NZ254785A - Heterocyclically-condensed indoles and medicaments - Google Patents
Heterocyclically-condensed indoles and medicamentsInfo
- Publication number
- NZ254785A NZ254785A NZ254785A NZ25478593A NZ254785A NZ 254785 A NZ254785 A NZ 254785A NZ 254785 A NZ254785 A NZ 254785A NZ 25478593 A NZ25478593 A NZ 25478593A NZ 254785 A NZ254785 A NZ 254785A
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- NZ
- New Zealand
- Prior art keywords
- methyl
- indole
- dihydropyrrolo
- pyridylcarbamoyl
- formula
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Indole Compounds (AREA)
Description
New Zealand Paient Spedficaiion for Paient Number £54785
254785
New Zealand No. 254785 International No. PCT/EP93/02031
Priority Date(s):
Complete Specification Filed: ..2.3.-.3.:33
Class;
.ft.^V.^xYw^.VMrtv.Sa.Sr..JW^.
Publication Dale:... 26.SEP.t995
P.O. Journal No: j
NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION
Title of Invention:
Condensed indole derivatives as 5HT2C and 5HT2B antagonists
Name, address and nationality of applicant(s) as in international application form:
SMITHKLINE BEECHAM P.L.C., a British Brentford, Middlesex TW8 9EP, England company of New Horizons Court,
WO 94/04533 254785 PCT/EP93/02031
Condensed Indole derivatives as 5HT2Q aRd ^1"2B antagonists
This invention relates to compounds having pharmacological activity, to a process 5 for their preparation, to compositions containing them and to their use in the treatment of mammals.
P. Fludzinski et. al., J. Med. Chem. 1986 29 2415-2418 describes N-(l,2-dimethyl-3-ethyl-lH-indol-5-yl)-N - (3-trifluoromethylphenyl)urea which shows selectivity for the rat stomach fundus serotonin receptor.
WO 92/05170 describes certain urea derivatives which are described as possessing 5HTjc receptor antagonist activity. The 5HTreceptor has recently been reclassified as the 5HT2C receptor [P. Hartig et al.. Trends in Pharmacological Sciences (TIPS) 1993].
A structurally distinct class of compounds has now been discovered, which 15 compounds have been found to have 5HT2C receptor antagonist activity. Certain compounds of the invention also show 5HT2B receptor antagonist activity, the 5HT2B receptor being previously known as the fundus receptor [P.Hartig et al., Trends in Pharmacological Sciences (TIPS) 1993]. 5HT2C /5HT2B receptor antagonists are believed to be of potential use in the treatment of CNS disorders such as anxiety, 20 depression, obsessive compulsive disorders, migraine, anorexia, Alzheimers disease, sleep disorders, bulimia, panic attacks, withdrawal from drug abuse such as cocaine, ethanol, nicotine and benzodiazepines, schizophrenia, and also disorders associated with spinal trauma and/or head injury such as hydrocephalus.
Accordingly, in a first aspect, the present invention provides a compound of 25 formula (I) or a salt thereof:
R
13 14
(CR R )n
■P .
(0
R R
wherein:
P represents a quinoline or isoquinoline residue, or a 5- or 6-membered aromatic heterocyclic ring containing up to three heteroatoms selected from nitrogen, oxygen or sulphur;
Rl is hydrogen orC^.g alkyl;
1 -
^VO 94/04533 PCT/EP93/02031
w
R^, r3, r10 an£i r 11 are independently hydrogen or Cj.g alkyl, or R*0 and R* 1 together form a bond, or R^ and R^ or R^ and R^ together form a C2-6 aikylene chain; R4 is hydrogen, Cj.g alkyl, halogen, NR^R^ or OR^ where R^, R^ and R^ are independently hydrogen or C 1.5 alkyl;
r5 is hydrogen or C alkyl;
R7 is hydrogen, alkyl, OR*2 or halogen, where R^ is hydrogen or alkyl; and n is 2 or 3; and the groups Rl3 and R*4 are independently hydrogen or Cj.g alkyl.
alkyl moieties can be straight chain or branched and are preferably 10 C1.3 alkyl, such as methyl, ethyl, n- and iso- propyl.
Suitable R4 and R7 halogens include chloro and bromo.
Suitably R^ is hydrogen or C j.g alkyl such as methyl, ethyl or propyl. Preferably Rl is methyl or ethyl.
Suitably R^, r3, rIO an(j r1 1 are independently hydrogen or C^.g alkyl, or R*0 15 and Rl 1 together form a bond, or and R*0 or R^ and R^ together form a
C2-6 aikylene chain. Preferably R^ is hydrogen or methyl. Preferably R^ is hydrogen.
In an indoline structure, R^ and R^ are preferably hydrogen. Most preferably RlO and R^ form a bond so as to give an indole structure.
Suitably R4 is hydrogen, C^.5 alkyl, halogen, NR^r9 or OR 12 where R^, R^ 20 and R12 are independently hydrogen or Cj.g alkyl. Preferably R4 is hydrogen or methyl. Suitably R^ is hydrogen or C 1.5 alkyl. Preferably R^ is hydrogen.
Suitably R7 is hydrogen, Cj.g alkyl, OR*2 or halogen, where Rl2 is hydrogen or Cj.g alkyl. The group R7 can be attached to any vacant position in the phenyl part of the indole or indoline rings, that is to say, the 4-, 6- or 7-positions of the indole or indoline 25 rings. Preferably R7 is hydrogen.
Suitably P represents a quinoline or isoquinoline residue, or a 5- or 6-membered aromatic heterocyclic ring containing up to three heteroatoms selected from nitrogen, oxygen or sulphur. Suitable moieties when the ring P is a 5-membered aromatic heterocyclic ring include, for example, isothiazolyl, isoxazolyl, thiadiazolyl and triazolyl. 30 Suitable moieties when the ring P is a 6-membered aromatic heterocyclic ring include, for example, pyridyl, pyrimidyl or pyrazinyl. When P is a quinoline or isoquinoline residue, the urea moiety can be attached at any position of the ring, preferably to the 4-position. Preferably P is a 4-quinoline or 3-pyridyl group.
The urea moiety can be attached to a carbon or any available nitrogen atom of the 35 ring P, preferably it is attached to a carbon atom.
Suitably the group -(CR^rI^. forms an ethylene or propylene group each of which can be substituted by Ci.galkyl. The group -(CR^R^)n- can be attached to the 4-or 6-position of the indole or indoline ring, preferably it is attached to the
WO 94/04533 PCT/EP93/02031
6-position. Preferably the group -(CR^Rl4)n. js ethylene.
Particularly preferred compounds of formula (I) include:
-Methyl-1 -(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole
6-Methyl-3-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole
5,7-Dimethyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f)indole l-(3-Pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f] indole 6-Methyl-3-(4-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole 6-Methyl-3-(2-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole 5-Methyl-1 -(2-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole 10 5-Methyl-l-(4-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f] indole
-Methyl-1-(3-pyridylcarbamoyl)-2,3,6,7-tetrahydropyrrolo[2,3-f] indole 5-Ethyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f] indole
-n-Propyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f] indole 5,6-Dimethyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f] indole
6,7-Dimethyl-3-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole l-Methyl-N-(3-pyridyl)-5,6,7,8-tetrahydro-lH-pyrrolo[2,3-g]quinoline-5-carboxamide 3-Methyl-N-(3-pyridyl)-6,7,8,9-tetrahydro-3H-pyirolo[3,2-f]quinoline-6-carboxamide
6-Methyl-3-(2-methyl-4-quinolinylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole, 6-Methyl-3-(5-quinolinylcarbamoyl)-2,3-dihydro-pyrrolo[3,2-e]indole,
6-Methyl-3-(3-quinolinylcarbamoyl)-2,3-dihydropyrrolo [3,2-e]indole,
-Methyl-l-(2-methyl-4-quinolinylcarbamoyl)-2,3-dihydropyrrolo[2,3-f] indole, 6,8-Dimethyl-3-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole,
6-Methyl-3-(3-pyridylcarbamoyl)-2,3,7,8-tetrahydropyrrolo[3,2-e]-indole,
-Methyl-1 -(2-pyrazinylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole,
2,3-Dihydro-5-methyl-1 -(3-methyl-5-isothiazolylcarbamoyl)- lH-pyrrolo[3,2-e]indole, 2,3-Dihydro-5-methyl-1 -(3-methyl-5-isothiazolylcarbamoyl)-lH-pyrrolo[2,3-f] indole, 2,3-Dihydro-5-methyl- l-(5-quinolylcarbamoyl)- lH-pyrrolo[2,3-f]indole, 2,3-Dihydro-5-methyl-1-(3-methyl-5-isoxazolylcarbamoyl)-lH-pyrrolo[2,3-f] indole, N-(5-Isoquinolyl)-5-methyl-2,3-dihydropyrrolo[2,3-f] indole-1-carboxamide, 30 N-(6-Quinolyl)-5-methyl-2,3-dihydro-pyrrolo [2,3-f]indole-1-carboxamide; or pharmaceutically acceptable salts thereof.
The compounds of the formula (I) can form acid addition salts with acids, such as conventional pharmaceutically acceptable acids, for example maleic, hydrochloric, hydrobromic, phosphoric, acetic, fumaric, salicylic, citric, lactic, mandelic, tartaric and 35 methanesulphonic.
Compounds of formula (I) may also form N-oxides or solvates such as hydrates, and the invention also extends to these forms. When referred to herein, it is understood that the term 'compound of formula (I)' also includes these forms.
When R* (in an indole) and/or are hydrogen or when R4 is hydroxy or NR8r9 and at least one of R^ and R^ are hydrogen the compounds of formula (I) may exist tautomerically in more than one form. The invention extends to these and any other tautomeric forms and mixtures thereof.
Certain compounds of formula (I) are capable of existing in stereoisomeric forms including enantiomers and the invention extends to each of these stereoisomeric forms and to mixtures thereof including racemates. The different stereoisomeric forms may be separated one from the other by the usual methods, or any given isomer may be obtained by stereospecific or asymmetric synthesis.
The present invention also provides a process for the preparation of a compound of formula (I) or a pharmaceutically acceptable salt thereof, which process comprises
(a) the coupling of a compound of formula (II);
4'
R A (||)
with a compound of formula (HI);
13' 14'
(CR R )n
("0
wherein A and R*> contain the appropriate functional group(s) necessary to form the moiety, -NR^'co when coupled, wherein R^' is R^ as defined in formula (I) or a group convertible thereto, n is as defined in formula (I), and the variables R*', R2', R3', RlO', R1 r, R13', R14', R4', R5' and R7' are R1, R2, R3, R10, R11, R13, R14, R4 and R7 respectively, as defined in formula (I), or groups convertible thereto, and thereafter optionally and as necessary and in any appropriate order, converting any R*', R2', R3', R10', R11', R13', R*4', R4', R5' and R7' when other than R*, R2, R3, RlO, r11, r13, R14, R4, R5, and R7 respectively to R1, R2, R3, R10, R11, R13, R14, R4, R5 and R7, interconverting R*, R2, R3, R*0, R**, R*3, R^4, R4, R^ and R7, and forming a pharmaceutically acceptable salt thereof;
WO 94/04533 PCT/EP93/02031
or (b) cyciising a compound of formula (IV):
wherein R^', R^', r7'? r13'5 r14' ^ as defined in formulae (II) and (III), n is as defined in formula (I), and C and D contain the appropriate functional group(s) necessary to form the indole or indoline ring substituted by R*, R2, R3 , R*0 and R^ as defined in formula (HI), and thereafter optionally and as necessary in any appropriate order,
converting any R* , R2, R3', RlO', Rll, r!3 ? r14'5 r4? r5 ancj r7 when other than Rl, 10 R2, R3, RlO, Rll, R13, r14 r4 r5 and r7? to Rl, R2 r3j RIO, r1 1t r13> R14 R4t R5
and R7, interconverting R*, R2, R3, R^, R^, R*3, r14^ r4? r5 an(j r7^ ^ forming a pharmaceutically acceptable salt.
Suitable examples of groups A and R*> include:
(i) A is -N=C=0 and R6 is -H,
(ii) A is -NR^'COL and R^ is -H,
(iii) A is -NHR5' and R*> is COL, or
(iv) A is halogen and R^ is -CONHR^,
wherein R^' is as defined above and L is a leaving group. Examples of suitable leaving groups L include imidazole, halogen such as chloro or bromo or phenoxy or phenylthio 20 optionally substituted for example with halogen.
When A is -N=C=0 and R*> is H the reaction is suitably carried out in an inert solvent for example dichloromethane or toluene at ambient temperature.
When A is -NR^ COL and R^ is H or when A is -NHR^ and R^ is COL, the reaction is suitably canied out in an inert solvent such as dichloromethane at ambient 25 temperature optionally in the presence of a base, such as triethylamine or in dimethylformamide at ambient or elevated temperature.
When A is halogen and R*> is CONHR^, the reaction is suitably carried out in an inert solvent such as toluene at elevated temperature, optionally in the presence of a base.
The cyclisation of the compound of formula (IV) to prepare indoles (R^ and R^ 1 30 are a bond) may be effected using standard methodology such as described in
AVO
94/04533
Comprehensive Heterocyclic Chemistry 1984 4, 313 et. seq. or J. Het. Chem. 1988 25 p.l et seq.
Examples of the more important routes include the Leimgruber synthesis, the Fischer synthesis, the Japp-Klingemann variation, the Madelung synthesis and the 5 Nordlander synthesis.
Examples of the groups C and D in the preparation of indoles include:
(v) C is NO2 and D is CH=CH-nz2 where each Z is independently C^.g alkyl or together represent C2-7 aikylene;
(vi) C is NR1 -N=C(r2')-CH2R3 and D is H;
(vii) C is NH-N=C(C02X)-CH2R3' and D is H where X is C!_6 alkyl;
(viii) C is NR1 COR2' and D is CH2R3'.
(ix) C is NHCH2CR3'(OR)2 and D is H where R is a Cj.galkyl group.
Indolines may also be prepared by reduction, e.g. with NaCNBH3, of indoles produced by variants (vi) to (ix) above.
In reaction variant (v) (Leimgruber synthesis) the compound of formula (IV) is prepared from the 2-methyinitrophenyl urea by treatment with a dialkylacetal of the dialkylformamide OHCNZ2 with heating and the product of formula (TV) cyclised by hydrogenation over a suitable catalyst such as palladium and charcoal optionally under pressure to yield the compound of formula (I) where R^=R2=R3=H. 20 In reaction variant (vi) (Fischer synthesis) the compound of formula (TV) is prepared from the hydrazinophenyl urea by dehydration, preferably by heating, with the appropriate ketone R2 COCE^R^ and the product of formula (TV) cyclised by heating with an acid catalyst such as hydrochloric or sulphuric acid.
In reaction variant (vii) (Japp-Klingemann synthesis) the compound of formula 25 (IV) is prepared from the aminophenyl urea by diazotisation followed by treatment for example with CH3C0CH(C02X)-CH2R^ where X is Cj.g alkyl under basic conditions in aqueous alcohol as solvent
The product of formula (IV) may then be cyclised as in the Fischer synthesis above.
In reaction variant (viii) (Madelung synthesis) the compound of formula (TV) is cyclised with base in an inert solvent optionally with heating.
In reaction variant (ix) (Nordlander synthesis), the compound of formula (TV) is cyclised by heating in a mixture of trifluoroacetic anhydride/acid.
It will be appreciated that when D is hydrogen, either or both indole isomers may 35 be formed during the cyclisation process.
WO 94/04533 PCI7EP93/02031
Suitable examples of groups R2, R3, r4 ? r7 whjch are convertible to R2, R3, R^, and R7 alkyl groups respectively, include acyl groups which are introduced conventionally and may be converted to the corresponding alkyl group by conventional reduction, such as using sodium borohydride in an inert solvent followed by 5 hydrogenolysis in an inert solvent. Hydrogen substituents may be obtained from alkoxycarbonyl groups which may be converted to hydrogen by hydrolysis and decarboxylation. When R^ is hydroxy it is preferably protected in the compound of formula (II) as, for example, benzyl which is removed by hydrogenation.
Suitable examples of a group R*' which is convertible to R*, include typical 10 N-protecting groups such as alkoxycarbonyl, in particular t-butyloxycarbonyl, acetyl, trifluoroacetyl, benzyl and para-methoxybenzyl which are converted to R* hydrogen using conventional conditions.
Suitable examples of a group R^' which is convertible to R^ include alkoxycarbonyl and benzyl or para-methoxybenzyl which are converted to R^ is 15 hydrogen using conventional conditions.
Interconversions of R*, R2, R3, R^, R^, R*3, R^, R^, R^ and R7 are carried out by conventional procedures.
For example, in the case wherein R1, R2 and R3 are Cj_6 alkyl and R^ is hydrogen it is possible to introduce a Cj.g alkyl group at the R5 position by conventional 20 alkylation using 1 molar equivalent of aCj.g alkyl halide and 1 molar equivalent of a suitable base in an inert solvent R* Ci_g alkyl groups may also be introduced by conventional alkylation, for example using a Cj.g alkyl halide and base such as sodium hydride, or by reduction of C^.g acyl.
R^ halo and R7 halo may be introduced by selective halogenation of the ring P or 25 indole/indoline ring respectively using conventional conditions.
It should be appreciated that it may be necessary to protect any R* to R*2 hydrogen variables which are not required to be interconverted.
Protection, especially of a R*' hydrogen, may also be necessary during coupling reaction (a) and ring-forming reaction (b) above.
Suitable protecting groups and methods for their attachment and removal are conventional in the art of organic chemistry, such as those described in Greene T.W. 'Protective groups in organic synthesis' New York, Wiley (1981).
It is preferable, however, to introduce and interconvert the groups R* to R*2 before coupling compounds of formulae (II) and (HI) together, or cyclising the compound 35 of formula (IV).
Compounds of formula (I) which are substituted indoles, and their appropriate derivatives, can be converted to the corresponding indolines, and vice versa, by
Ik
H
conventional methods, e.g. reduction with NaCNBH3 in acetic acid and oxidation using Mn02 in an inert solvent.
Compounds of formula (II) in which A is NHR^' are known compounds or can be prepared analogously to known compounds, see, for example, WO 92/05170.
Compounds of formula (II) in which A is -N=C=0 may be prepared by treating a compound of formula (II) in which :
i) A is amino, with phosgene or a phosgene equivalent, in the presence of excess base in an inert solvent ii) A is acylazide (i.e. CON3), via the nitrene, by thermal rearrangement using conventional conditions (ref L.S. Trifonov et al, Helv. Chim. Acta 1987 70 262).
iii) A is CONH2- v*a nitrene intermediate using conventional conditions.
Compounds of formula (II) in which A is -NR^ COL may be prepared by reacting a compound of formula (II) in which A is -NHR^' with phosgene or a phosgene equivalent in an inert solvent at low temperature, if necessary in the presence of one equivalent of a base such as triethylamine.
Compounds of formula (HI) may be prepared:
(a) by cyclisation of compounds of formula (V), followed by reduction to the amine if necessary
13" 14'
CHCR R ),
HRe'
Rn" Ra"
(V)
wherein Q is CR^rMj^ CRl30 or CO2R where L is a leaving group and R*3 and R^ are as defined in formula (I), m is 1 or 2, R*', r^', r3\ RlO', r! rl3' and r14' ^ as defined in formula (IE) above, R^' is a group R^ as defined in formula (ID) and R is an aryl or
Cj.galkyl group,
or (b) cyclisation of compounds of formula (VI)
13' 14'
(CR R )n
R
(VI)
io 94/04533 PCT/EP93/02031
wherein , R^', R7', r13'? r14' and n are as defined in formula (V) and C and D are as defined in formula (IV) above.
The cyclisation of a compound of formula (V) may be suitably carried out in an inert solvent at ambient or elevated temperatures, optionally in the presence of a base. 5 Reduction may be carried out using conventional reduction techniques. The cyclisation of a compound of formula (VI) may be suitably carried out using the procedures outlined for the cyclisation of a compound of formula (TV), above.
Compounds of formula (II) in which A is halogen and R4' is hydrogen are commercially available.
Novel intermediates of formulae (HI) and (IV) also form part of the invention.
Pharmaceutically acceptable salts may be prepared conventionally by reaction with the appropriate acid or acid derivative.
N-oxides may be formed conventionally by reaction with hydrogen peroxide or percarboxylic acids.
Compounds of formula (I) and their pharmaceutically acceptable salts have
5HT2C receptor antagonist activity, and certain compounds show 5HT2B antagonist activity. Compounds of formula (I) are therefore believed to be of potential use in the treatment or prophylaxis of anxiety, depression, migraine, anorexia, obsessive compulsive disorders, Alzheimer's disease, sleep disorders, bulimia, panic attacks, withdrawal from 20 drug abuse, schizophrenia, and also disorders associated with spinal trauma and/or head injury such as hydrocephalus.
Thus the invention also provides a compound of formula (I) or a pharmaceutically acceptable salt thereof, for use as a therapeutic substance, in particular in the treatment or prophylaxis of the above disorders.
The invention further provides a method of treatment or prophylaxis of the above disorders, which comprises administering to the sufferer a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof.
In another aspect, the invention provides the use of a compound of formula (I) or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for the 30 treatment or prophylaxis the above disorders.
The present invention also provides a pharmaceutical composition, which comprises a compound of formula (I) or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
A pharmaceutical composition of the invention, which may be prepared by 35 admixture, suitably at ambient temperature and atmospheric pressure, is usually adapted for oral, parenteral or rectal administration and, as such, may be in the form of tablets, capsules, oral liquid preparations, powders, granules, lozenges, reconstitutable powders,
injectable or infusable solutions or suspensions or suppositories. Orally administrate compositions are generally preferred.
Tablets and capsules for oral administration may be in unit dose form, and may contain conventional excipients, such as binding agents, fillers, tabletting lubricants, 5 disintegrants and acceptable wetting agents. The tablets may be coated according to methods well known in normal pharmaceutical practice.
Oral liquid preparations may be in the form of, for example, aqueous or oily suspension, solutions, emulsions, syrups or elixirs, or may be in the form of a dry product for reconstitution with water or other suitable vehicle before use. Such liquid preparations 10 may contain conventional additives such as suspending agents, emulsifying agents, non-aqueous vehicles (which may include edible oils), preservatives, and, if desired, conventional flavourings or colourants.
For parenteral administration, fluid unit dosage forms are prepared utilising a compound of the invention or pharmaceutically acceptable salt thereof and a sterile 15 vehicle. The compound, depending on the vehicle and concentration used, can be either suspended or dissolved in the vehicle. In preparing solutions, the compound can be dissolved for injection and filter sterilised before filling into a suitable vial or ampoule and sealing. Advantageously, adjuvants such as a local anaesthetic, preservatives and buffering agents are dissolved in the vehicle. To enhance the stability, the composition 20 can be frozen after filling into the vial and the water removed under vacuum. Parenteral suspensions are prepared in substantially the same manner, except that the compound is suspended in the vehicle instead of being dissolved, and sterilization cannot be accomplished by filtration. The compound can be sterilised by exposure to ethylene oxide before suspension in a sterile vehicle. Advantageously, a surfactant or wetting agent is 25 included in the composition to facilitate uniform distribution of the compound.
The composition may contain from 0.1% to 99% by weight, preferably from 10 to 60% by weight, of the active material, depending on the method of administration.
The dose of the compound used in the treatment of the aforementioned disorders will vary in the usual way with the seriousness of the disorders, the weight of the sufferer, 30 and other similar factors. However, as a general guide suitable unit doses may be 0.05 to 1000 mg, more suitably 0.05 to 20.0 mg, for example 0.2 to 5 mg; and such unit doses may be administered more than once a day, for example two or three a day, so that the total daily dosage is in the range of about 0.01 to 100 mg; and such therapy may extend for a number of weeks or months.
When administered in accordance with the invention, no unacceptable toxicological effects are expected with the compounds of the invention.
94/04533 PCT/EP93/02031
The following Examples illustrate the preparation of pharmacologically active compounds of the invention. The following Descriptions illustrate the preparation of intermediates to compounds of the present invention.
94/04533 PCT/EP93/02031
Description 1
l-AcetyJ-5-aminoindoline (Dl)
1 - Acetyl-5-nitroindoline (12.77g, 62 mmol), cyclohexene (62 ml, 610 mmol), and 5% palladium on charcoal (2.34g) were stirred at reflux under nitrogen for 18h. A further 5 portion of catalyst (0.5g) was then added, and reflux was continued for a further 3h. The mixture was cooled, filtered through Kieselguhr, and evaporated to give the tide compound (9.33g, 85%) as an orange-yellow solid.
NMR (D6-DMSO) 8: 2.05 (3H, s), 3.0 (2H, t, J 8), 3.97 (2H, t, J 8), 4.97 (2H, bs), 10 6.33 (1H, dd, J 7,1), 6.46 (1H, d, J 1), 7.72 (1H, d, J 7).
Description 2
N-(l-Acetyl-5-indolinyl)-2,2-diethoxyethylamine (D2)
l-Acetyl-5-aminoindoline (Dl) (9.33g, 53 mmol), bromoacetaldehyde diethyl acetal (6.0 15 ml, 40 mmol) and sodium hydrogen carbonate (4.58g, 54 mmol) was stirred at reflux under nitrogen for 64h. Further acetal (2.0 ml, 13 mmol) was then added, and reflux was continued for a further 24h. The mixture was cooled, filtered, and evaporated to near-dryness. Chromatography on silica gel using ethyl acetate/petroleum ether (b.p. 60-80°C) (50-100% ethyl acetate) gave the tide compound (6.59g) as a yellow-brown solid, in 20 addition to recovered starting amine (3.09g). The yield of product was 63%, based on consumed starting material.
NMR (CDCI3) 6: 1.25 (6H, t, J 7), 2.2 (3H, s), 3.13 (2H, t, J 8), 3.22 (2H, d, J 5),
3.5-3.65 (2H, m), 3.65-3.8 (2H, m), 4.01 (2H, t, J 8), 4.68 (1H, t, J 5), 6.5 (2H, m), 8.03 25 (1H, d, J 7).
Alternative Procedure l-Acetyl-5-aminoindoline (Dl) was reductively alkylated with glyoxal monomethyl acetal in ethanol at 45°C using 10% palladium on charcoal and hydrogen at 50 p.s.i. Removal of 30 the catalyst by filtration followed by evaporation of the solvent afforded the corresponding dimethyl acetal which was used directly in Description 3 instead of the diethyl acetal.
O 94/04533 PCT/EP93/02031
Description 3
l-Acetyl-5-trifluoroacetyl-2,3-dihydropyrrolo[23-r|indoie (D3)
N-(l-Acetyl-5-indolinyl)-2,2-diethoxyethylamine (D2) (6.5 lg, 22 mmol) was added to an ice-cold, stirred mixture of trifluoroacetic acid (25 ml) and trifluoroacetic anhydride (25 5 ml). The mixture was stirred at 0°C under nitrogen for 0.5h, after which time further trifluoroacetic acid (40 ml) was added. The mixture was then heated at reflux for 64h, cooled, and evaporated to dryness. Chromatography on silica gel using ethyl acetate/chloroform (0-60% ethyl acetate) then gave the title compound (6.28, 89%) as a light cream solid which darkened slightly on standing.
NMR (CDCI3) 5: 2.33 (3H, s), 3.37 (2H, t, J 8), 4.17 (2H, t, J 7), 6.76 (1H, d, J
3), 7.45 (1H, m), 8.27 (1H, s), 8.44 (1H, s).
Description 4
l-Acetyl-2^-dihydropyrrolo[23-f]indole (D4)
l-Acetyl-5-trifluoroacetyl-2,3-dihydropyrrolo[2,3-f]indole (D3) (2.80g, 9.4 mmol) was suspended with stirring in methanol (100 ml), and anhydrous potassium carbonate (1.96g, 14.2 mmol) was added. The mixture was stirred for 0.5h, evaporated to near-dryness, and partitioned between ethyl acetate and water. After separation, the aqueous portion was 20 extracted with 5% methanol/chloroform, and the combined organics were dried (Na2SC>4), filtered and evaporated, giving the title compound (1.53g, 80%) as a cream solid.
NMR (D6-DMSO) 5: 2.15 (3H, s), 3.18 (2H, t, J 8), 4.08 (2H, t, J 8), 6.33 (1H, bs), 7.2 (2H, m), 8.22 (1H, s), 10.9 (1H, bs).
Description 5
l-Acetyl-5-methyl-2T3-dihydropyrrolo[23-f]'ndole (D5)
Sodium hydride (80%, 0.25g, 8.3 mmol) was stirred under nitrogen in dry N,N-dimethylformamide (DMF) (5 ml), as l-acetyl-2,3-dihydropyrrolo[2,3-f]indole (D4) 30 (1.52g, 7.6 mmol) was added in DMF (20 ml), with effervescence. The mixture was stirred for 0.5h, and iodomethane (0.52 ml, 8.3 mmol) was then added in DMF (5 ml). After stirring for a further lh, excess sodium hydride was quenched by addition of water (1 ml), and the mixture was partitioned between ethyl acetate and water, and separated. The organic portion was washed with water and brine, dried (Na2SC>4) and evaporated. 35 Chromatography on silica gel using ethyl acetate/chloroform (0-50% ethyl acetate) then gave the title compound (0.80g, 49%) as a pale yellow solid.
t
/O 94/04533 PCT/EP93/02031
NMR (cdci3) ca.5:l mixture of rotamers 8:
2.26 (major, 3H, s), 2.51 (minor, 3H, s), 3.16 (minor, 2H, t, J 8), 3.3 (major, 2H, t, J 8), 3.74 (major, 3H, s), 3.77 (minor, 3H, s), 4.1 (major, 2H, t, J 8), 4.19 (minor, 2H, t, J 8),
6.44 (both, 1H, d, J 2), 6.98 (major, 1H, d, J 2), 7.0 (minor, m), 7.09 (major, 1H, s), 7.18 (minor, 1H, s), 7.31 (minor, 1H, s), 8.48 (major, 1H, s).
Description 6
-Methyl-2,3-dihvdropyrrolo[2,3-f]indole (D6)
l-Acetyl-5-methyl-2,3-dihydropyrrolo[2,3-f]indole (D5) (0.70g, 3.3 mmol) was stirred at reflux under nitrogen in 10% sodium hydroxide solution (50 ml) for 4h. The mixture was cooled, diluted with water (200 ml), and extracted with ethyl acetate. The extract was dried (Na2SC>4) and evaporated to give the title compound (0.58g) as a light brown gum, still containing ca. 20% of the starting amide (NMR). This material was used in the next 15 step without purification.
NMR (cdci3) 8: 3.12 (2H, t, J 9), 3.33 (1H, bs), 3.56 (2H, t, J 9), 3.7 (3H, s),
6.27 (1H, d, J 3), 6.85 (1H, s), 6.9 (1H, d, J 3), 7.08 (1H, s).
Description 7
(l-MethyI-5-nitro-4-indolyl)acetonitrile (D7)
1-Methyl-5-nitroindole (0.77g, 4.4 mmol) and (4-chlorophenoxy)acetonitrile (0.88g, 5.2 mmol) were stirred in dry DMF (10 ml) at 0°C, and potassium t-butoxide (1.47g, 13.1 mmol) was added in dry DMF (10 ml). The mixture was stirred at 0°C for 15 rain, poured
into 1M hydrochloric acid (200 ml), and stirred until the precipitate coagulated. The solid was then filtered off and dried. Chromatography on silica gel using chloroform then gave the title compound (0.48g, 51 %) as a yellow solid.
NMR (CDCI3) 8: 3.9 (3H, s), 4.37 (2H, s), 6.78 (1H, d, J 3), 7.31 (1H, d, J 3), 30 7.38 (1H, d, J 8), 8.12 (1H, d, J 8).
Description 8
2-(l-Methyl-5-nitro-4-indoIyl)ethanol
(l-Methyl-5-nitro-4-indolyl)acetonitrile (D7) (3.36g, 15.6 mmol) was stirred in dry 35 tetrahydrofuran (THF) (100 ml) under nitrogen, as diisobutylaluminium hydride (1.5M in toluene, 21 ml, 31.5 mmol) was added. The mixture was stirred for 6h, and methanol (25
^WO 94/04533 PCT/EP93/02031
ml) was added. After a further 5 min, it was diluted with water (500 ml), acidified with 5M hydrochloric acid, and extracted with chloroform. The extract was dried (NaoSO^, evaporated to a blackish gum, and suspended in ethanol (100 ml). Sodium borohydride (0.88g, 23.1 mmol) was added, and the mixture was stirred for 0.5h, when a second similar 5 portion of sodium borohydride was added. After a further 0.5h, the mixture was diluted with water (500 ml), acidified with 5M hydrochloric acid, and extracted with chloroform. The extract was washed with brine, dried (Na2S(>4) and evaporated to a brown gum. Chromatography on silica gel using ethyl acetate/petroleum ether (b.p. 60-80°C) (20-60% ethyl acetate) gave the title compound (0.50g, 15%) as a brown oil.
NMR (CDC13) 8: 3.47 (2H, t, J 7), 3.78 (3H, s), 4.02 (2H, t, J 7), 6.73 (1H, d. J
3), 7.2 (2H, m), 7.89 (1H, d,J8).
Description 9
2-(l-Methyl-5-nitro-4-indolyl)ethyl metiianesulphonate (D9)
2-(l-Methyl-5-nitro-4-indolyl)ethanol (D8) (0.50g, 2.3 mmol) and triethylamine (0.38 ml, 2.7 mmol) were stirred in dichloromethane (10 ml), and methanesulphonyl chloride (0.21 ml, 2.7 mmol) was added. The mixture was stirred for 10 min, when water (10 ml) was added, and then stirred vigorously for a further 10 min. After acidification with 5M 20 hydrochloric acid, the layers were separated, and the organic portion was dried (NaoSC^) and evaporated to give a dark oil. Chromatography on silica gel using chloroform followed by dichloromethane gave the title compound (0.54g, 79%) as an orange solid.
NMR (CDCI3) 8: 2.44.(3H, s), 3.68 (2H, t, J 7), 3.85 (3H, s), 4.63 (2H, t, J 7), 25 6.81 (1H, d, J 3), 7.25 (1H, d, J 3), 7.3 (1H, d, J 8), 8.0 (1H, d, J 8).
Description 10
6-MethyI-2,3-dihydropyrrolo[3,2-e]indole (D10)
2-(l-Methyl-5-nitro-4-indolyl)ethyl methanesulphonate (D9) (0.38g, 1.3 mmol) was 30 hydrogenated over 5% palladium on charcoal (0.23g) in dry DMF (20 ml) at 80 p.s.i. H2 for 2h, diluted with ethanol (80 ml), filtered through Kieselguhr, and evaporated to a brown gum. The title compound can be purified by preparation of the HC1 salt to give 6-Methyl-2,3-dihydropyrrolo[3,2-e]indolehydrochloride.
Description 11
N-(l-Acetyl-5-indolinyl)-2-chloroallylainine (Dll)
l-Acetyl-5-amino indoline (Dl) (4.36g, 24.8 mmol), anhydrous potassium carbonate (5.1g, 37 mmol) and 2,3-dichloro-l-propene (4.5 ml, 48.9 mmol) were stirred in dry DMF (50 5 ml) at 70°C for 16 h. The mixture was then diluted with water (500 ml), and stirred for 10 min. Filtration and air drying then gave the tide compound (5.7 lg, 92%) as a dark olive solid.
NMR (CDC13) 5 2.19 (3H, s), 3.13 (2H, t, J 8), 3.9-4.2 (5H, m), 5.32 (1H, m),
5.41 (1H, m), 6.4-6.6 (2H, m), 8.05 (1H, d, J 9)
Description 12
N-(l-Acetyl-5-indolinyl)-2-chloro-N-trifluoroacetylallylamine (D12)
N-(l-Acetyl-5-indolinyl)-2-chloroallylamine (Dll) (5.71g, 24.8 mmol) and triethylamine 15 (3.8 ml, 27.3 mmol) were stirred in chloroform (100 ml), and trifluoroacetic anhydride (3.8 ml, 27.3 mmol) was added dropwise over 1 min. The mixture was stirred for 1 h, when water (100 ml) was added. This mixture was stirred vigorously for 20 min, acidified with 5 M hydrochloric acid, and separated. The organic portion was dried (Na2S04) and evaporated to give the title compound as a dark oil (7.49 g, 95%), which solidified on 20 standing.
NMR (CDCI3) 5 : 2.25 (3H, s), 3.24 (2H, t, J 8), 4.16 (2H, t, J 8), 4.52 (2H, s),
.23 (1H, s), 5.36 (1H, s), 7.1 (2H, m), 8.23 (1H, d, J 8)
Description 13
1 AcetyI-7-methyl-5-trifluoroacetyl-2^-dihydropyrrolo[2,3-flindole (D13)
N-(l-Acetyl-5-indolinyl)-2-chloro-N-trifluoroacetylallylamine (D12) (7.63 g, 22 mmol) was stirred in polyphosphoric acid (38 g) at 140° C for 1.5h. The mixture was cooled, dispersed in water (200 ml) and extracted with ethyl acetate. The extract was filtered 30 through Kieselguhr, dried (Na2S04) and evaporated to give a dark gum (ca. 3g).
Chromatography on silica gel, eluting with 0-20% ethyl acetate in chloroform gave the title compound (0.49g, 7%) as a light yellow solid.
NMR (CDCI3) 5 : 2.28 (3H, s), 2.33 (3H, s), 3.36 (2H, t, J 8), 4.18 (2H, t, J 8),
7.19 (1H, s), 8.24 (1H, s), 8.36 (1H, s).
^94/04533 PCT/EP93/02031
Description 14
l-Acetyl-7-methyl-2,3-dihydropyrrolo[2,3-f]indole (D14)
This was prepared from l-acetyl-7-methyl-5-trifluoroacetyl-2,3-dihydropyrrolo[2t3-f]indole (D13) (0.49g, 1.58 mmol) following the procedure of Description 4, but working 5 up by dilution with water. The title compound (0.3 lg, 91%) was then isolated by filtration and drying, as a yellow solid.
NMR (D6-DMSO) 5 : 2.15 (3H, s), 2.18 (3H, s), 3.17 (2H, t, J 8), 4.09 (2H, t, J 8), 7.00 (1H, s), 7.14 (1H, s), 8.16 (1H, s), 10.55 (1H, b s)
Description 15
l-AcetyI-5,7-dimethyI-23-dihydropyrrolo[23-f]>ndole (D15)
This was prepared from l-acetyl-7-methyl-2,3-dihydropyrrolo[2,3-f]indole (D14) (0.3 lg, 1.46 mmol) following the procedure of Description 5, but working up by dilution with 15 water. The title compound (0.26g, 79%) was then isolated by filtration and drying, as an orange-yellow solid.
NMR (CDCI3) ca 5:1 mixture of rotamers, 5 :
2.27 & 2.30 (major, 3H, s + both, 3H, s), 2.53 (minor, 3H, s), 3.15 (minor, 2H, t J 8), 3.30 20 (major, 2H, t, J 8), 3.68 (major, 3H, s), 3.70 (minor, 3H, s), 4.10 (major, 2H, t J 8), 4.20 (minor, 2H, t, J 8), 6.76 (major, 1H, s), 6.80 (minor, 1H, s), 7.05 (major, 1H, s), 7.13 (minor, 1H, s), 7.19 (minor, 1H, s), 8.42 (major, 1H, s).
Description 16
5,7-DimethyI-23-dihydropyrrolo[2,3-f]indole (D16)
This was prepared from l-acetyl-5,7-dimethyl-2,3-dihydropyrrolo[2,3-f]indole (D15) (0.44g, 1.93 mmol) following the procedure of Description 6, using 5:1 10% sodium hydroxide solution/ethanol as solvent NMR after 7h reaction time showed ca. 60% reaction, but this material (0.30g) was used in the next step without separation of the 30 starting material.
Description 17
l-Acetyl-5-ethyl-23-dihydropyrrolo[2^3-f]indole (D17)
The title compound was prepared from l-acetyl-2,3-dihydropyrrolo[2,3-f]indole (D4), 35 sodium hydride and ethyl iodide in 90% yield using a procedure similar to that for D5.
NMR (cdci3) (mixture of rotamers) 5 major signals:
1.44 (3H, t, J 8), 2.23 (3H, s), 3.29 (2H, t, J 10), 4.0-4.25 (4H, m), 6.43 (1H, d, J 3), 7.03 (1H, d, J 3), 7.10 (1H, s), 8.48 (1H, s)
Description 18
-Ethyl-2,3-dihydropyrrolo[2,3-f]indole (D18)
The title compound was prepared from l-acetyl-5-ethyl-2,3-dihydropyrrolo[2,3-f]indole (D17) in 100% yield using a procedure similar to that for D6.
NMR (CDCI3) 5: 1.41 (3H, t, J 8), 3.12 (2H, t, J 10), 3.58 (2H, t, J 10),
4.08 (2H, q, J 8), 6.26 (1H, d, J 3), 6.84 (1H, s), 6.97 (1H, d, J 3), 7.12 (1H, s)
Description 19
l-Acetyl-5-n-propyi-2,3-dihydropyrrolo[23-flindole (D19)
Prepared as in Description 5 using sodium hydride (80%, 0.08g, 2.8 mmol), l-acetyl-2.3-dihydropyrrolo[2,3-f]indole (D4) (0.4g, 2 mmol) and 1-iodopropane (0.27 ml, 2.8 mmol). The mixture was partitioned between ether/H20. The organic portion was separated, dried and evaporated to afford the title compound (0.48 g, 99%) as a yellow solid.
NMR (CDCI3) ca 4:1 mixture of rotamers, 5 :
0.92 (t, 3H, J=8.4Hz), 1.84 (m, 2H, J=8.4Hz), 2.25 (major, s, 3H), 2.50 (minor, s, 3H). 3.14 (minor, t, 2H, J=8.4Hz), 3.29 (major, t, 2H, J=8.4Hz), 4.02 (t, 2H, J=8.4Hz), 4.09 (major, t, 2H, J=8.4Hz), 4.19 (minor, t, 2H, J=8.4Hz), 6.44 (d, 1H, J=5Hz), 7.02 (d, 1H. 25 J=5Hz), 7.10 (s, 1H), 8.46 (s, 1H).
Description 20
-n-Propyl-2,3-dihydropyrrolo[2,3-f]indole (D20)
Prepared as in Description 6 using l-acetyl-5-propyl-2,3-dihydropyrrolo[2,3-f]indole 30 (D19) (0.48g, 1.9 mmol) in ethanol (30 ml) and 10% NaOH solution (5 ml).
Chromatography over silica gel eluting with 3% MeOH/CH2Cl2 afforded the title compound (0.23g, 60%).
NMR (CDCI3) 5: 0.93 (t, 3H, J=8.4Hz), 1.86 (m, 2H, J=8.4Hz),
3:12 (t, 2H, J=8.4Hz), 3.56 (t, 2H, J=8.4Hz), 4.01 (t, 2H, J=8.4Hz),
6.27 (d, 1H, J=5Hz), 6.87 (s, 1H), 6.97 (d, 1H, J=5Hz), 7.02 (s, 1H).
AVO 94/04533
Description 21
N-(l-Acetyl-5-indoIinyl)-2-chloro-N-methylallylamine (D21)
Formaldehyde (40% aq. solution, 2.8 ml, 36 mmol) and 3M sulphuric acid (5ml, 15 mmol) 5 were stirred in ice. To this was added portionwise a suspension of sodium borohydride (1.66g, 44 mmol) and N-(l-acetyl-5-indolinyl)-2-chloroallylamine (Dll) (3.08g, 12.2 mmol) in tetrahydrofuran (60 ml), maintaining temperature below 20° C. The mixture was then stirred at ambient temperature for 0.25 h, and basified with excess solid sodium hydroxide. The supernatant was decanted, and the solid residue was dissolved in water 10 (150 ml) and extracted with ethyl acetate. The combined organics were dried (Na2S04) and evaporated to a brown tar, which was dissolved in chloroform, re-dried (Na2SC>4), filtered and evaporated to give the title compound (3.80g, >100%) as a brown solid. This was used without purification.
NMR (CDC13) 5: 2.20 (3H, s), 3.00 (3H, s), 3.16 (2H, t, J 7), 3.95-4.20 (4H, m),
.22 (1H, m), 5.30 (1H, m), 6.56 (2H, m), 8.08 (1H, d, J 8)
Description 22
l-Acetyl-5,6-dimethyl-2,3-dihydropyrrolo[2,3-f|indole and l-acetyI-6,7-dimethyl-2,3-20 dihydropyrrolo[3^2-e]indole (D22)
N-(l-Acetyl-5-indolinyl)-2-chloro-N-methylallylamine (D21) (2.1g, 7.9 mmol) was stirred in polyphosphoric acid (44g) at 140° C for 24h, cooled, dispersed in water (200 ml), and extracted with ethyl acetate. The extract was washed with brine, dried (Na2SC>4) and evaporated to give a pink solid. Chromatography on silica gel, eluting with 0-20% 25 ethyl acetate in dichloromethane, gave:
1) faster-eluting material, the linear [2,3-f]indole (0.21g, 11.6%) as a white solid. NMR showed a mixture of rotamers, in approximate ratio 5:1
NMR (CDCI3) 8 : 2.25 (3H, major, s), 2.39 (3H, major, s), 2.41 (3H, minor, s),
2.50 (3H, minor, s), 3.15 (2H, minor, t, J 7), 3.29 (2H, major, t, J 7), 3.62 (3H, major, s), 3.64 (3H, minor, s), 4.10 (2H, major, t, J 7), 4.19 (2H, minor, t, J 7), 6.22 (1H, both, s), 7.03 (1H, major, s), 7.11 (1H, minor, s), 7.21 (1H, minor, s), 8.38 (1H, major, s).
2) slower-eluting material, the angular [3,2-e]indole (0.1 Og, 5.5%) as a white solid. 35 NMR showed a mixture of rotamers, in approximate ratio 8:1
94/04533 PCT/EP93/02031
NMR (CDCI3) 8 : 2.25 (3H, major, s), 2.4-2.5 (3H, minor, + 3H, both:m), 3.18
(2H, minor, t, J 8), 3.33 (2H, major, t, J 8), 3.56 (3H, both, s), 4.15 (2H, major, t, J 8), 4.26 (2H, minor, t, J 8), 6.1 (IH, both, m), 7.0-7.15 (IH, both, + IH, minor: m), 8.20 (IH, major,d,J8).
Description 23
.6-Dimethyl-2,3-<lihydropyrrolo[2,3-f]indole (D23)
This was prepared from l-acetyl-5,6-dimethyl-2,3-dihydropyrrolo[2,3-f]indole (D22) (0.42g, 1.84 mmol), following the procedure of D6. This gave the title compound (0.30g) 10 as a brown gum. NMR indicated ca. 60% conversion to the desired material. This was used without purification.
NMR (CDCI3) 8 : 2.36 (3H, s), 3.12 (2H, t, J 7), 3.56 (2H, t, J 7), 3.58 (3H, s),
6.06 (IH, s), 6.78 (IH, s), 7.03 (IH, s).
Description 24
6.7-Dimethyl-23-dihydropyrrolo[3,2-e]indole (D24)
This was prepared from l-acetyl-6,7-dimethyl-2,3-dihydropyrrolo[3,2-e]indole (D22) (0.156g, 0.68 mmol), follwing the procedure of D6. This gave the title compound 20 (0.124g, 97%) as a dark oil.
NMR (CDCI3) 8 : 2.38 (3H, s), 3.16 (2H, t, J 7), 3.6 (5H, m), 6.04 (IH, s), 6.63
(IH, d, J 8), 6.95 (IH, d, J 8)
Description 25
N-(6-Quinolyi)trifluoroacetamide (D25)
6-Aminoquinoline (5.75g, 40 mmol) and triethylamine (6.7 ml, 48 mmol) were stirred in chloroform (100 ml), and trifluoroacetic anhydride (6.7 ml, 48 mmol) was added over 2 rain. The mixture was stirred for 1 h., when water (100 ml) was added. After stirring for 30 5 min, the gummy precipitate was filtered off, washed with chloroform and water, and dried in vacuo at 50° C. This gave the title compound (7.68g, 80%) as a straw-coloured semi-solid, containing residual triethylamine (NMR).
NMR (CDCI3) 8 : 7.57 (IH, dd, J 9,4), 7.97 (IH, dd, J 9,2), 8.08 (IH, d, J 9), 8.4
(2H, m), 8.90 (IH, dd, J 5, 2), 11.63 (IH, s).
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Description 26
N-(lr2,3,4-Tetrahydro-6-quinolyl)trifluoroacetamide (D26)
N-(6-Quinolyl)trifluoroacetamide (D25) (6.84g, 28.5 mmol) and nickel chloride hexahydrate (1.36g, 5.71 mmol) were stirred in methanol (100 ml), and sodium 5 borohydride (4.3g, 113 mmol) was added portionwise over 0.5h. After stirring for a further 0.5h, another portion of sodium borohydride (l.Og, 26 mmol) was added. After another 0.5 h, the mixture was evaporated to dryness, partitioned between 5M hydrochloric acid (25 ml) and ethyl acetate (100 ml), and stirred until clear. This mixture was neutralised with excess sodium hydrogen carbonate, and separated. The aqueous 10 portion was extracted with further ethyl acetate, and the combined organics were washed with brine, dried (Na2SC>4) and evaporated. Chromatography on silica gel, eluting with 0-30% ethyl acetate/chloroform, gave the title compound (5.07g, 73%) as a pale greenish solid.
NMR (CDC13) 8 : 1.44 (2H, m), 2.75 (2H, t, J 6), 3.31 (2H, t, J 6), 3.92 (IH, b s),
6.45 (IH, d, J 9), 7.09 (IH, dd, J 9, 2), 7.16 (IH, d, J 2), 7.65 (IH, b s).
Description 27
N-(1-Acetyl-1,2,3,4-tetrahydro-6-quinolyl)trifluoroacetamide (D27)
N-(l,2,3,4-Tetrahydro-6-quinolyl)trifluoroacetamide (D26) (5.64g, 23.1 mmol) and acetyl chloride (2.0 ml, 28 mmol) were stirred in dichloromethane (100 ml) as pyridine (2.25 ml, 28 mmol) was added. The mixture was stirred for 0.5h, when water (100 ml) was added. After vigorous stirring for 0.25 h, it was acidified with 5M hydrochloric acid, and separated. The organic portion was washed with brine, dried (Na2SC>4), and evaporated, 25 giving the title compound (5.24 g, 79%) as a cream solid.
NMR (CDCI3) 8 : 1.99 (2H, m), 2.25 (3H, s), 2.57 (2H, t, J 6), 3.78 (2H, t, J 6),
7.3 (b), 7.52 (IH, b s), 8.08 (IH, b s).
Description 28
l-Acetyl-6-amino-l,2,3,4-tetrahydroqiiinoline (D28)
N-( 1-Acetyl-1,2,3,4-tetrahydro-6-quinolyl)trifluoroacetamide (D27) (1.85g, 6.5 mmol) was stirred in ethanol (15 ml), and sodium hydroxide (0.52g, 13.0 mmol) was added in water (3ml). The mixture was stirred at ambient temperature for 0.5 h, and then heated to 35 reflux over 0.25 h. After 0.5 h at reflux, the mixture was cooled, acidified with 5M
hydrochloric acid, basified with solid sodium carbonate, diluted with water (100 ml), and
kWO 94/04533 PCT/EP93/02031
extracted with chloroform. The extract was dried (Na2SC>4) and evaporated to give the title compound (1.38g, >100%) as a brown oil containing residual chloroform (NMR).
NMR (CDCI3) 5 : 1.92 (2H, m), 2.27 (3H, s), 2.60 (2H, m), 3.67 (2H, b s), 3.79
(2H, b m), 6.5 (2H, m), 6.87 (IH, b d, J 6).
Description 29
l-Acety!-6-(2,2-diethoxyethyl)aniino-l,2,3,4-tetrahydroquinoline (D29)
l-Acetyl-6-amino-l,2,3,4-tetrahydroquinoline (D28) (2.35g, 12.4 mmol) and N,N-10 diisopropylethylamine (2.7 ml, 15.5 mmol) were stirred in 1,2-dichloroethane (50 ml) under Ar. 2,2-Diethoxyethyl trifluoromethanesulphonate (3.78g, ca. 90% purity, ca 13 mmol) was added dropwise in 1,2-dichloroethane (10 ml) over 5 min. The mixture was then stirred at reflux for 0.5 h, cooled, washed with water, dried (Na2SC>4) and evaporated to give a black oil. This material was combined with that obtained by an identical 15 procedure using 1.40g of the aminoquinoline reagent, and chromatographed on silica gel using 0-100% ethyl acetate/chloroform. This gave the title compound (3.72g, 61%) as an amber oil, contaminated with a little dialkylated material (NMR).
NMR (CDCI3) 5 : 1.25 (6H, t, J 7), 1.92 (2H, m), 2.20 (3H, s), 2.63 (2H, b m),
3.25 (2H, t, J 5), 3.5-3.9 (7H, m), 4.69 (IH, t, J 6), 6.45 (2H, m), 6.89 (IH, b d, J 6)
Description 30
-Acetyl-l-trifluoroacetyl-5,6,7,8-tetrahydro-lH-pyrrolo[2,3-g]quinoline (D30)
l-Acetyl-6-(2,2-diethoxyethyl)amino-l,2,3,4-tetrahydroquinoline (D29) (3.72g, 12.2 25 mmol) was stirred at 0° C under Ar in a mixture of trifluoroacetic acid (20 ml) and trifluoroacetic anhydride (20 ml) for 0.5 h. Further trifluoroacetic acid (30 ml) was added, and the solution was then stirred at reflux for 90 h, cooled, and evaporated to give a black gum. Chromatography on silica gel, eluting with 0-60% ethyl acetate/chloroform, gave the title compound (2.77g, 73%) as an amber oil.
NMR (CDCl3/D6-DMSO) 5 : 2.03 (2H, m), 2.25 (3H, s), 2.87 (2H, t, J 6), 3.80 (2H, t, J 7), 6.83 (IH, d, J 4), 7.51 (2H, m), 8.25 (IH, s)
^94/04533 PCT/EP93/02031
Description 31
-Acetyl-5,6,7,8-tetrahydro-lH-pyrrolo[23-g]quinoiine (D31)
-Acetyl-1 -trifluoroacetyl-5,6,7,8-tetrahydro-1 H-pyrrolo[2,3-g]quinoline (D30) (2.76g, 8.9 mmol) and anhydrous potassium carbonate (3.7g, 27 mmol) were stirred in methanol 5 (50 ml) for 1 h. The mixture was then concentrated in vacuo, diluted with water (100 ml), and extracted with chloroform. The extract was dried (Na2SC>4) and evaporated, giving the title compound (1.40g, 73%) as an orange-brown solid. NMR showed a mixture of rotamers in approximate ratio 9:1.
NMR (CDCI3) 8 : 1.97 (2H, major, m), 2.07 (2H, minor, m), 2.22 (3H, both, s),
2.73 (2H, major, t, J 6), 3.01 (2H, minor, t, J 6), 3.86 (2H, both, t, J 7), 6.52 (IH, both, m), 7.20 (2H, both, m), 7.34 (IH, major, s), 8.33 (IH, both, b).
Description 32
5-Acetyl-l-methyl-5,6,7,8-tetrahydro-lH-pyrrolo[2r3-g]quinoline (D32)
-Acetyl-5,6,7,8-tetrahydro-lH-pyrrolo[2,3-g]quinoline (D31) (1.39g, 6.5 mmol) in dry dimethylformamide (DMF) (20ml) was added, with stirring under Ar, to a suspension of sodium hydride (80% in mineral oil, 0.25g, 8.3 mmol) in DMF (5ml). After stirring for 20 min, iodomethane (0.61 ml, 9.8 mmol) was added. The resulting suspension was stirred 20 for lh, diluted with water (100 ml), and extracted with ethyl acetate. The extract was washed with water and brine, dried (Na2SC>4) and evaporated to give a gum. Chromatography on silica gel, eluting with 0-100% ethyl acetate/chloroform, gave the title compound (0.97g, 65%) as a pale, straw coloured oil which solidified on standing. NMR showed a mixture of rotamers in approximate ratio 6:1.
NMR (CDCI3) 5 : 1.97 (2H, both, m), 2.20 (3H, both, s), 2.75 (2H, major, t, J 6),
2.98 (2H, minor, t, J 6), 3.78 (3H, both, s), 3.84 (2H, both, t, J 7), 6.45 (IH, both, d, J 3), 7.04 (IH, both, d, J 3), 7.12 (IH, both, s), 7.31 (IH, both, s).
Description 33
l-MethyI-5,6,7,8-tetrahydro-lH-pyrroIo[2,3-g]quinoline (D33)
-Acetyl-l-methyl-5,6,7,8-tetrahydro-lH-pyrrolo[2,3-g]quinoline (D32) (0.96g, 4.2 mmol) was dissolved in ethanol (10 ml), and 2.5 M sodium hydroxide (90 ml) was added. This mixture was stirred at reflux under Ar for 23h, cooled, diluted with water (200 ml), 35 and extracted with ethyl acetate. The extract was dried (Na2SC>4) and evaporated to give the title compound (0.64g, 81%) as a light brown gum.
NMR (CDCI3) 5 : 2.00 (2H, m), 2.95 (2H, t, J 6), 3.0 (IH, b), 3.30 (2H, t, J 5.5),
3.68 (3H, s), 6.20 (IH, d, J 3), 6.72 (IH, s), 6.87 (IH, d, J 3), 6.92 (IH, s).
Description 34
3-(l -Methyl-5-nitro-4-indoIyl)propionitrile (D34)
2-(l-Methyl-5-nitro-4-indolyl)ethane methanesulphonate (D9) (1.60g, 5.4 mmol) and sodium cyanide (0.53g, 10.8 mmol) were stirred in dry dimethyl sulphoxide (15 ml) at 100° C under Ar for 5h. After cooling, the mixture was diluted with ethyl acetate (150
ml), washed with water, dried (Na2SC>4) and evaporated to give the title compound (1.16g, 94%) as a brown solid.
NMR (CDCI3) 5 : 2.93 (2H, t, J 7), 3.60 (2H, t, J 7), 3.87 (3H, s), 6.80 (IH, d, J
3), 7.3 (2H, m), 8.05 (IH, d, J 8).
Description 35
3-(l-Methyl-5-nitro-4-indolyl)propanoic acid (D35)
3-(l-Methyl-5-nitro-4-indolyl)propionitrile (D34) (1.16g, 5.1 mmol) was stirred at reflux in concentrated hydrochloric acid (150 ml) for 7.5 h, After cooling, the dark mixture was 20 extracted with ethyl acetate; the extract was dried (Na2SC>4) and evaporated to give the title compound (0.74 g, 59%) as a brown solid.
NMR (CDCI3) 6 : 2.88 (2H, t, J 7), 3.55 (2H, t, J 7), 3.84 (3H, s), 6.76 (IH, d, J
3), 7.21 (IH, d, J 3), 7.25 (IH, d, J 8), 7.98 (IH, d, J 8).
Description 36
Methyl 3-(l-methyl-5-nitro-4-indolyl)propanoate (D36)
3-(l-Methyl-5-nitro-4-indolyl)propanoic acid (D35) (0.94g, 3.8 mmol) was stirred in methanol (10 ml) as thionyl chloride (1 ml) was added drop wise. The mixture was then 30 stirred at reflux for 2h, and evaporated to a dark oil. Chromatography on silica gel, eluting with dichloromethane, gave the title compound (0.58g, 58%) as a pale yellow solid.
NMR (CDCI3) 6 : 2.81 (2H, t, J 7), 3.55 (2H, t, J 7), 3.70 (3H, s), 3.84 (3H, s),
6.73 (IH, d, J 3), 7.20 (IH, d, J 3), 7.24 (IH, d, J 8), 7.97 (IH, d, J 8).
*VO 94/04533 PCT/EP93/02031
Description 37
3-(l-MethyI-5-nitro-4-indoIyl)-l-propanol (D37)
Methyl 3-(l-raethyl-5-nitro-4-indolyl)propanoate (D36) (0.46g, 1.8 mmol) was stirred under Ar in tetrahydrofuran (25 ml) as lithium aluminium hydride (0.10g, 2.6 mmol) was 5 added portionwise. After 3h, water (0.5 ml), 2.5M sodium hydroxide solution (0.75 ml) and water (1.5 ml) were successively added. The mixture was then dried (Na2SC>4) and evaporated to a brown oil. Chromatography on silica gel, eluting with 0-20% ethyl acetate in dichloromethane, then gave the title compound (0.39g, 95%) as an orange solid.
NMR (CDCI3) 5 : 2.05 (2H, m), 3.34 (2H, t, J 7), 3.78 (2H, q, J 6), 3.85 (4H, m), 6.77 (IH, d, J 3), 7.18 (IH, d, J 3), 7.22 (IH, d, J 8), 7.96 (IH, d, J 8)
Description 38
3-(l-Methyl-5-nitro-4-indolyI)-l-propyI methanesuiphonate (D38)
This was prepared from 3-(l-methyl-5-nitro-4-indolyl)-l-propanol (D37) (0.39g, 1.7 mmol), following the procedure of Description 8. This gave the title compound (0.54g, >100%) as a brown oil, which was used without purification.
NMR (CDCI3) 5 : 2.25 (2H, m), 3.05 (3H, s). 3.36 (2H, I J 7), 3.84 (3H, s), 4.37 20 (2H, t, J 7), 6.73 (IH, d, J 3), 7.21 (IH, d, J 3), 7.25 (IH, d, J 8), 7.98 (IH, d, J 8).
Description 39
3-Methyl-6,7,8,9-tetrahydro-3H-pyrrolo[3,2-f]quinoline (D39)
This was prepared from 3-(l-methyl-5-nitro-4-indolyl)-l-propyI methanesuiphonate (D38) 25 (0.54g, 1.7 mmol), following the procedure of Description 10. Neutralisation with sodium hydrogen carbonate solution gave the title compound (Q.21g, 65%), as a brown oil.
NMR (CDCI3) 8 : 2.05 (2H, m), 2.95 (2H, t, J 6), 3.32 (2H, t, J 6), 3.63 (IH, b), 3.73 (3H, s), 6.70 (IH, d, J 3), 6.86 (IH, d, J 8), 6.96 (IH, d, J 3), 7.00 (IH, d, J 8)
Description 40
6-Methyl-8-(N,N-dimethylaminomethyl)-3-(3-pyridyl-carbainoyl)-2,3-
dihydropyrrolo[3,2-e]indole (D40)
6-Methyl-3-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo [3,2-e]indole (E2) (0.65g, 35 0.0022moles) suspended in 1,4-dioxan (10ml) was added to a mixture of 37% aqueous
formaldehyde (0.2ml) and 33% dimethylamine in ethanol (0.46ml) in a mixture of 1,4-dioxan (3.5ml) and glacial acetic acid (3.5ml) at 5°C with stirring. The mixture was stirred at ambient temperature for 20hrs then diluted with water (80ml) and basified with 10% aqueous sodium hydroxide. Filtration gave the title compound (D40) (0.66g, 85%) 5 as an off white solid.
NMR (D6-DMSO) 5: 2.17 (6H,s), 3.41 (2H, s), 3.50 (2H, t, J=8Hz), 3.71 (3H, s), 4.19 (2H, t, J=8Hz). 7.11-7.17 (IH, m), 7.26-7.34 (IH, m), 7.88 (IH, d, J=8Hz), 7.95-8.01 (IH, m), 8.16-8.22 (IH, m), 8.58 (IH, s), 8.74 (IH, d, J=4Hz)
Description 41
2j3-Dihydro-l-(l-imidazolylcarbonyl)-5-methyl-lH-pyrrolo[2,3-f]indole (D41)
To a solution of carbonyldimidazole (0.7lg, 4.4mmol) in DMF (25ml) was added dihydropyrroloindole (D6) (0.69g, 4mmol) in DMF (5ml). The mixture was stirred for lh 15 at 110-140°C, then cooled and poured into water. After allowing the precipitate to form, solid material was filtered off, washed with water and dried. Crude product was recrystallised from dichloromethane/petrol to give the title compound (0.45g, 42%), m.p. 178-180°C.
NMR (D6-DMSO) 6: 3.22 (2H, t, J=8), 3.77 (3H, s), 4.24 (3H, t, J=8), 6.40 (IH, d, J=4), 7.08 (IH, s), 7.28 (IH, d, J=4), 7.38 (IH, s), 7.69 (IH, s), 7.83 (IH, broad s), 8.24 (IH, s).
Description 42
l-Acetyl-2-methyl indoline (D42)
2-methylindoline (5.0g, 0.037 mol) in acetic anhydride (40 ml) and pyridine (2 ml) was heated under argon at reflux for 4 h. The mixture was cooled, poured into water (100 ml), allowed to stand for 30 mins, extracted (EtOAc 2x 250 ml), the combined organic solution washed (K2CO3 solution), and dried (Na2SC>4). The solution was filtered, evaporated to 30 dryness under reduced pressure and purified by column chromatography (Si02, Et20) to afford the product as a yellow oil (6.57 g, 96%) which crystallised on standing.
NMR (CDCI3) 5 : 1.30 (3H, d), 2.30 (3H, s), 2.68 (IH, d), 3.41 (IH, dd), 4.49
(IH, m), 7.04 (IH, t), 7.24 (2H, m), 8.18 (IH, d).
:WO 94/04533 PCT/EP93/02031
Description 43 l-Acetyl-2-methyI-5-nitroindoline (D43)
l-Acetyl-2-methylindoline (D42) (6.57g, 37.5 mmol) was dissolved in AcOH (56 ml) and a mixture of conc. HNO3 (16 ml) and AcOH (8 ml) was added. The blue solution was 5 heated to 50° C under Ar, whereupon the solution was red/brown and began to emit brown fumes. After stirring for 2h at 50° C, the solution was poured into water (500 ml), extracted with EtOAc (300 ml), washed with sat. aq. K2CO3 solution (200 ml), dried (Na2S04), evaporated under reduced pressure to give an orange oil. This was purified by column chromatography (Si02) to afford an orange oil (7.82g, 95%) which solidified on 10 standing.
NMR (CDCI3) 5:
1.3 (3H, d), 2.30 (3H, s), 2.72 (IH, d), 3.41 (IH, dd), 4.58 (IH, m), 8.10 (3H, m).
Description 44
l-AcetyI-5-amino-2-methylindoline (D44)
l-Acetyl-2-methyl-5-nitroindoline (D43), (16g, 0.073 mol) was dissolved in EtOH (180 ml), 10% Pd-C (0.3g) added and the suspension hydrogenated at 50° C and 50 psi on a Parr rocker hydrogenator for 6 h. The mixture was filtered through celite and evaporated 20 to dryness to afford the product (D44) (14.0g, 100%) as a red oil.
NMR (CDCI3) 8 : 1.30 (3H, d), 2.24 (3H, s), 2.58 (IH, d), 3.38 (IH, dd), 4.41
(IH, m), 6.58 (2H, m), 7.98 (IH, d).
Description 45
l-AcetyI-5-[(2,2-dimethoxyethyl)-aniino]-2-methyIindoline (D45)
l-Acetyl-5-amino-2-methylindoline (D44), (5.0g, 0.027 mol) was dissolved in EtOH (100 ml), 10% Pd-C (0.5g) added followed by glycolaldehyde dimethyl acetal (5.53g of a 60% solution in water, 1.2 equiv.) The mixture was hydrogenated at rtp with stirring overnight, 30 filtered through celite, evaporated to near dryness, taken up in EtOAc (200 ml), washed (H2O, brine), dried (Na2S04), and evaporated to dryness under reduced pressure to afford the product (D45) as a brown oil (7.69g, 95%).
NMR (CDCI3) 5 : 1.30 (3H, d), 2.24 (3H, s), 2.58 (IH, d), 3.23 (2H, d), 3.33 (IH,
dd), 3.41 (6H, s), 4.41 (IH, m), 4.58 (IH, t), 6.51 (2H, m), 7.98 (IH, d).
O 94/04533 PCT/EP93/02031 ,
Description 46
1 - Acetyl-2-methyl-2,3-dihydropyrrolo-[2,3-f)-indole (D46)
1-Acetyl-5-[(2,2-dimethoxyethyl)amino}-2-methylindoline (D45) (7.5g, 0.027 mol) was dissolved in TFA (32 ml) and cooled to 0° C under Ar. TFAA (30 ml) was added and the
brown solution stirred at 0° C for 30 mins. TFA (50 ml) was added and the mixture heated at reflux for 6 days, evaporated to dryness and purified by column chromatography (SiC>2, CH2Cl2/MeOH 0.5-0.75%) to afford the product as a pale pink solid (4.84 g, 58%). 2.84 g, (9.2 mmol) was dissolved in MeOH (70 ml) and anhydrous K2CO3 (1.90 g, 1.5 equiv.) added. The mixture was stirred vigorously for lht heated briefly to 40° C, 10 cooled, evaporated to dryness and partitioned between water and CHCI3. The organic layer was dried (Na2SC>4) and evaporated to dryness under reduced pressure to afford the product (D46) (1.89g, 96%) as a pale brown solid.
NMR (CDCI3) 8 : 0.72 (3H, d), 2.17 (IH, d), 2.52 (3H, s), 2.91 (IH, m), 3.98 (IH,
m), 5.80 (IH, s), 6.58 (IH, s), 6.68 (IH, s), 7.70 (IH, s), 9.95 (IH, s, N-H)
Description 47
2-Methyl-2,3-dihydropyrrolo[2,3-flindole (D47)
l-Acetyl-2-methyl-2,3-dihydropyrrolo [2,3-f] indole (D46) (2.55g, 0.0119 mol) in EtOH 20 (30 ml) and 10% NaOH (120 ml) was heated at reflux under Ar overnight The mixture was extracted with EtOAc (2 x 200 ml) the organic solution dried (Na2S04), evaporated to dryness and purified by column chromatography (Si02, Et20/Me0H 1%) to afford the product (D47) (1.4g, 68%).
NMR (CDCI3) 8 : 1.32 (3H, d), 2.71 (IH, dd), 3.19 (IH, dd), 3.98 (IH, m), 6.38
(IH, s), 6.83 (IH, s), 7.07 (IH, s), 7.12 (IH, s), 7.92 (IH, bs, NH)
Description 48
l-Acetyl-2,5-dimethyl-2,3-dihydro-pyrTolo[23-f]indole (D48)
As for Description 5 using l-acetyl-2-methyl-2,3-dihydropyrrolo[2,3-f]indole (D46)
(1.35g, 6.3 mmol) in dry DMF (10 ml), NaH (265 mg of 80% suspension in oil) in DMF (10 ml) and Mel (0.55 ml, 1.4 equiv.). After the reaction was complete, the mixture was evaporated to dryness, partitioned between sat aq K2CO3 (100 ml) and CH2CI2 (3 x 100 ml), the organic solutions dried, combined and evaporated to dryness with subsequent 35 purification by column chromatography (Si02, Et20/Me0H 2-20%) to afford the product (D48) as a pale yellow solid (1.16g, 81%).
wO 94/04533
NMR (CDCI3) 8 : 1.30 (3H, d), 2.32 (3H, s), 2.40 (IH, d), 2.75 (IH, dd), 3.76
(3H, s, NMe), 4.50 (IH, m), 6.47 (IH, s), 7.00 (IH, s), 7.12 (IH, s), 8.41 (IH, s).
Description 49
2,5 Diinethyl-2,3-dihydropyrrolo[2,3-f]indole (D49)
l-Acetyl-2,5-dimethyl-2,3-dihydropyrrolo[2,3-f]indole (D48) (l.lg, 4.82 mmol) in EtOH (40 ml) and 10% NaOH (3.45 ml, 1.8 eq) with solid NaOH (1.93,10 eq) was heated at reflux under an Ar atmosphere (Firestone valve) for 6 h, partitioned between H2O and 10 CH2CI2, the organic solutions dried (Na2S04), evaporated to dryness and purified by column chromatography (Si02, CHClg/MeOH 10%) to afford the product as an oil (370 mg, 37%).
NMR (CDCI3) 8 : 1.30 (3H, d), 2.72 (IH, dd), 3.22 (IH, dd), 3.78 (3H, s, NMe),
4.00 (IH, m), 6.28 (IH, d), 6.89 (IH, d), 6.80 (IH, s), 7.08 (IH, s).
Example 1
-Methyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-flindole (El)
Nicotinoyl azide (0.56g, 3.8 mmol) was stirred at reflux under nitrogen in dry toluene (20 20 ml) for 0.75h, and cooled to ambient temperature. 5-Methyl-2,3-dihydropyrrolo[2.3-fjindole (D6) (0.59g, nominally 3.4 mmol) was added in dichloromethane (20 ml) was stirring, with immediate precipitation. The suspension was stirred for 2.5h, and the solid was then filtered off, washed with 1:1 dichloromethane/toluene, and thoroughly dried. This gave the title compound (0.60g, 60%) as a light grey powder.
NMR (D6-DMSO) 8: 3.28 (2H, t, J 8), 3.73 (3H, s), 4.17 (2H, t, J 8),
6.81 (IH, d, J 3), 7.1-7.35 (3H, m), 8.0 (IH, m), 8.03 (IH, s), 8.21 (IH, m), 8.63 (IH, s),
8.76 (IH, d, J 2).
Found: C, 70.1; H, 5.6; N, 18.8%
Ci7Hi6N40 requires C, 69.8; H, 5.5; N, 19.2%
Found: M+ 292, C17H16N4O requires 292
WO 94/04533 PCT/EP93/02031 ,~
Example 2
6-MethyI-3-(3-pyridylcarbamoyl)-2,3-diliydropyrrolo[3,2-e]indoIe (E2)
2-(l-Meihyl-5-niiro-4-indolyl)eihyl methanesuiphonate (D9) (0.38g, 1.3 mmol) was hydrogenated over 5% palladium on charcoal (0.23g) in dry DMF (20 ml) at 80 p.s.i. H2 5 for 2h, diluted with ethanol (80 ml), filtered through Kieselguhr, and evaporated to a brown gum. This was dissolved in dichloromethane (10 ml), and reacted with 3-pyridyl isocyanate, formed from pyrolysis of nicotinoyl azide (0.20g, 2.35 mmol) as described in Example 1, but adding triethylamine (0.18g, 1.3 mmol) to the isocyanate before addition of the crude mesylate salt. After a reaction time of 16h, filtration, washing, and drying as 10 before, gave the tide compound (0.16g, 44%) as a light green powder.
NMR (D6-DMSO) 8: 3.33 (2H, t, J 8), 3.77 (3H, s), 4.22 (2H, t, J 8), 6.28 (IH, d, J 3), 7.23 (IH, d, J 8), 7.3 (2H, ra), 7.89 (IH, d, J 8), 8.0 (IH, d, J 8), 8.2 (IH, d, J 5), 8.61 (IH, s), 8.75 (IH, d, J 2).
Found: C, 66.1; H, 5.4; N, 17.8%
C17H16N4O. H2O requires C, 65.8; H, 5.8; N, 18.0%
Found: M+292, C17H16N4O requires 292
Example 3
,7-Dimethyl-H3-pyridylcarbamoyl)-2,3-diliydropyrrolo[2,3-f]indole (E3)
This was prepared from 5,7-dimethyl-2,3-dihydropyrrolo[2,3-f]indole (D16) (0.30g, nominally 1.6 mmol) following the procedure of Example 1. This gave the title compound (0.19g, 42% from (D15)) as a white solid, still containing traces of toluene (NMR).
NMR (D6-DMSO) 8 : 2.19 (3H, s), 3.27 (2H, t, J 8), 3.67 (3H, s), 4.18 (2H, t, J 8), 6.96 (IH, s), 7.21 (IH, s), 7.32 (IH, dd, J 7,4), 8.00 (IH, s), 8.02 (IH, dd, J 7, 2), 8.22 (IH, dd, J 4, 2), 8.62 (IH, s), 8.77 (IH, s).
Found: C, 70.6; H, 6.0%, CigHjg^O requires C, 70.6; H, 5.9%
Found: M+306, CigHig^O requires 306
Example 4
l-(3-PyridylcarbamoyI)-2,3-dihydropyrrolo[2,3-flindole (E4)
This material was isolated by chromatography on silica gel, eluting with 0-5% methanol in chloroform, as an impurity in a sample of 5-methyl-l-(3-pyridylcarbamoyl)-2,3-
WQ 94/04533 PCT/EP93/02031
t dihydropyrrolo[2,3-f]indole (El). Recrystallisation from ethanol/petroleura ether (b.p. 60-80° C) gave the compound as fine grey needles, m.p. 207-8° C (dec.), still containing ethanol of crystallisation. It can also be prepared by hydrolysing D4 and then coupling with 3-pyridylisocyanate.
NMR (D6-DMSO) 5 : 1.15 (t, J 7; EtOH), 3.34 (2H, t, J 8), 3.55 (quintet, J 7; EtOH), 4.26 (2H, t, J 8), 4.48 (t, J 6; EtOH), 6.42 (IH, s), 7.31 (2H, s), 7.42 (IH, dd, J 7,4), 8.05-8.2 (2H, m), 8.31 (IH, d, J 4), 8.72 (IH, s) 8.86 (IH, s), 10.95 (IH, s)
Found: C, 67.2; H, 6.1; N, 17.6%
c16Hi4N40. 0.75(C2H60) requires C, 67.2; H, 6.0; N, 17.9%
Found: M+278, C16H14N4O requires 278
Example 5
6-MethyI-3-(4-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole (E5)
The title compound was prepared from 4-aminopyridine, 1,1 '-carbonyldiimidazole, 6-methyl-(2,3-dihydropyirolo[3,2-e]indole) hydrochloride (D10) and triethylamine in methylene chloride/dimethylformamide. The reaction mixture was poured onto water to afford the title compound in 98% yield, m.p >230° C.
NMR (D6-DMSO) 8 : 3.30 (2H, t, J 7), 3.75 (3H, s), 4.25 (2H, t, J 7), 6.30 (IH, d, J 4), 7.21 (IH, d, J 10), 7.30 (IH, d, J 4), 7.58 (IH, s), 7.62 (IH, s), 7.90 (IH, d, J 10), 8.31 (IH, s), 8.36 (IH, s), 8.75 (IH, s).
Found: C, 69.5; H, 5.6; N, 19.1%, C17H16N4O requires C, 69.8; H, 5.5; N, 19.1% Found M+292, C47H16N4O requires 292.
Example 6
6-Methyl-3-(2-pyridylcarbainoyl)-2,3-dihydropyrrolo[3,2-e]indole (E6)
The title compound was prepared from 2-aminopyridine, 1,1 '-carbonyldiimidazole, 6-methyl-(2,3-dihydropyiTolo[3,2-e]indole) hydrochloride (D10) and triethylamine using a procedure similar to that described for Example 5, in 39% yield, m.p 143-4° C.
NMR (D6-DMSO) 8 : 3.35 (2H, t, J 7), 3.85 (3H, s), 4.38 (2H, t, J 7), 6.40 (IH, d, J 35 4), 7.08-7.15 (IH, m), 7.33 (IH, d, J 7), 7.41 (IH, d, J 4), 7.79-7.89 (IH, m), 7.95-8.05 (2H, m), 8.39 (IH, d, J 4), 9.00 (IH, s).
PCT/EP93/02031 -
Found: C, 69.6; H, 5.6; N, 19.1%, C17H16N40 requires C, 69.8, H, 5.5; N, 19.2%
Found M+ 292, C17H15N4O requires 292
Example 7
-Methyl-l-(2-pyridylcarbamoyl)-2,3-dihydropyrrolo[23-nindoIe (E7)
The title compound was prepared from 2-aminopyridine, l,l'-carbonyldiimidazole and 5-methyl-(2,3-dihydropyrrolo[2,3-f]indole) (D7) using a procedure similar to that described for Example 5, in 75% yield, m.p 137-8° C.
NMR (D6-DMSO) 8 : 3.25 (2H, t, J 7), 3.75 (3H, s), 4.21 (2H, t, J 7), 6.31 (IH, d, J4), 7.03 (IH, t, J 4), 7.20 (IH, s), 7.30 (IH, s), 7.75 (IH, t, J 7), 7.95 (IH, d, J 7), 8.04 (IH, s), 8.30 (IH, d, J 4), 8.95 (IH, s).
Found: C, 66.0; H, 5.6; N, 18.0%, C17H16N4O. H2O requires C,65.8; H,5.8; N,18.0% Found: M+292, C17H16N4O requires 292
Example 8
-Methyl-l-(4-pyridylcarbanK)yI)-23-dihydropyrrolo[2r3-f]indole (E8)
The title compound was prepared from 4-aminopyridine, l,r-carbonyldiimidazole and 5-methyl-(2,3-dihydropyrrolo[2,3-f]indole) (D7) using a procedure similar to that described for Example 5, in 84% yield, m.p 251-3° C.
NMR (D6-DMSO) 8 : 3.25 (2H, t, J 7), 3.72 (3H, s), 4.18 (2H, t, J 7), 6.32 (IH. d. J 25 4), 7.18 (IH, d, J 4), 7.27 (IH, s), 7.62 (2H, d, J 7), 8.05 (IH, s), 8.35 (2H, d, J 7), 8.85 (IH, s).
Found: C, 69.2; H, 5.7; N, 19.0%, C17H16N4O requires C, 69.8; H, 5.5; N, 19.2% Found: M+292, ^nHig^O requires 292
Example 9
-Methyl-1 -(3-pyridylcarbamoyI)-2,3,6,7-tetrahydropyrrolo[2,3-f]indole (E9)
-Methyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole (El) (0.8g, 2.7 mmol) was treated with sodium cyanoborohydride (0.86g, 13.7 mmol) in glacial acetic acid (20 35 ml) at room temperature for 4h. Water (100 ml) was added and the mixture basified with 10% aqueous sodium hydroxide. Extraction with dichloromethane followed by drying
WO 94/04533 PCT/EP93/02031
>
(Na2S04) and evaporation to diyness gave a solid. Recrystallisation from methanol/60-80 petrol gave the title compound (E9) (0.43g, 53%) as a white crystalline solid, m.p. 153-155° C.
NMR (D6-DMSO) 8 : 2.62 (3H, s), 2.80 (2H, t, J 8), 3.05 (2H, t, J 8), 3.17 (2H, t, J 8), 4.10 (2H, t, J 8), 6.40 (IH, s), 7.30 (IH, q, J 4), 7.65 (IH, s), 7.91-7.98 (IH, m), 8.19 (IH, d, J 4), 8.55 (IH, s), 8.72 (IH, d, J 4)
Found: C, 68.7; H, 6.2; N, 18.9%, CnHxg^O requires C, 69.4; H, 6.2; N, 19.0% 10 Found: M+294, CiyHjg^O requires 294
Example 10
-Ethyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2T3-f]indole (E10)
The title compound was prepared from 5-ethyl-2,3-dihydropyrrolo[2,3-f]indole (D18) and 15 3-pyridylisocyanate (prepared in situ from nicotinoyl azide) in 58% yield using a procedure similar to that for El, m.p. 202-203° C.
NMR (DgDMSO) 8 : 1.33 (3H, t, J 8), 3.28 (2H, t, J 10), 4.16 (4H, m), 6.31 (IH, d, J 3), 7.24 (IH, d, J 3), 7.30 (IH, s), 7.32 (IH, m), 8.00 (IH, m), 8.03 (IH, s), 8.22 (IH, m), 20 8.65 (IH, s), 8.77 (IH, s).
Found: C, 70.70; H, 6.01; N, 18.46%, QgHig^O requires C, 70.57; H, 5.92;
N, 18.29%
Found: M+306, CjgHig^Orequires 306
Example 11
-n-Propyl-l-(3-pyridylcarbamoyl)-23-dihydropyrrolo[2^-f]indole (Ell)
Prepared as in Example 1 using nicotinoyl azide (0.19g, 1.4 mmol) and 5-propyl-2,3-dihydropyrrolo[2,3-f]indole (0.23g, 1.2 mol). Chromatography over silica gel eluting with 30 5% MeOH/CH2Cl2 afforded the title compound (0.27g, 70%) as a pale green powder.
NMR (CDCI3) 8: 0.93 (t, 3H, J=8.4Hz), 1.87 (m, 2H, J=8.4Hz), 3.31 (t, 2H,
J=8.4Hz), 4.05 (t, 2H, J=8.4Hz), 4.28 (t, 2H, J=8.4Hz), 6.45 (d, IH, J=2.8Hz), 6.77 (br s, IH), 7.06 (d, IH, J=2.8Hz), 7.18 (s, IH), 7.29 (m, IH,), 7.92 (s, IH), 7.85 (m, IH), 8.30 35 (dd, IH, J=2.8Hz), 8.51 (s, IH)
WO 94/04533 PCT/EP93/02031
Found: C; 70.54 H; 6.34 N; 17.39 C19H20N4O.'/sH20 requires C; 70.58, H; 6.39, N: 17.33 Found: M+ = 320, C19H20N4O requires 320
Example 12
.6-Dimethyl-l-(3-pyridylcarbamoyl)-2,3-<iihydropyrrolo[2,3-flindole (E12)
This was prepared from 5,6-dimethyl-2,3-dihydropyrrolo[2,3-fjindole (D23) (0.30g, nominally 1.61 mmol), following the procedure of Example 1. This gave the title compound (0.219g, 39% from D22), as a buff powder, containing residual CH2CI2 10 (NMR), and which decomposed at ca. 225° C.
NMR (D6-DMSO) 8 : 2.36 (3H, s), 3.26 (2H, t, J 8), 3.60 (3H, s), 4.17 (2H, t, J 8), 6.11 (IH, s), 7.21 (IH, s), 7.32 (IH, dd, J 7,4), 7.93 (IH, s), 8.00 (IH, d, J.7), 8.21 (IH, d, J 4), 8.63 (IH, s), 8.75 (IH, d, J 2).
Found: C, 69.2; H, 5.9; N, 17.6%
CigH18N40.(0.08 CH2C12) requires C, 69.3; H, 5.8; N, 17.9%
Found: M+306, CigHigN40 requires 306
Example 13
6.7-Dimethyl-3-(3-pyridylcarbanioyl)-2r3-dihydropyiTolo[3^2-e]indole (E13)
This was prepared from 6,7-dimethyl-2,3-dihydropyrrolo[3,2-e]indole (D24) (0.124g, 0.67 mmol), following the procedure of Example 1. This gave the title compound (0.128g, 62%), as a light brown powder, containing residual CH2CI2 (NMR), m.p. 216-8° C 25 (decomp).
NMR (D6-DMSO) 8 : 2.45 (3H, s), 3.33 (2H, t, J 8), 3.70 (3H, s), 4.28 (2H, t, J 8), 6.15 (IH, s), 7.21 (IH, d, J 9), 7.37 (IH, dd, J 8, 5), 7.86 (IH, d, J 9), 8.06 (IH, dm, J 9), 8.26 (IH, d, J 5), 8.67 (IH, s), 8.81 (IH, d, J 2).
Found: C, 69.4; H, 5.9; N, 17.7%
c18h18n40.(0.°8 CH2C12) requires C, 69.3; H, 5.8; N, 17.9%
Found: M+306, CigHjgN40 requires 306
>
Example 14
l-Methyl-N-(3-pyridyl)-5,6,7,8-tetrahydro-lH-pyrrolo[2,3-g]quinoline-5-carboxamide (E14)
This material was prepared from l-methyl-5,6,7,8-tetrahydro-lH-pyrrolo[2,3-g]quinoline 5 (D33) (0.64g, 3.4 mmol), following the procedure of Example 1. This gave a pale orange solid, 0.64g (60%). Recrystallisation from ethanol/petroleum ether (b.p. 60-80° C) gave lustrous pale orange flakes (0.56g), m.p. 154.5-155.5° C.
NMR (D6-DMSO) 5 : 1.93 (2H, m), 2.80 (2H, t, J 7), 3.72 (2H, t, J 7), 3.77 (3H, s), 10 6.34 (IH, d, J 3), 7.25 (3H, m), 7.49 (IH, s), 7.89 (IH, dt, J 8, 2), 8.15 (IH, dd, J 4, 2), 8.65 (2H, m).
Found: C, 70.2; H, 5.4; N, 18.0%, CigHigN40 requires C, 70.6; H, 5.9; N, 18.3% Found: M+306, CigHigN40requires 306
Example 15
3-Methyl-N-(3-pyridyl)-6,7,8,9-tetrahydro-3H-pyrrolo[3,2-f]quinoIine-6-carboxamide (E15)
This was prepared from 3-methyl-6,7,8,9-tetrahydro-3H-pyrrolo[3,2-f]quinoline (D39) 20 (0.21g, 1.1 mmol), following the procedure of Example 1. The reaction was worked up by evaporation to give a brown oil, which was chromatographed on silica gel, eluting with 0-10% methanol/dichloromethane. Finally, recrystallisation from ethanol/petroleum ether (b.p. 60-80°C) gave the title compound (0.26g, 75%) as a cream solid, m.p. 174-5° C, containing residual ethanol (NMR)
NMR (D6-DMSO) 5 : 1.98 (2H, m), 2.94 (2H, t, J 7), 3.75 (5H, m), 6.41 (IH, d, J 3), 7.13 (IH, d, J 8), 7.23 (IH, d, J 8), 7.25-7.30 (2H, m), 7.89 (IH, m), 8.15 (IH, d, J 3), 8.64 (IH, m) 8.77 (IH, s)
Found: C, 70.2; H, 6.1; N, 17.8%
Ci8HigN40. (0.14 C2H60) requires C, 70.2; H, 6.1; N, 17.9%
Found: M+306, CjgHigN40 requires 306.
^VVO 94/04533
Example 16
PCT/EP93/02031 ,~
6-Methyl-3-(2-methyl-4-quinolinylcarbamoyl)-2r3-dihydro-pyrrolo[3,2-e]indole (E16)
The title compound was prepared from 2-methyl-4-aminoquinoline, 1,1 -carbonyl diimidazole, 6-methyl-(2,3-dihydropyrrolo-[3,2-e]indole)hydrochloride (D10) and 5 triethylamine, in 76% yield, m.p. > 230° C.
NMR (D6-DMSO)5: 2.60 (3H, s), 3.34 (2H, t, J 7), 3.75 (3H, s), 4.42 (2H, t, J 7), 6.31
(IH, d, J 3), 7.25 (IH, d, J 8), 7.35 (IH, d, J 3), 7.52 (IH, t, J 7), 7.70 (IH, t, J 7), 7.80 10 (IH, s), 7.88 (IH, s), 7.92 (IH, s), 8.17 (IH, d, J 7), 8.70 (IH, s)
Found: C, 73.3; H, 5.8; N, 15.5
C22 H20 N^.1^ H20 requires C, 73.3; H, 5.7; N, 15.5
Found: M+ 356, C22H20N4O requires 356
Example 17
6-Methyl-3-(5-quinolinylcarbamoyl)-2t3-dihydro-pyrrolo[3>2-e]indole (E17)
The title compound was prepared from 5-aminoquinoline, 1,1 -carbonyldiimidazole, 6-methyl-(2,3-dihydropyrrolo-[3,2-e]iiidole)hydrochloride (D10) and triethylamine, in 42% 20 yield, m.p. >240° C.
NMR(D6-DMSO)6: 3.35 (2H, t, J 7), 3.75 (3H, s), 4.38 (2H, t, J 7), 6.30 (IH, d, J 4), 7.19 (IH, d, J 8), 7.30 (IH, d, J 4), 7.50-7.58 (IH, m), 7.62 (IH, d, J 7), 7.75 (IH, t, J 7), 7.83-7.93 (2H, ra), 8.45 (IH, d, J 7), 8.70 (IH, s), 8.92 (IH, d, J 4).
Found: C, 73.6; H, 5.50; N, 16.3 C21H18N4° requires C, 73.7; H, 5.3; N, 16.4 Found: M+ 342, C2iHjgN40 requires 342
Example 18
6-Methyl-3-(3-quinolinylcarbamoyl)-23-dihydropyrrolo [3,2-e]indole (E18)
The title compound was prepared from 3-aminoquinoline, 1,1 -carbonyl diimidazole, 6-methyl-(2,3-dihydropyrrolo-[3,2-e]-indole hydrochloride (D10) and triethylamine in 53% yield, m.p. 222-4° C.
94/04533 PCT/EP93/02031
NMR(D6-DMSO)6: 3.35 (2H, d, J 7), 3.78 (3H, s), 4.32 (2H, d, J 7), 6.30 (IH, d, J 4), 7.25 (IH, d, J 8), 7.32 (IH, d, J 4), 7.50-7.68 (2H, m), 7.83-8.00 (3H, m), 8.54 (IH, d, J 4), 8.82 (IH, s), 9.05 (IH, s)
FoundrC, 72.9; H, 5.5; N, 16.2,
C2lHi8N40.,/4 H2O requires C, 72.7; H, 5.3; N, 16.2 Found: M+ 342, C21H18N4O requires 342
Example 19
5-Methyl-l-(2-methyl-4-quinolinylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole (E19)
The title compound was prepared from 2-methyl-4-aminoquinoline, 1,1 -carbonyl diimidazole and 5-methyl-(2,3-dihydropyrrolo[2,3-f]indole) (D6), in 57% yield, m.p.>240° C.
NMR (D6-DMSO)8: 2.64 (3H, s), 3.30 (2H, t, J 7), 3.72 (3H, s), 4.38 (2H, t, J 7), 6.3 (IH, d, J 4), 7.20 (IH, d, J 4), 7.30 (IH, s), 7.53 (IH, t, J 7), 7.70 (IH, t, J 7), 7.78 (IH, s), 7.90 (IH, d, J 7), 8.08 (IH, s), 8.15 (IH, d, J 7), 8.73 (lH,s)
Example 20
6y8-Dimethyl-3-(3-pyridylcarbamoyl)-2T3-dihydropyrrolo[3,2-e]indole (£20)
6-Methyl-8-(N,N-dimethylaminomethyl)-3-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo [3,2-e] indole (D40) (0.5g, 0.0014 moles) was hydrogenated at STP in ethanol (50ml) over 10% palladium on charcoal catalyst (0.5g) for 24hrs then at 50p.s.i. for 4hrs. Filtration through kieselguhr followed by evaporation to dryness gave the crude product. Flash 25 chromatography on silica gel eluting with 0-5% methanol/dichloromethane followed by recrystallisation from ethyl acetate/methanol give the title compound (E20) (0.174g, 40%) as white crystals, m.p. 228-230°C.
NMR (D6-DMSO) 8: 2.32 (3H, s), 3.55 (2H, t, J=8Hz), 3.65 (3H, s), 4.21 (2H, t, 30 J=8Hz), 7.00 (IH, s), 7.10 (IH, d, J=8Hz), 7.24-7.33 (IH, m), 7.83 (IH, d, J=8Hz), 7.94-8.03 (IH, m), 8.19 (IH, d, J=4Hz), 8.57 (IH, s), 8.73 (IH, d, J=3Hz).
Found: C, 69.77; H, 6.00; N, 18.08%
C18H18N4O 1/5H20 requires: C, 69.77, H, 5.94; N, 18.09%
Found: M+ 306, CigHjg^O requires 306
Example 21
6-Methyl-3- (3-py ridylcarbamoy 1 )-2,3,7 3- tetrahydropyrrolo[3,2-e]-indole (E21)
6-Methyl-3-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo [3,2-e]indole (E2) (l.Og, 0.0034 5 moles) was dissolved in glacial acetic acid (25ml) and treated with sodium cyanoborohydride (l.Og, 0.016 moles) at ambient temperature. The mixture was stirred for 4 hrs then diluted with water (100ml). The mixture was basified with 10% aqueous sodium hydroxide and the product extracted into dichloromethane, drying with sodium sulphate. Evaporation of the solvent followed by flash chromatography on silica gel 10 eluting with 0-5% methanol/dichloromethane gave a white solid residue. Recrystallisation from ethyl acetate/60-80 petrol gave the title compound (E21) as white crystals (0.68g, 67%) m.p. 201-203°C.
NMR (D6-DMSO) 6: 2.75 (3H, s), 2.89 (2H, t, J=8Hz), 3.15 (2H, t, J=8Hz), 3.31 15 (2H, t, J=8Hz), 4.22 (2H, t, J=8Hz), 6.40 (IH, d, J=7Hz), 7.33- 7.45 (IH, m), 7.70 (IH, d, J=7Hz), 8.03-812 (IH, m), 8.30 (IH, d, J=4Hz), 8.65 (IH, s), 8.85 (IH, d, J=4Hz).
Found: C, 69.07; H, 6.29; N, 18.90%, C17Hi8N40 requires C, 69.37; H, 6.16; N, 19.03% Found: M+ 294, C17H18N4O requires 294
Example 22
-Methyl-l-(2-pyrazinylcarbainoyl)-2,3-dihydropyrrolo[2,3-f]indole (E22)
The title compound was prepared from 2-aminopyrazine anion (prepared using sodium hydride), 1,1 '-carbonyldiimidazole, and 5-methyl-2,3-dihydropyrrolo[ 2,3-f]indole in 25 dimethylformamide using a procedure similar to that described for Example 5, in 75% yield, m.p. 196-198°C.
NMR (D6DMSO) 5: 3.26 (2H, t, J=10), 3.76 (3H, s), 4.25 (2H, t, J=10), 6.33 (IH, d, J=3), 7.20 (IH, d, J=3), 7.28 (IH, s), 8.07 (IH, s), 8.28 (IH, d, J=2), 8.37 (IH, d, J=2), 30 9.19 (lH,m), 9.38 (lH,s).
Found: C, 65.55; H, 5.36; N, 23.54%, CjgH^NjO requires C, 65.52; H, 5.15; N, 23.88% Found: M+ 293, C16H15N5O requires 293
WO 94/04533 PCT/EP93/02031
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Example 23
2,3-Dihydro-5-methyl-1 -(3-methy 1-5-isothiazoIylcarbamoyl)-1 H-pyrrolo[3,2-e]indole (E23)
To an ice-cooled solution of carbonyldiimidazole (CDI) (0.445g, 2.75 mmol) in 5 dichloromethane (15ml) was added a solution of 5-amino-3-methylisothiazole hydrochloride (0.38g, 2.5mmol) and triethylamine (0.35ml, 2.5 mmol) in dichloromethane (15ml). The mixture was stirred for lh at 0°C, then evaporated to dryness. The residue was dissolved in dimethyl formamide (DMF) (15ml) and to this solution was added dihydropyrroloindole hydrochloride (D10) (0.52g,2.5mmol) and triethylamine (0.35ml) in 10 DMF (2.5ml). The mixture was heated at approx. 130°C, with stirring, for lh, then cooled and poured into water. Solid product was filtered off, washed with water and dried, then triturated with dichloromethane/methanol. Trituration liquor was concentrated, with addition of petrol, to give a precipitate which was filtered off and combined with the trituration residue. Drying in vacuo gave the title compound, (0.42g, 54%) m.p. >250°C.
NMR (D6-DMSO) 8: 2.29 (3H, s), 3.33 (2H, t, J=7), 3.75 (3H, s), 4.20 (2H, t, J=7), 6.29 (IH, d, 1=4), 6.74 (IH, s), 7.25 (IH, d, J=9), 7.32 (IH, d, J=4), 7.90 (IH, d, J=9), 10.41 (IH, s).
Found: C, 61.13; H, 5.16; N, 17.84%, C^H^N^S requires C, 61.52; H, 5.16; N,
17.93%
Example 24
2r3-Dihydro-5-methyl-l-(3-methyl-5-isothiazolylcarbamoyI)-lH-pyrrolo[2,3-f]indole
(E24)
The title compound was prepared by the method of E23, using 5-amino-3-methylisothiazole hydrochloride (0.60g, 4 mmol), CDI (0.7lg, 4.4 mmol), triethylamine (0.56ml, 4 mmol) and dihydropyrroloindole (D6) (0.69g, 4 mmol). Triethylamine was added only with the isothiazole hydrochloride.
After pouring the final mixture into water and filtering off the product, the crude material was recrystallised from dichloromethane/methanol/petrol to give the title compound (0.76g, 61%), m.p. 254-255°C.
NMR (D6-DMSO) 8: 2.30 (3H, s), 3.30 (2H, t, 1=1), 3.74 (3H, s), 4.14 (2H, t, J=7), 35 6.35 (IH, d, J=4), 6.76 (IH, s), 7.20 (IH, d, J=4), 7.29 (IH, s), 8.08 (IH, s), 10.48 (IH, s).
^WO 94/04533 PCT/EP93/02031
Found: C, 61.31; H, 5.24; N, 17.74%, C16H16N4OS requires: C, 61.52, H, 5.15; N, 17.93%
Example 25
2,3-Dihydro-5-methyl-l-(5-quinoIylcarbamoyl)-lH-pyrrolo[23-nindole (E25)
The title compound was prepared by the method of E23, using 5-aminoquinoline (0.58g, 4 mmol), CDI (0.7 lg, 4.4 mmol), and dihydropyrroloindole (D6) (0.69g, 4 mmol). No triethylamine was used, and the initial reaction mixture was stirred for lh at 0°C and 0.5h at room temperature.
After pouring the final mixture into water and filtering off the product, the crude material was recrystallised from dichloromethane/methane/petrol to give the title compound (0.48g, 35%), m.p. 240-243°C.
NMR (D6-DMSO) 6: 3.43 (2H, t, J=8), 3.84 (3H, s), 4.42 (2H, t, J=8), 6.37 (IH, d, 15 J=4), 7.27 (IH, d, J=4), 7.38 (IH, s), 7.63 (IH, dd, J=8.5), 7.72 (IH, d, J=8), 7.87 (IH, t, J=8), 7.99 (IH, d, J=8), 8.08 (IH, s), 8.55 (IH, d, J=8), 8.84 (IH, s), 9.00 (IH, d, J=5).
Found: C, 72.85; H, 5.45; N, 16.36%, C2iH18N40 requires C, 73.67; H, 5.30; N, 16.36%
Example 26
23-Dihydro-5-methyl-l-(3-methyl-5-isoxazolylcarbamoyl)-lH-pyrrolo[2r3-f]indole (E26)
To a suspension of sodium hydride (80% in oil, 40mg, 1.33 mmol) in dry DMF (10ml) was added 5-amino-3-methylisoxazole (0.12g, 1.24 mmol), and the mixture was stirred for 25 20 min at 0°C. Imidazolylcarbamoyl pynoloindole (D41) (0.32g, 1.20 mmol) was then added and the mixture was stirred for 1.5h at 100-130°C, then cooled and poured into water. The precipitate was filtered off, washed with water and dried to give the title compound (0.17g, 48%), m.p. 212-215°C.
NMR (D6-DMSO) 8: 2.19 (3H, s), 3.24 (2H, t, J=7), 3.73 (3H, s), 4.14 (2H, t, J=7), 6.07 (IH, s,), 6.33 (IH, d, J=4), 7.20 (IH, d, J=4), 7.28 (IH, s), 8.05 (IH, s), 10.20 (IH, s).
Found: C, 64.83; H, 5.51; N, 18.83%, Ci6H16N4C>2 requires: C, 64.85; H, 5.44; N, 35 18.91%
-WO 94/04533
Example 27
N-(5-Isoquinolvl)-5-methyl-23-<iihytiropyrTolo[2,3-f] indole-1-carboxamide (E27)
The title compound was prepared from 5-aminoisoquinoline, carbonyl diimidazole and 1-amino-5-methyl- 2,3-dihydropyrrolo [2,3-f]indole, using a procedure similar to that 5 described for Example 25, in 15% yield, m.p. 245-250°C.
NMR (D6 DMSO) 8: 3.48 (2H, t, J=6), 3.86 (3H, s), 4.42 (2H, t, J=6), 6.38 (IH, d, J=2), 7.28 (IH, d, J=2), 7.40 (IH, s), 7.80 , (IH, t, d=6), 7.91 (IH, d, J=6), 7.99 (IH, d, J=6), 8.08 (2H, d, J=6), 8.60 (IH, d, J=6), 8.79 (IH, s), 9.42 (IH, s).
Found: M+ 342.40, C2iHigN40 requires 342.40 Example 28
N-(6-Quinolyl)-5-methyl-2,3-dihydro-pyrrolo [2,3-f] indole-1-carboxamide (E28)
The title compound was prepared from 6-aminoquinoline, carbonyl diimidazole, and 1-amino-5-methyl-2,3-dihydro-pyrrolo [2,3-f] indole using a procedure similar to that described for Example 25, in 12% yield, m.p. 217-220°C.
NMR (D6 DMSO) 8: 3.30 (2H, t, J=6), 3.74 (3H, s), 4.23 (2H, t, J=6), 6.32 (IH, d, 20 J=2), 7.20 (IH, d, J=2), 7.29 (IH, s), 7.42-7.49 (IH, m), 7.94 (2H, s),8.09 (IH, s), 8.27 (2H, m), 8.74-8.79 (2H, m).
Found: M+ 342-40, C21H18N4O requires 342.40
Example 29
2-Methyl-l-(3-pyridylcarbamoyI)-23-dihydropyrrolo[23-f)-indole (E29)
Nicotinoyl azide (0.142g, 0.96 mmol) was stirred at reflux under Ar in dry toluene (40 ml) for lh, allowed to cool and 2-methyl-2,3-dihydropyrrolo[2,3-f]indole (D47) (0.15g, 0.87 mmol) in dry toluene (10 ml) was added. The solution was stirred for 1 h, the resulting 30 precipitate filtered off, washed with a small quantity of Et20 and dried thoroughly to afford the title compound (E29) (70 mg, 28%).
NMR (D6-DMSO) 8 : 1.25 (3H, d), 2.75 (IH, d), 3.46 (IH, dd), 4.82 (IH, m), 6.32 (IH, s), 7.20 (IH, s), 7.33 (IH, dd), 8.01 (IH, m), 8.01 (IH, s), 8.21 (IH, d), 8.68 (IH, s) 35 8.78 (IH, d), 10.83 (IH, bs, NH).
WO 94/04533 PCT/EP93/02031 /
Found: C, 69.69; H, 5.71; N, 19.16%
C17H16N4O requires C, 69.85; H, 5.52; N, 19.16%
Found: M+ 292 C17H16N4O requires 292
Example 30
2,5-Dimethyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2r3-f]-indole (E30)
Nicotinoyl azide (28.7 mg, 1.1 eq.) was stirred at reflux under Ar in dry toluene (40 ml) for lh, allowed to cool and 2,5-dimethyl-2,3-dihydropyrrolo[2,3-f]indole (D49) (0.37g, 1.76 mmol) in dry toluene (10 ml) added. The solution was stirred for lh, the solution 10 evaporated to dryness, and purified by column chromatography (SiC>2, CHCiyMeOH 9:1) to afford the product as a pale yellow oil which was triturated with Et20 to give a pale yellow solid (170 mg).
NMR (CDCI3) 5 : 1.33 (3H, d), 2.89 (IH, d), 3.62 (IH, dd), 3.84 (3H, s, NMe),
4.96 (IH, m), 6.42 (IH, d), 7.30 (IH, d), 7.39 (IH, s), 7.42 (IH, dd), 8.08 (IH, s), 8.13 (IH, s), 8.32 (1H, d), 8.80 (IH, s), 8.85 (IH, s, NH).
r
Found: C, 69.98; H, 6.11; N, 17.72%
C18H18N4° 1/6 H2° requires C, 69.90; H, 6.04; N, 18.10%
Found: M+ 306, CigHjg^O requires 306.
Example 31
-Ethyl-l-(3-pyridylcarbamoyl) 2T3,6,7-tetrahydropyn-olo-[2?3-f|indole (E31)
-Ethyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo-[2,3-f]indole (E 10) (0.7g, 0.0023 25 moles) was dissolved in glacial acetic acid (15 ml) and treated with sodium cyanoborohydride (0.72g, 0.0114 moles) at ambient temperature with stirring. The mixture was stirred for 1 h then diluted with water (100 ml), basified with 10% aqueous sodium hydroxide and extracted with dichloromethane (2x 100 ml). The organic solution was dried (Na2SC>4), filtered and evaporated to dryness. Flash chromatography on silica 30 gel eluting with 2-5% methanol/dichloromethane followed by recrystallisation of the solid obtained from ethyl acetate/40-60 petrol gave the title compound (E31) as a white crystalline solid (0.45 g, 64%) m.p. 151-153° C.
NMR (D6-DMSO) 5 : 1.10 (3H, t, J 7), 2.81 (2H, t, J 7), 2.98-3.11 (4H, m), 3.21 (2H, 35 t, J 7), 4.07 (2H, t, J 7), 6.41 (IH, s), 7.29 (1H, q, J 5), 7.62 (IH, s), 7.93-7.96 (IH, m), 8.19 (IH, d, J 2), 8.51 (IH, s), 8.70 (IH, s).
94/04533
Found: C, 69.56; H, 6.50; N, 18.04%
CigH2oN40. x/8 H2O requires: C, 69.58; H, 6.57; N, 18.03%
Found: M+308, CjgH2oN40 requires 308
Example 32
-Methyl-l-(2-methyl-4-quinolinylcarbamoyl)-2,3,6,7-tetrahydropyrrolo[2,3-f]indole (E32)
-Methyl-l-(2-methyl-4-quinolinylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole (E 19) (0.7 10 g, 0.002 moles) in glacial acetic acid (15 ml) was treated with sodium cyanoborohydride (0.58 g, 0.009 moles) as in the method of Example 9 to give the title compound (E32) as pale yellow crystals (0.44g, 63%) m.p. 242-244° C.
NMR (D6-DMSO) 5 : 2.61 (3H, s), 2.69 (3H, s), 2.80 (2H, t, J 7),3.10-3.22 (4H. m). 15 4.29 (2H, t, J 7), 6.45 (1H, s), 7.45-7.53 (1H, m), 7.64-7.77 (3H, m), 7.88 (IH, d. J 8). 8.12 (IH, d, J 8), 8.54 (1H, s)
Found: C, 72.69; H, 6.37; N, 15.36%
C22H22N4O »/4 H20 requires: C, 72.83; H, 6.21; N, 15.45%
Found: M+ 358, C22H22N4O requires 358
Example 33
-Methyl-l-(2-methyl-4-pyridylcarbamoyl)-23-dihydropyrrolo[2?3-f]indole (E33)
The title compound was prepared from 2-methyl-4-aminopyridine anion (prepared using 25 sodium hydride) 1,1'-carbonyldiimidazole, and 5-methyl-2,3-dihydropyrrolo[2,3-fjindole in dimethylformamide using a procedure similar to that described for Example 5, in 45% yield.
NMR (D6-DMSO) 6 : 2.40 (3H, s), 3.27 (2H, t, J 7), 3.72 (3H, s), 4.18 (2H, t, J 7), 30 6.32 (IH, d, J 3), 7.19 (IH, d, J 3), 7.26 (IH, s), 7.43 (IH, d, J 8), 7.50 (IH, s), 8.05 (IH, s), 8.22 (IH, d, J 8), 8.74 (IH, s).
Found: M+306, CigHig^O requires 306
PCT/EP93/02031 —
Example 34
Pharmaceutical compositions for oral administration may be prepared by combining the following:
1) Solid Dosage Formulation
% w/w
Compound of formula 1
%
Magnesium stearate
0.5%
Starch
2.0%
HPM cellulose
1.0%
Microcrystalline cellulose
86.5%
The mixture may be compressed to tablets, or filled into hard gelatin capsules.
The tablet may be coated by applying a suspension of film former (e.g. HPM cellulose), pigment (e.g. titanium dioxide) and piasticiser (e.g. diethyl phthalate) and drying the film 15 by evaporation of the solvent The film coat can comprise 2.0% to 6.0% of the tablet weight preferably about 3.0%.
2) Capsule
%w/w
Compound of formula 1 20%
Polyethylene glycol 80%
The medicinal compound is dispersed or dissolved in the liquid carrier, with a thickening agent added, if required. The formulation is then enclosed in a soft gelatin capsule by suitable technology.
Example 35
A pharmaceutical composition for parenteral administration may be prepared by combining the following:
Preferred Level
Compound of formula 1 1.0%
Saline 99.0%
The solution is sterilised and sealed in sterile containers.
94/04533
Pharmacological Data
[3H]-mesulergine binding to rat or human 5-HT2C clones expressed in 293 cells in vitro
Evidence from the literature suggests that 5-HT2C antagonists may have a 5 number of therapeutic indications including the treatment of anxiety, migraine, depression, feeding disorders and obsessive compulsion disorders. (Curzon and Kennett, 1990; Fozard and Gray, 1989) and Alzheimer's Disease (Lawlor, 1989, J. Arch. Gen. Psychiat. Vol. 46 p.542).
The affinity of test drugs for the 5-HT2C binding site can be determined by 10 assessing their ability to displace [3H]-mesulergine from 5-HT2C clones expressed in 293 cells (Julius et al., 1988). The method employed was similar to that of Pazos et al, 1984.
The cells suspension (400ml) was incubated with [3H]-mesulergine (0.5nM) in Tris HQ buffer (pH 7.4) at 37°C for 30 minutes. Non-specific binding was measured in the presence of mianserin (10"^M). Ten concentrations of test drug (3 x 10"9 to 10"^M 15 final concentration) were added in a volume of 50ml. The total assay volume was 500ml. Incubation was stopped by rapid filtration using a Brandel cell harvester and radioactivity measured by scintillation counting. The IC50 values were determined using a four parameter logistic program (DeLean 1978) and the pKj (the negative logarithm of the inhibition constant) calculated from the Cheng Prusoff equation where: 20 Ki = IC50
l+_£
Kd
Kj = inhibition constant.
C = concentration of [3H]-mesulergine
Kd = Affinity of mesulergine for 5-HT2C binding sites.
Curzon, G.A. and Kennett, G.A. (1990). TIPS, Vol. 11,181-182.
Fozard, J.R. and Gray, J.A. (1989). TIPS, Vol. 10, 307-309.
Pazos, A. et al. (1984). Eur. J. Pharmacol., 106, 531-538.
Julius et al. (1988) Science 241, 558-564
DeLean A, Munson P.J., Rodbaud D (1978) Am. J. Physiol 235, E97-E102.
Results: The compound of examples 1 to 11 have pKj values of 6.04 to 9.29.
wo
94/04533
Reversal of MCPP-induced Hypolocomotion
Administration of m-(chlorophenyl)piperazine (mCPP) to rats induces hypolocomotion (Kennett and Curzon 1988, Luckie et al. 1989) as seen with the related drug l-(m-trifluoromethylphenyl)piperazine (TFMPP) (Lucki and Frazer 1982, Kennett 5 and Curzon 1988). This effect was blocked by the non specific 5-HT2C/5-HT2A receptor antagonists mianserin, cyproheptadine and metergoline and perhaps by mesulergine. It was not blocked by the 5-HT2A receptor antagonists ketanserin and ritanserin at relevant doses (Kennett and Curzon 1991) nor by antagonists of 5-HT^, 5-HTijj, 5-HT3, ct2 adrenoceptors or dopamine D2 receptors. The effect of mCPP is therefore considered to 10 be mediated by 5-HT2C receptors (Kennett and Curzon 1988) as confirmed by subsequent studies (Lucki et al., 1989). Since mCPP causes hypolocomotion when infused into the cerebral ventricles this effect is probably centrally mediated (Kennett and Cuizon 1988).
mCPP-induced hypolocomotion was measured in automated locomotion cages of dimensions 56 cm long x I6V2 cm wide x 25 cm high and made of black perspex. Two 15 photobeams traversed the width of the cages at either end at ground level. Sequential breaking of these beams allowed the measurement of cage transits.
Male Sprague Dawley rats (200-250g) (Charles River) were housed in groups of six. They were given drugs orally lh pretest and 40 mins later mCPP (7 mg/kg i.p.).
After a further 20 min they were placed in individual automated cages in groups of four 20 under red light in an adjacent room. After 10 min the test was terminated. Reversal of mCPP-induced hypolocomotion was considered as evidence of in vivo central 5-HT2C receptor antagonist properties.
Kennett, G.A., Curzon, G., (1991). Brit. J. Pharmacol. 103,2016-2020.
Lucki, I., Frazer, A., (1982). Am. Soc. Neurosci. 8 (abstr), 101. 25 Lucki, I., Ward, H.R., Frazer, A., (1989). J. Pharmacol. Exp. Therap. 249,155-
164.
Results: The compounds of examples 1,2 and 4 had H^o's of 5.5 to 22.3mg/kg p.o.
Social Interaction Test
Potential anxiolytic properties have been evaluated using the social interaction test based on that described by File (1980 J.Neurosci.Meth., 2,219). Active social interaction between male rats is usually quantitated by counting interactive behaviours such as following, grooming, sniffing, climbing over or under, biting, mounting and boxing. This 35 behaviour is supressed when the rats encounter each other in an environment which is novel and brightly lit- Under these circumstances anxiolytic drugs will enhance the level of social interaction.
^W'O
94/04533
Rats were housed in groups of 8 in a holding room adjacent to the experimental chamber for 8 days. They were then housed singly in the same room for 3 days prior to the experimental day. On the experimental day rats were injected p.o. lh pretest with vehicle or drug in pairs at 15 min intervals beginning at 10.00 am. 60 Mins later they were placed 5 with a weight matched pair mate (encountered for the first time) in the social interaction box in a separate room. The box was made of white perspex 54 x 37 x 26 cm with no lid. The floor was divided into 24 equal squares and the cage was brightly lit Active social interaction was scored blind over the next 15 min by remote video monitoring to give total interaction scores. The number of squares crossed by each rat was also scored and 10 summed. At the end of each test the box was carefully wiped with a damp cloth. Unlike anxiolytic drugs, treatments that enhance social interaction by stimulant action will also increase locomotion. Treatments that are sedative reduce locomotion.
The compound of Example 2 showed a significant increase in social interaction at doses of 15 lOmg/kg.
Geller-Seifter Procedure
Potential anxiolytic properties are evaluated using the Geller-Seifter procedure based on that originally described by Geller and Seifter, (1960) Psychopharmacologia, 1, 20 482-492. This procedure has been shown to be selective for drugs with anxiolytic properties (Cook and Sepinwall, (1975) "Mechanism of Action of Benzodiazepines" ed. Costa, E. and Greengard, P., Raven Press, New York; pp. 1-28).
Rats are trained on a variable interval 30 sec schedule (VI30) to press a lever in order to obtain food reward. The 5 min sessions of the VI30 schedule alternate with 2-5 25 min of a schedule (FR5) in which every 5th lever press is followed by presentation of a food pellet paired with a 0.5 sec mild footshock. The total study lasts approximately 30 mins. Rats typically respond with high rates of lever pressing under the VI30 schedule and low response rates under the FR5 'conflict' session. Anxiolytic drags increase the suppressed response rates of rats in a 'conflict' session.
Drugs are administered intraperitoneally or orally to groups of 3-8 rats 30 min before testing. The results are expressed as the percentage increase in the square root of the total number of lever presses in the FR5 'conflict' session. Square root transformation is necessary to normalise the data for statistical analysis using parametric methods.
The compound of Example 2 showed a significant increase in responding in the 35 'conflict' session at dose levels in the range 5 mg/kg p.o.
Claims (5)
- A compound of formula (I) or a salt thereof: »■ (0 wherein: P represents a quinoline or isoquinoline residue, or a 5- or 6-membered aromatic heterocyclic ring containing up to three heteroatoms selected from nitrogen, oxygen or sulphur; 10 R1 is hydrogen or C i_g alkyl; R2, r3, RlO and R^ are independently hydrogen or Cj-g alkyl, or R*0 and R*1 together form a bond, or R2 and R*0 or R3 and R* * together form a C2-6 aikylene chain; r4 is hydrogen, Cj.g alkyl, halogen, Nr8r9 or OR*2 where R^, R^ and R*2 are independently hydrogen or C|.g alkyl; 15 R5 is hydrogen orC^.g alkyl; R7 is hydrogen, alkyl, OR12 or halogen, where R12 is hydrogen or Ci_$ alkyl; n is 2 or 3; and the groups R^ and are independently hydrogen or alkyl. 20
- 2. A compound according to claim 1 in which R* is methyl or ethyl.
- 3. A compound according to claim 2 in which R2 and R3 are hydrogen and RlO ^ r1 1 together form a bond. 25
- 4. A compound according to claim 3 in which R4 is hydrogen or methyl. 5. A compound according to claim 4 in which R^ and R7 are hydrogen. 6. A compound according to claim 5 in which (CR13R14)n is an ethylene 30 group. 7. A compound according to claim 1 which is selected from: t 94/04533 PCT/EP93/02031 5-Methyl-1 -(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole 6-Methyl-3-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole 5,7-Dimethyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f] indole l-(3-Pyridylcarbamoyl)-2,3-dihydropyirolo[2,3-f] indole 5 6-Methyl-3-(4-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole 6-Methyl-3-(2-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole 5-Methyl-l-(2-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole 5-Methyl-1 -(4-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole 5-Methyl-1 -(3-pyridylcarbamoyl)-2,3,6,7-tetrahydropyrrolo[2,3-f] indole 10 5-Ethyl-1 -(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole 5-n-Propyl-l-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f]indole 5.6-Dimethyl-1 - (3-pyridylcarbamoyl)-2,3-dihydropyrrolo[2,3-f] indole 6.7-Dimethyl-3-(3-pyridylcarbamoyl)-2,3-dihydropyrrolo[3,2-e]indole l-Methyl-N-(3-pyridyl)-5,6,7,8-tetrahydro-lH-pyirolo[2,3-g]quinoline-5-carboxamide 15 3-Methyl-N-(3-pyridyl)-6,7,8,9-tetrahydro-3H-pyrrolo[3,2-f]quinoline-6-carboxamide 6-Methyl-3-(2-methyl-4-quinolinylcarbamoyl)-2,3-dihydropynolo[3,2-e]indole, 6-Methyl-3-(5-quinolinylcarbamoyl)-2,3-dihydro-pyrrolo[3,2-e]indole, 6-Methyl-3-(3-quinoliny lcarbamoyl)-2,3-dihydropyrrolo [3,2-e] indole, 5-Methyl-1 -(2-methyl-4-quinolinylcarbamoyl)-2,3-dihydropynolo[2,3-f] indole, 20 6,8-Dimethyl-3-(3-pyridylcarbamoyl)-2,3-dihydropyiTolo[3,2-e]indole, 6-Methyl-3-(3-pyridylcarbamoyl)-2,3,7,8-tetrahydropyrrolo[3,2-e]-indole, 5-Methyl-1 -(2-pyrazinylcarbamoyl)-2,3-dihydropyiTolo[23-f] indole, 2,3-Dihydro-5-methyl-l-(3-methyI-5-isothiazolylcarbamoyl)-lH-pyrrolo[3,2-e]indole, 23-Dihydro-5-methyl-1 -(3-methyl-5-isothiazolylcarbamoyl)- lH-pyrrolo[23-f] indole, 25 2,3-Dihydro-5-methyl-l-(5-quinolylcarbamoyl)-lH-pyrrolo[23-flindole, 2,3-Dihydro-5-methyl-l-(3-methyl-5-isoxazolylcarbamoyl) -lH-pyrrolo[23-f]indole, N-(5-Isoquinolyl)-5-methyl-2,3-dihydropyrrolo[23-f] indole- 1-carboxamide, N-(6-Quinolyl)-5-methyl-2,3-dihydro-pyrrolo [2,3-fjindole-1 -carboxamide; or a pharmaceutically acceptable salt thereof. 30 35 8. A compound according to any one of claims 1 to 7 for use in therapy. 9. A pharmaceutical composition which comprises a compound according to any one of claims 1 to 7 and a pharmaceutically acceptable carrier or excipient 10. A process for the preparation of a compound of formula (I) or a salt thereof, which process comprises: -49- WO 94/04533 PCT/EP93/02031 (a) the coupling of a compound of formula (II); — A (||) 5 with a compound of formula (HI); 13* 14' (CR R )n (III) wherein A and R*> contain the appropriate functional group(s) necessary to form the 10 moiety, -NR^CO when coupled, wherein R^' is R^ as defined in formula (I) or a group convertible thereto, n is as defined in formula (I), and the variables R* , R2, R3, R*0, R11', R13', R14', R4', R5' andR7' are R1, R2, R3, R10, R11, R13, R14, R4 and R7 respectively, as defined in formula (I), or groups convertible thereto, and thereafter optionally and as necessary and in any appropriate order, converting any R*, R2, R3, 15 R10', R11', R13', R14', R4', R5' and R7' when other than R1, R2, R3, R™, RU, R*3, R14, R4, R5, and R7 respectively to R1, R2, R3, R10, R1R13, R14, R4, R5 and R7, interconverting R*, R2, R3, R*0, R^, R*3, R^4, R4, R^ and R7, and forming a pharmaceutically acceptable salt thereof; 20 or (b) cyclising a compound of formula (IV): R
- 5. 13' 14' R (CR R )n (IV) wherein R4, R^', R7', R*3' and R*4 are as defined in formulae (II) and (III), n is as 25 defined in formula (I), and C and D contain the appropriate functional group(s) necessary to form the indole or indoline ring substituted by R*, R2, R3 , and R* * as defined in -50- * 94/04533 PCT/EP93/02031 (HI), and thereafter optionally and as necessary in any appropriate order, converting any R1', R2', R3', RiO', R11', R13', R14', R4', R5' and R7' when other than R1, R2, R3, R10, R1R13, R14, R4, R5 and R7, to R1, R2, R3, R10, R11, R13, R14 R4, r5 and R7, interconverting R*, R2, R3, R^t R^, R*3, R^4, R4, R^ and R7, and forming a 5 pharmaceutically acceptable salt -51 -
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KR19980701879A (en) * | 1995-02-02 | 1998-06-25 | 피터 기딩스 | Indole derivatives as 5-hydroxytryptamine receptor antagonists |
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UA77650C2 (en) | 1999-12-06 | 2007-01-15 | Lundbeck & Co As H | Use of serotonin reuptake inhibitor in combination with deramcyclane |
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GB0305553D0 (en) * | 2003-03-11 | 2003-04-16 | Glaxo Group Ltd | Compounds |
WO2014049153A1 (en) * | 2012-09-28 | 2014-04-03 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antagonists of the 5-ht2b receptor for use in the prevention or treatment of spasticity |
US20230312562A1 (en) * | 2020-07-02 | 2023-10-05 | Purdue Research Foundation | Tetrahydro-3h-pyrazolo quinolone and tetrahydro-3h-pyrrolo[3,2-f]quinoline -containing compounds and uses thereof |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH06500551A (en) * | 1990-09-13 | 1994-01-20 | ビーチャム・グループ・パブリック・リミテッド・カンパニー | Indoleurea as a 5HT receptor antagonist |
-
1993
- 1993-07-29 WO PCT/EP1993/002031 patent/WO1994004533A1/en not_active Application Discontinuation
- 1993-07-29 JP JP6505828A patent/JPH08500580A/en active Pending
- 1993-07-29 EP EP93917699A patent/EP0656003A1/en not_active Ceased
- 1993-07-29 NZ NZ254785A patent/NZ254785A/en unknown
- 1993-07-29 CA CA002142721A patent/CA2142721A1/en not_active Abandoned
- 1993-07-29 AU AU47046/93A patent/AU4704693A/en not_active Abandoned
- 1993-08-18 MA MA23262A patent/MA22955A1/en unknown
- 1993-08-18 MX MX9305037A patent/MX9305037A/en unknown
- 1993-08-19 AP APAP/P/1993/000560A patent/AP9300560A0/en unknown
- 1993-08-19 IL IL10673793A patent/IL106737A0/en unknown
- 1993-08-19 TW TW082106679A patent/TW248557B/zh active
- 1993-08-19 CN CN93116553A patent/CN1086819A/en active Pending
- 1993-08-20 SI SI9300438A patent/SI9300438A/en unknown
Also Published As
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TW248557B (en) | 1995-06-01 |
EP0656003A1 (en) | 1995-06-07 |
AU4704693A (en) | 1994-03-15 |
MX9305037A (en) | 1994-03-31 |
CA2142721A1 (en) | 1994-03-03 |
CN1086819A (en) | 1994-05-18 |
MA22955A1 (en) | 1994-04-01 |
WO1994004533A1 (en) | 1994-03-03 |
IL106737A0 (en) | 1994-05-30 |
JPH08500580A (en) | 1996-01-23 |
SI9300438A (en) | 1994-03-31 |
AP9300560A0 (en) | 1995-02-19 |
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