EP0516658A1 - Benzopyranes avec activite pharmacologique - Google Patents

Benzopyranes avec activite pharmacologique

Info

Publication number
EP0516658A1
EP0516658A1 EP91903810A EP91903810A EP0516658A1 EP 0516658 A1 EP0516658 A1 EP 0516658A1 EP 91903810 A EP91903810 A EP 91903810A EP 91903810 A EP91903810 A EP 91903810A EP 0516658 A1 EP0516658 A1 EP 0516658A1
Authority
EP
European Patent Office
Prior art keywords
formula
compound
group
alkyl
benzopyran
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP91903810A
Other languages
German (de)
English (en)
Inventor
Frederick Smithkline Beecham Pharm. Cassidy
John Morris Smithkline Beecham Pharmaceut. Evans
Geoffrey Smithkline Beecham Pharmaceutical Stemp
Gordon Burrell
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beecham Group PLC
Original Assignee
Beecham Group PLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beecham Group PLC filed Critical Beecham Group PLC
Publication of EP0516658A1 publication Critical patent/EP0516658A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • C07D311/68—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with nitrogen atoms directly attached in position 4

Definitions

  • the present invention relates to novel benzopyrans having pharmacological activity, to a process and intermediates for preparing them and to their use as pharmaceuticals.
  • EP-A-250077 (Beecham Group p.I.e.) and EP-A-298452
  • EP-A-412760 (Beecham Group p.I.e.) discloses
  • a class of pharmaceutically active compounds which are 4-substituted benzopyran derivatives substituted in the 6-position by an alkenyl or alkynyl group.
  • K + channel activators which indicates that they are of potential use in the treatment of disorders associated with smooth muscle
  • disorders include hypertension, including pulmonary hypertension, and cardiovascular disorders other than hypertension, such as congestive heart failure, angina, peripheral vascular disease and cerebral vascular disease.
  • cardiovascular disorders other than hypertension, such as congestive heart failure, angina, peripheral vascular disease and cerebral vascular disease.
  • Other disorders include those of the gastro-intestinal tract, respiratory system, uterus and urinary tract.
  • Such disorders include irritable bowel syndrome and diverticular disease; reversible airways obstruction such as asthma;
  • the compounds may also be of potential use as anticonvulsants in the treatment of epilepsy.
  • R 1 and R 2 are hydrogen or C 1-4 alkyl and the other is C 1- 4 alkyl or R 1 and R 2 together are C 2-5
  • R 3 is hydrogen, hydroxy, C 1-6 alkoxy or C 1-7 acyloxy
  • R 4 is a C 2-6 alkenyl or C 2-6 alkynyl group
  • E is a moiety of structure E 1 :
  • Y is N or (when R 3 is hydroxy, C 1-6 alkoxy or C 1-7
  • R 5 is hydrogen, C 1-6 alkyl optionally substituted by hydroxy, C 1-6 alkoxy, C 1-6 alkoxycarbonyl or carboxy, C 1-6 alkyl substituted by halogen, or C2-6 alkenyl; aryl or heteroaryl either being optionally substituted by one or more groups or atoms selected from the class of C 1-6 alkoxy, hydroxy, halogen, trifluoromethyl, nitro, cyano, C 1-12 carboxylic acyl, or amino or aminocarbonyl optionally substituted by one or two C 1-6 alkyl groups; and
  • R 6 is hydrogen or C 1-6 alkyl
  • R 5 and R 6 are joined together to form C 3-4 polymethylene optionally substituted by one or two C 1-6 alkyl groups or -CH 2 -(CH 2 ) n -Z-(CH 2 ) m - wherein m and n are integers 0 to 2 such that m+n is 1 or 2 and Z is oxygen, sulphur or NR 9 wherein R 9 is hydrogen, C 1- 9 alkyl, C 2-7 alkanoyl, phenyl C 1-4 alkyl, naphthylcarbonyl, phenylcarbonyl or benzylcarbonyl optionally
  • R 5 is NR 7 R 8 wherein R 7 and R 8 are independently C 1-6 alkyl, R 7 is hydrogen and R 8 is C 1-6 alkyl or R 7 and
  • R 8 together are C 4-5 polymethylene
  • R 6 is hydrogen or C 1-6 alkyl
  • R 6 and R 7 together are -(CH 2 ) p - wherein p is 2 or 3, and R 8 is hydrogen or C 1-6 alkyl; or
  • R 5 is CH 2 R 10 wherein R 10 is hydrogen or C 1-5 alkyl or R 6 and
  • R 10 together are -(CH 2 ) q - wherein q is 2 or 3; and X is oxygen or sulphur; or
  • E is 2-pyridine-N-oxide, 2-pyrazinyl-1-oxide, or 2- or
  • the nitrogen-containing group in the 4-position being trans to the R 3 group when R 3 is hydroxy, C 1-6 alkoxy or C 1-7 acyloxy.
  • Y is preferably N.
  • R 1 and R 2 are both C 1-4 alkyl, in particular both methyl.
  • R 3 is C 1-6 alkoxy
  • preferred examples of R 3 include methoxy and ethoxy, of which methoxy is more preferred.
  • R 3 is C 1-7 acyloxy a preferred class of R 3 is
  • R 3 is hydroxy
  • R 4 examples include vinyl, prop-2-enyl, 1-methylvinyl, but-1-enyl, but-2-enyl, but-3-enyl, 1-methylenepropyl,
  • R 5 when C 1-6 alkyl, include methyl, ethyl and n- and iso-propyl. Preferably such R 5 is methyl.
  • a sub-group of R 5 when C 1-6 alkyl substituted by halogen is C 1-6 alkyl substituted by chloro or bromo. Examples thereof include methyl or ethyl terminally substituted by chloro or bromo.
  • R 5 when C 1-6 alkyl substituted by hydroxy, include methyl or ethyl terminally substituted by hydroxy.
  • a sub-group of R 5 when C 1-6 alkyl substituted by alkoxy is C 1-6 alkyl substituted by methoxy or ethoxy. Examples thereof include methyl or ethyl terminally substituted by methoxy or ethoxy.
  • a sub-group of R 5 when C 1-6 alkyl substituted by C 1-6 alkoxycarbonyl is C 1-6 alkyl substituted by methoxycarbonyl or ethoxycarbonyl. Examples thereof include methyl or ethyl terminally substituted by methoxycarbonyl or ethoxycarbonyl.
  • R 5 when C 1-6 alkyl substituted by carboxy include methyl or ethyl terminally substituted by carboxy.
  • R 5 when alkyl substituted by amino optionally substituted by one or two independent C 1-6 alkyl groups include a group (CH 2 ) r NR a R b where r is 1 to 6, and R a and R b are each independently hydrogen or C 1-6 alkyl. Examples of r include 1 and 2, in particular 1.
  • R a and R b are each independently selected from hydrogen and methyl.
  • R 5 when C 2-6 alkenyl include vinyl,
  • prop-1-enyl prop-2-enyl, 1-methylvinyl, but-1-enyl,
  • trichloroacetyl group or by a phenyl group optionally substituted by one methyl, methoxy or chloro group or atom, in particular amino, methylamino, and phenylamino optionally substituted in the phenyl ring by one methyl, methoxy or chloro group or atom.
  • R 5 when aryl include phenyl and naphthyl, of which phenyl is preferred.
  • heteroaryl preferably contains one, two or three heteroatoms which are selected from the class of oxygen, nitrogen and sulphur and which, in the case of there being more than one heteroatom, are the same or different.
  • heteroatoms which are selected from the class of oxygen, nitrogen and sulphur include furyl, thienyl, pyrryl, oxazolyl, thiazolyl, imidazolyl and thiadiazolyl, and pyridyl, pyridazyl, pyrimidyl, pyrazyl and triazyl.
  • Preferred examples of such groups include furanyl, thienyl, pyrryl and pyridyl, in particular 2- and 3-furyl, 2- and 3-pyrryl, 2- and 3-thienyl, and 2-, 3- and 4-pyridyl.
  • 9- or 10-membered bicyclic heteroaryl containing one, two or three heteroatoms which are selected from the class of oxygen, nitrogen and sulphur examples include benzofuranyl, benzothienyl, indolyl and indazolyl, quinolyl and
  • Preferred examples of such groups include 2- and 3-benzofuryl, 2- and 3-benzothienyl, and 2- and 3-indolyl, and 2- and 3-guinolyl.
  • the number of groups or atoms for optional substitution of aryl or heteroaryl is one, two, three or four.
  • Preferred examples of the groups or atoms for optional substitution of aryl or heteroaryl include methyl, methoxy, hydroxy, bromo, chloro, fluoro, nitro or cyano.
  • a sub-group of R 5 is phenyl or naphthyl or a 5- or
  • 6-membered monocyclic or a 9- or 10-membered bicyclic heteroaryl the phenyl, naphthyl or heteroaryl group being optionally substituted by one, two, three or four groups or atoms selected from the class of C 1-6 alkyl, C 1-6 alkoxy, halogen, (such as chloro, bromo or, in particular, fluoro), trifluoromethyl, nitro or cyano.
  • phenyl optionally substituted as hereinbefore defined is phenyl, 4-substituted phenyl,
  • a preferred sub-group of 5- or 6-membered monocyclic or 9- or 10-membered bicyclic heteroaryl optionally substituted as hereinbefore defined is unsubstituted or mono-substituted 5- or 6-membered monocyclic or 9- or 10-membered bicyclic heteroaryl, in particular unsubstituted 5- or 6-membered monocyclic or 9- or 10-membered bicyclic heteroaryl.
  • R 5 and R 6 when together are -CH 2 - (CH 2 ) n -Z- (CH 2 ) m - as defined the resulting radical substituting thebenzopyran in the 4-position is preferably either pyrrolidonyl or
  • R when Z is other than CH 2 m is often 0 or 1 and n is often 0 or 1.
  • Suitable examples of R when Z is NR 9 include
  • R 9 is hydrogen, methyl, n-butyl, acetyl, benzyl, benzylcarbonyl, phenylcarbonyl or furylcarbonyl. Most preferably R 9 is methyl.
  • R 5 and R 6 are R 5 methyl and R 6 hydrogen and R 5 and R 6 together are C 3 or C 4 polymethylene.
  • Y is CH
  • R 6 is preferably hydrogen and R 5 is NR 7 R 8 .
  • R 7 and R 8 examples include hydrogen (for R 7 ), methyl, ethyl, n- and iso-propyl, and n-, iso-, sec- and t-butyl, C 4 or C 5 polymethylene or R 7 together with R 6 is -(CH 2 ) 2 - or -(CH 2 ) 3 -, and R 8 is hydrogen or an alkyl group as described above.
  • R 7 and R 8 are each methyl or R 6 CHCXNR 7 R 8 forms a pyrrolidone or piperidone ring and R 8 is methyl.
  • X is oxygen
  • Examples of a pharmaceutically acceptable salt of a compound of formula (I), when the compound contains a salifiable group which is an optionally substituted amino group, include acid addition salts such as the hydrochloride and hydrobromide salts. Such a salifiable group may be within an R 4 or R 5 group. A carboxy group within R 5 may also be salified to form metal salts, such as alkali metal salts, or optionally substituted ammonium salts.
  • the invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof, other than the compound E5 hereinbefore defined.
  • the compounds of formula (I) may also exist as hydrates and these are included wherever a compound of formula (I) or a salt thereof is herein referred to.
  • the compounds of formula (I), are asymmetric, and,
  • optical isomers therefore, can exist in the form of optical isomers.
  • the present invention extends to all such isomers individually and as mixtures, such as racemates.
  • Examples of compounds of formula (I) include the compounds prepared in the Examples 1-4 hereinafter.
  • a process for the preparation of a compound of formula (I) wherein E is a moiety of structure E 1 as defined, or, when the compound of formula (I) contains a salifiable group, a pharmaceutically acceptable salt thereof, comprises; i) (When Y is N) acylating a compound of formula (II) :
  • R 4 ' is R 4 or a group convertible thereto; R 1 R 2 and
  • R 3 are as hereinbefore defined, and R 6 1 is hydrogen or C 1-6 alkyl, the R 6 1 NH group being trans to the R 3 group, a) with an acylating agent of formula (III)
  • L 1 is a leaving group
  • R 11 is hydrogen, C 1-6 alkyl optionally substituted by halogen, hydroxy, C 1-6 alkoxy, C 1-6 alkoxycarbonyl, carboxy or amino optionally. substituted as hereinbefore defined for R 5 , C 2-6 alkenyl or optionally substituted aryl or heteroaryl a hereinbefore defined for R 5 , or a group convertible to R 5 as hereinbefore defined, and thereafter, when R 6 is hydrogen and R 11 is
  • YHCOR 13 is tetrahydroisoquinolinone; or (when Y is CH) R 13 is NR 7 'R 8 or CHR 10 CO 2 R 15 wherein R 15 is C 1-6 alkyl or benzyl, R 7 ' is R 7 or an amino protecting group and the remaining variables are as hereinbefore defined; and thereafter, if necessary, converting R 13 to R 5 , converting R 7 ' to R 7 ; optionally converting R 3 in the resulting compound into another R 3 ; converting R 4 ' to R 4 and
  • the leaving group L 1 is a group that is displaceable by a primary or secondary amino nucleophile. Examples of such a group include C 1-4 alkanoyloxy, and halogen, such as chloro and bromo.
  • the acylating agent of formula (III) is either an acid anhydride or an acid halide. When it is an acid anhydride, it may be a mixed or simple anhydride. If it is a mixed anhydride, it may be prepared in situ from a
  • R 11 is a group convertible to the R 5
  • R 11 halo substituent in the resultant compound of process variant i) a) may be converted to an R 5 substituent which is amino Optionally substituted as hereinbefore defined by a conventional animation reaction with ammonia or a corresponding alkyl- or dialkylamine.
  • R 11 may be C 1-6 alkyl substituted by protected amino, protected C 1-6 alkylamino or amino
  • the acylation of the compound of formula (II) may be carried out in the presence of an acid acceptor, such as sodium acetate, optionally using the anhydride as the solvent.
  • an acid acceptor such as sodium acetate
  • a non-aqueous medium such as dichloromethane
  • an acid acceptor such as triethylamine, trimethylamine, pyridine, picoline or calcium, potassium or sodium carbonate.
  • R 3 in a compound of formula (II) is hydroxy
  • the reaction may be carried out under controlled conditions such that only the R 6 1 YH- is acylated, for example, by using a C 2-9 acyloxy group as the leaving group L 1 , in the acylating agent of formula (III) in the manner as previously described for an acid anhydride, and/or effecting the reaction at relatively low temperature, e.g. at below 10°C.
  • R 3 may be C 1-7 acyloxy in a compound of formula (II), although less preferably if R 3 in the resultant compound of formula (I) is to be hydroxy, and, after reaction with the acylating agent of formula (III), be converted into hydroxy, as described hereinafter.
  • R 9 is Q(CH2) Z where the variables are as hereinbefore defined
  • the leaving group Q is a group that is displaceable by a secondary amino nucleophile adjacent to a carbonyl function.
  • a preferred example is chloro.
  • reaction between the compounds of formulae (II) and (IV) is, preferably, carried out using a corresponding alkali metal cyanate or thiocyanate, for example that of sodium or potassium, in an optionally methanolic aqueous medium acidified with a mineral acid, such as dilute hydrochloric acid.
  • a slightly elevated temperature such as 50 to 90°C is apt.
  • reaction of a compound of formula (V) with a compound of formula (VI) it is particularly preferred that the reaction is carried out under basic conditions so as to facilitate the formation of the anion of the compound of; formula (VI), for example, in the presence of sodium hydride.
  • the reaction is preferably carried out in a solvent such as tetrahydrofuran at a temperature of -70°C to reflux, depending on the anion of the compound of formula. (VI).
  • the anion is generated by use of a base, such as lithium diisopropylamide.
  • An intermediate compound wherein R 13 is CHR 10 CO 2 R 15 may be converted to a compound of formula (I) wherein R 5 is CH 2 R 10 , by deesterification followed by decarboxylation.
  • Deesterification may be effected conventionally, the most appropriate method depending to some extent on the nature of the group R 14 .
  • basic reaction conditions will generally be applicable.
  • the process conditions described hereinafter for the decarboxylation in the presence of base are in general suitable for this deesterification.
  • R 14 is, for example, a tert-butyl group
  • deesterification may also be effected conventionally in the presence of acid such as trifluoroacetic acid or aqueous hydrochloric acid. Reaction may be effected at ambient temperature or a slightly higher temperature.
  • R 14 is for example a benzyl group
  • deesterification may also be effected conventionally by hydrogenolysis, for example by transition-metal catalysed hydrogenation, such as that using palladium/charcoal.
  • the decarboxylation is conveniently effected by treatment with a moderately strong base optionally in an aqueous reaction medium.
  • bases for the reaction include inorganic bases such as sodium hydroxide.
  • reaction media include water, usually in admixture with a water-miscible solvent such that the compound is soluble therein.
  • aqueous alcohols such as aqueous ethanol and aqueous polyethers such as aqueous dioxan.
  • Reaction is conveniently effected at a moderately elevated temperature, such as 50 to 150°C, conveniently at the boiling point of the reaction medium.
  • the decarboxylation may be effected by heating to a non-extreme temperature, for example 60 to 150°C in an inert solvent, such as benzene, toluene or xylene, for example at solvent boiling point.
  • Spontaneous decarboxylation may occur under the reaction conditions for the deesterification. Even where this is not the case, it is convenient to decarboxylate the CHR 10 CO 2 H compound in situ without isolation. It is especially convenient to carry out the conversion CHR 10 CO 2 R 12 to CH 2 R 10 as a single-step one-pot process, by treatment with a moderately strong base optionally in an aqueous reaction medium. Suitable conditions are as hereinbefore described for decarboxylation.
  • R 3 when R 3 is hydroxy, it may be alkylated using an alkyl iodide in an inert solvent, such as toluene, in the presence of a base, such as potassium hydroxide, or it may be acylated using a carboxylic acid chloride or anhydride in a non-hydroxylic solvent in the presence of antacid
  • R 3 is C 1-7 acyloxy or C 1-6 alkoxy, it may be converted into hydroxy by conventional hydrolysis with, for example, dilute mineral acid.
  • R 4 ' may be formyl which may be converted to R 4 by
  • the thiation reaction conditions are conventional for the thiation agent employed.
  • the use of hydrogen sulphide is, preferably, acid catalysed by, for example, hydrogen chloride in a polar solvent, such as acetic acid or ethanol.
  • the preferred use of Lawesson's reagent is, preferably, carried out under reflux in a dry solvent, such as toluene or methylene chloride.
  • a compound of formula (II) wherein R 3 is hydroxy, C 1-6 alkoxy or C 1-7 acyloxy may be prepared by reacting a
  • the reaction is normally carried out in a solvent, such as a C 1-4 alcohol, in particular methanol, ethanol or propanol at an ambient or an elevated temperature, for example 12 to 100°C.
  • a solvent such as a C 1-4 alcohol, in particular methanol, ethanol or propanol
  • the reaction proceeds particularly smoothly if carried out in ethanol under reflux.
  • the resulting compound of formula (II) may be removed from the reaction mixture by removal of the solvent, for example. by evaporation under reduced pressure. Any epoxide impurity may be removed conventionally, for example by
  • a compound of formula (II) wherein R 3 is hydrogen may be prepared by known methods, for example as described in Khim. Geterot. Soed 5(3), 434, 1969.
  • a compound of formula (V) may be prepared in accordance with the methods described in the patent publications herein referred to in the name of Beecham Group p. I.e.
  • the compounds of formula (I) may be prepared in accordance with the processes described in EP-A-298452.
  • the invention provides the foregoing process for preparing compounds in formula (I) and pharmaceutically acceptable salts thereof, other than compound E5.
  • the intermediates of formulae (II) represent part of the present invention.
  • the intermediates of formulae (III), (IV), (V), (VI), (VII), (VIII) and (IX) are known or may be prepared in accordance with an appropriate known process.
  • the present invention accordingly provides a pharmaceutical composition which comprises a compound of formula (I) or a pharmaceutically acceptable salt thereof, and a
  • compositions are preferably adapted for oral
  • a composition- may be in the form of spray, aerosol or other conventional method of inhalation, for treating respiratory tract disorders.
  • compositions may be in the form of tablets, capsules, powders, granules, lozenges, suppositories, reconstitutable powders, or liquid preparations, such as oral or sterile parenteral solutions or suspensions.
  • composition of the invention is in the form of a unit dose .
  • the present invention further provides a method of
  • a unit dose form of a composition of the invention may contain from 1 to 100 mg of a compound of the invention and more usually from 1 to 50 mg, for example 1 to 25 mg such as 1, 2, 5, 10, 15 or 20mg.
  • Such compositions may be administered from 1 to 6 times a day, more usually from 1 to 4 times a day, in a manner such that the daily dose is from 1 to 200 mg for a 70 kg human adult and more particularly from 1 to 100 mg. No toxicological effects are indicated at the aforementioned dosage ranges.
  • the present invention further provides a compound of formula (I) or a pharmaceutically acceptable salt thereof for use in the treatment or prophylaxis of hypertension.
  • the invention also provides the use of a benzopyran
  • benzopyran derivatives may be prepared in a similar manner to the known benzopyran derivatives having other 6-substituents and according to the methods described hereinbefore. Such compounds are described in EP-A-372998 (Beecham Group p.l.c).
  • chloroform-methanol gave a mixed fraction containing the required product and starting material. This mixture was dissolved in ethyl acetate and thoroughly washed with saturated sodium metabisulphate solution. The chloroform solution was washed with water then brine and dried over anhydrous magnesium sulphate. Evaporation of the solvent in vacuo gave the title compound as a mixture of E and Z.
  • 1,8-Diazabicyclo[5,4,0]-undec-7-ene (10 g) was added and the solution heated in an oil-bath at 140°C under a nitrogen atmosphere for 12 h. After cooling ethyl acetate (120 ml), and water (100 ml) were added, the mixture then made acidic (pH 4) with dilute sulphuric acid. The two phases were separated, and the aqueous phase was further extracted with ethyl acetate (100 ml). The combined organic phase was thoroughly washed with water, then brine and dried over anhydrous magnesium sulphate. Evaporation of the solvent in vacuo and column chromatography (Kieselgel 60, eluting with chloroform-methanol) gave a white crystalline solid.
  • Antihypertensive Activity Systolic blood pressures were recorded by a modification of the tail cuff method described by I.M. Claxton, M.G.
  • the compounds of the Examples and compound E5 were shown to have blood pressure lowering activity in the above test, at a dose of 10 mg/kg or less.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Cardiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

L'invention se rapporte à de nouveaux benzopyranes ayant une activité pharmacologique, à un procédé et à des intermédiaires permettant la préparation de ces composés, ainsi qu'à leur utilisation comme produits pharmaceutiques.
EP91903810A 1990-02-03 1991-01-31 Benzopyranes avec activite pharmacologique Withdrawn EP0516658A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB909002458A GB9002458D0 (en) 1990-02-03 1990-02-03 Pharmaceuticals
GB9002458 1990-02-03

Publications (1)

Publication Number Publication Date
EP0516658A1 true EP0516658A1 (fr) 1992-12-09

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Application Number Title Priority Date Filing Date
EP91903810A Withdrawn EP0516658A1 (fr) 1990-02-03 1991-01-31 Benzopyranes avec activite pharmacologique

Country Status (5)

Country Link
EP (1) EP0516658A1 (fr)
JP (1) JPH05503938A (fr)
AU (1) AU7237591A (fr)
GB (1) GB9002458D0 (fr)
WO (1) WO1991011446A1 (fr)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8409745D0 (en) * 1984-04-14 1984-05-23 Beecham Group Plc Active compounds
PT84806B (pt) * 1986-05-03 1989-12-29 Beecham Group Plc Processo para a preparacao de benzopiranos

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9111446A1 *

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AU7237591A (en) 1991-08-21
GB9002458D0 (en) 1990-04-04
JPH05503938A (ja) 1993-06-24
WO1991011446A1 (fr) 1991-08-08

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