrogen,
hydroxyl, NH.sub.2, NH(C.sub.1-C.sub.4-alkyl),
N(C.sub.1-C.sub.4-alkyl).sub.2, halogen, C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy or C.sub.1-C.sub.4-alkylthio; [0008] X
nitrogen or CR.sup.14 where R.sup.14 is hydrogen or
C.sub.1-5-alkyl, or CR.sup.14 forms together with CR.sup.3 a 5- or
6-membered alkylene or alkenylene ring which can be substituted by
one or two C.sub.1-4-alkyl groups and in which in each case a
methylene group can be replaced by oxygen, sulfur, --NH or
--NC.sub.1-4-alkyl; [0009] R.sup.3 hydrogen, hydroxyl, NH.sub.2,
NH(C.sub.1-C.sub.4-Alkyl), N(C.sub.1-C.sub.4-alkyl).sub.2, halogen,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy,
C.sub.1-C.sub.4-alkylthio or CR.sup.3 is linked to CR.sup.14 as
indicated above to give a 5- or 6-membered ring; [0010] R.sup.4 and
R.sup.5 (which can be identical or different): [0011] phenyl or
naphthyl, which can be substituted by one or more of the following
radicals: halogen, nitro, cyano, hydroxyl, C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy, phenoxy, C.sub.1-C.sub.4-alkylthio,
amino, C.sub.1-C.sub.4-alkylamino or C.sub.1-C.sub.4-dialkylamino;
or [0012] phenyl or naphthyl, which are connected together in the
ortho positions via a direct linkage, a methylene, ethylene or
ethenylene group, an oxygen or sulfur atom or an SO.sub.2--, NH--
or N-alkyl group, or C.sub.3-C.sub.7-cycloalkyl; [0013] R.sup.6
hydrogen, C.sub.1-C.sub.8-alkyl, C.sub.3-C.sub.6-alkenyl,
C.sub.3-C.sub.6-alkynyl or C.sub.3-C.sub.8-cycloalkyl, where each
of these radicals can be substituted one or more times by: halogen,
nitro, cyano, C.sub.1-C.sub.4-alkoxy, C.sub.3-C.sub.6-alkenyloxy,
C.sub.3-C.sub.6-alkynyloxy, C.sub.1-C.sub.4-haloalkoxy,
C.sub.1-C.sub.4-alkylcarbonyl, C.sub.1-C.sub.4-alkoxycarbonyl,
C.sub.3-8-alkylcarbonylalkyl, di-C.sub.1-C.sub.4-alkylamino, phenyl
or phenyl or phenoxy which is substituted one or more times, eg.
one to three times, by halogen, mitro, cyano,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy or C.sub.1-C.sub.4-alkylthio; [0014]
phenyl or naphthyl, each of which can be substituted by one or more
of the following radicals: halogen, nitro, cyano, hydroxyl, amino,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy, phenoxy, C.sub.1-C.sub.4-alkylthio,
C.sub.1-C.sub.4-alkylamino, C.sub.1-C.sub.4-dialkylamino,
dioxomethylene [sic] or dioxoethylene [sic]; [0015] a five- or
six-membered heteroaromatic moiety containing one to three nitrogen
atoms and/or one sulfur or oxygen atom, which can carry one to four
halogen atoms and/or one or two of the following radicals:
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy,
C.sub.1-C.sub.4-alkylthio, phenyl, phenoxy or phenylcarbonyl, it
being possible for the phenyl radicals in turn to carry one to
five, halogen atoms and/or one to three of the following radicals:
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy and/or
C.sub.1-C.sub.4-alkylthio; [0016] with the proviso that R.sup.6 can
be hydrogen only when Z is not a single bond; [0017] Y sulfur or
oxygen or a single bond; [0018] Z sulfur or oxygen or a single
bond.
[0019] The compounds, and the intermediates for preparing them,
such as IV and VI, may have one or more asymmetrical substituted
carbon atoms. Such compounds may be in the form of the pure
enantiomers or pure diastereomers or a mixture thereof. The use of
an enantiomerically pure compound as active substance is
preferred.
[0020] The invention furthermore relates to the use of the
abovementioned carboxylic acid derivatives for producing drugs, in
particular for producing endothelin receptor inhibitors.
[0021] The invention furthermore relates to the preparation of the
compounds of the formula IV in enantiomerically pure form.
Enantioselective epoxidation of an olefin with two phenyl
substituents is known (J. Org. Chem. 59, 1994, 4378-4380). We have
now found, surprisingly, that even ester groups in these systems
permit epoxidation in high optical purity.
[0022] The preparation of the compounds according to the invention
where Z is sulfur or oxygen starts from the epoxides IV, which are
obtained in a conventional manner, eg. as described in J. March,
Advanced Organic Chemistry, 2nd ed., 1983, page 862 and page 750,
from the ketones II or the olefins III:
##STR00003##
[0023] Carboxylic acid derivatives of the general formula VI can be
prepared by reacting the epoxides of the general formula IV (eg.
with R.dbd.ROOR.sup.10 [sic]) with alcohols or thiols of the
general formula V where R.sup.6 and Z have the meanings stated in
claim 1.
##STR00004##
[0024] To do this, compounds of the general formula IV are heated
with compounds of the formula V, in the molar ratio of about 1:1 to
1:7, preferably 1 to 3 mole equivalents, to 50-200.degree. C.,
preferably 80-150.degree. C.
[0025] The reaction can also take place in the presence of a
diluent. All solvents which are inert toward the reagents used can
be used for this purpose.
[0026] Examples of such solvents or diluents are water, aliphatic,
alicyclic and aromatic hydrocarbons, which may in each case be
chlorinated, such as hexane, cyclohexane, petroleum ether, naphtha,
benzene, toluene, xylene, methylene chloride, chloroform, carbon
tetrachloride, ethyl chloride and trichloroethylene, ethers such as
diisopropyl ether, dibutyl ether, methyl tert-butyl ether,
propylene oxide, dioxane and tetrahydrofuran, ketones such as
acetone, methyl ethyl ketone, methyl isopropyl ketone and methyl
isobutyl ketone, nitriles such as acetonitrile and propionitrile,
alcohols, such as methanol, ethanol, isopropanol, butanol and
ethylene glycol, esters such as ethyl acetate and amyl acetate,
amides such as dimethylformamide, dimethylacetamide and
N-methylpyrrolidone, sulfoxides and sulfones, such as dimethyl
sulfoxide and sulfolane, bases such as pyridine, cyclic ureas such
as 1,3-dimethylimidazolidin-2-one and
1,3-dimethyl-3,4,5,6-tetra-hydro-2(1H)-pyrimidinone.
[0027] The reaction is preferably carried out at a temperature in
the range from 0.degree. C. to the boiling point of the solvent or
mixture of solvents.
[0028] The presence of a catalyst may be advantageous. Suitable
catalysts are strong organic and inorganic acids, and Lewis acids.
Examples thereof are, inter alia, sulfuric acid, hydrochloric acid,
trifluoroacetic acid, p-toluenesulfonic acid, boron trifluoride
etherate and titanium(IV) alcoholates.
[0029] Compounds of the formula VI where R.sup.4 and R.sup.5 are
cycloalkyl can also be prepared by subjecting compounds of the
formula VI where R.sup.4 and R.sup.5 are phenyl, naphthyl, or
phenyl or naphthyl substituted as described above, to a nuclear
hydrogenation.
[0030] Compounds of the formula VI can be obtained in
enantiomerically pure form by starting from enantiomerically pure
compounds of the formula IV and reacting them in the manner
described with compounds of the formula V.
[0031] It is furthermore possible to obtain enantiomerically-pure
compounds of the formula VI by carrying out a classical racemate
resolution on racemic or diastereomeric compounds of the formula VI
using suitable enantiomerically pure bases such as brucine,
strychnine, quinine, quinidine, chinchonidine [sic], chinchonine
[sic], yohimbine, morphine, dehydroabietylamine, ephedrine (-),
(+), deoxyephedrine (+), (-),
threo-2-amino-1-(p-nitrophenyl)-1,3-propanediol (+), (-),
threo-2-(N,N-dimethylamino)-1-(pnitrophenyl)-1,3-propanediol (+),
(-) threo-2-amino-1-phenyl-1,3-propanediol (+), (-),
.alpha.-methylbenzylamine (+), (-), .alpha.-(1-naphthyl)ethylamine
(+), (-), .alpha.-(2-naphthyl)ethylamine (+), (-),
aminomethylpinane, N,N-dimethyl-1-phenylethylamine,
N-methyl-1-phenylethylamine, 4-nitrophenylethylamine,
pseudoephedrine, norephedrine, norpseudoephedrine, amino acid
derivatives, peptide derivatives.
[0032] The compounds according to the invention where Y is oxygen,
and the remaining substituents have the meanings stated under the
general formula I, can be prepared, for example, by reacting the
carboxylic acid derivatives of the general formula VI where the
substituents have the stated meanings with compounds of the general
formula VII
##STR00005##
where R.sup.15 is halogen or R.sup.16--SO.sub.2--, where R.sup.16
can be C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl or phenyl.
The reaction preferably takes place in one of the abovementioned
inert diluents with the addition of a suitable base, ie. of a base
which deprotonates the intermediate VI, in a temperature range from
room temperature to the boiling point of the solvent.
[0033] Compounds of the formula VII are known, some of them can be
bought, or they can be prepared in a generally known manner.
[0034] It is possible to use as base an alkali metal or alkaline
earth metal hydride such as sodium hydride, potassium hydride or
calcium hydride, a carbonate such as an alkali metal carbonate, eg.
sodium or potassium carbonate, an alkali metal or alkaline earth
metal hydroxide such as sodium or potassium hydroxide, an
organometallic compound such as butyllithium, or an alkali metal
amide such as lithium diisopropylamide.
[0035] The compounds according to the invention where Y is sulfur,
and the remaining substituents have the meanings stated under the
general formula I, can be prepared, for example, by reacting
carboxylic acid derivatives of the general formula VIII, which can
be obtained in a known manner from compounds of the general formula
VI and in which the substituents have the abovementioned meanings,
with compounds of the general formula IX, where R.sup.2, R.sup.3
and X have the meanings stated under general formula I.
##STR00006##
[0036] The reaction preferably takes place in one of the
abovementioned inert diluents with the addition of a suitable base,
ie. a base which deprotonates the intermediate IX, in a temperature
range from room temperature to the boiling point of the
solvent.
[0037] It is possible to use as base, besides those mentioned
above, organic bases such as triethylamine, pyridine, imidazole or
diazabicycloundecane [sic].
[0038] Carboxylic acid derivatives of the formula VIa (Z in formula
VI=direct linkage) can be prepared by reacting epoxides of the
formula IV with cuprates of the formula XI:
##STR00007##
[0039] The cuprates can be prepared as described in Tetrahedron
Letters 23, (1982) 3755.
[0040] Compounds of the formula I can also be prepared by starting
from the corresponding carboxylic acids, ie. compounds of the
formula I where R is COOH, and initially converting these in a
conventional manner into an activated form, such as a halide, an
anhydride or imidazolide, and then reacting the latter with an
appropriate hydroxy compound HOR.sup.10. This reaction can be
carried out in the usual solvents and often requires addition of a
base, in which case those mentioned above are suitable. These two
steps can also be simplified, for example, by allowing the
carboxylic acid to act on the hydroxy compound in the presence of a
dehydrating agent such as a carbodiimide.
[0041] In addition, it is also possible for compounds of the
formula I to be prepared by starting from the salts of the
corresponding carboxylic acids, ie. from compounds of the formula I
where R is COR.sup.1 and R.sup.1 is OM, where M can be an alkali
metal cation or the equivalent of an alkaline earth metal cation.
These salts can be reacted with many compounds of the formula
R.sup.1-A where A is a conventional nucleofugic leaving group, for
example halogen such as chlorine, bromine, iodine or aryl- or
alkylsulfonyl which is unsubstituted or substituted by halogen,
alkyl or haloalkyl, such as toluenesulfonyl and methylsulfonyl, or
another equivalent leaving group. Compounds of the formula
R.sup.1-A with a reactive substituent A are known or can be easily
obtained with general expert knowledge. This reaction can be
carried out in conventional solvents and advantageously takes place
with the addition of a base, in which case those mentioned above
are suitable.
[0042] The radical R in formula I may vary widely. For example, R
is a group
##STR00008##
where R.sup.1 has the following meanings: [0043] a) hydrogen;
[0044] b) succinylimidoxy [sic]; [0045] c) a five-membered
heteroaromatic moiety linked by a nitrogen atom, such as pyrrolyl,
pyrazolyl, imidazolyl and triazolyl, which may carry one or two
halogen atoms, in particular fluorine and chlorine and/or one or
two of the following radicals: [0046] C.sub.1-C.sub.4-alkyl such as
methyl, ethyl, 1-propyl, 2-propyl, 2-methyl-2-propyl,
2-methyl-1-propyl, 1-butyl, 2-butyl; [0047]
C.sub.1-C.sub.4-haloalkyl, in particular C.sub.1-C.sub.2-haloalkyl
such as fluoromethyl, difluoromethyl, trifluoromethyl,
chlorodifluoromethyl, dichlorofluoromethyl, trichloromethyl,
1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl,
2,2,2-trifluoroethyl, 2-chloro-2,2-difluoroethyl,
2,2-dichloro2-fluoroethyl, 2,2,2-trichloroethyl and
pentafluoroethyl; [0048] C.sub.1-C.sub.4-haloalkoxy, in particular
C.sub.1-C.sub.2-haloalkoxy such as difluoromethoxy,
trifluoromethoxy, chloradifluoromethoxy, 1-fluoroethoxy,
2-fluoroethoxy, 2,2-difluoroethoxy, 1,1,2,2-tetrafluoroethoxy,
2,2,2-trifluoroethoxy, 2-chloro-1,1,2-trifluoroethoxy and
pentafluoroethoxy, in particular trifluoromethoxy; [0049]
C.sub.1-C.sub.4-alkoxy such as methoxy, ethoxy, propoxy,
1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy,
1,1-dimethylethoxy, in particular methoxy, ethoxy, 1-methylethoxy;
[0050] C.sub.1-C.sub.4-alkylthio such as methylthio, ethylthio,
propylthio, 1-methylethylthio, butylthio, 1-methylpropylthio,
2-methylpropylthio, 1,1-dimethylethylthio, . . . in particular
methylthio and ethylthio; [0051] d) R.sup.1 furthermore a
radical
[0051] ##STR00009## [0052] where m is 0 or 1 and R.sup.7 and
R.sup.8, which can be identical or different, have the following
meanings: [0053] hydrogen [0054] C.sub.1-C.sub.8-alkyl, in
particular C.sub.1-C.sub.4-alkyl as mentioned above; [0055]
C.sub.3-C.sub.6-alkenyl such as 2-propenyl, 2-butenyl, 3-butenyl,
1-methyl-2-propenyl, 2-methyl-2-propenyl, 2-pentenyl, 3-pentenyl,
4-pentenyl, 1-methyl-2-butenyl, 2-methyl2-butenyl,
3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl,
3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl,
1,2-dimethyl-2-propenyl; 1-ethyl-2-propenyl, 2-hexenyl, 3-hexenyl,
4-hexenyl, 5-hexenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl,
3-methyl-2-pentenyl, 4-methyl2-pentenyl, 3-methyl-3-pentenyl,
4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl,
3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl,
1,1-dimethyl-3-butenyl, 1,2-dimethyl-2-butenyl,
1,2-dimethyl-3-butenyl, 1,3-dimethyl-2-butenyl,
1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl,
2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 1-ethyl-2-butenyl,
1-ethyl-3-butenyl, 2-ethyl2-butenyl, 2-ethyl-3-butenyl,
1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl and
1-ethyl-2-methyl-2-propenyl, in particular 2-propenyl, 2-butenyl,
3-methyl-2-butenyl and 3-methyl-2-pentenyl; [0056]
C.sub.3-C.sub.6-alkynyl such as 2-propynyl, 2-butynyl, 3-butynyl,
1-methyl-2-propynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl,
1-methyl-3-butynyl, 2-methyl-3-butynyl, 1-methyl-2-butynyl,
1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 2-hexynyl, 3-hexynyl,
4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-2-pentynyl,
1-methyl-3-pentynyl, 1-methyl-4-p ntynyl, 2-methyl-3-pentynyl,
2-methyl-4-pentynyl, 3-methyl-4-pentynyl, 4-methyl-2-pentynyl,
1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl,
1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 1-ethyl-2-butynyl,
1-ethyl-3-butynyl, 2-ethyl-3-butynyl and
1-ethyl-1-methyl-2-propynyl, preferably 2-propynyl, 2-butynyl,
1-methyl-2-propynyl and 1-methyl-2-butynyl, in particular
2-propynyl [0057] C.sub.3-C.sub.8-cycloalkyl such as cyclopropyl,
cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl, cyclooctyl,
where these alkyl, cycloalkyl, alkenyl and alkynyl groups can each
carry one to five halogen atoms, in particular fluorine or chlorine
and/or one or two of the following groups: [0058]
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-alkylthio, C.sub.1-C.sub.4-haloalkoxy as mentioned
above, C.sub.3-C.sub.6-alkenyloxy, C.sub.3-C.sub.6-alkenylthio,
C.sub.3-C.sub.6-alkynyloxy, C.sub.3-C.sub.6-alkynylthio, where the
alkenyl and alkynyl constituents present in these radicals
preferably have the abovementioned meanings; [0059]
C.sub.1-C.sub.4-alkylcarbonyl such as, in particular,
methylcarbonyl, ethylcarbonyl, propylcarbonyl,
1-methylethylcarbonyl, butyl-carbonyl, 1-methylpropylcarbonyl,
2-methylpropylcarbonyl, 1,1-dimethylethylcarbonyl; [0060]
C.sub.1-C.sub.4-alkoxycarbonyl such as methoxycarbonyl,
ethoxycarbonyl, propyloxycarbonyl, 1-methylethoxycarbonyl,
butyloxycarbonyl, 1-methylpropyloxycarbonyl,
2-methylpropyloxycarbonyl, 1,1-dimethylethoxycarbonyl; [0061]
C.sub.3-C.sub.8-alkenylcarbonyl, C.sub.3-C.sub.6-alkynylcarbonyl,
C.sub.3-C.sub.8-alkenyloxycarbonyl and
C.sub.3-C.sub.6-alkynyloxycarbonyl, where the alkenyl and alkynyl
radicals are preferably defined as detailed above; [0062] phenyl,
unsubstituted or substituted one or more times, eg. one to three
times, by halogen, nitro, cyano, C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy or C.sub.1-C.sub.4-alkylthio, such as
2-fluorophenyl, 3-chlorophenyl, 4-bromophenyl, 2-methylphenyl,
3-nitrophenyl, 4-cyanophenyl, 2-trifluoromethylphenyl,
3-methoxyphenyl, 4-trifluoroethoxyphenyl, 2-methylthiophenyl,
2,4-dichlorophenyl, 2-methoxy-3-methylphenyl, 2,4-dimethoxyphenyl,
2-nitro-5-cyanophenyl, 2,6-difluorophenyl; [0063]
di-C.sub.1-C.sub.4-alkylamino such as, in particular,
dimethylamino, dipropylamino, N-propyl-N-methylamino,
N-propyl-N-ethylamino, diisopropylamino, N-isopropyl-N-methylamino,
N-isopropylN-ethylamino, N-isopropyl-N-propylamino; [0064] R.sup.7
and R.sup.8 furthermore phenyl which can be substituted by one or
more, eg. one to three, of the following radicals: halogen, nitro,
cyano, C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy or
C.sub.1-C.sub.4-alkylthio, as mentioned above in particular; [0065]
or R.sup.7 and R.sup.9 together form a C.sub.4-C.sub.7-alkylene
chain which is closed to form a ring, is unsubstituted or
substituted, eg. substituted by C.sub.1-C.sub.4-alkyl, and may
contain a heteroatom selected from the group consisting of oxygen,
sulfur or nitrogen, such as --(CH.sub.2).sub.4--,
--(CH.sub.2).sub.5--, --(CH.sub.2).sub.6--, --(CH.sub.2).sub.7--,
--(CH.sub.2).sub.2--O--(CH.sub.2).sub.2--,
--CH.sub.2--S--(CH.sub.2).sub.3--,
--(CH.sub.2).sub.2--O--(CH.sub.2).sub.3--,
--NH--(CH.sub.2).sub.3--, --CH.sub.2--NH--(CH.sub.2).sub.2--,
--CH.sub.2--CH.dbd.CH--CH.sub.2--, --CH.dbd.CH--(CH.sub.2).sub.3--;
[0066] e) R.sup.1 furthermore a group
[0066] ##STR00010## [0067] where k is 0, 1 and 2, p is 1, 2, 3 and
4 and R.sup.9 is [0068] C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.3-C.sub.6-alkenyl,
C.sub.3-C.sub.6-alkynyl or unsubstituted or substituted phenyl, as
mentioned above in particular. [0069] f) R.sup.1 furthermore a
radical OR.sub.10, where R.sup.10 is: [0070] hydrogen, the cation
of an alkali metal such as. lithium, sodium, potassium or the
cation of an alkaline earth metal such as calcium, magnesium and
barium or an environmentally compatible organic ammonium ion such
as tertiary C.sub.1-C.sub.4-alkylammonium or the ammonium ion;
[0071] C.sub.3-C.sub.8-cycloalkyl as mentioned above, which may
carry one to three C.sub.1-C.sub.4-alkyl groups; [0072]
C.sub.1-C.sub.8-alkyl such as, in particular, methyl, ethyl,
propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl,
1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl,
3-methylbutyl, 1,2-dimethylpropyl, 1,1-dimethylpropyl,
2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1-methylpentyl,
2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,2-dimethylbutyl,
1,3-dimethylbutyl, 2,3-dimethylbutyl,
1,1-dimethyl-inaty-1,-2,2-dimethylbutyl, 3,3-dimethylbutyl,
thylpropyl, 1,2,2-trimethylpropyl, 1-ethylbutyl, 2-ethylbutyl,
1-ethyl-2-methylpropyl, which can carry one to five halogen atoms,
in particular fluorine and chlorine and/or one of the following
radicals: [0073] C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-alkylthio,
cyano, C.sub.1-C.sub.4-alkylcarbonyl, C.sub.3-C.sub.9-cycloalkyl,
C.sub.1-C.sub.4-alkoxycarbonyl, phenyl, phenoxy or phenylcarbonyl,
where the aromatic radicals in turn can carry in each case one to
five halogen atoms and/or one to three of the following radicals:
nitro, cyano, C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy and/or
C.sub.1-C.sub.4-alkylthio, as mentioned above in particular; [0074]
a C.sub.1-C.sub.8-alkyl as mentioned above, which can carry one to
five halogen atoms, in particular fluorine and/or chlorine, and
carries one of the following radicals: a 5-membered heteroaromatic
moiety containing one to three nitrogen atoms, or a 5-membered
heteroaromatic moiety containing a nitrogen atom and an oxygen or
sulfur atom, which can carry one to four halogen atoms and/or one
or two of the following radicals: [0075] nitro, cyano,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, phenyl, C.sub.1-C.sub.4-haloalkoxy and/or
C.sub.1-C.sub.4-alkylthio. Particular mention may be made of:
1-pyrazolyl, 3-methyl-1-pyrazolyl, 4-methyl-1-pyrazolyl,
3,5-dimethyl-1-pyrazolyl, 3-phenyl-1-pyrazolyl,
4-phenyl-1-pyrazolyl, 4-chloro-1-pyrazolyl, 4-bromo-1-pyrazolyl,
1-imidazolyl, 1-benzimidazolyl, 1,2,4-triazol-1-yl,
3-methyl-1,2,4-triazol-1-yl, 5-methyl-1,2,4-triazol-1-yl,
1-benzotriazolyl, 3-isopropyl-5-isoxazolyl, 3-methyl-5-isoxazolyl,
2-oxazolyl, 2-thiazolyl, 2-imidazolyl, 3-ethyl-5-isokazolyl,
3-phenyl5-isoxazolyl, 3-tert-butyl-5-isoxazolyl; [0076] a
C.sub.2-C.sub.6-alkyl group which carries one of the following
radicals in position 2: C.sub.1-C.sub.4-alkoxyimino,
C.sub.3-C.sub.6-alkynyloxyimino,
C.sub.3-C.sub.6-haloalkenyloxylmino or benzyloxyimino; [0077] a
C.sub.3-C.sub.6-alkenyl or C.sub.3-C.sub.6-alkynyl group, it being
possible for these groups in turn to carry one to five halogen
atoms; [0078] R.sup.10 furthermore a phenyl radical which can carry
one to five halogen atoms and/or one to three of the following
radicals: nitro, cyano, C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy and/or C.sub.1-C.sub.4-alkylthio, as
mentioned above in particular; [0079] a 5-membered heteroaromatic
moiety which is linked via a nitrogen atom, contains one to three
nitrogen atoms and can carry one or two halogen atoms and/or one or
two of the following radicals: C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy, phenyl,
C.sub.1-C.sub.4-haloalkoxy and/or C.sub.1-C.sub.4-alkylthio.
Particular mention may be made of: 1-pyrazolyl,
3-methyl-1-pyrazolyl, 4-methyl-1-pyrazolyl,
3,5-dimethyl-1-pyrazolyl, 3-phenyl-1-pyrazolyl,
4-phenyl-1-pyrazolyl, 4-chloro-1-pyrazolyl, 4-bromo-1-pyrazolyl,
1-imidazolyl, 1-benzimidazolyl, 1,2,4-triazol-1-yl,
3-methyl-1,2,4-triazol-1-yl,
5-methyl-1,2,4-triazol-1-yl4-1-benzotriazolyl,
3,4-dichloro-1-imidazolyl; [0080] R.sup.10 furthermore a group
[0080] ##STR00011## [0081] where R.sup.11 and R.sup.12, which can
be identical or different, are: [0082] C.sub.1-C.sub.8-alkyl,
C.sub.3-C.sub.6-alkenyl, C.sub.3-C.sub.6-alkynyl,
C.sub.3-C.sub.8-cycloalkyl, it being possible for these radicals to
carry a C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-alkylthio and/or an
unsubstituted or substituted phenyl radical, as mentioned above in
particular; [0083] phenyl which can be substituted by one or more,
eg. one to three, of the following radicals: halogen, nitro, cyano,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.1-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy or
C.sub.1-C.sub.4-alkylthio, where these radicals are, in particular,
those mentioned above; [0084] or R.sup.11 and R.sup.12 together
form a C.sub.3-C.sub.12-alkylene chain which can carry one to three
C.sub.1-C.sub.4-alkyl groups and contain a heteroatom from the
group consisting of oxygen, sulfur and nitrogen, as mentioned in
particular for R.sup.7 and R.sup.8. [0085] g) R.sup.1 furthermore a
radical
[0085] ##STR00012## [0086] where R.sup.13 is: [0087]
C.sub.1-C.sub.4-alkyl, C.sub.3-C.sub.6-alkenyl,
C.sub.3-C.sub.6-alkynyl, C.sub.3-C.sub.8-cycloalkyl as mentioned
above in particular, it being possible for these radicals to carry
a C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-alkylthio and/or a phenyl
radical as mentioned above; [0088] phenyl, unsubstituted or
substituted, in particular as mentioned above. [0089] h) R.sup.1 a
radical
[0089] ##STR00013## [0090] where R.sup.13 has the abovementioned
meaning. [0091] R can furthermore be: [0092] tetrazole [sic] or
nitrile [sic].
[0093] In respect of the biological effect, preferred carboxylic
acid derivatives of the general formula I, both as pure enantiomers
and pure diastereomers or as mixture thereof, are those where the
substituents have the following meanings: [0094] R.sup.2 hydrogen,
hydroxyl, N(C.sub.1-C.sub.4-alkyl).sub.2, the C.sub.1-C.sub.4alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy, C.sub.1-C.sub.4-alkylthio groups and
halogen atoms mentioned in detail for R.sup.1, especially chlorine,
methyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy; [0095]
X nitrogen or CR.sup.14 where [0096] R.sup.14 is hydrogen or alkyl,
or CR.sup.14 forms together with CR.sup.3 a 4- to
5-memberedalkylene or alkenylene ring in which, in each case, a
methylene group can be replaced by oxygen or sulfur, such as
--CH.sub.2--CH.sub.2--O--, --CH.dbd.CH--O--,
--CH.sub.2--CH.sub.2--CH.sub.2--O--, --CH.dbd.CH--CH.sub.2O--, in
particular hydrogen, --CH.sub.2--CH.sub.2--O--,
--CH(CH.sub.3)--CH(CH.sub.3)--O0-,
--C(CH.sub.3).dbd.C(CH.sub.3)--O--, --CH.dbd.C(CH.sub.3)--O-- or
--C(CH.sub.3).dbd.C(CH.sub.3)--S; [0097] R3 the hydrogen, hydroxyl,
N(C.sub.1-C.sub.4-alkyl).sub.2, C.sub.1-C.sub.4haloalkyl,
C.sub.1-C.sub.4alkoxy, C.sub.1-C.sub.4-haloalkoxy,
C.sub.1-C.sub.4-alkylthio groups and halogen atoms mentioned for
R.sup.1, especially chlorine, methyl, methoxy, ethoxy,
difluoromethoxy, trifluoromethoxy or is linked to R.sup.14 as
mentioned above to give a 5- or 6-membered ring; [0098] R.sup.4 and
R.sup.5 phenyl or naphthyl, which can be substituted by one or
more, eg. one to three, of the following radicals: halogen, nitro,
cyano, hydroxyl, mercapto, amino, C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4alkoxy,
C.sub.1-C.sub.4-haloalkoxy, C.sub.1-C.sub.4-alkylamino,
di-C.sub.1-C.sub.4-alkylamino, C.sub.1-C.sub.4alkylcarbonyl,
C.sub.1-C.sub.4alkoxycarbonyl; phenyl or naphthyl, which are
connected together in the ortho positions by a direct linkage, a
methylene; ethylene or ethenylene group, an oxygen or sulfur atom
or an SO.sub.2, NH or N-alkyl group, or C.sub.3-C.sub.7-cycloalkyl;
[0099] R.sup.6 C.sub.1-C.sub.8-alkyl, C.sub.3-C.sub.6-alkenyl,
C.sub.3-C.sub.6-alkynyl or C.sub.2-C.sub.8-cycloalkyl as mentioned
above in particular, it being possible for these radicals in each
case to be substituted one or more times by: halogen, hydroxyl,
nitro, cyano, C.sub.1-C.sub.4-alkoxy, C.sub.3-C.sub.6-alkenyloxy,
C.sub.3-C.sub.6-alkyhyloxy, C.sub.1-C.sub.4-alkylthio,
C.sub.1-C.sub.4-haloalkoxy, C.sub.1-C.sub.4-alkylcarbonyl,
hydroxycarbonyl, C.sub.2-C.sub.4-alkoxycarbonyl,
C.sub.1-C.sub.4-alkylamino, di-C.sub.1-C.sub.4-alkylamino or
unsubstituted or substituted phenyl or phenoxy, as mentioned above
in particular; [0100] phenyl or naphthyl, which can be substituted
by one or more of the following radicals: halogen, nitro, cyano,
hydroxyl, amino, C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy, C.sub.1-C.sub.4-haloalkoxy, phenoxy,
C.sub.1-C.sub.4-alkylthio, C.sub.1-C.sub.4-alkylamino [sic] or
C.sub.2-C.sub.4-dialkylamino, as mentioned in particular for
R.sup.7 and R.sup.4; [0101] a five- or six-membered heteroaromatic
moiety which contains one to three nitrogen atoms and/or one sulfur
or oxygen atom and which can carry one to four halogen atoms and/or
one or two of the following radicals: C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy, C.sub.1-C.sub.4-alkylthio, phenyl,
phenoxy or phenylcarbonyl, it being possible for the phenyl
radicals in turn to carry one to five halogen atoms and/or one to
three of the following radicals: C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-haloalkoxy and/or C.sub.1-C.sub.4-alkylthio, as
mentioned for R.sup.4 in particular; [0102] Y sulfur, oxygen or a
single bond; [0103] Z sulfur, oxygen, --SO--, --SO.sub.2-- or a
single bond.
[0104] Particularly preferred compounds of the formula I, both as
pure enantiomers and pure diastereomers or as mixture thereof, are
those in which the substituents have the following meanings: [0105]
R.sup.2 C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-alkoxy [0106] X
nitrogen or CR.sup.14, where [0107] R.sup.14 is hydrogen or alkyl,
or CR.sup.14 forms together with CR.sup.3 a 4- or 5-membered
alkylene or alkenylene ring such as
--CH.sub.2--CH.sub.2--CH.sub.2--, --CH.dbd.CH--CH.sub.2--, in which
in each case a methylene group can be replaced by oxygen or sulfur,
such as --CH.sub.2--CH.sub.2--O--, --CH.dbd.CH--O--,
--CH.sub.2--CH.sub.2--CH.sub.2--O--, --CH.dbd.CH--CH.sub.2O--, in
particular hydrogen, --CH.sub.2--CH.sub.2--O--,
--CH(CH.sub.3)--CH(CH.sub.3)--O--,
--C(CH.sub.3).dbd.C(CH.sub.3)--O--, --CH.dbd.C(CH.sub.3)--O-- or
--C(CH.sub.3).dbd.C(CH.sub.3)--S; [0108] R.sup.3 the
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-alkylthio groups mentioned for R.sup.1, or is
linked to R.sup.14 as mentioned above to give a 5- or 6-membered
ring; [0109] R.sup.4 and R.sup.5 phenyl (identical or different)
which can be substituted by one or more, eg. one to three, of the
following radicals: halogen, nitro, hydroxyl,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-alkylthio or [0110] R.sup.4 and R.sup.5 are phenyl
groups which are connected together in the ortho positions by a
direct linkage, a methylene, ethylene or ethenylene group, an
oxygen or sulfur atom or an SO.sub.2, NH or N-alkyl group; or
[0111] R.sup.4 and R.sup.5 are C.sub.3-C.sub.7-cycloalkyl; [0112]
R.sup.6 C.sub.1-C.sub.8-alkyl, C.sub.3-C.sub.6-alkenyl or
C.sub.3-C.sub.8-cycloalkyl, it being possible for these radicals in
each case to be substituted one or more times by: halogen,
hydroxyl, nitro, cyano, C.sub.1-C.sub.4-alkoxy,
C.sub.3-C.sub.6-alkenyloxy, C.sub.1-C.sub.4-alkylthio; phenyl or
naphthyl, which can be substituted by one or more of the following
radicals: halogen, nitro, cyano, hydroxyl, amino,
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
--C.sub.1-C.sub.4-alkowy, C.sub.1-C.sub.4-haloalkoxy, phenoxy,
C.sub.1-C.sub.4-alkylthio, C.sub.1-C.sub.4-alkylamino [sic] or
C.sub.1-C.sub.4-dialkylamino; [0113] a five- or six-membered
heteroaromatic moiety which contains a nitrogen atom and/or a
sulfur or oxygen atom and which can carry one to four halogen atoms
and/or one or two of the following radicals: C.sub.1-C.sub.4-alkyl,
C.sub.1-C.sub.4-haloalkyl, C.sub.1-C.sub.4-alkoxy,
C.sub.1-C.sub.4-alkylthio, phenyl, phenoxy or phenylcarbonyl, it
being possible for the phenyl radicals in turn to carry one to
five. halogen atoms and/or one to three of the following radicals:
C.sub.1-C.sub.4-alkyl, C.sub.1-C.sub.4-haloalkyl,
C.sub.1-C.sub.4-alkoxy and/or C.sub.1-C.sub.4-alkylthio; [0114] Y
sulfur, oxygen or a single bond; [0115] Z sulfur, oxygen, --SO--,
--SO.sub.2-- or a single bond.
[0116] The compounds of the present invention provide a novel
therapeutic potential for the treatment of hypertension, pulmonary
hypertension, myocardial infarct, angina pectoris, acute kidney
failure, renal insufficiency, cerebral vasospasms, cerebral
ischemia, subarachnoid hemorrhages, migraine, asthma,
atherosclerosis, endotoxic shock, endotoxin-induced organ failure,
intra vascular coagulation, restenosis after angioplasty, benign
prostate hyperplasia, or hypertension or kidney failure caused by
ischemia or intoxication.
[0117] The good effect of the compounds can be shown in the
following tests:
Receptor Binding Studies
[0118] Cloned human ET.sub.A receptor-expressing CHO cells and
guinea pig cerebellar membranes with >60% ET.sub.B compared with
ET.sub.A receptors were used for binding studies.
[0119] The ET.sub.A receptor-expressing CHO cells were grown in
F.sub.12 medium containing 10% fetal calf serum, 1% glutamine, 100
U/ml penicillin and 0.2% streptomycin (Gibco BRL, Gaithersburg,
Md., USA). After 48 h, the cells were washed with PBS and incubated
with 0.05% trypsin-containing PBS for 5 min. Neutralization was
then carried out with F.sub.12 medium, and the cells were collected
by centrifugation at 300.times.g. To lyze the cells, the pellet was
briefly washed with lysis buffer (5 mM Tris-HCl, pH 7.4 with 10%
glycerol) and then incubated at a concentration of 10.sup.7
cells/ml of lysis buffer at 4.degree. C. for 30 min. The membranes
were centrifuged at 20,000 xsg-for 10 min, and the pellet was
stored in liquid nitrogen.
[0120] Guinea pig cerebella were homogenized in a Potter-Elvejhem
homogenizer and [lacuna] obtained by differential centrifugation at
1000.times.g for 10 min and repeated centrifugation of the
supernatant at 20,000.times.g for 10 min.
Binding Assays
[0121] For the ET.sub.A and ET.sub.B receptor binding assay, the
membranes were suspended in incubation buffer (50 mM Tris-HCl, pH
7.4 with 5 mM MnCl.sub.2, 40 .mu.g/ml bacitracin and 0.2% BSA) at a
concentration of 50 Rg of protein per assay mixture and incubated
with 25 pM [125I)-ET.sub.1 (ET.sub.A receptor assay) or 25 pM
[125I]-RZ.sub.3 (ET.sub.B receptor assay) in the presence and
absence of test substance at 25.degree. C. The nonspecific binding
was determined using 10.sup.-7 M ET.sub.1. After 30 min, the free
and bound radioligand were separated by filtration through GF/B
glass fiber filters (Whatman, England) on a Skatron cell collector
(Skatron, Lier, Norway) and the filters were washed with ice-cold
Tris-HCl buffer, pH 7.4 with 0.2% BSA. The radioactivity collected
on the filters was quantified using a Packard 2200 CA liquid
scintillation counter.
Functional In Vitro Assay System to Look for Endothelin Receptor
(Subtype A) Antagonists
[0122] This assay system is a functional, cell-based assay for
endothelin receptors. When certain cells are stimulated with
endothelin 1 (ET1) they show an increase in the intracellular
calcium concentration. This increase Can be measured in intact
cells loaded with calcium-sensitive dyes.
[0123] 1-Fibroblasts which had been isolated from rats and in which
an endogenous endothelin receptor of the A subtype had been
detected were loaded with the fluorescent dye Fura 2-an as follows:
after trypsinization, the cells were resuspended in buffer A (120
mM NaCl, 5 mM KCl, 1.5 mM MgCl.sub.2, 1 mM CaCl.sub.2, 25 mM HEPES,
10 mM glucose, pH, 7.4.) to a density of 2.times.10.sup.6/ml and
incubated with Fura 2-am (2 .mu.M), Pluronics F-127 (0.04%) and
DMSO (0.2%) at 37.degree. C. in the dark for 30 min. The cells were
then washed twice with buffer A and resuspended at
2.times.10.sup.6/ml.
[0124] The fluorescence signal from 2.times.10.sup.5 cells per ml
with Ex/Em 380/510 was recorded continuously at 30.degree. C. The
test substances and, after an incubation time of 3 min, ET1
[lacuna] to the cells, the maximum change in the fluorescence was
determined. The response of the cells to ET1 without previous
addition of a test substance was used as control and was set equal
to 100%.
Testing of ET Antagonists In Vivo
[0125] Male SD rats weighting 250-300 g were anesthetized with
amobarbital, artificially ventilated, vagotomized and pithed. The
carotid artery and jugular vein were cathetized [sic].
[0126] In control animals, intravenous administration of 1 .mu.g/kg
ET1 led to a distinct rise in blood pressure which persisted for a
lengthy period.
[0127] The test animals received an i.v. injection of the test
compounds (1 ml/kg) 5 min before the administration of ET1. To
determine the ET-antagonistic properties, the rise in blood
pressure in the test animals was compared with that in the control
animals.
Endothelin-1-Induced Sudden Death in Mice
[0128] The principle of the-test is the inhibition of the sudden
heart death caused in mice by endothelin, which is probably induced
by constriction of the coronary vessels, by pretreatment with
endothelin receptor antagonists. Intravenous injection of 10
nmol/kg endothelin in a volume of 5 ml/kg of body weight results in
death of the animals within a few minutes.
[0129] The lethal endothelin-1 dose is checked in each case on a
small group of animals. If the test substance is administered
intravenously, the endothelin-1 injection which was lethal in the
reference group usually takes place 5 min thereafter. With other
modes of administration, the times before administration are
extended, where appropriate up to several hours.
[0130] The survival rate is recorded, and effective doses which
protect 50% of the animals (ED 50) from endothelin-induced heart
death for 24 h or longer are determined.
Functional Test on Vessels for Endothelin Receptor Antagonists
[0131] Segments of rabbit aorta are, after an initial tension of 2
g and a relaxation time of 1 h in Krebs-Henseleit solution at
37.degree. C. and pH-7.3-7.4, first induced to contract with K+.
After washing out, an endothelin dose-effect plot up to the maximum
is constructed.
[0132] Potential endothelin antagonists are administered to other
preparations of the same vessel 15 min before starting the
endothelin dose-effect plot. The effects of the endothelin are
calibrated as a % of the K+-induced contraction. Effective
endothelin antagonists result in a shift to the right in the
endothelin dose-effect plot.
[0133] The compounds according to the invention can be administered
orally or parenterally (subcutaneously, intravenously,
intramuscularly, intraperotoneally) in a conventional way.
Administration can also take place with vapors or sprays through
the nasopharyngeal space.
[0134] The dosage depends on the age, condition and weight of the
patient and on the mode of administration. The daily dose of active
substance is, as a rule, about 0.5-50 mg/kg of body weight on oral
administration and about 0.1-10 mg/kg of body weight on parenteral
administration.
[0135] The novel compounds can be used in conventional solid or
liquid pharmaceutical forms, eg. as uncoated or (film-)coated
tablets, capsules, powders, granules, suppositories, solutions,
ointments, creams or sprays. These are produced in a conventional
way. The active substances can for this purpose be processed with
conventional pharmaceutical aids such as tablet binders, fillers,
preservatives, tablet disintegrants, flow regulators, plasticizers,
wetting agents, dispersants, emulsifiers, solvents, release-slowing
agents, antioxidants and/or propellent gases (cf. H. Sucker. et
al.: Pharmazeutische Technologie, Thieme-Verlag, Stuttgart, 1991).
The administration forms obtained in this way normally contain from
0.1 to 90% by weight of the active substance.
SYNTHESIS EXAMPLES
Example 1
Methyl 2-hydroxy-3-methoxy-3,3-diphenylpropionate
[0136] 5 g (19.6 mmol) of methyl 3,3-diphenyl-2,3-epoxypropionate
were dissolved in 50 M1 of absolute methanol and, at 0.degree. C.,
0.1 ml of boron trifluoride etherate was added. The mixture was
stirred at 0.degree. C. for 2 h and at room temperature for a
further 12 h. The solvent was distilled out, the residue was taken
up in ethyl acetate, washed with sodium bicarbonate solution and
water and dried over magnesium sulfate. After removal of the
solvent by distillation there remained 5.5 g (88%) of a, pale
yellow oil.
Example 2
Methyl 2-hydroxy-3-phenoxy-3,3-diphenylpropionate
[0137] 5 g (19.6 mmol) of methyl 3,3-diphenyl-2,3-epoxypropionate
and 5.6 g (60 mmol) of phenol were heated together at 100.degree.
C. for 6 h. Removal of the excess phenol by distillation under high
vacuum and purification of the residue by chromatography on silica
gel with hexane/ethyl acetate mixtures resulted in 4.9 g (77%) of a
pale yellow oil.
Example 3
Methyl
2-(4,6-dimethoxy-pyrimidin-2-yloxy)-3-methoxy-3,3-diphenylpropionat-
e
[0138] 2.86 g (10 mmol) of methyl
2-hydroxy-3-methoxy-3,3-diphenylpropionate were dissolved in 40 ml
of dimethylformamide, and 0.3 g (12 mmol) of sodium hydride was
added. The mixture was stirred for 1 h and then 2.2 g (10 mmol) of
4,6-dimethoxy-2-methylsulfonylpyrimidine were added. After stirring
at room temperature for 24 h, cautious hydrolysis was carried out
with 10 ml of water, the pH was adjusted to 5 with acetic acid, and
the solvent was removed by distillation under high vacuum. The
residue was taken up in 100 ml of ethyl acetate, washed with water
and dried over magnesium sulfate, and the solvent was distilled
out. The residue was mixed with 10 ml of ether, and the resulting
precipitate was filtered off with suction. After drying, 3.48 g
(82%) of a white powder remained.
[0139] Melting point 81.degree. C.
Example 4
2-(4,6-Dimethoxy-pyrimidin-2-yloxy)-3-methoxy-3,3-diphenylpropionic
acid
[0140] 2.12 g (5 mmol) of methyl
2-(4,6-dimethoxy-pyriMidin-2-yloxy)-3-methoxy-3,3-diphenylpropionate
were dissolved in 50 ml of dioxane, 10 ml of 1 N KOH solution were
added, and the mixture was stirred at 100.degree. C. for 3 h. The
solution was diluted with 300 ml of water and extracted with ethyl
acetate to remove unreacted ester. The aqueous phase was then
adjusted to pH 1-2 with dilute hydrochloric acid and extracted with
ethyl acetate. After drying over magnesium sulfate and removal of
the solvent by distillation, the residue was mixed with an
ether/hexane mixture, and the precipitate which formed was filtered
off with suction. After drying, 1.85 g (90%) of a white powder
remained.
[0141] Melting-point 16-7.degree. C.
Example 5
2-(4,6-Dimethoxy-2-pyrimidinyloxy)-3-methoxy-3,3-diphenyl sodium
[sic] propionate
[0142] 1.68 g (4 mmol) of
2-(4,6-dimethoxy-2-pyrimidinyloxy)-3-methoxy-3,3-diphenylpropionic
acid are dissolved in 4 ml of 1N NaOH 4 100 ml of water. The
solution is freeze-dried, and the sodium salt of the carboxylic
acid used is obtained quantitatively.
[0143] 10 g (34.9 mmol) of methyl
2-hydroxy-3-methoxy-3,3-diphenylpropionate were dissolved in 50 ml
each of methanol and glacial acetic acid, 1 ml of RuO(OH).sub.2 in
dioxane was added, and hydrogenation was carried out with H.sub.2
in an autoclave at 100.degree. C. under 100 bar for 30 h. The
catalyst was filtered off, the mixture was concentrated, mixed with
ether and washed with NaCl solution, and the organic phase was
dried and concentrated. 10.1 g of methyl
3,3-dicyclohexyl-2-hydroxy-3-methoxypropionate were obtained as an
oil.
Example 7
Methyl
2-[(4,6-dimethoxy-pyrimidin-2-yl)thio]-3-methoxy-3,3-diphenylpropio-
nate [sic]
[0144] 7.16 g (25 mmol) of methyl
2-hydroxy-3-methoxy-3,3-diphenylpropionate were dissolved in 50 ml,
of dichloromethane, 3 g (30 mmol) of triethylamine were added, and
3.2 g (28 mmol) of methanesulfonyl chloride were added dropwise
while stirring. The mixture was stirred at room temperature for 2
h, washed with water, dried over magnesium sulfate and concentrated
under reduced pressure. The residue was taken up in DMF and added
dropwise at 0.degree. C. to a suspension of 12.9 g (75 mmol) of
4,6-dimethoxypyrimidine-2-thiol and 8.4 g (100 mmol) of sodium
bicarbonate in 100 ml of DMF. After stirring at room temperature
for 2 h and at 60.degree. C. for a further 2 h, the mixture was
poured into 1 liter of ice-water, and the resulting precipitate was
filtered off with suction. After drying, 3.19 g (29%) of a white
powder remained.
Example 8
Methyl 2-hydroxy-3,3-diphenylbutyrate
[0145] 1.5 g (5.9 mmol) of methyl 3,3-diphenyl-2,3-epoxypropionate
dissolved in 10 ml of absolute ether were added dropwise to a
cup-rate solution which had been prepared from 635 mg (7 mmol) of
copper(I) cyanide dissolved in 10 ml of absolute ether and 8.14 ml
(13 mmol) of a 1.6 normal methyllithium solution and had been
cooled to -78.degree. C. The solution was stirred at -78.degree. C.
for 1 h and then allowed to warm to room temperature. It was
subsequently diluted with 100 ml of ether and 100 ml of water, and
the ether phase was washed with dilute citric acid and with sodium
bicarbonate solution and dried over magnesium sulfate. The crude
product was purified by chromatography on silica gel with
cyclohexane/ethyl acetate mixtures to result in 250 mg (16%) of a
pale yellow oil.
Example 9
2-Hydroxy-3-methoxy-3,3-diphenylpropionic acid
[0146] 91.11 g (0.5 mol) of benzophenone and 45.92 g (0.85 mol) of
sodium methoxide were suspended in 150 ml of methyl tert-butyl
ether (MTB) at room temperature. After cooling to -10.degree. C.,
92.24 g (0.85 mol) of methyl chloroacetate were added in such a way
that the internal temperature rose to 40.degree. C. while
continuing to cool in a bath at -10.degree. C. The mixture was then
stirred without cooling at the autogenous temperature for one hour.
After addition of 250 ml of water, and brief stirring, the aqueous
phase was separated off. The MTB phase was washed with 250 ml of
dilute sodium chloride solution. After the solvent had been changed
to methanol (250 ml), a solution of 1 g of p-toluenesulfonic acid
in 10 ml of methanol was added at room temperature. The mixture was
stirred at autogenous temperature for one hour and then heated to
reflux. While distilling out the methanol, 400 g of a 10% strength
sodium hydroxide solution was added dropwise, and finally 60 ml of
water were added. The methanol was distilled out until the bottom
temperature reached 97.degree. C. After cooling to 55.degree. C.,
190 ml of MTB were added and the mixture was acidified to pH 2 with
about 77 ml of concentrated HCl. After cooling to room temperature,
the aqueous phase was separated off and the organic phase was
concentrated, by distilling, out 60 ml of MtB [sic]. The product
was crystallized by adding 500 ml of heptane and slowly cooling to
room temperature. The coarsely crystalline solid was filtered off
with suction, washed with heptane and dried to constant weight in a
vacuum oven at 40.degree. C.
[0147] Yield: 108.9 g (80%), HPLC >99.5% area.
Example 10
S-2-Hydroxy-3-methoxy-3,3-diphenylpropionic acid (facemate
resolution with L-proline methyl ester)
[0148] 148.8 g of a 30% strength methanolic sodium methanolate
solution (0.826 mol) were added dropwise to 240 g of a 57.%
strength methanolic L-proline methyl ester hydrochloride solution
(0.826 mol) at room temperature, and 2.4 l of MTB and 225 g (0.826
mol) of 2-hydroxy-3-Methoxy-3,3-diphenylpropionic acid were added.
After 2680 ml of MTB/methanol mixture had been distilled out with
simultaneous dropwise addition of 2.4 l of MTB, the mixture was
slowly cooled to room temperature, the crystals
(R-2-hydroxy-3-methoxy-3,3-diphenylpropionic acid.times.L-proline
methyl ester) were filtered off with suction, and the solid was
washed with 150 ml of MTB. The filtrate was concentrated by
distilling out 1.5 l of MTB, and 1.0 l of water was added. The pH
was adjusted to 1.2 with concentrated hydrochloric acid at room
temperature and, after stirring and phase separation, the aqueous
phase was separated off and extracted with 0.4 l of MTB. The
combined organic phases were extracted with 0.4 l of water. The
residue after the MTB had been stripped off was dissolved in 650 ml
of toluene under reflux, and the product was crystallized by
seeding and slow cooling. Filtration with suction, washing with
toluene and drying in a vacuum oven resulted in 78.7 g of
S-2-hydroxy-3-methoxy-3,3-diphenylpropionic acid (yield 35% based
on the racemate).
[0149] Chiral HPLC: 100% pure
[0150] HPLC: 99.8%
Example 11
S-2-Hydroxy-3-methoxy-3,3-diphenylpropionic acid (racemate
resolution with (S)-1-(4-nitrophenyl)ethylamine)
[0151] 30.5 g J0.184 mol) of (S)-1-(4-nitrophenyl)ethylamine were
added to 100 g (0.368 mol) of
2-hydroxy-3-methoxy-3,3-diphenylpropionic acid in 750 ml of acetone
and 750 ml of MTB under reflux, the mixture was seeded, boiled
under reflux for one hour and slowly cooled to room temperature for
crystallization. The crystals
(S-2-hydroxy-3-methoxy-3,3-diphenylpropionic
acid.times.(S)-1-(4-nitrophenyl)ethylamine) were filtered off with
suction and washed with MTB. The residue was suspended in 500 ml of
water and 350 ml of MTB and then the pH was adjusted to 1.2 with
concentrated hydrochloric acid at room temperature, and, after
stirring and phase separation, the aqueous phase was separated off
and extracted with 150 ml of MTB. The combined organic phases were
extracted with 100 ml of water. 370 ml of MTB were distilled out
and then 390 ml of n-heptane were added under reflux, and the
mixture was slowly cooled to room temperature while the product
crystallized. Filtration with suction, washing with n-heptane and
drying in a vacuum oven resulted in 35.0 g of
S-2-hydrory-3-methoxy-3,3-diphenylpropionic acid (yield 35% based
on the race-mate).
[0152] Chiral HPLC: 100% pure
[0153] HPLC: 99.8%
Example 12
Benzyl
3-methoxy-2-(4-methoxy-6,7-dihydro-5H-cyclopentapyrimidin-2-yloxy)--
3,3-diphenylpropionate
[0154] 24.48 g (90 mmol) of
3-methoxy-3,3-diphenyl-2-hydroxypropionic acid were dissolved in
150 ml of DMF, and 13.7 g (99 mmol) of potassium carbonate were
added. The suspension was stirred at room temperature for 30. min.
Then 10.7 ml (90 mmol) of benzyl bromide were added dropwise over
the course of 5 min, and the mixture was stirred for 1 h, during
which the temperature rose to 32.degree. C.
[0155] To this mixture were successively added 24.84 g (180 mmol)
of K.sub.2CO.sub.3 and 20.52 g (90 mmol) of
2-methanesulfonyl-4-methoxy6,7-dihydro-5H-cyclopentapyridine [sic],
and the mixture was stirred at 80.degree. C. for 3 h.
[0156] For workup, the contents of the flask were diluted with
about 600 ml of H.sub.2O and cautiously acidified with concentrated
HCl, and 250 ml of ethyl acetate were added. 31.4 g of pure product
precipitated and were filtered off.
[0157] The ethyl acetate phase was separated from the mother
liquor, the aqueous phase was extracted again with ethyl acetate,
and the combined organic phases were concentrated. The oily residue
(19 g) was purified by chromatography (cyclohexane/ethyl
acetate=9/1) to result in a further 10.5 g of pure product.
[0158] Total yield: 41.9 g (82.2 mmol)=191%
[0159] Melting point 143-147.degree. C.
[0160] MS: MH.sup.+=511
Example 13
3-Methoxy-2-(4-inethoxy-(6,7-dihydro-5H-cyclopeniapyrimidin-2-yloxy)-3,3-d-
iphenylpropionic [sic] acid
[0161] 40 g (78.4 mmol) of benzyl
3-methoxy-2-(4-methoxy-6,7-dihydro-5H-cyclopentapyrimidin-2-yloxy)-3,3-di-
phenylpropionate were dissolved in 400 ml of ethyl acetate/methanol
(4:1), about 500 mg of palladium on active carbon (10%) were added,
and the mixture was exposed to a hydrogen atmosphere until no
further gas was taken up. The Catalyst was-filtered off, the
solution was evaporated, and the residue was crystallized from
ether.
Example 14
Ethyl 2S-3,3-diphenyloxirane-2-carboxylate
[0162] 2.57 g (10.2 mmol) of ethyl 3,3-diphenylacrylate and 464 mg
of 4-phenylpyridine N-oxide were dissolved in 24 ml of methylene
chloride, and 432 mg (6.5 mol %) of
(5,5)-(+)-N,N'-bis(3,5-ditert-butylsalicylidene)-1,2-cyclohexanediaminoma-
nganese(III) chloride were added. While cooling in ice, 6.4 ml of a
12% strength sodium hypochloride [sic] solution were added, and the
mixture was stirred while cooling in ice for 30 min and at room
temperature overnight. The solution was diluted to 200 ml with
water, extracted with ether, dried and evaporated. 2.85 g of a
colorless oil were obtained. Purification by NPLC [sic]
(cyclohexane:ethyl acetate=9:1) resulted in 1.12 g of oil with an
enantiomer ratio of about 8:1 in favor of the S configuration.
[0163] .sup.1H-NMR [CDCl.sub.3],
[0164] .delta.=1.0 (t, 3H); 3.9 (m, 3H); 7.3 (m, 10H)
Example 15
2-Methylsulfonyl-6,7-dihydro-5H-cyclopentapyrimidin-4-ol [sic]
[0165] 46.9 g (330 mmol) of methyl cyclopentanone-2-carboxylate and
53.5 g (192 mmol) of 5-methylisothiourea [sic] sulfate were
successively added to 29.6 g (528 mmol) of KOH in 396 ml of
methanol, and the mixture was stirred at room temperature
overnight, acidified with 1N hydrochloric acid and diluted with
water. The crystals which separated out were filtered off with
suction and dried. 20 g of crystals were obtained.
Example 16
sulfanyl 4-Chloro-2-methyl-6,7-dihydro-5H-cyclopentapyrimidine
[sic]
[0166] 255 ml of phosphorus oxychloride were added to 20 g (110
mmol) [lacuna], and the mixture was stirred at 80.degree. C. for 3
hours. Phosphorus oxychloride was evaporated off, ice was added to
the residue, and the crystals which separated out were filtered off
with suction. 18.5 g of a brownish solid were obtained.
Example 17
4-Methoxy-2-methylsulfonyl-6,7-dihydro-5H-cyclopenipyrimidine
[sic]
[0167] 18.05 g (90 mmol) of
4-chloro-2-methylsulfonyl-6,7-dihydro-5H-cyclopentapyrimidine [sic]
were dissolved in 200 ml of methanol. At 45.degree. C., 16.7 g of
sodium methoxide (as 30% strength solutions [sic] in methanol) were
added dropwise, and the mixture was stirred for 2 hours. The
solution was evaporated, taken up in ethyl acetate and acidified
with dilute hydrochloric acid, and the ethyl acetate extract was
evaporated. 15.5 g of an oil remained.
[0168] .sup.1H-NMR [DMSO],
[0169] .delta.=2.1 (quintet, 2H); 2.5 (s, 3H);
[0170] 2.8 (dt, 4H); 3.9 (s, 3H) ppm.
Example 18
2-methylsulfonyl-4-methoxy-6,7-dihydro-5H-cyclopentopyrimidine
[sic]
[0171] 15 g (76.2 mmol) of
4-methoxy-2-methylsulfonyl-6,7-dihydro-5Hcyclopentapyrimidine [sic]
were dissolved in 160 ml of glacial acetic acid/methylene chloride
(1:1), and 1.3 g of sodium tungstate were added. At 35.degree. C.,
17.5 ml (170 ml [sic]) of a 30% strength H202 solution were added
dropwise. The mixture was then diluted with 500 ml of water and 100
ml of methylene chloride, and the organic phase was separated off,
dried and evaporated. 14 g of oil remained and were crystallized
from ether.
[0172] .sup.1H-NMR [CDCl.sub.3],
[0173] .delta.=2.2 (quintet, 2H); 3.0 (dt., 4H);
[0174] 3.3 (s, 3H); 4.1 (s, 3H) ppm
Example 19
1-Benzenesulfonyl-3-(4,6-dimethoxy-2-pyrimidinyloxy)-4-methoxy-4,4-dipheny-
l-2-butanone
[0175] 0.37 g (2.4 mmol) of phenyl methane [sic] sulfone were
dissolved in 10 ml of dry THE and then, at -70.degree. C., 2 eq. of
butyllithium (2.94. ml; 1.6 molar solution in hexane) were added
dropwise. After 1 h at -70.degree. C., 1 g (2.4 mmol) of methyl
2-(4,6-dimethoxy-2-pyrimidinyloxy)-3-methoxy-3,3-diphenylpropynoate
[sic] dissolved in 5 ml of THF was added dropwise. The reaction
mixture was then stirred at -70.degree. C. for 1 h and at
-10.degree. C. for 1 h and then warmed to room temperature.
[0176] For workup, about 10 ml of saturated NH.sub.4Cl solution
were added dropwise, thorough extraction with ethyl acetate was
carried out, and the-combined organic phases [lacuna] with
saturated N--Cl [sic] solution and dried over Na.sub.2SO.sub.4. The
residue obtained after drying and concentration was purified by
chromatography on silica gel (n-heptane/ethyl acetate
15%.fwdarw.30%) and subsequently MPLC on RP silica gel
(acetonitrile/H.sub.2O+TFA); 0.3 g of a white amorphous powder was
obtained as product.
Example 20
3,3-Diphenyloxiram-2-carbonitrile [sic]
[0177] 3.1 g (54.9 mmol) of sodium methoxide were suspended in 20
ml of dry THF and then, at -10.degree. C., a mixture of 5-g (27.4
mmol) of benzophenone and 4.2 g (54.9 mmol) of chloroacetonitrile
was added dropwise.
[0178] The reaction mixture was stirred at -10.degree. C. for about
2 h, then poured into water and extracted several times with ethyl
acetate. The combined organic phases were dried over
Na.sub.2SO.sub.4 and concentrated, and the residue was purified by
chromatography on silica gel (n-heptane/ethyl acetate).
[0179] Yield: 1.2 g (20%)
[0180] .sup.1H-NMR (CDCl.sub.3],
[0181] .delta.=3.9 (s, 1H); 7.4-7.5 (m, 10H) ppm
Example 21
2-Hydroxy-3-methoxy-3,3-diphenylpropionitrile
[0182] 6.5 [lacuna] (29.4 mmol) of
3,3-diphenyloxirane-2-carbonitrile were dissolved in 60 ml of
methanol and, at 0.degree. C., about 2 ml of boron trifluoride
etherate solution were added. The mixture was stirred further at
0.degree. C. for 1 h and then at room temperature overnight. For
workup it was diluted with diethyl ether and washed with saturated
NaCl solution, and the organic phase was dried over Na2SO4 and
concentrated. The residue comprised 7.3 g of a white amorphous
powder which was used directly in the subsequent reactions.
[0183] .sup.1H-NMR.[CDCl.sub.3],
[0184] .delta.=2.95 (broad s, OH), 3.15 (s, 3H),.sup.-
[0185] 5.3 (s, 1H), 7.3-7.5 (m, 10) ppm
Example 22
2-(4,6-Dimethoxy-2-nyrimidinyloxy)-3-methoxy-3,3-diphenylpropionitrile
[0186] 7.3 g (28.8 mmol) of
2-hydroxy-3-methoxy-3,3-diphenylpropionitrile were dissolved in 90
ml of DMF, and 4 g (28.8 mmol) of K.sub.2CO.sub.3 and 6.3 g (28
mmol) of 2-methanesulfonyl-4,6-dimethoxypyrimidine were added. The
mixture was stirred at room temperature for about 12 h, then poured
into water and extracted with ethyl acetate. The combined organic
phases were washed again with H.sub.2O, dried and concentrated. The
residue obtained in this way was then purified by chromatography on
silica gel (n-hepane/ethyl acetate.
[0187] Yield: 6.9 g of white amorphous powder
[0188] FAB-MS: 392 (M+H.sup.+)
[0189] .sup.1H-NMR [CDCl.sub.3],
[0190] .delta.=3.3 (s, 3H); 4.95 (s, 6H), 5.85 (s, 1H);
[0191] 6.3 (s, 1H); 7.3-7.5 (m, 10H) ppm
Example 23
5-[2-(4,6-Dimethoxy-2-pyrimidinyloxy)-3-methoxy-3,3-diphenyl)-propyl]-1H-t-
etrazole [sic]
[0192] 0.5 g (1.3 mmol) of nitrile was dissolved in-10 ml of
toluene, and 85 mg (1.3 mmol) of NaN.sub.3 and 460 mg (1.4 mmol) of
Bu.sub.3SnCl were successively added, and then the mixture was
refluxed for about 40 h. Cooling was followed by dilution with
ethyl acetate and washing with 10% aqueous KF solution and with
NaCl solution. After drying over MgSO.sub.4 and concentration there
remained 1.0 g of a yellow oil, which was purified by
chromatography on silica gel (n-heptane/ethyl acetate).
[0193] Concentration of the fractions resulted in 60 mg of the
1H-tetra; zole and 110 mg of the 1-methyltetrazole, each as
amorphous white solids.
5-12-(4,6-Dimethoxy-2-pyrimidinyloxy)-3-methoxy-3,3-diphenyl)-propyl]-1H-t-
etrazole [sic]
[0194] Electrospray-MS: 435 (M+H.sup.+)
[0195] .sup.1H-NMR (CDCl.sub.3):
[0196] .delta. (ppm) 3.28 (s, 3H), 3.85 (s, 6H), 5.75 (s, 1H),
7.25-7.40
[0197] (m, 10H), 7.50 (s, 1H).
5-[2-(4,6-Dimethoxy-2-pyrimidinyloxy)-3-methoxy-3,3-diphenyl)-propyl]-1-me-
thyltetrazole [sic]
[0198] Electrospray-MS; 471 (M+H.sup.+)
[0199] .sup.1H-NMR (CDCl.sub.3):
[0200] .delta. (ppm) 3.0 (s, 3H), 3.35 (s, 3H9 [sic], 3.80 (s, 6H),
5.75 (s, 1H), 7.30-7.40 (m, 11H).
Example 24
2-(4,6-Dimethoxy-2-pyrimidinyloxy)-3-methylsulfinyl-3,3-diphenylpropionic
acid
[0201] 1.2 g (2.9 mmol) of
2-(4,6-dimethoxy-2-pyrimidinyloxy)-3-methylsulfonyl-3,3-diphenylpropionic
[sic] acid were introduced into 15 ml of glacial acetic acid at
0.degree. C. and 294 .mu.l of 30% strength H.sub.20.sub.2 were
added dropwise. The mixture was stirred at room temperature
overnight, poured into water, extracted with CH.sub.2Cl.sub.2 and
washed with sodium thiosulfate solution and brine. After drying, 1
g of substance was isolated as a white foam.
Example 25
2-(4,6-Dimethoxy-2-pyrimidinyloxy)-3-methylsulfonyl-3,3-diphenylpropionic
acid
[0202] 0.6 g (1.45 mmol) of
2-(4,6-dimethoxy-2-pyrimidinyloxy)-3-methylsulfonyl-3,3-diphenylpropionic
[sic] acid was introduced into 15 ml of glacial acetic acid at room
temperature, and 294 .mu.l of 30% strength H.sub.2O.sub.2 were
added dropwise. The mixture was stirred at room temperature
overnight, heated at 50.degree. C. for a further 3 h, poured into
water and washed with sodium thiosulfate solution and brine. After
drying, 400 mg were isolated as a white solid.
[0203] The compounds listed in Table 1 [sic] can be prepared in a
similar way.
TABLE-US-00001 TABLE I ##STR00014## No R.sup.1 R.sup.4, R.sup.5
R.sup.6 R.sup.2 R.sup.3 X Y Z m.p. [.degree. C.] I-195 OMe Phenyl
Methyl OMe OMe CH O O 61 I-196 OH Phenyl Methyl OMe OMe CH O O 167
I-197 OH Phenyl CH.sub.2--CH.sub.2--S--CH.sub.3 OMe OMe CH O O
I-198 OH Phenyl Ethyl OMe OMe CH O O 81 (decomp.) I-199 OH Phenyl
iso-Propyl OMe OMe CH O O 182 I-200 OH Phenyl Methyl OMe OMe CH O S
163 I-201 OH Phenyl
CH.sub.2--CH.sub.2--SO.sub.2--CH(CH.sub.3).sub.2 OMe OMe CH O O
I-202 OH Phenyl CH.sub.2--CH.sub.2--SO.sub.2--CH(CH.sub.3).sub.2
OMe OMe CH S O I-203 OH Phenyl
CH.sub.2--CH.sub.2--SO.sub.2--CH(CH.sub.3).sub.2 OMe OMe
C--CH(CH.sub.3).sub.2 O O I-204 OH Phenyl
CH.sub.2--CH.sub.2--SO.sub.2--CH(CH.sub.3).sub.2 OMe OMe
C--CH(CH.sub.3).sub.3 O O I-205 OH Phenyl
CH.sub.2--CH.sub.2--SO.sub.2--CH(CH.sub.3).sub.2 OMe NH--OCH.sub.3
CH O O I-206 OH Phenyl n-Propyl OMe OMe CH O O 174 I-207 OMe Phenyl
n-Propyl OMe OMe CH O O I-208 OH Phenyl n-Propyl OEt OEt CH O O
I-209 OH Phenyl n-Butyl OMe OMe CH O O I-210 OH Phenyl iso-Butyl
OMe OMe CH O O I-211 OH Phenyl iso-Butyl OMe
O--CH.sub.2--CH.sub.2--C O O I-212 OH Phenyl tert-Butyl OMe OMe CH
O O I-213 OH Phenyl Cyclopropyl OMe OMe CH O O I-214 OH Phenyl
Cyclopentyl OMe OMe CH O O I-215 OH Phenyl Cyclohexyl OMe OMe CH O
O I-216 OH Phenyl (CH.sub.3).sub.3C--CH.sub.2--CH.sub.2 OEt OEt CH
O O I-217 OH Phenyl
(CH.sub.3).sub.2CH--CH.sub.2--CH.sub.2--CH.sub.2 OMe OMe CH O O 173
I-218 OH Phenyl HO--CH.sub.2--CH.sub.2 OMe OMe CH O O I-219 OH
Phenyl HO.sub.2C--(CH.sub.2).sub.2-- OMe OMe CH O O I-220 OH Phenyl
Cyclopropylmethylene OMe OMe CH O O 115 [sic] I-221 OH Phenyl H OMe
OMe CH O O I-222 OH Phenyl Methyl OMe OMe CH O -- I-223 OH Phenyl
Phenyl OMe OMe CH O O 136 I-224 OH Phenyl Phenyl OMe
O--CH(CH.sub.3)--CH.sub.2--C O O I-225 OMe Phenyl Phenyl OMe OMe CH
O O I-226 OH Phenyl 4-Isopropyl-Phenyl OMe OMe CH O O I-227 OH
Phenyl 4-Me-S-Phenyl OMe OMe CH O O I-228 OH Phenyl 4-Me-O-Phenyl
OMe OMe CH O O I-229 OH Phenyl 3-Et-Phenyl OMe OMe CH O O I-230 OH
Phenyl 2-Me-Phenyl OMe OMe CH O O I-231 OH Phenyl 2-Cl-Phenyl OMe
OMe CH O O I-232 OH Phenyl 3-Br-Phenyl OMe OMe CH O O I-233 OH
Phenyl 4-F-Phenyl OMe OMe CH O O I-234 OH Phenyl 4-F-Phenyl OMe OMe
CH S O I-235 OH Phenyl 4-CH.sub.3-Phenyl OMe OMe CH O O I-236 OH
Phenyl 3-NO.sub.2-Phenyl OMe OMe CH O O I-237 OH Phenyl 2-HO-Phenyl
OMe OMe CH O O I-238 OH Phenyl 3,4-Dimethoxyphenyl OMe OMe CH O O
I-239 OH Phenyl 3,4-Dioxomethylenephenyl OMe OMe CH O O [sic] I-240
OH Phenyl 3,4,5-Trimethoxyphenyl OMe OMe CH O O I-241 OH Phenyl
Benzyl OMe OMe CH O O I-242 OH Phenyl 2-Cl-Benzyl OMe OMe CH O O
I-243 OH Phenyl 3-Br-Benzyl OMe OMe CH O O I-244 OH Phenyl
4-F-Benzyl OMe OMe CH O O I-245 OH Phenyl 2-Me-Benzyl OMe OMe CH O
O I-246 OH Phenyl 2-Me-Benzyl OMe O--CH.dbd.CH--C O O I-247 OH
Phenyl 3-Et-Benzyl OMe OMe CH O O I-248 OH Phenyl
4-iso-Propyl-Benzyl OMe OMe CH O O I-249 OH Phenyl
4-NO.sub.2-Propyl-Benzyl OMe OMe CH O O I-250 OH Phenyl
2-Me-5-Propyl-Benzyl OMe OMe CH O O I-251 OH Phenyl
2-Me-5-Propyl-Benzyl OEt OEt CH O O I-252 OH Phenyl
4-Me-2-Propyl-Benzyl OMe OMe CH O O I-253 OH Phenyl
3,4-Dioxomethylene- OMe OMe CH O O benzyl [sic] I-254 OH 4-F-Phenyl
Methyl OMe OMe CH O O 163-165 (decomp.) I-255 OMe 4-F-Phenyl Methyl
OEt OEt CH O O I-256 OH 4-Cl-Phenyl Methyl OMe OMe CH O O I-257 OH
4-Me--O-Phenyl Methyl OMe OMe CH O O I-258 OH 4-Me--O-Phenyl Ethyl
OMe OMe CH O O I-259 OH 4-Me-Phenyl Methyl OMe OMe CH O O I-260 OH
4-Me-Phenyl Methyl OMe O--CH.sub.2--CH.sub.2--C O O I-261 OH
3-CF.sub.3-Phenyl n-Propyl OMe OMe CH O O I-262 OH
3-CF.sub.3-Phenyl n-Propyl OMe O--CH(CH.sub.2)--CH.sub.2--C O O
I-263 OH 4-NO.sub.2-Phenyl Methyl OMe OMe CH O O I-264 OH
4-NO.sub.2-Phenyl Methyl OMe O--CH.dbd.CH--C O O I-265 OH
3-Cl-Phenyl Ethyl OMe OMe CH O O I-266 OH 2-F-Phenyl Methyl OMe OMe
CH O O 193-194 (decomp.) I-267 OH 2-F-Phenyl Methyl OMe OMe CH S O
I-268 OH 2-Me--O-Phenyl Methyl OMe OMe CH O O I-269 OH
2-Me--O-Phenyl Methyl OMe OMe CH O S I-270 OH 3,4-Dimethoxyphenyl
Methyl OMe OMe CH O O I-271 OH 3,4-Dioxomethylenephenyl Methyl OMe
OMe CH O O [sic] I-272 OH p-CF.sub.3-Phenyl Methyl OMe OMe CH O O
I-273 OH Phenyl Methyl OMe OEt CH O O I-274 OMe Phenyl Methyl OMe
OEt CH S O I-275 OH Phenyl Ethyl OMe NH--OMe CH O O I-276 OH
p-Me--O-Phenyl n-Propyl OMe OCF.sub.3 CH O O I-277 OH Phenyl Methyl
OMe CF.sub.3 CH O O I-278 OH Phenyl Methyl OMe CF.sub.3 N O O I-279
OH 3,4-Dimethoxyphenyl Benzyl Me Me O O I-280 OH
3,4-Dimethoxyphenyl Methyl OMe O--CH.sub.2--CH.sub.2--C O O I-281
OH Phenyl Methyl OMe O--CH.sub.2--CH.sub.2--C O O 126 (decomp.)
I-282 OH Phenyl Methyl OMe O--CH(CH.sub.3)--CH.sub.2--C O O I-283
OH Phenyl Methyl OMe N(CH.sub.3)--CH.dbd.CH--C O O 118 I-284 OH
Phenyl Methyl OMe S--C(CH.sub.3).dbd.C(CH.sub.3)--C O O I-285 OH
Phenyl Methyl OMe O--C(CH.sub.3).dbd.CH--C O O I-286 OH Phenyl
Methyl Me O--C(CH.sub.3).dbd.C--C O O I-287 OH Phenyl Methyl Me
O--CH.dbd.CH--C O O I-288 OH 4-F-phenyl Methyl Me S--CH.dbd.CH--C O
O I-289 OH 4-F-phenyl H OMe OMe CH O O I-290 OH Phenyl Methyl OMe
CH.sub.2--CH.sub.2--CH.sub.2--C O O 149-151 (decomp.) I-291 OH
Phenyl Methyl Methyl CH.sub.2--CH.sub.2--CH.sub.2--C O O 157
(decomp.) I-292 OH Phenyl Methyl Ethyl
CH.sub.2--CH.sub.2--CH.sub.2--CH.sub.2--C O O I-293 OH Phenyl
Methyl OMe CH.sub.2--CH.sub.2--CH.sub.2--CH.sub.2--C O O I-294 OH
Phenyl Methyl Me Me CH O O I-295 OH Phenyl Methyl Et Et CH O O
I-296 OH Phenyl Methyl Me Me C--CH.sub.3 O O I-297 OH Phenyl Methyl
OMe Me CH O O I-298 OH Cyclohexyl Methyl OMe OMe CH O O I-299 OH
Cyclohexyl Methyl OMe CH.sub.2--CH.sub.2--CH.sub.2--C O O I-300 OH
Phenyl Methyl OCH.sub.3 OCH.sub.3 CH S S I-301 OH Phenyl Methyl
OCH.sub.3 OCH.sub.3 CH O S 134 I-302 OCH.sub.3 Phenyl Methyl
OCH.sub.3 OCH.sub.3 CH S S I-303 OH Phenyl Methyl OCH.sub.3
OCH.sub.3 CH O O I-304 OCH.sub.3 2-Fluorophenyl Methyl OCH.sub.3
OCH.sub.3 CH O O I-305 OC.sub.2H.sub.5 3-Chlorophenyl Methyl
OCH.sub.3 OCH.sub.3 N O O I-306 ON(CH.sub.3).sub.2 4-Bromophenyl
Methyl CF.sub.3 CF.sub.3 CH S O I-307 O--CH.sub.2--C.dbd.CH Phenyl
Ethyl OCH.sub.3 CF.sub.3 CH O O I-308 OH Phenyl Propyl OCH.sub.3
OCF.sub.3 CH O S I-309 OCH.sub.3 Phenyl i-Propyl OCH.sub.3 CH.sub.3
CH O O I-310 OC.sub.2H.sub.5 Phenyl s-Butyl OCH.sub.3 Cl CH S O
I-311 ON(CH.sub.3).sub.2 2-Methylphenyl Methyl OCH.sub.3 OCH.sub.3
CH O O I-312 ON(CH.sub.3).sub.2 3-Methoxyphenyl Methyl OCH.sub.3
OCH.sub.3 CH O O I-313 ON.dbd.C(CH.sub.3).sub.2 4-Nitrophenyl
Methyl OCH.sub.3 OCH.sub.3 CH O O I-314 ON(CH.sub.3).sub.2 Phenyl
1-Phenylpropyn-3-yl OCH.sub.3 OCF.sub.3 N O S I-315
ON.dbd.C(CH.sub.3).sub.2 2-Hydroxyphenyl Methyl OCH.sub.3 CH.sub.3
N O O I-316 ONSO.sub.2C.sub.6H.sub.5 3-Trifluoromethylphenyl Methyl
OCH.sub.3 Cl N O O I-317 NHPhenyl 4-Dimethylaminophenyl Methyl
OCH.sub.3 OCH.sub.3 CH S O I-318 OC.sub.2H.sub.5 Phenyl
Trifluoroethyl CH.sub.3 CH.sub.3 CH O O I-319 ON(CH.sub.3).sub.2
Phenyl Benzyl Cl Cl CH O O I-320 ON(CH.sub.3).sub.2 Phenyl
2-Methoxyethyl OCH.sub.3 --O--CH.sub.2--CH.sub.2-- S O I-321 OH
Phenyl Phenyl OCH.sub.3 OCH.sub.3 CH O O I-322 OH Phenyl Phenyl
OCH.sub.3 --O--CH.sub.2--CH.sub.2 -- O O I-323 OH Phenyl Phenyl
OCH.sub.3 OCH.sub.3 N O O I-324 OH Phenyl Phenyl OCH.sub.3
OCH.sub.3 CH S O I-325 OH Phenyl Phenyl OCH.sub.3 OCH.sub.3 CH S S
I-326 OH Phenyl Phenyl OCH.sub.3 OCH.sub.3 CH O S I-327 OH Phenyl
Phenyl OCH.sub.3 OCH.sub.3 CH O O I-328 OH Phenyl Phenyl OCH.sub.3
OCH.sub.3 CH O O I-329 OH --(CH.sub.2).sub.5-- Phenyl Phenyl
OCH.sub.3 CH O O I-330 OH Phenyl 2-Thiazolyl OCH.sub.3 OCH.sub.3 CH
O O I-331 OCH.sub.3 2-Fluorophenyl Phenyl OCH.sub.3 OCH.sub.3 CH O
O I-332 OC.sub.2H.sub.5 3-Chlorophenyl Phenyl OCH.sub.3 OCH.sub.3 N
O O I-333 ON(CH.sub.3).sub.2 4-Bromophenyl Phenyl CF.sub.3 CF.sub.3
CH O O I-334 O--CH.sub.2.ident.CH Phenyl 2-Fluorophenyl OCH.sub.3
CF.sub.3 CH O O I-335 OH Phenyl 3-Chlorophenyl OCH.sub.3 OCF.sub.3
CH O S I-336 OCH.sub.3 Phenyl 4-Bromophenyl OCH.sub.3 CH.sub.3 CH O
O I-337 OC.sub.2H.sub.5 Phenyl 4-Thiazolyl OCH.sub.3 Cl CH S O
I-338 ON(CH.sub.3).sub.2 2-Methylphenyl Phenyl OCH.sub.3 OCH.sub.3
CH O O I-339 ON.dbd.C(CH.sub.3).sub.2 3-Methoxyphenyl Phenyl
OCH.sub.3 OCH.sub.3 CH O O I-340 OH Phenyl Methyl OCH.sub.3
--CH.sub.2--CH.sub.2--CH.sub.2--C O O I-341 OH 4-Fluorophenyl
Methyl OCH.sub.3 OCH.sub.3 CH O O 168 (decomp.) I-342 OH
4-Fluorophenyl Methyl OCH.sub.3 --CH.sub.2--CH.sub.2--CH.sub.2--C O
O I-343 NH--SO--C.sub.6H.sub.5 4-Nitrophenyl Phenyl OCH.sub.3
OCH.sub.3 CH O O I-344 OCH.sub.3 Phenyl 3-Imidazolyl OCH.sub.3
--O--CH.sub.2--CH.sub.2 O O I-345 OC.sub.2H.sub.5 Phenyl
4-Imidazolyl OCH.sub.3 CF.sub.3 N S O I-346 ON(CH.sub.3).sub.2
Phenyl 2-Pyrazolyl OCH.sub.3 OCF.sub.3 N O S I-347
ON.dbd.C(CH.sub.3).sub.2 2-Hydroxyphenyl Phenyl OCH.sub.3 CH.sub.3
N O O I-348 NH--SO.sub.2--C.sub.6H.sub.5 3-Trifluoromethylphenyl
Phenyl OCH.sub.3 Cl N O O I-349 NHPhenyl 4-Dimethylaminophenyl
Phenyl OCH.sub.3 OCH.sub.3 CH S O I-350 ONa Phenyl Phenyl OCH.sub.3
OCH.sub.3 CH S S I-351 O--CH.sub.2--C.ident.C Phenyl Phenyl
OCH.sub.3 OCH.sub.3 N S S I-352 OH Phenyl Phenyl CF.sub.3 CF.sub.3
CH O S I-353 OCH.sub.3 Phenyl Phenyl OCF.sub.3 OCF.sub.3 CH O O
I-354 OC.sub.2H.sub.5 Phenyl 2-Dimethylaminophenyl CH.sub.3
CH.sub.3 CH O O I-355 ON(CH.sub.3).sub.2 Phenyl 3-Hydroxyphenyl Cl
Cl CH O O I-356 ON.dbd.C(CH.sub.3).sub.2 Phenyl
4-Trifluoromethylphenyl OCH.sub.3 --O--CH.sub.2--CH.sub.2-- S O
I-357 NH--SO.sub.2--C.sub.6H.sub.5 Phenyl 2-Oxazolyl OCH.sub.3
CF.sub.3 N S S I-358 OH Phenyl Methyl CH.sub.3 CH.sub.3 CH O O
I-359 OH Cyclohexyl Methyl OCH.sub.3 OCH.sub.3 CH O O I-360 OH
Cyclohexyl Methyl OCH.sub.3 --CH.sub.2--CH.sub.2--CH--C O O I-361
OH Phenyl Methyl N(CH.sub.3).sub.2 N(CH.sub.3).sub.2 CH O O I-362
OH Phenyl Methyl OCH.sub.3 OCH.sub.3 CH O SO.sub.2 I-363 OH Phenyl
Methyl OCH.sub.3 OCH.sub.3 CH O SO.sub.2 I-364 OH 3-F-Phenyl Me OMe
OMe CH O O I-365 OH 3-F-Phenyl Me OMe
CH.sub.2--CH.sub.2--CH.sub.2--C O O I-366 OH 4-F-Phenyl Me OMe
CH.sub.2--CH.sub.2--CH.sub.2--C O O 142-143 191.degree. C. I-367 OH
3-MeO-Phenyl Me OMe CH.sub.2--CH.sub.2--CH.sub.2--C O O 158-161
(decomp.) I-368 OH 3-MeO-Phenyl Me OMe OMe CH O O I-369 OH
3-MeO-Phenyl Et OMe CH.sub.2--CH.sub.2--CH.sub.2--C O O I-370 OH
Phenyl HO--CH.sub.2--CH.sub.2 OMe CH.sub.2--CH.sub.2--CH.sub.2--C O
O I-371 OH Phenyl Me NMe.sub.2 NMe.sub.2 N O O 181 I-372 OH Phenyl
Me OMe OMe N O O I-373 OH I-374 NH--SO.sub.2-Phenyl Phenyl Me OMe
OMe CH O O I-375 NH--SO.sub.2--Me Phenyl Me OMe OMe CH O O I-376
CH.sub.2--SO.sub.2-Phenyl Phenyl Me OMe OMe CH O O I-377
CH.sub.2--SO.sub.2--Me Phenyl Me OMe OMe CH O O I-378 --CN Phenyl
Me OMe OMe CH O O I-379 Tetrazole [sic] Phenyl Me OMe OMe CH O O
I-380 NH--SO.sub.2-Phenyl Phenyl Me OMe OMe CH O O 167 I-381
N-Methyltetra- Phenyl Me OMe OMe CH O O zole [sic] I-382 ONa Phenyl
Me OMe --O--CH.sub.2--CH.sub.2--C-- O O 122-139 (zers.) I-383 OH
o-F-Phenyl Me OMe --O--CH.sub.2--CH.sub.2--C-- O O 140-144
(decomp.) I-384 OH m-Me-Phenyl Me OMe OMe CH O O 169-177 I-385 OH
m-Me-Phenyl Me OMe --O--CH.sub.2--CH.sub.2--C-- O O 119-135
(decomp.) I-386 OH p-F-Phenyl Me OMe Me CH O O 137-140 (decomp.)
I-387 OH m-F-Phenyl Me Me --O--CH.sub.2--CH.sub.2--C-- O O 150-152
I-388 OH p-F-Phenyl Me Me --O--CH.sub.2--CH.sub.2--C-- O O
169-170
TABLE-US-00002 TABLE II ##STR00015## No. R.sup.1 A R.sup.6 R.sup.2
R.sup.3 X Y Z m.p. [.degree. C.] II-1 OH Bond Methyl OMe OMe CH O O
96-98 II-2 OH CH.sub.2 Methyl OMe OMe CH O O II-3 OH
CH.sub.2--CH.sub.2 Methyl OMe OMe CH O O II-4 OH CH.dbd.CH Methyl
OMe OMe CH O O II-5 OH O Methyl OMe OMe CH O O II-6 OH S Methyl OMe
OMe CH O O II-7 OH NH(CH.sub.3) Methyl OMe OMe CH O O II-8 OH Bond
Isopropyl OMe OMe CH O O 137-139 II-9 OH Bond p-Isopropylphenyl OMe
OMe CH O O II-10 OH Bond Benzyl OMe OMe CH O O II-11 OH CH.dbd.CH
Ethyl OMe OMe CH O O II-12 OH CH.dbd.CH
(CH.sub.3).sub.2--CH.sub.2--CH.sub.2 OMe OMe CH O O II-13 OH
CH.dbd.CH Cyclopropylmethylene [sic] OMe OMe CH O O II-14 OH
CH.dbd.CH Methyl OMe O--CH.sub.2--CH.sub.2--C O O II-15 OH
CH.sub.2--CH.sub.2 Ethyl OMe O--CH.dbd.CH--C O O II-16 OH
CH.sub.2--CH.sub.2 Methyl OMe CH.sub.2--CH.sub.2--CH.sub.2--C O O
II-17 OH Bond Methyl OMe CH.sub.2--CH.sub.2--CH.sub.2--C O O
147
Example 35
[0204] Receptor binding data were measured by the binding assay
described above for the compounds listed below.
[0205] The results are shown in Table 2 [sic].
TABLE-US-00003 TABLE 2 [sic] Receptor binding data (K.sub.i values)
Compound ET.sub.A [nM] ET.sub.B [nM] I-2 6 34 I-29 86 180 I-5 12
160 I-4 7 2500 I-87 1 57 I.89 86 9300 I-103 0.4 29 I-107 3 485 I-12
19 1700 I-26 23 2000 I-23 209 1100 I-47 150 1500 I-60 33 970 I-96
0.6 56 II-3 107 7300 II-1 28 2300
* * * * *