AP479A

AP479A - Amine derivatives.

Info

Publication number: AP479A
Application number: APAP/P/1994/000642A
Authority: AP
Inventors: Duncan Robert Amour; Philip Charles Box; Primton Shah
Original assignee: Glaxo Group Ltd
Priority date: 1994-05-17
Filing date: 1994-05-17
Publication date: 1996-03-21
Also published as: AP9400642A0

Abstract

Compounds of general formula (1)

Description

Amine Derivatives

This invention relates to novel amine derivatives, to processes for their 5 preparation, to pharmaceutical compositions containing them and to their use in medicine.

In particular the invention relates to 5-aminoalkyl-1,4-benzodiazepine derivatives which modulate the effects of gastrin and/or cholecystokinin (CCK) in mammals.

Thus the invention provides compounds of general formula (I)

NRjR, and physiologically acceptable salts thereof;

wherein R-| represents CH2CONR5R5 or CH2COR7;

R2 represents a phenyl group optionally substituted by 1 or 2 substituents selected from halogen, alkyl, nitro, cyano, trifluoromethyl, trifluoromethoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, amino, substituted amino, hydroxy, alkoxy, methylenedioxy, alkoxycarbonyl, oxazolyl or oxadiazolyl;

A represents a C-|_4 straight or branched alkylene chain;

R3 and R4 independently represent hydrogen or C^alkyl or R3 and R4 together with the nitrogen atom to which they are attached form a saturated 5-7 membered heterocyclic ring, which ring may contain an additional heteroatom selected from oxygen, sulphur or nitrogen;

R5 represents hydrogen or Cf _4alkyl;

Rg represents C^alkyl or phenyl, optionally substituted by halogen,

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When NR3R4 represents a 5-7 membered saturated heterocyclic ring this may be for example pyrrolidino, piperidino, hexamethylenimino, morpholino, thiomorpholino and oxides thereof, piperazino or an N-substitued derivative thereof e.g. N-methyl piperazino or N-alkoxycarbonyl piperazino.

When R3 and R4 represent Ci_4alkyl examples of suitable groups include methyl, ethyl, ispropyl, propyl or n-butyl.

The alkylene chain A in the compounds of formula (I) is preferably a straight chain alkylene such as methylene, ethylene, propylene or butylene.

When Rg represents halogen examples of suitable groups include chlorine or fluorine.

The term oxazolyl refers to a 1,3 oxazolyl group which is linked to the rest of the molecule via the carbon atom in the 2 or 5 position.

The term oxadiazolyl refers to a 1,2, 4 oxadiazolyl group which is linked to the rest of the molecule via the carbon atom in the 3 or 5 position.

In compounds of formula (I) the term substituted amino means C-i^alkylamino, e.g. isopropylamino, diCi.4alkylamino e.g. dimethylamino, Ci^alkanoylamino or C-j_4alkoxycarbonylamino e.g. t-butoxycarbonylamino .

When R2 is phenyl containing a single substituent this is preferably in the meta or para position.

A preferred class of compounds of formula (I) include those wherein R-| represents the group Cb^CONRgRg . Within this class particularly preferred compounds are those wherein R5 represents methyl or ethyl and Rg represents

Ν.

or

When R3 and R4 represent C-|_4alkyl examples of suitable groups include methyl, ethyl, ispropyl, propyl or n-butyl.

In compounds of formula (I) the term substituted amino means C-^alkylamino, e.g. isopropylamino, diCi-4alkylamino e.g. dimethylamino, Ci-4alkanoylamino or C-j .4alkoxycarbonylamino e.g. t-butoxycarbonylamino .

A preferred class of compounds of formula (I) include those wherein R-| represents the group CH2CONR5R5 . Within this class particularly preferred compounds are those wherein R5 represents methyl or ethyl and Rg represents

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A further preferred group of compounds of formula (I) are those wherein R₁represents the group CH₂CONR₅R₆ A represents a methylene chain, NR₃R₄represents a saturated 5-7 membered heterocyclic ring which may contain an additional heteroatom selected from oxygen, sulphur or nitrogen. From within this group particularly preferred compounds include those wherein R₅ is methyl or ethyl and R₆ is phenyl optionally substituted by fluorine or chlorine or NR₅R₆represents a pyrrolidino, 2,5-dimethylpyrrolidino, 3,3-dimethylpyrrolidino, piperidino, 3,3-dimethylpiperidino, or 1-tetrahydroquinolino, R₂ represents phenyl optionally substituted by one or 2 groups selected from fluorine, methyl, methoxy, trifluoromethyl amino, cyano, hydroxy, oxazol-5-yl or 1,2,4-oxadiazol3-yl and R₈ represents hydrogen or R₈ represents fluorine or chlorine and n is 1.

Particularly preferred compounds of the invention include

2-{3-[3-(3-Methoxy-phenyl)-ureido]-5-morpholin-4-ylmethyl-2-oxo-2,3-dihydro15 benzo [e] [1,4]diazepin-1 -yl}-N-methyl-N-phenyl-acetamide;

N-Methyl-2-[5-morpholin-4-ylmethyl-2-oxo-3-(3-phenyl-ureido)-2,3 -dihydrobenzo[e] [1,4]diazepin-1 -yl]-N-phenyl-acetamide;

N-Methyl-2-{5-morpholin-4-ylmethyl-2-oxo-3-[3-(3-trifluoromethyl -phenyl)ureido]-2,3- dihydro-benzo[e][ i ,4]diazepin-1 -yl}-N-phenyl-acetamide;

2-{3-[3-(3-Cyano-phenyl)-ureido]-5-morpholin-4-ylmethyl-2-oxo-2,3-dihydrobenzo[e] [1,4]diazepin-1-yl}-N-methyl-N-phenyl-acetamide;

-[5-(Morpholin-4-yl-methyl)-2-oxo-1 -(2-oxo-2-pyrrolidin-1 -y l-ethy l)-2,3-di hydro1 H-benzo[e][1,4]diazepin-3-yl]-3-(3-oxazol-5-yl-phenyl)-urea; N-Ethyl-N-(4-fluoro-phenyl)-2-{3-[3-(4-fluoro-phenyl)-ureido]-5-(morpholin-4-yl25 methyl)-2-oxo-2,3-dihydro-benzo[e][1,4]diazepin-1 -yl}-acetamide;

and the enantiomers thereof; and physiologically acceptable salts thereof.

The physiologically acceptable salts of the compounds of formula (I) include conventional salts formed for example from pharmaceutically acceptable inorganic or organic acids as well as quaternary ammonium acid addition salts. Examples of suitable salts include hydrochloric, hydrobromic, sulfuric, phosphoric, nitric, perchloric, fumaric, acetic, propionic, succinic, glycolic, formic, lactic, maleic, tartaric, citric, pamoic, malonic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, fumaric, toluenesulphonic, methanesulphonic, naphthalene-2-sulphonic, benzenesulphonic and the like. Other acids such as

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A further preferred group of compounds of formula (I) are those wherein Rt represents the group CH₂CONR₅R₆ A represents a methylene chain, NR₃R₄represents a saturated 5-7 membered heterocyclic ring which may contain an additional heteroatom selected from oxygen, sulphur or nitrogen. From within this group particularly preferred compounds include those wherein R₅ is methyl or ethyl and R₆ is phenyl optionally substituted by fluorine or chlorine or NR₅R₆represents a pyrrolidino, 2,5-dimethylpyrrolidino, 3,3-dimethylpyrrolidino, piperidino, 3,3-dimethylpiperidino, or 1-tetrahydroquinolino, R₂ represents phenyl optionally substituted by one or 2 groups selected from fluorine, methyl, methoxy, trifluoromethyl amino, cyano, hydroxy, oxazol-5-yl or 1,2,4-oxadiazolC 3-yl and R₈ represents hydrogen or R₈ represents fluorine or chlorine and nisi.

Particularly preferred compounds of the invention include

N-Methyl-2-[5-morpholin-4-ylmethyl-2-oxo-3-(3-phenyl-ureido)-2,3 -dihydrobenzo[ej [1,4]diazepin-1-yl]-N-phenyl-acetamide;

-[5-(Morpholin-4-yl-methyl)-2-oxo-1 -(2-oxo-2-pyrrolidin-1 -yl-ethyl)-2,3-dihydro1 H-benzo[e][1,4]diazepin-3-yl]-3-(3-oxazol-5-yl-phenyl)-urea; N-Ethyl-N-(4-fluoro-phenyl)-2-{3-[3-(4-fluoro-phenyl)-ureido]-5-(morpholin-4-yl25 methyl)-2-oxo-2,3-dihydro-benzo[e][1,4]diazepin-1 -yl}-acetamide;

and the enantiomers thereof; and physiologically acceptable salts thereof.

BAD ORIGINAL $ the invention are useful for the treatment of gastrointestinal disorders especially those where there is an advantage in lowering gastric acidity. Such disorders include peptic ulceration, reflux oesophagitis and Zollinger Ellison syndrome. They may also be useful for the treatment of gastrointestinal disorders such as irritable bowel syndrome, excess pancreatic secretion, acute pancreatitis, motility disorders, antral G cell hyperplasia, fundic mucosal hyperplasia or gastrointestinal neoplasms. The compounds of the invention are also useful for the treatment of central nervous system disorders where CCK and/or gastrin are involved. For example anxiety disorders (including panic disorder, agoraphobia, social phobia, simple phobia, obsessive compulsive disorders, post traumatic stress disorder, and general anxiety disorder), depression, tardive dyskinesia, Parkinson's disease or psychosis. They may also be useful for the treatment of dependency on drugs or substances of abuse and withdrawal, Gilles de la Tourette syndrome, or dysfunction of appetite regulatory systems; as well as the treatment of certain tumours of the lower oesophagus, stomach, intestines and colon. Compounds of the invention are also useful for directly inducing analgesia, or enhancing opiate or non-opiate mediated analgesia, as well as anaesthesia or loss of the sensation of pain.

The invention therefore provides a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof for use in therapy, in particular in human medicine.

According to another aspect the invention provides the use of a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for the treatment of conditions where modification of the effects of gastrin and/or CCK is of therapeutic benefit.

According to a further aspect of the invention we provide a method for the treatment of a mammal, including man, in particular in the treatment of conditions where modification of the effects of gastrin and/or CCK is of therapeutic benefit which method comprises administering an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof to the patient.

the invention are useful for the treatment of gastrointestinal disorders especially those where there is an advantage in lowering gastric acidity. Such disorders include peptic ulceration, reflux oesophagitis and Zollinger Ellison syndrome. They may also be useful for the treatment of gastrointestinal disorders such as irritable bowel syndrome, excess pancreatic secretion, acute pancreatitis, motility disorders, antral G cell hyperplasia, fundic mucosal hyperplasia or gastrointestinal neoplasms. The compounds of the invention are also useful for the treatment of central nervous system disorders where CCK and/or gastrin are involved. For example anxiety disorders (including panic disorder, agoraphobia, social phobia, simple phobia, obsessive compulsive disorders, post traumatic ( stress disorder, and general anxiety disorder), depression, tardive dyskinesia,

Parkinson's disease or psychosis. They may also be useful for the treatment of dependency on drugs or substances of abuse and withdrawal, Gilles de la Tourette syndrome, or dysfunction of appetite regulatory systems; as well as the treatment of certain tumours of the lower oesophagus, stomach, intestines and colon. Compounds of the invention are also useful for directly inducing analgesia, or enhancing opiate or non-opiate mediated analgesia, as well as anaesthesia or loss of the sensation of pain.

ί'

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Tablets and capsules for oral administration may contain conventional excipients such as binding agents, for example, syrup, acacia, gelatin, sorbitol, tragacanth, mucilage of starch or polyvinylpyrrolidone; fillers, for example, lactose, sugar, microcrystalline cellulose, maize-starch, calcium phosphate or sorbitol; lubricants, for example, magnesium stearate, stearic acid, talc, polyethylene glycol or silica; disintegrants, for example, potato starch or sodium starch glycollate, or wetting agents such as sodium lauryl sulphate. The tablets may be coated according to methods well known in the art. Oral liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions emulsions, syrups or elixirs, or may be presented as a dry product for constitution with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents, for example, sorbitol syrup, methyl cellulose, glucose/sugar syrup, gelatin, hydroxyethylcellulose, carboxymethyl cellulose, aluminium stearate gel or hydrogenated edible fats; emulsifying agents, for example, lecithin, sorbitan mono-oleate or acacia; non-aqueous vehicles (which may include edible oils), for example, almond oil, fractionated coconut oil, oily esters, propylene glycol or ethyl alcohol; and preservatives, for example, methyl or propyl βhydroxybenzoates or ascorbic acid. The compositions may also be formulated as suppositories, e.g. containing conventional suppository bases such as cocoa butter or other glycerides.

For buccal administration the composition may take the form of tablets or lozenges formulated in conventional manner.

The composition according to the invention may be formulated for parenteral administration by injection or continuous infusion. Formulations for injection may be presented in unit dose form in ampoules, or in multi-dose containers with an added preservative. The compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising and/or dispersing agents. Alternatively the active ingredient may be in powder form for constitution with a suitable vehicle, e.g. sterile, pyrogen-free water, before use.

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Tablets and capsules for oral administration may contain conventional excipients such as binding agents, for example, syrup, acacia, gelatin, sorbitol, tragacanth, mucilage of starch or polyvinylpyrrolidone; fillers, for example, lactose, sugar, microcrystalline cellulose, maize-starch, calcium phosphate or sorbitol; lubricants, for example, magnesium stearate, stearic acid, talc, polyethylene glycol or silica; disintegrants, for example, potato starch or sodium starch glycollate, or wetting agents such as sodium lauryl sulphate. The tablets may be coated according to methods well known in the art. Oral liquid preparations may be in the form of, for example, aqueous or oily suspensions, solutions emulsions, syrups or elixirs, or may be presented as a dry product for constitution with water or other suitable vehicle before use. Such liquid preparations may contain conventional additives such as suspending agents, for example, sorbitol syrup, methyl cellulose, glucose/sugar syrup, gelatin, hydroxyethylcellulose, carboxymethyl cellulose, aluminium stearate gel or hydrogenated edible fats; emulsifying agents, for example, lecithin, sorbitan mono-oleate or acacia; non-aqueous vehicles (which may include edible oils), for example, almond oil, fractionated coconut oil, oily esters, propylene glycol or ethyl alcohol; and preservatives, for example, methyl or propyl phydroxybenzoates or ascorbic acid. The compositions may also be formulated as suppositories, e.g. containing conventional suppository bases such as cocoa butter or other glycerides.

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In a particular aspect of the process with a compound of formula (II) wherein R₉is a 1-imidazole group, this compound may be formed in situ, in which case the amine R2NH2 will be reacted with the compound of formula (III)

in the presence of carbonyl diimidazole under the aforementioned conditions.

Compounds of formula (II) may be prepared from compounds of formula (III).

Thus a compound of formula (II) wherein R_g is 1- imidazole may be prepared by reacting a compound of formula (III) with carbonyldiimidazole in a suitable solvent such as a halogenated hydrocarbon (e.g. dichloromethane) or an ether (e.g. tetrahydrofuran) at a temperature ranging from Οθ to 80°C, conveniently at room temperature.

Compounds of formula (II) wherein R1, R3, R4 and A have the meanings defined in formula (I) and R_g is an optionally substituted phenoxy group may be prepared by reaction of a compound of formula (III) with the appropriate haloformate R_gCOHal wherein Hal is chlorine or bromine. The reaction is preferably carried out in the presence of a base such as a tertiary amine e.g. triethylamine or pyridine, and in a solvent such as a halohydrocarbon e.g. dichloromethane.

Compounds of formula (I) may also be prepared by reacting a compound of formula (III) wherein R1, R3, R4 and A have the meanings defined above for formula (I) with the isocyanate R2NCO or carbamoyl chloride R₂NHCOCI (wherein R2 has the meaning defined in formula (I)). The reaction conveniently takes place in the presence of a suitable solvent such as a halohydrocarbon (e.g. dichloromethane), an ether (e.g. tetrahydrofuran) or a nitrile (e.g.

acetonitrile) or a mixture thereof at a temperature in the range of 0° to 80° C.

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In a particular aspect of the process with a compound of formula (II) wherein R_gis a 1-imidazole group, this compound may be formed in situ, in which case the amine R2NH2 will be reacted with the compound of formula (III)

in the presence of carbonyl diimidazole under the aforementioned conditions.

Compounds of formula (II) may be prepared from compounds of formula (III).

Thus a compound of formula (II) wherein R₉ is 1- imidazole may be prepared by reacting a compound of formula (III) with carbonyldiimidazole in a suitable solvent such as a halogenated hydrocarbon (e.g. dichloromethane) or an ether (e.g. tetrahydrofuran) at a temperature ranging from 0° to 80θ0, conveniently at room temperature.

Compounds of formula (II) wherein R-|, R3, R4 and A have the meanings defined in formula (I) and R_g is an optionally substituted phenoxy group may be prepared by reaction of a compound of formula (III) with the appropriate haloformate RgCOHal wherein Hal is chlorine or bromine. The reaction is preferably carried out in the presence of a base such as a tertiary amine e.g. triethylamine or pyridine, and in a solvent such as a halohydrocarbon e.g. dichloromethane.

Compounds of formula (I) may also be prepared by reacting a compound of formula (III) wherein R-|, R3, R4 and A have the meanings defined above for formula (I) with the isocyanate R2NCO or carbamoyl chloride R₂NHCOCI (wherein R2 has the meaning defined in formula (I)). The reaction conveniently takes place in the presence of a suitable solvent such as a halohydrocarbon (e.g. dichloromethane), an ether (e.g. tetrahydrofuran) or a nitrile (e.g.

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The reaction is preferably carried out at a temperature within the range -30° to 40°C.

The compound of formula (V) may be prepared by cyclisation of the ketone 5 derivative (VI)

The cyclisation may be carried out by treating the compound (VI) with ammonia in a suitable solvent such as an ether e.g. tetrahydrofuran followed by reaction with sodium acetate in glacial acetic acid.

Compounds of formula (IV) wherein A is a methylene group may also be prepared by reaction of the compound of formula (VII) wherein R-| is as defined in formula (I)

with an amine R3R4NH, preferably in a solvent such as halohydrocarbon e.g. dichloromethane.

Compounds of formula (VII) may be prepared by bromination of the compound of formula (VIII)

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The bromination reaction may be carried out using a reagent such as Nbromosuccinimide or 5,5-dibromobarbituric acid.

Compounds of formula (IV) wherein A is an ethylene group may be prepared from a compound of formula of (VIII) with the amine HNR3R4 and formaldehyde under conventional Mannich reaction conditions.

The compounds of formula (VIII) may be prepared by alkylation of the compound of formula (IX)

using the same conditions as that described above for preparing the corresponding compound of formula (IV) from compound (V).

The compounds of formula (VI) may be prepared by condensation of the amino ketone (X) with the benzotriazole derivative (XI)

COANR-,^

HO,C-CH-NHCO,CHjPh (X) (XT)

r™—> ·· - - ·

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The condensation reaction may be carried out using conventional procedures, for example by the reaction of (X) with (XI) in the presence of dicyclohexylcarbodiimide in a solvent such as tetrahydrofuran.

The compounds of formula (X) are either known compounds or may be prepared by analogous methods described for preparing known compounds.

Compounds of formula (I) wherein A represents a methylene group may also be prepared by reaction of the bromomethyl derivative (XII)

wherein R-| and R2 are as defined in formula (I) with the amine R3R4NH, wherein R3 and R4 are as defined in formula (I). The reaction is preferably carried out in an aprotic solvent such as a halohydrocarbon e.g.

dichloromethane. The bromomethyl derivatives (XII) may be prepared by bromination of the corresponding methyl compound (XIII)

The bromination reaction may be carried out using a reagent such as 5,520 dibromobarbituric acid in a solvent such as a halohydrocarbon e.g.

dichloromethane, or chloroform or mixtures thereof.

The methyl derivative (XIII) may be prepared from the corresponding intermediate (VIII) using the general procedures described above for converting the compound of formula (IV) into a compound of formula (I).

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Compounds of the invention may be converted into other componds of the invention. Thus compounds of formula (I) wherein R2 is a phenyl group substituted by amino may be prepared from the corresponding compound wherein R2 is a phenyl group substituted by an alkoxycarbonylamino group by conventional means such as acid hydrolysis. For example compounds wherein R2 is phenyl substituted by amino may be prepared by reaction of the corresponding t-butylcarbonylamino compound with trifluroacetic in a suitable solvent such as dichloromethane.

Acid addition salts of compounds of formula (I) may be prepared by reaction with the appropriate physiologically acceptable acid in a suitable solvent followed if necessary by addition of suitable non solvent.

The compounds of formulae (II), (III), (IV), (V), (VI) and (VII) are novel and form further aspects of the invention.

In general, the compounds R2NH2, R2NCO or R₂HNCOCI are either known or may be prepared according to methods used for the preparation of known compounds. For example the amines R2NH2 may be prepared by reduction of the corresponding nitro compounds R2NO2. The reduction may be effected for example by catalytic hydrogenation using a suitable metal catalyst such as palladium on carbon in a suitable solvent such as an alcohol (e.g. ethanol) at room temperature.

Compounds of formula (I) contain at least one asymmetric carbon atom, namely the carbon atom of the diazepine ring to which the substituted urea grouping is attached. Specific enantiomers of the compounds of formula (I) may be obtained by resolution of the racemic compound using conventional procedures such as salt formation with a suitable optically active acid or by the use of chiral H.P.L.C.

Alternatively the required enantiomer may be prepared from the corresponding enantiomeric amine of formula (III) using any of the processes described above for preparing compounds of formula (I) from the amine (III). The enantiomers of the amine (III) may be prepared from the racemic amine (III) using conventional procedures such as salt formation with a suitably optically active acid.

carbonate ester to yield an optically active carbamate thereof. The resultant diastereoisomers may then be separated by conventional means. Each separate diastereosiomeric carbamate may then be converted into the corresponding enantiomeric amine (III) by conventional processes.

The following examples, which are non-limiting, illustrate the invention. Temperatures are in °C. Dried refers to drying with anhydrous Mg2SO4. All chromatography was carried out on silica gel. The following abbreviations are used. T.I.c. - thin layer chromatography; CDI-carbonyldiimidazole; DCM dichloromethane; DE - Diethyl ether; THF - tetrahydrofuran; DMF - Ν,Νdimethylformamide; EA - ethyl acetate; MeOH - methanol; CHCI₃ - chloroform; NaH - sodium hydride; ir - infra red spectra determined as a mull in mineral oil unless otherwise stated.

Intermediate 1

Phenylmethyl (2[(2-acetylphenyl)amino]-1 -[(1 -methylethvl)thio]-2-oxoethyl] carbamate

A suspension of ((l-methylethyl)thio]- [(phenylmethoxy)carbonyl]amino]acetic acid (10.49g) in dry DCM (175ml) at 0° under nitrogen was treated with 4methylmorpholine (3.93g) followed by the dropwise addition of isobutyl chloroformate (5.31 g). The mixture was stirred at 0° for 40min and a solution of

2-aminoacetophenone (5.00g) in dry DCM (60ml) was added dropwise. The mixture was stirred at 0° for 1h then at 23° for 18h. The mixture was washed with 2N hydrochloric acid, 2N sodium carbonate solution, saturated brine and dried. Solvent evaporation in vacuo gave the title compound (14.82g) which was used without further purification.

T.I.c. (1:1 DE-hexane) Rf 0.3

Intermediate 2

Phenylmethyl [2.3-dihydro-5-methyl-2-oxo-1 H-1.4-benzodiazepin-3vQcarbamate

Ammonia gas was passed through a solution of phenylmethyl[2-[(2acetylphenyl)amino]-1 -[(1 -methylethyl)thio]-2-oxoethyl]carbamate (14.74g) in dry THF (250ml) at 0° for 0.5h. Mercury (II) chloride (10.00g) was added and

BAD ORIGINAL ft the mixture was rapidly stirred for 6h whilst continuing to pass ammonia gas through the mixture. The mixture was filtered through hyflo and the solvent removed from the filtrate by evaporation in vacuo. The residue was treated with acetic acid (290ml) and sodium acetate (13.35g) and the resulting mixture stirred at 23° for 18h. The solvent was evaporated in vacuo and the residue was purified by chromatography. Elution with EA gave the title compound (5.70g).

T.I.c. (3:2 EA-hexane) Rf 0.4

Intermediate 3

Phenvlmethyl [2.3-dihydro-5-methyl-1-[2-(methylphenylamino)-2-oxoethyl3-2axo-- ,4zbe.niPdiazgpin-3-yllcarbamate.

80% Sodium hydride in oil (102mg) was added to a solution of phenylmethyl (2,3-dihydro-5-methyl-2-oxo-1H-1,4-benzodiazepin-3- yljcarbamate (1.00g) in dry DMF (10ml) under nitrogen. The mixture was stirred for 0.5h at 23° and was treated with a solution of 2- bromo-N-methyl-N-phenylacetamide (707mg) in dry DMF (1ml). The mixture was stirred at 23° for 1 h, partitioned between phosphate buffer solution (pH6.5) and EA, the organic phase was washed with water and dried. The solvent was evaporated in vacuo and the residue was purified by chromatography on alumina. Elution with MeOH-DCM (1:50) gave the title compound (568mg).

T.I.c. (1:50 MeOH-DCM) Rf 0.2

Intermediate 4

3-Amino-2.3-dihydro-N.5-dimethyl-2-oxo-N-phenyl-1 H-1.4-benzodia zepine-1 acetamide

A mixture of 5% palladium on carbon (300mg) and phenylmethyl (2,3- dihydro5-methyl-1-[2-(methylphenylamino)-2-oxoethyl]-2-oxo-1 H-1,4- benzodiazepin-3yljcarbamate (500mg) in MeOH-water 4:1 (40ml) at 40° under nitrogen was treated with ammonium formate (201 mg) and the mixture stirred at 40° for 1 h. The mixture was cooled to 23° and was filtered through hyflo. The filtrate was evaporated in vacuo and the residue partitioned between 2N sodium carbonate solution and chloroform. The organic phase was dried and the solvent evaporated in vacuo. The residue was purified by chromatography, elution with

MeOH-DCM (1:9) gave the title compound (302mg).

T.I.c. (1:9 MeOH-DCM) Rf 0.3

Intermediate 5

2.3-Dihydro-N.5-dimethyl-2-oxo-N-phenyl-[3[[(3-cyanophenyl)amino1carbonyl]a mine!-1H-1.4-benzodiazepine-1 -acetamide

3-Cyanophenyl isocyanate (144mg) was added to a solution of intermediate 4 (336mg) in dichloromethane (10ml) under nitrogen and the mixture stirred for 4h. The reaction mixture was filtered to give the title compound (305mg) as a white solid, m.p. 210-211°.

Intermediate 6

2-f5-BromQmethYl_-3-J3-(3-cvano-phenyl)-ureido]-2-oxo-2.3-dihydrobenzo(e1f1.41 diazepin- 1-yl)-N-methyl-N-phenyl-acetamide.

A solution of intermediate 5 (2.99g) in dry DCM (300ml) and CHCI3 (100ml) at

23° under nitrogen was treated with 5,5-dibromobarbituric acid (0.93g). After 18 hours silica (Merck 9385; 20g) was added and the mixture evaporated in vacuo. The mixture was purified by flash chromatography eluting with (1 to 2 to 5%) MeOH in DCM to give the title compound as a white foam (1.89g), m.p. 100° dec.

T.I.c. (5%MeOH-DCM) Rf 0.29

Intermediate 7

5-Bromomethyl-2-oxo-2.3-dihydro-1 H-benzofelfl ,41diazeoine-3-carba mic acid benzyl ester,

5,5-Dibromobarbituric acid (5.1 g) was added to a solution of 2,3-dihydro-5methyl- 2-oxo-1 H-benzo[e][1,4]-diazepine-3-carbamic acid benzyl ester (1 lg) in dry DCM (750ml) at 23° under nitrogen. The solution grew progressively cloudier and deeper orange over 20h whereupon silica (50g) was added and the mixture evaporated to dryness. The residue was chromatographed on silica (EtgN-deactivated, Merck 9385) with 1% MeOH in DCM as eluent to give the title compound (7.1 g) as a pale yellow solid, m.p. 154°dec.

T.I.c. Et₃N-deactivated SiO₂ (100:1 DCM-MeOH) Rf 0.55

Intermediate 8

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5-Morpholin-4-ylmethyl-2-oxo-2.3-dihydro-1 H-benzoie][1.4]diazepin e-3carbamic acid benzyl ester.

Morpholine (7.5ml) was added to a solution of intermediate 7 (6.9g) in dry DCM (190ml) at 23° under nitrogen. After 3h the cloudy orange mixture was poured into water (200ml) and the layers separated. The aqueous phase was reextracted with DCM (150ml) and the combined, dried organic extracts evaporated. The residue was chromatographed with 2 to 3% MeOH in DCM as eluent to give the title compound (3.38g) as a beige foam, m.p. 91⁰ dec.

T.I.c. (95:5 DCM-MeOH) Rf 0.28

I. r. 3235; 1698; 1500; 1456; 1241; 1116cm-¹

Intermediate 9

1-(3-Cvano-Phenyl)-3-(5-morpholin-4-vlmethyl-2-oxo-2.3-dihydro-1H-benzo[e]

II, 4]diazepin;3-yl):urea,

A solution of intermediate 8 (3.38g) in absolute EtOH (160ml) was hydrogenated at 23° and 1 atmosphere pressure in the presence of 10% palladium on charcoal as catalyst (1g). After 3h the mixture was filtered through hyflo and the filtrate evaporated to give a purple foam. A solution of the foam in MeCN (54ml) was treated with 3- cyanophenyl isocyanate (1.21g) and after 1h DE was added to the resulting suspension. The solid was filtered off and dried at 50° in vacuo to give the title compound (1.44g) as an off-white solid, m.p. 249-50°.

T.I.c. (9:1 DCM-MeOH) Rf 0.46

Intermediate 10

1-(3-Cyano-phenyl)-3-[1-(3.3-dimethyl-2-oxo-butyl)-5-methyl-2-oxo-2.3-dihydro1 H-benzo[e] (1.4Jdiazepin-3-yl]-urea,

3-Cyanophenyl isocyanate (278mg) was added to a solution of 3-amino-2,3dihydro- 1-(3,3,-dimethyl-2-oxo-butyl)-5-methyl-2-oxo-1 H-1,4-benzodiazep ine (500mg) in dry MeCN (13ml) at 23° under nitrogen. After 30 min the resulting thick slurry was stirred with DE (5ml) filtered and the filtercake washed with EA and DE then dried in vacuo at 50° to give the title compound (571 mg) as a white solid, m.p. 246-7°

T.I.c. (9:1 DCM-MeOH) Rf 0.51

l.r. 3340; 2229; 1719; 1678; 1646; 1557; 1517cm-¹

BAD ORIGINAL ft

Intermediate 11

-[5-Bromomethyl-1 -(3.3-dimethyl-2-oxo-butylV2-oxo-2.3-dihydro-1 H-benzo[e] [1.4]diazepin-3-yl]-3-(3-cyano-phenyO-urea,

5,5-Dibromobarbituric acid (38mg) was added to a suspension of intermediate (100mg) in dry DCM (10ml) at 23° under nitrogen. After 6.5h, dry THF (4ml) was added to induce solubility and stirring was continued for 17h. Silica (2g) was added to the pale orange solution and the mixture evaporated to dryness. The residue was chromatographed with 0 to 0.25 to 0.5 to 1 to 2% MeOH in

DCM as eluent to give the title compound (80mg) as a white solid, m.p.

135°dec.

T.I.c. (2% MeOH-DCM) Rf 0.23

Intermediate 12

5-Bromomethyl-1-(methyl-phenvl-carbamoylmethyh-2-oxo-2.3-dihydro-1Hbenzo[e] [1,4]diazepine-3-carbamic acid, benzyl ester A solution of intermediate 3 (200mg) in DE (5ml) and chloroform (5ml) under nitrogen, was trated with 5,5-dibromobarbituric acid (61 mg) and the mixture stirred at 23° for 18h. MeOH (5ml) and silica (1 g) were added and the solvent was evaporated in vacuo. The residue was chromatographed with MeOH-DCM (0.2:10) as eluent to give the title compound (175mg) as a white foam.

T.I.c. (10:0.5 DCM-MeOH) Rf 0.69

l.r. 3418; 3325; 1727; 1670; 1496; 1453cm*¹.

Intermediate 13

1-(Methyl-ρhenyl-caΓbamovlmethvh-5-morDholin-4-ylmethyl·2-oxo-2.3-d^hvdro1 H-benzo(e) (1.4]diazepine-3-carbamic acid, benzyl ester A solution of intermediate 12 (2.75g) in DCM (50ml) was treated with morpholine (2.18g) and the mixture was stirred at 23° under nitrogen for 1h.

The mixture was washed with water (2x40ml), brine (40ml) and dried then evaporated in vacuo. The residue was chromatographed with DCM-MeOH (10:0.3) as eluent to give the title compound (2.38g) as an orange foam,

l.r. (Solution in CHCI3) 3425; 1723; 1670; 1497; 1452; 1394cm*¹.

Intermediate 14

BAD ORIGINAL

2-(3-Amino-5-morDholin-4-ylmethyl-2-oxo-2.3-dihydro-benzoie1 (1.4]diazeoin-1 yl)-N- methyl-N-phenyl-acetamide

A solution of intermediate 13 (1.82g) in EtOH (50ml) was hydrogenated over 10% palladium on carbon (250mg) at 23θ and 1 atmosphere pressure. After 4h the mixture was filtered through hyflo and the filtrate evaporated to give the title compound (1.35g) as a pale yellow foam.

T.I.c. (9:1 DCM-MeOH) Rf 0.25

l.r. (Solution in CHCI3) 3395; 1669; 1598; 1497; 1451; 1116cm-1.

intermsdiateJS

R-Carbonic acid (4-nitro-phenyl) ester (1-phenyl-ethyl) ester.

A solution of (fi)-sec-phenethyl alcohol (500mg) and pyridine (324mg) in DCM (15ml) at 0-5° under nitrogen was treated dropwise with a solution of 4nitrophenyl chloroformate (825mg) in DCM (10ml). The mixture was allowed to warm to 23° and was stirred for 18h. The mixture was partitioned between phosphate buffer (pH 6.5) and DCM. The organic phase was washed with 8% sodium bicarbonate solution and was dried (Na2SO4). Solvent evaporation in vacuo gave a residue which was azeotroped with toluene and then purified by chromatography. Elution with EA-hexane (1:9) gave the title compound as a colourless oil (290mg).

T.I.c. (1:4 EA-hexane) Rf 0.45

l.r. (film) 3086; 2986; 1765; 1526; 1349; 1258; 1220; 1064; 861; 700cm-¹.

Intermediate 16

R-5-Methyl-1-(methyl-phenyl-carbamoylmethyl)-2-oxo-2.3-dihydro-1Hbenzo(e][k4]diazepine-3-carbamic acid 1-Dhenvl-ethvl ester.

A solution of intermediate 4 (200mg) and intermediate 15 (256mg) in MeCN (14ml) under nitrogen was treated with ΕίβΝ (60mg) and the mixture was heated under reflux for 18h. The mixture was cooled to 23° and was partitioned between phosphate buffer (pH 6.5) and EA. The organic phase was dried (Na2SO4) and the solvent evaporated in vacuo. The residue was purified by chromatography. Elution with EA-hexane (7:3) gave the title compound as a white foam (79mg).

T.I.c. (7:3 EA-Hexane) Rf 0.26

l.r. 3425;3318; 1724; 1669; 1632; 1596; 1270; 1244; 1206; 1071; 766;

701cm’¹.

Intermediate 17

2-(3-Amino-5-methyl-2-oxo-2.3-dihydro-benzo[e][1.4]diazepin-1 -vl) -N-methvl-Nphenvl- acetamide. (Isomer 2)

A solution of intermediate 16 (442mg) in EtOH (14ml) was hydrogenated over 10% palladium on carbon (90mg). After 7h the mixture was filtered through hyflo and the solvent evaporated in vacuo to give the title compound as a white foam (311 mg).

T.I.c. (1:20 MeOH-DCM) Rf 0.24

l.r. 1660; 1595; 1317; 1275; 1251; 1200; 1122; 964; 770; 724; 702; 558cm’¹.

Intermediate 18

2-{3-[3-(3-Methoxy-phenyl)-ureido]-5-methyl-2-oxo-2.3-dihydro-benzo[e] [1.4]diazepin-1 -yl)-N-methyl-N-phenyl-acetamide, (isomer 1)

A solution of intermediate 17 (208mg) in DCM (5ml) under nitrogen was treated with 3-methoxyphenyl isocyanate (92mg) and the mixture was stirred for 4h at 23°. The solvent was evaporated in vacuo and the residue was purified by chromatography. Elution with MeOH-DCM (1:20) gave the title compound as a white solid (221 mg), m.p. 238-9°.

T.I.c. (1:20 MeOH-DCM) Rf 0.30

l.r. 3311;1666; 1637; 1612; 1558; 1523; 1496; 1158; 1036; 766; 701; 557cm’¹.

Intermediate 19

1-(Methyl-phenyl-carbamoylmethyl)-5-(4-methyl-piperazin-1-ylmethyl)-2-oxo2.3- dihydro-1 H-benzo[e)[1,4)diazeDine-3-carbamic acid benzvl ester.

N-Methyl piperazine (0.51ml) was added to a stirred solution of intermediate 12 (0.5g) in dry DCM (10ml) at 23° under nitrogen. After 3 hours the mixture was poured into water (75ml) and extracted with EA (50ml x 3). The combined organic extracts were washed with saturated brine, dried and evaporated in vacuo. The crude product was purified by flash chromatography on silica (Merck 9385 - Et₃N deactivated) eluting with 2 to 4% MeOH in DCM to give the title compound as an orange foam (385mg), m.p. 65-70°.

T.I.c. SiO2-Et₃N deactivated (2% MeOH-DCM) Rf 0.39.

BAD ORIGINAL

Intermediate 2Q

2- (3-i3-(3-Methoxv-Dhenvl)-ureido1-5-methvl-2-oxo-2.3-dihvdro-benzofel [1,4]diazepin-1 -yl}-N-methyl-N-phenyl-acetamide.

A solution of intermediate 4 (500mg) in dry MeCN (10ml) was treated with 3methoxyphenylisocyanate (195μΙ) and the mixture was stirred at 23° under nitrogen for 5 hours. DE (10ml) was added and the resultant mixture was filtered, washing the filter-cake with hexane to give the title compound as a cream solid (599mg), m.p. 215.

T.I.c. (EA) Rf 0.38 l

intermediate 21

3- Amino-2.3-dihvdro-1-(3.3-dimethvl-2-oxo-butvl)-5-methvl-2-oxo -1H-1.4benzodiazpine (a) N-[5-Methyl-1 -(3.3-dimethyl-2-oxo-butvl)-2-oxo-1.3-dihvdrobenzoJeirK41dtazepin-3-yn-carbamic acid benzyl ester

Sodium hydride (80% in oil, 235mg) was added to a solution of Intermediate 2, (2g) in dry DMF (20ml) under nitrogen and cooled in an ice-bath. After 45min, a solution of 1-bromopinacolone (1.23g) in dry DMF (5ml) was added and stirred for 2h 20min as the ice-bath was allowed to melt. The reaction mixture was partioned between water (150ml) and EA (2x150ml) and the combined EA extracts were washed with water (100ml), saturated brine (100ml) and dried.

( The solution was evaporated and the residue chromatographed with hexane-EA (1:2) as eluent to give the title compound (2.47g) as a white foam, m.p. 68°.

b. 3-AminQ-2.3-dihvdro-1-(3.3-dimethyl-2-oxo-butvn-5-methvl-2-oxo -1 H-1.4benzodiazpine

A 3-necked flask was flushed thoroughly with nitrogen and charged successively with 5% palladium on carbon (50%) wet paste; 1.66g) water (45ml), a solution of Intermermediate 21a (2.42g) in methanol (180ml) and ammonium formate (1.09g). The mixture was stirred at 40° under nitrogen for 1.5h then cooled and filtered through hyflo. The filtrate was evaporated and the residue partioned between 2N sodium carbonate solution (100ml) and EA (2 x 150ml). The combined organic extracts were washed with saturated brine

r ¹⁰ (

(100ml), dried and evaporated to give the title compound (1.63g) as a fawn solid, m.p. 96-8°.

T.I.c. (9:1 DCM-MeOH) Rf 0.33.

Intermediate 22

N-[5-Methyl-1 -(2-oxo-2-pvrrolidin-1 -yl-ethyl)-2-oxo-1.3-dihvdro-benzo[elf 1.4] diazepin-3-vl]-carbamic acid benzyl ester

NaH (80% in oil; 102mg) was added to a solution of intermediate 2(1.00g) in dry DMF (10ml) at 0°. The mixture was stirred at 0° for 0.5h and a solution of 2-Npyrrolidinyl-2-oxo-ethylbromide (596mg) in DMF (1 ml) was added. The mixture was stirred at 23° for 4h. Phosphate buffer (pH 6.5;50ml) was added and the mixture extracted with ethyl acetate (50ml). The organic phase was washed with water (2x50ml) and dried (Na2SO4). Solvent evaporation in vacuo gave a residue which was chromatographed with EA then MeOH-EA (1:9) as eluent to give the title compound (959mg) as a white solid, m.p. 165-6°.

T.I.c. (EA) Rf0.16

l.r. (Solution in CHBr3) 3147; 2974; 2874; 1719; 1683; 1654; 1057; 1449; 1079; 765cm-¹

Intermediate .23

N-f5-(Bromo-methyl)-1 -(2-oxo-2-Dvrrolidin-1 -vl-ethyl)-2-oxo-1.3-dihvdrobenzo[e][1.4]diazepin-3-yl]-carbamic acid benzyl ester.

A solution of intermediate 22(4.00g) in DE (50ml) and CHCI3 (50ml) under nitrogen at 23° was treated with 5,5-dibromobarbituric acid (1.32g) and the mixture stirred at 23° for 18h. MeOH (20ml) and silica (Merck 9385;15g) were added and the solvent evaporated in vacuo. The residue was chromatographed with MeOH-DCM (0.2:10) as eluent to give the title compound as a white solid (3.88g).

T.I.c. (10:0.2 DCM-MeOH) Rf 0.36

l.r. 3389; 1733; 1686; 1662; 1650; 1596; 1330; 1217; 1200; 1084; 777cm*¹

Intermediate 24

N-f5-(MorDholin-4-yl-methyl)-1-(2-oxo-2-pyrrolidin-1-yl-ethyl)-2-oxo-1.3-dihvdrobenzo[e][1.4]diazepin-3-yl]-carbamic acid benzyl ester.

BAD ORIGINAL Si

A solution of intermediate 23 (3.78g) in DMF (20ml) under nitrogen at 23° was treated with morpholine (3.21 g) and the mixture was stirred for 1 h. Water was added and the mixture extracted with EA. The extract was washed with water and saturated brine then was dried (Na2SC>4). The solvent was evaporated in vacuo and the residue purified by chromatography. Elution with DCM-MeOH (100:3) gave the title compound as a pale orange foam (1.095g).

T.I.c. (100:3 DCM - MeOH) Rf 0.27

l.r. (KBr disc) 3426; 2979; 1723; 1688; 1661; 1510; 1453; 1394; 1323; 1116; 1090; 929cm'¹ lntermediate.25

3-Amino-5-(morpholin-4-yl-methyl)-1 -(2-oxo-2-pyrrolidin-1 -vl-ethvl)-1.3-dihydroΕ6ΡΖΡ[9][1,4Μ&Ζ£ΡΪ0ς2ςΡ0£,

A solution of intermediate 24 (3.584g) in EtOH (100ml) was hydrogenated over 15 10% palladium on carbon (500mg) at 23°. After 3.5h the mixture was filtered through hyflo and the filtrate evaporated in vacuo to give the title compound as a beige foam (2.536g).

T.I.c. (9:1 DCM-MeOH) Rf 0.22

l.r (KBr disc) 3396; 2981; 1657; 1448; 1322; 1256; 1116; 865cm'¹

Intermediate 26 Ethyl-(4-fluoro-phenyl)-amine, lodoethane (3.6ml) was added to a mixture of 4-fluoroaniline (4.26ml) and potassium carbonate (6.9g) in dry DMF (100ml). After 18.5h at 23°, the resulting suspension was poured into water (400ml) and extracted with EA (400ml). The organic extract was washed with water (200ml) then saturated brine (200ml), dried and evaporated. The residual oil was chromatographed with 2 to 3 to 4% EA in hexane as eluent to give the title compound (3.667g) as a yellow oil.

T.I.c. (4:1 Hexane-EA) Rf 0.62

Intermediate 27

2-Bromo-N-ethyl-N-(4-fluoro-Phenyl)-acetamide·

A solution of bromoacetyl bromide (2.24ml) in dry DCM (15ml) was added dropwise over 20 min to a solution of intermediate 26 (3.58g) and ΕΐβΝ (3.59ml)

BAD ORIGINAL in dry DCM (30ml) at 0° under nitrogen. After 2.5h at 0° the solution was partitioned between water (200ml) and DCM (200 + 100ml). The combined organic extracts were dried and evaporated and the residue chromatographed with 10 to 15 to 20% EA in hexane as eluent to give the title compound (2.641 g) as a pale orange oil.

T.I.c. (9:1 hexane-EA) Rf 0.15

Intermediate 28

N-(1-{[Ethyl-(4-fluQrQ-phenyl)-carbamQyl3-methyl}-5-methyl-2-Qxg-1.3-dihydrQbenzo[e][1.4]diazepin-3-yl)-carbamic acid, benzyl ester,

NaH (80% in oil; 348mg) was added to a solution of intermediate 2 (2.92g) in dry DMF (30ml) at 0° under nitrogen. After 1 h, the orange solution was treated with a solution of intermediate 27 (2.608g) in dry DMF (10ml). Stirring was continued at 0° for 2h whereupon the solution was poured into water (200ml) and extracted with EA (200 + 100ml). The combined extracts were washed with saturated brine (200ml), dried and evaporated. The residue was chromatographed with EA-DCM (4:1) as eluent to give the title compound (3.75g) as a pale yellow foam.

T.I.c. (4:1 EA-DCM) Rf0.26

l.r. (Solution in CHCI₃) 3425; 1724; 1671; 1515; 1510; 1248; 1094; 845cm'¹ lntgrmediate-29

N-{1-[Ethvl-(4-fluoro-Dhenvn-carbamovl-methvn-5-fmorpholin-4-vl-methvh-2oxo-1,3-dihydro-benzo(e1[1,4]diazepin-3-yl)-carbamic acid benzyl ester.

5,5-Dibromobarbituric acid (765mg) was added to a solution of intermedaite 28 (2.69g) in CHCI3 (30ml) and DE (30ml) at 23° under nitrogen. After 30h morpholine (2.3ml) was added and stirring continued for a further 16h whereupon the cloudy orange solution was poured into water (100ml). The layers were separated and the aqueous phase extracted with CHCI3 (100ml). The combined, dried organic extracts were evaporated and the residue chromatographed with EA-DCM (3:1) as eluent to give the title compound (2.22g) as a crunchy orange foam.

T.I.c. (4:1 EA-DCM) Rf 0.17

l.r. (Solution in CHCI3) 3621; 3425; 1726; 1672; 1510; 1233; 1202; 1116; 845cm'¹

BAD ORIGINAL ft tntermediaie.3Q

2- [3-Amino-5-(morDholin-4-yl-methyl)-2-oxo-2.3-dihydro-benzo[e1f1.4)diazeoin1- yl]-N-ethyl-N-(4-fluoro-phenyl)-acetamide,

A solution of intermediate 29(1.144g) in absolute EtOH (25ml) was hydrogenated at 23° and 1 atmosphere pressure in the presence of 10% palladium on charcoal as catalyst (160mg). After stirring for 6h and allowing to stand under hydrogen overnight the mixture was filtered through hyflo and the filtrate evaporated to give the title compound (879mg) as a crunchy green-brown foam, m.p. 95-9° dec.

T.I.c. (9:1 DCM-MeOH) Rf 0.18

InleimadiateJl

3- XL2J.:Q2adia£Ql^ylhfiheiiylamine,

A solution of 3-(1,2,4-oxidazol-3-yl)nitrobenzene (3.Og) in EA (50ml) was hydrogenated at 1atm. and 23° over Raney nickel (1 pipette-full). After 4.5h the catalyst was removed by filtration through hyflo. The filtrate was evaporated to give a pale cream solid (2.57g) identified as the hydroxylamine.

T.I.c. (1:1 EA - Hexane) Rf 0.27

A solution of the hydroxylamine (2.54g) in EA (40ml) was further hydrogenated at room temperature and pressure over Raney nickel (1 pipette-full). After 4.5h the catalyst was removed by filtration through hyflo and the filtrate evaporated to give a yellow solid.Crystallization from EA gave pure product.The mother liquors were chromatographed with hexane - DE (3:1) as eluent to give more product which was combined with the crystallized material to give the title compound (548mg) as a cream solid.

T.I.c. (2:1 DE-Hexane) Rf 0.35

Example 1.

2- ]3-(3-(3-Cyano-phenyll-ureidofc2-oxo-5-piperidin-1-ylmethyl-2· 3-dihvdrobenzoLel f 1,41 diazepin-l-vn--N-methvl-N-Dhenvl-acetamide·

A solution of intermediate 6 (300mg) in DCM (5ml) at 23° under nitrogen was treated with piperidine (0.27ml). After 2 hours the mixture was poured into

BAD ORIGINAL ft water (75ml) and extracted with EA (100mlx2). The combined organic extracts were washed with saturated brine, dried and evaporated in vacuo. The crude product was partially purified by flash chromatography on silica (Merck 9385Et3N deactivated) eluting with 2% MeOH in DCM. Complete purification was obtained by flash chromatography on silica (Merck 9385 - Et₃N deactivated) eluting with 1 to 2% MeOH in DCM to give the title compound as a cream solid (135mg), m.p. 145-150°

l.r. 3260; 2222; 1704; 1686; 1591; 1383; 1223; 1125cm’¹

2-ί3-Γ3-(3-Ον3ηο-ρΐΊθπνΙ)-ιΐΓ6ίάο1-2-οχο-5-ρνπΌ^ϊη-Ι-νΙηηθίΙινΙ-2 .3-dihvdrobenzofel M Aldiazepin-l-vD-N-methvl-N-DhenvI-acetamide.

A solution of intermediate 6 (300mg) in DCM (5ml) at 23° under nitrogen was treated with pyrrolidine (0.22ml). After 2 hours the mixture was evaporated in vacuo to give a brown oil which was purified by flash chromatography on silica (Merck 9385 - Et₃N deactivated) eluting with 2% MeOH in DCM. Product fractions, after evaporation in vacuo, were triturated with EA - hexane. The solid was dissolved in EA-THF (4:1; 100ml) and the solution was washed with water and saturated brine then was dried and evaporated in vacuo to give the title compound as a pale peach solid (154mg), m.p. 140 - 145° dec.

T.I.c. Et₃N deactivated SiO₂ (2%MeOH-DCM) Rf 0.22

l.r. 3342; 2226; 1685; 1593; 1559; 1496; 1381cm’¹

Example 3

2-(3-f3-(3-Cvano-phenvn-ureidQl-5-(isQDroDvlamino-methvl)-2-oxo -2.3-dihvdrobenzo[e] [1.4]diazepin-1-yl)-N-methvl-N-phenyl-acetamide,

A splution pf intermediate 6 (300mg) in DCM (5ml) at 23° under nitrogen was treated with isopropylamine (0.23ml). After 2 hours the mixture was evaporated in vacuo to give an oil which was purified by flash chromatography on silica (Merck 9385 - Et₃N deactivated) eluting with 2% MeOH - DCM. Trituration with EA - hexane gave a cream solid which was dissolved in EA - THF (4:1; 100ml) and washed with water (100ml) and saturated brine, dried and evaporated in vacuo to give the title compound as a cream solid (132mg), m.p. 160° dec.

T.I.c. Et₃N deactivated SiO₂(2% MeOH-DCM) Rf 0.16

l.r. 3316;2231; 1674; 1591; 1561; 1455; 1432; 1384; 1240; 1198cm’¹

BAD ORIGINAL £

Exampte-4

243--l3r(3-CyaDO^phenvl)-ureido]-2-oxo-5-[1.4]thiazinan-4-ylmethv l-2.3-dihydrobenzo[e][1.4] diazepin-1-yl)-N-methyl-N-phenyl-acetamide,

A solution of intermediate 6 (1 g) in dry DCM (20ml) was treated with thiomorpholine (0.90ml) at 23° under nitrogen. After 2 hours the mixture was poured into water (75ml) and extracted with EA (3x75ml). The combined organic extracts were washed with saturated brine, dried and evaporated in vacuo. The crude product was purified by flash chromatography eluting with EA to give, after trituration with EA-hexane, the title compound as a white solid ( (458mg), m.p. 165°.

T.I.c. ΕίβΝ deactivated S1O2 (EA) Rf 0.52

l.r. 3267; 2229; 1687; 1557; 1450; 1382; 1221cm-¹

Example 5 t-(3-C van o-Dhenvh-3-l 1-12-(cis-2.5-di met hvl-pvrrolidin-Ι-νΠ-2-oxo-eth vl]-5moroholin- 4-.ylmethvl-2-oxo-2.3-dihvdro-1 H-benzofe1(1.41diazeDin-3-vl}urea.

NaH (80% in oil; 23mg) was added to a suspension of intermediate 9 (253mg) in dry DMF (3ml) at 0° under nitrogen. After 30min the resulting solution was treated with a solution of 2-(cis-2,5-dimethylpyrrolidin-1-yl)-2-oxo-ethyl bromide (145mg) in dry DMF (0.5ml) and stirring was continued at 0° for 2.25h and at 23° for 20h. The dark solution was poured into water (20ml) and extracted with ( EA (2x30ml) then the combined extracts were washed with water (20ml) then saturated brine (40ml), dried and evaporated. Trituration of the residue with EA25 DE gave the title compound (196mg) as a white solid, m.p. 234-5° dec.

T.I.c. (95:5 DCM-MeOH) Rf 0.26

l.r. 3263; 2224; 1685; 1650; 1590; 1557; 1449; 1378; 1115; 1001 cm*¹

Example 6

2-{3-(3-(3-Cyano-phenyl)-ureido]-5-morpholin-4-ylmethvl-2-oxo-2.3-dihvdrobenzofel f1.4ldiazepin-1 -yl)-N-(4-fluoro-phenvn-N-methvl-acetamide.

NaH (80% in oil; 23mg) was added to a suspension of intermediate 9 (250mg) in dry DMF (3ml) at 0°under nitrogen. After 40 min a solution of 2-bromo-N-(4fluorophenyl)-N-methyl-acetamide (162mg) in dry DMF (0.5ml) was added to the

resulting solution and stirring was continued at 23° for 22h. The yellow solution was then poured into water (20ml) and extracted with EA (2x30ml) and the combined extracts were washed with water (20ml) then saturated brine (40ml) dried and evaporated. A solution of the residue in MeOH was preadsorbed onto silica and chromatographed with 0 to 1 to 2 to 3 to 4% MeOH in DCM as eluent to give the title compound (260mg) as an orange solid, m.p. 182-4° dec.

T.I.c. (95:5 DCM-MeOH) Rf 0.19

l.r. 3341; 2229; 1674; 1510; 1223; 1116cm*¹

Example 7

2-f3-f3-f3-Cvano-Dhenyl)-ureido1-5-morPholin-4-ylmethyl-2-oxo-2. 3-dihvdrobenzo(e) [1.4]diazepin-1-vl)-N-ethyl-N-phenyl-acetamide.

NaH (80% in oil; 23mg) was added to a suspension of intermediate 9 (250mg) in dry DMF (3ml) at 0° under nitrogen. After 40 min a solution of 2-bromo-N15 ethyl-N-phenyl acetamide (160mg) in dry DMF (0.5ml) was added to the resulting solution and stirring was continued at 23° for 22h. The orange solution was then poured into water (20ml) and extracted with EA (2x30ml) and the combined extracts were washed with water (20ml) then saturated brine (30ml) dried and evaporated. Trituration of the residue with EA-DE gave the title compound (239mg) as a white solid, m.p. 211 - 2° dec.

T.I.c. (95:5 DCM-MeOH) Rf 0.26

l.r. 3294; 2225; 1684; 1666; 1456; 1203; 777cm*¹

Example 8

1 -(3-Cyano-phenyl)-3-[1 -(3.3-dimethyi-2-oxo-butyn-5-moroholin-4 -ylmethvl-2oxo-2.3-dihydro-1 H-benzo[e)[1.4]diazepin-3-vl]-urea,

Morpholine (62μI) was added to a suspension of intermediate 11 (72mg) in dry DCM (2ml) at 23° under nitrogen. After 1 h the mixture was poured into water (20ml) and extracted with EA (20+15ml). The combined extracts were washed with saturated brine (20ml) dried and evaporated. The residue was triturated with EA-DE, filtered off and dried in vacuo to give the title compound (53mg) as a white solid, m.p. 168-9°dec.

T.I.c. (95:5 DCM-MeOH) Rf 0.26

l.r. 3279; 2229; 1688; 1455 cm-¹

BAD ORIGINAL ft

Example 2

2- f3-f3-(3-Methoxv-Phenvl)-ureidol-5-morpholin-4-ylmethyl-2-oxo-2.3-dihydrobenzo [e] [1.4)diazepin-1-vl}-N-methyl-N-Dhenyl-acetamide.

3- Methoxyphenyl isocyanate (53mg) was added to a solution of intermediate 14 (150mg) in DCM (5ml) under nitrogen. The solution was stirred at 23° for 3h. The solvent was evaporated in vacuo and the residue purified by chromatography. Elution with MeOH-DCM (1:20) gave the title compound as a pale straw coloured solid (176mg), m.p. 164-6° dec.

T.I.c. (1:20 MeOH-DCM) Rf 0.25

l.r. (Solution in CHCI3) 3431; 1670; 1599; 1495; 1454; 1425; 1392; 1289; 1158; 1116cm-¹.

Example 1Ώ

N-Methvl-2J5-morDholiD-4--Vlmethvl-2-oxo-3-(3-phenvl-ureido)-2.3 -dihvdrobenzole] [1,4]diazepin-1-yl]-N-phenyl-acetamide.

Phenyl isocyanate (42mg) was added to a solution of intermediate 14 (150mg) in MeCN (5ml) under nitrogen and the mixture was stirred at 23 for 2h. DE was added and the mixture was filtered to give the title compound as a white solid (160mg), m.p. 157-8° dec.

T.I.c. (1:20 MeOH-DCM) Rf 0.33

l.r. (Solution in CHCI₃) 3430; 1670; 1599; 1498; 1452; 1392; 1311; 1292; 1116; 1002cm’¹.

Example 11 hL·Methyl-245-mQTDholiOr4.-ylmethyl-2-oxo-3-[3-f3-trifluoromethyl -phenvl)ureido]-2.3- dihydrQd3enzofe][1.4]diazepin-1 -yl)-N-phenyl-acetamide.

3-Trifluoromethylphenyl isocyanate (103μΙ) was added dropwise to a stirred solution of intermediate 14 (300mg) in dry DCM (3ml). The mixture was stirred at room temperature under nitrogen for 18 hrs. Purification by column chromatography eluting with DCM-MeOH-. 880 ammonia (94.5:5:0.5), gave the title compound (87mg) as a white solid, m.p. 190° dec.

T.I.c. (94.5:5:0.5 DCM-MeOH-880 ammonia) Rf 0.22

l.r. 2924; 2854; 1688; 1671; 1450; 1339; 1116 cm¹

Example 12

BAD (3-{3-(1-(Methyl-phenvl-carbamoylmethyl)-5-morpholin-4-ylmethyl-2-oxo-2.3dihvdro-1 H-benzo[eH1.41diazeDin-3-vl]-ureido)-phenvl)-carbamic acid tert-butvl ester.

Carbonyl diimidazole (97mg) was added to a solution of intermediate 14 5 (230mg) in THF (10ml) under nitrogen and the mixture was stirred at 23 for 1 h.

(3-Amino-phenyl)-carbamic acid t-butyl ester (114mg) was added and the mixture was heated under reflux for 18h. The mixture was cooled to 23 and was partitioned between water and EA. The organic phase was dried (Na2SC>4) and the solvent evaporated in vacuo to give a residue which was purified by chromatography. Elution with MeOH-DCM (1:20) gave the title compound as a straw coloured solid (78mg).

T.I.c. (1:20 MeOH-DCM) Rf 0.32 Mass spectrum MH+ (observed) 656

Example 13

2- {3-[3-(3-Amino-phenyl)-ureido]-5-morpholin-4-ylmethyl-2-oxo-2, 3-dihvdrobenzo[e] [1.4]diazepin-1-yl)-N-methyl-N-phenyl-acetamide.

A solution of Example 12 (70mg) in DCM (5ml) was treated with trifluoroacetic acid (0.3ml) and stirred for 1 h. EA was added, the mixture washed with 2N sodium carbonate solution, dried (NagSO^ and evaporated in vacuo. The residue was triturated with DE to give the title compound as a beige solid (31 mg), m.p. 158-60°.

T.I.c. (1:20 MeOH-DCM) Rf 0.22

l.r. 3353; 1667; 1613; 1596; 1556; 1496; 1321; 1204; 1115; 773cm-¹.

Exampi.e_L4 (+)-2-{3-[3-(3-Methoxy-Dhenyl)-ureidol-5-morpholin-4-ylmethyl-2-oxo-2.3dihydrp-benzo [e][1,4]diazepin-1-yl}-N-mgthyl-N-phenyl-acetamide,

3- Methoxyphenyl isocyanate (106mg) was added to a stirred solution of intermediate 14 (300mg) in DCM (10ml) under nitrogen and the mixture was stirred at 23° for 2h. The solvent was evaporated in vacuo and the residue purified by chromatography. Elution with MeOH-DCM (1:20) gave a straw coloured solid (205mg) a portion (75mg) of which was further purified by chiral h.p.I.c. to give the title compound as a white solid (26mg), m.p. 169-70 dec.

T.I.c. (1:20 MeOH-DCM) Rf 0.25

BAD ORIGINAL.

l.r. (Solution in CHCI₃) 3431; 1670; 1600; 1496; 1454; 1427; 1289; 1158; 1116; 1002cm*¹.

H.p.I.c. Column: CHIRALCEL-OD 25cm x 4.6mmid Eluent; EtOH-Hexane (1:1)

Flow: 1 ml/min.

Wavelength: 230nm Temperature: 23°

Rt: 4.96 min

Example 15 f-h)2-.(3Tf3--(3-A1ethQxy-Dhenyl)-ureido]-5-morpholin-4-ylmethyl-2-oxo-2.3dihydro- benzo (e)[1.4ldiazepin-1-yl}-N-methyl-N-phenyl-acetamide.

A solution of intermediate 18 (189mg) in chloroform (8ml) and DE (3ml) under nitrogen was treated with 5,5-dibromobarbituric acid (56mg) and the mixture stirred at 23° in the dark for 18h. Morpholine (68mg) was added and the mixture was stirred for 2h at 23°. The mixture was partitioned between EA and phosphate buffer (pH6.5). The organic phase was dried (NagSO^ and the solvent evaporated in vacuo to give a residue which was purified by chromatography. Elution with EA then MeOH-DCM (1:20) gave the title compound as a white solid (147mg), m.p. 164-6° dec.

T.I.c. (1:20 MeOH-DCM) Rf 0.35

l.r. 3339; 1668; 1598; 1549; 1290; 1203; 1156;1115,771 ;703cm*¹

Example 16

243-i3-f3-.CvanQ-Dhenyl)-ureido]-5-(4-methyl-piperazin-1-ylmethyB-2-oxo-2.3dihydro- benzQ[e][1.4]diazepin-1-vl}-N-methyl-N-Dhenvl-acetamide.

A solution of intermediate 19 (352mg) in EtOH (20ml) was hydrogenated at 23°and 1 atm pressure using 10% palladium on carbon (80mg) as a catalyst. After 7 hours the mixture was filtered through hyflo and evaporated to give crude amine (319mg) as an orange-red oil. This was redissolved in dry MeCN (3ml) and treated with 3-cyanophenyl isocyanate (85mg) at 23° under nitrogen. After 2 hours the mixture was evaporated in vacuo to give a red oil which was purified by flash chromatography on silica (Merck 9385-Et3N deactivated) eluting with 2 to 5 to 10% MeOH in DCM. Trituration with DE-hexane gave the title compound as a cream solid (171 mg), m.p. 152-155°.

BAD ORIGINAL

T.I.c. SiO₂-Et3N deactivated (5% MeOH-DCM) Rt 0.20.

I.r. 3338; 2228; 1671; 1594; 1557; 1496; 1455cm*¹.

Example 17

2-(3-f3-(3-MethPxv-phenvn-ureido]-5-(2-dimethylamino-ethyl)-2-oxo-2.3dihvdro- benzofe) [1.4]diazepin-1-yl}-N-methyl-N-phenyl-acetamide,

A mixture of intermediate 20 (100mg) and Eschenmoser's salt (46mg) in dimethoxyethane (5ml) was heated to reflux for 4 hours then was poured into EA (50ml) and extracted with 2N HCI (25ml x 2). The combined aqueous extracts were basified to pH8 with 2N Na₂CO3 solution then extracted with EA (30ml x 2). The combined organic extracts were dried and evaporated in vacuo. The crude product was purified by flash chromatography on silica (Merck 9385 Et3N deactivated) eluting with 2 to 3 to 4 to 5% MeOH in DCM to give the title compound as a cream solid (31 mg), m.p. 134°.

T.I.c. SiO₂-Et₃N deactivated (5% MeOH-DCM) Rf 0.13.

I.r. (Solution in CHCI₃) 2954; 1670; 1600; 1495; 1455; 1158; cm*¹.

Example 18

2-{3-[3-(3-Cyano-phenyl)-ureido]-5-morpholin-4-ylmethyl-2-oxo-2. 3-dihvdro20 benzole] [1.4]diazepin-1-vl}-N-methyl-N-phenyl-acetamide

A solution of intermediate 14 (113mg) in DCM (5ml) was treated with 3cyanophenyl isocyanate (39mg) and the mxiture stirred at 23° under nitrogen for 18h. The solvent was removed in vacuo and the residue chromatographed with EA-EtOH (10:0.5) s eluent to give the title compound (64mg) as a white solid, m.p. 165-7°.

T.I.c. (10:0.5 EA-EtOH) Rf 0.24

I.r. 3264; 2225; 1677; 1460; 1378cm*¹.

Example 1.2

1 -|5-(Morpholiri-4-yl-methyl)-2-oxo-1 -(2-oxo-2-pyrrolidin-1 -yl-ethvl)-2.3-dihvdro1 H-benzo[e]|1.41diazepin-3-yl]-3-(3-oxazol-5-yl-phenyl)-urea.

A solution of 3-(oxazol-5-yl)phenylamine (250mg) in THF (6ml) under nitrogen at 0° was treated with Et3N (79mg) followed by triphosgene (77mg). More Et3N (79mg) was added and the mixture was stirrred at 0° for 0.5h. A solution of intermediate 25 (125mg)in THF (5ml), was added and the mixture was stirred at

BAD ORIGINAL ft

23° for 2h. Phosphate buffer (pH6.5;30ml) was added and the mixture extracted with EA (30ml). The organic phase was dried (Na2SO4) and the solvent evaporated in vacuo. The residue was chromatographed. Elution with MeOHEA (0.5:10) then MeOH-DCM (0.5:10) gave the title compoundas a pale straw solid (199mg), m.p. 208-9°.

T.I.c. (9.Ί DCM-MeOH) Rf 0.42

l.r. 3284; 1683; 1663; 1551; 1499; 1324; 1205; 1116; 1003; 774cm-¹ fxample_2Q

1 -(5-(Morpholin^ykmethvl)-2-oxo-1 -(2-oxo-2-pyrrolidin-1 -yl-ethyl)-2.3-dihydro1 H-benzofelM .41diazepin-3-yn-3-f3-(1.2.4-oxadiazoi-3-yn-phenyn]-urea.

A solution of intermediate 31 (100mg) in THF (6ml) at 0° under nitrogen was treated with Et3N (63mg). Triphosgene (62mg) was then added followed by more ΕίβΝ (62mg). The mixture was stirred at 0° for 0.5h. A solution of

Intermediate 25 (200mg) in THF (5ml) was added and the mixture stirred at 23° for 2h. Phosphate buffer (pH 6.5;30ml) was added and the mixture extracted with DCM (30ml). The organic phase was dried (Na2SC>4) and the solvent evaporated in vacuo to give a residue which was chromatographed with MeOHDCM (0.5:10 to 1:10) as eluent to give the title compound (97mg) as a pale straw coloured solid, m.p. 197-9°dec.

T.I.c. (10:0.5 DCM-MeOH) Rf 0.27

l.r. (Solution in DMSO) 1684; 1656; 1615; 1599; 1568; 1540; 1510; 1347; 1204cm'¹

Example 2t

N-Elhyl-N-(4-fluoro-phenYD-2J3-[3-(4-fluoro-phenyl)-ureido1-5-(morDholin-4-ylmethvh^-oxo^.S-dihydrQ-benzoteHMdiazeDin-l-vn-acetamide.

4-Fluorophenyl isocyanate (49mg) in dry MeCN (0.5ml) was added to a solution of intermediate 30(150mg) in dry MeCN (1ml) at 23° under nitrogen. After 1h

DE (3ml) was added and the solid filtered off and dried in vacuo to give the title compound (100mg) as a white solid, m.p. 197° dec.

T.I.c. (9:1 DCM-MeOH) Rf 0.51

l.r. 3340; 2926; 1672; 1509; 1461; 1378cm'¹

Example 22 (+)-2-(3-f3-(3T.MethQXV-Dhenvn-ureidol-5-morDholin-4-ylmethyl-2-oxo-2.3dihvdro-benzo (e)(1,4)diazepin-1 -yl)-N-methyl-N-phenvl-acetamide hydrochloride salt

A solution of the (+)-2-{3-[3-(3-Methoxy-phenyl)-ureido]-5-morpholin-4-ylmethyl2-oxo-2,3-dihydro-benzo [e][1,4]diazepin-1 -yl}-N-methyl-N-phenyl-acetamide (200mg) in dry DCM (20ml) under nitrogen was treated with 1M hydrogen chloride in diethyl ether (0.77ml) and the solution was stirred for 5 min. The solvent was removed in vacuo and the residue azeotroped with toluene (2 x

10ml) to give the title compound (215mg) as a pale straw coloured solid, m.p.

160-170° dec.

Pharmacy Examples 15 Tablets

a.	Active ingredient Lactose anhydrous USP Microcrystalline Cellulose NF Pregelatinised starch Ph.Eur. Magnesium stearate USP Compression weight	50mg 163mg 69mg 15mg 3 mg 300mg
The	active ingredient, microcrystalline cellulose, lactose	and pregelatinised
starch are sieved through a 500 micron sieve and blended in a suitable mixer.
The magnesium stearate is sieved through a 250 micron sieve and blended with
the active blend. The blend is compressed into tablets using suitable punches.
b.	Active ingredient	50mg
	Lactose monohydrate USP	120mg
	Pregelatinised starch Ph.Eur.	20mg
	Crospovidone NF	8mg
	Magnesium stearate USP	..,2mg
	Compression weight	200mg

BAD ORIGINAL £

The active ingredient, lactose and pregelatinised starch are blended together and granulated with water. The wet mass is dried and milled. The magnesium stearate and Crospovidone are screened through a 250 micron sieve and blended with the granule. The resultant blend is compressed using suitable tablet punches.

Capsules

	a.	Active ingredient	50 mg
10		Pregelatinised Starch Ph.Eur.	148mg
		Magnesium stearate USP	2mg
		Fill weight	200mg

The active ingredient and pregelatinised starch are screened through a 500 15 micron mesh sieve, blended together and lubricated with magnesium stearate (meshed through a 250 micron sieve). The blend is filled into hard gelatin capsules of a suitable size.

Active ingredient	50mg
Lactose monohydrate USP	223mg
Povidone USP	12mg
Crospovidone NF	12mg
Magnesium stearate	2ma
Fill weight	300mg

The active ingredient and lactose are blended together and granulated with a solution of Povidone. The wet mass is dried and milled. The magnesium stearate and Crospovidone are screened through a 250 micron sieve and blended with the granule. The resultant blend is filled into hard gelatin capsules of a suitable size.

A preferred active ingredient for use in the pharmacy examples is the compound of Example 14.

BAD ORIGINAL $ t

CCK-B- Receptor Binding

The binding affinity of the compounds of the invention for the CCK-B receptor (guinea pig cortex assay) was determined using the procedure of G Dal Forno et al J. Pharmacol. Exp & Ther. 261 - 1056-1063. The pKi values determined with respresentative compounds of invention were as follows:

Compound Ex No pKi_

9

2	8.4
3	8.6
4	8.8
5	8.5
6	8.7
7	8.8
8	8.8
9	8.9
10	9.1
11	9.3
13	8.2
14	9
16	8.3
17	8.6
18	8.9
19	8.5

The compounds of the invention are essentially non-toxic and therapeutically useful doses. Thus for example no untoward effects were observed when the compound of Example 14 was given to rats and dogs at doses at which the

Claims

1. Compounds of the general formula (I)

5 nr₃r<

and physiologically acceptable salts thereof; wherein R-j represents CH^CONRgRg or CH2COR7;

R2 represents a phenyl group optionally substituted by 1 or 2 substituents selected from halogen, alkyl, nitro, cyano, trifluoromethyl, trifluoromethoxy,

10 alkylthio, alkylsulphinyi, alkylsulphonyl, amino, substituted amino, hydroxy, alkoxy, methylenedioxy, alkoxycarbonyl, oxazolyl or oxadiazolyl;

A represents a C-|-4 straight or branched alkylene chain;

R3 and R4 independently represent hydrogen or Chalky I or R3 and R4 together with the nitrogen atom to which they are attached form a saturated 5-7

15 membered heterocyclic ring, which ring may contain an additional heteroatom selected from oxygen, sulphur or nitrogen;

R5 represents hydrogen or C-i^alkyl;

Rg represents C-|-4alkyl or phenyl, optionally substituted by halogen, or R5 and Rg together with the nitrogen atom to which they are attached

20 represent a saturated 5 to 7 membered heterocyclic ring which may be optionally substituted by 1 or 2 methyl groups or fused to a benzene ring.

R7 represents a group selected from C^alkyl, or optionally substituted phenyl; R8 represents hydrogen or a halogen atom;

n is zero, 1 or 2.

2. Compounds as claimed in Claim 1 wherein R, is CH₂CONR₅R₆ and R₅represents methyl or ethyl and R₆ represents phenyl optionally substituted by halogen or NR₅R₆ represents a saturated heterocyclic ring selected from bad original pyrrolidino, 2,5-dimethylpyrrolidino, 3,3-dimethylpyrrolidino, piperidino, 3,3dimethylpiperidino or 1-tetrahydroquinolino.

3. Compounds as claimed in Claims 1 and 2 wherein R2 is phenyl or phenyl substituted by one or 2 groups selected from halogen, alkyl, alkoxy, amino, cyano, hydroxy, trifluoromethyl, oxazolyl or 1,2,4-oxadiazol-3-yl.

4. Compounds claimed in any of Claims 1 to 3 wherein R₂ is phenyl substituted by fluorine, oxazol-5-yl or methoxy.

5. Compounds as claimed in any of Claims 1 to 4 wherein A is a methylene chain.

6. Compounds as claimed in any of Claims 1 to 5 wherein NR₃R₄represents a pyrrolidino, piperidino, hexamethyleneimino, morpholino, thiomorpholino or N-methylpiperazino group.

7. Compounds as claimed in any of Claims 1 to 6 wherein NR₃R₄ is morpholino.

8. Compounds as claimed in any of Claims 1 to 7 wherein R₈ is hydrogen.

9. 2-{3-[3-(3-Methoxy-phenyl)-ureido]-5-morpholin-4-ylmethyl-2-oxo-2,3dihydro-benzo [e] [1,4]diazepin-1-yl)-N-methyl-N-phenyl-acetamide, the (+) enantiomer thereof and physiologically acceptable salts thereof.

10. A compound selected from:

N-Methyl-2-[5-morpholin-4-ylmethyl-2-oxo-3-(3-phenyl-ureido)-2,3 -dihydrobenzo[e] [1,4]diazepin-1-yl]-N-phenyl-acetamide; N-Methyl-2-{5-morpholin-4-ylmethyl-2-oxo-3-[3-(3-trifluoromethyl -phenyl)ureido]-2,3- dihydro-benzo[e][1,4]diazepin-1 -yl}-N-phenyl-acetamide; 2-{3-[3-(3-Cyano-phenyl)-ureido]-5-morpholin-4-ylmethyl-2-oxo-2, 3-dihydrobenzo(e) [1,4]diazepin-1-yl}-N-methyl-N-phenyl-acetamide;

1 -[5-(Morpholin-4-yl-methyl)-2-oxo-1 -(2-oxo-2-pyrrolidin-1 -yl-ethyl)-2,3-dihydro1 H-benzo[e][1,4]diazepin-3-yl]-3-(3-oxazol-5-yl-phenyl)-urea;

BAD ORIGINAL

N-Ethyl-N-(4-fluoro-phenyl)-2-(3-[3-(4-fluoro-phenyl)-ureido]-5-(morpholin-4-ylmethyl)-2-oxo-2,3-dihydro-benzo[e][1,4]diazepin-1-yl}-acetamide; enantiomers thereof; and physiologically acceptable salts thereof.

5 11. A process for the preparation of compounds as defined in Claim 1 which comprises (a) reacting a compounds of formula (II) wherein R_v A. R₃, R₄ and R₈ have the meanings defined for formula (I) and R_g represents a leaving group.

with an amine R₂NH₂ wherein R₂ has the meanings defined in formula (I);

(b) reacting a compound of formula (III) wherein R_v R₃, R₄, R₈ and A have 15 the meanings defined in formula (I) with the isocyanate R₂NCO or carbamoyl chloride R₂HNCOCI (wherein R₂ has 20 the meanings defined in formula (I);

(c) reacting a compound of formula (XII) wherein R_n R₂ and R_e have the with the amine R₃R₄NH wherein R₃ and R₄ have the meanings defined in formula (I);

and thereafter if necessary or desired subjecting the resultant compound either before or after separation into its stereochemical isomers to one or more of the following operations.

(1) conversion of one compound of formula (I) into another compound of formula (I).

(2) conversion of a compound of formula (I) into an acid addition salt thereof.

12. Pharmaceutical compositions comprising a compound as defined in any of Claims 1 to 10 in admixture with one or more physiologically acceptable carriers or excipients.

13. Compounds as defined in any of claims 1 to 10 for use in therapy.

14. The use of a compound as defined in any one of Claims 1 to 10 in the manufacture of a medicament for the treatment of conditions where a modification of the effects of gastrin and or CCK is of therapeutic benefit.

15. A method of treatment of a mammal including man for conditions where modification of the effects of gastrin and or CCK is a therapeutic benefit comprising administration of an effective amount of a compound as defined in any of claims 1 to 10.