CA2072785C - Pharmacologically active hydrazine derivatives and processes for the preparation thereof - Google Patents

Pharmacologically active hydrazine derivatives and processes for the preparation thereof Download PDF

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CA2072785C
CA2072785C CA002072785A CA2072785A CA2072785C CA 2072785 C CA2072785 C CA 2072785C CA 002072785 A CA002072785 A CA 002072785A CA 2072785 A CA2072785 A CA 2072785A CA 2072785 C CA2072785 C CA 2072785C
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lower alkyl
substituted
alkyl
phenyl
hydroxy
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CA2072785A1 (en
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Alexander Faessler
Guido Bold
Marc Lang
Peter Schneider
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Novartis AG
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Novartis AG
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
    • C07C243/10—Hydrazines
    • C07C243/12—Hydrazines having nitrogen atoms of hydrazine groups bound to acyclic carbon atoms
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    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36—Radicals substituted by singly-bound nitrogen atoms
    • C07D213/40—Acylated substituent nitrogen atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
    • A61K31/175—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine having the group, >N—C(O)—N=N— or, e.g. carbonohydrazides, carbazones, semicarbazides, semicarbazones; Thioanalogues thereof
    • A—HUMAN NECESSITIES
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    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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    • C07C243/16—Hydrazines having nitrogen atoms of hydrazine groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
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    • C07C255/60—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton at least one of the singly-bound nitrogen atoms being acylated
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    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/12—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
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    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
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    • C07C281/02—Compounds containing any of the groups, e.g. carbazates
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    • C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
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    • C07C311/05—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms to acyclic carbon atoms of hydrocarbon radicals substituted by nitrogen atoms, not being part of nitro or nitroso groups
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
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    • C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
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    • C—CHEMISTRY; METALLURGY
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    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
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    • C07K5/06—Dipeptides
    • C07K5/06008—Dipeptides with the first amino acid being neutral
    • C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
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    • C07C2601/14—The ring being saturated

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Abstract

The invention relates to compounds of formula (see formula I) wherein R1 and R9 are each independently of the other hydrogen; aryl;
unsubstituted or substituted alkyl, alkenyl or alkynyl; heterocyclyl; sulfo; sulfonyl substituted by unsubstituted or substituted alkyl, aryl, heterocyclyl, alkoxy, which is unsubstituted or substituted, or by aryloxy; sulfamoyl that is unsubstituted or substituted at the nitrogen atom; or phosphoryl substituted by one or two radicals, which may be identical or different, selected from unsubstituted or substituted alkyl, from unsubstituted or substituted cycloalkyl, from aryl, from hydroxy, from unsubstituted or substituted alkoxy, from cycloalkoxy and from aryloxy; with the proviso that not more than one of the radicals R1 and R9 is hydrogen; and R2 and R8 are each independently of the other hydrogen or one of the radicals mentioned above for R1 and R9; or the pairs of substituents R1 and R2, and R8 and R9, each independently of the other, may form together with the nitrogen atom to which they are bonded certain heterocyclic rings;
R3 and R4 are each independently of the other hydrogen; unsubstituted or substituted alkyl or cycloalkyl; aryl; heterocyclyl; or unsubstituted or substituted alkenyl; or R3 and R4 together form unsubstituted or substituted alkylene, alkylidene or benzo-fused alkylene;
R5 is hydroxy; R6 is hydrogen;
or R5 and R6 together are oxo;

and R7 is unsubstituted or substituted alkyl or cycloalkyl; aryl;
heterocyclyl; or unsubstituted or substituted alkenyl;
and salts of the mentioned compounds where salt-forming groups are present, and to processes for the preparation thereof, to pharmaceutical compositions, to the use thereof as medicaments or for the preparation of pharmaceutical compositions, and to novel intermediates for the preparation of those compounds.

Description

2~~w"~~~

Pharmacolo~icallv active hydrazine derivatives and processes for the preparation thereof The invention relates to a novel class of non-hydrolysable analogues of peptides that are cleavable by aspartate proteases, namely hydrazine derivatives, to processes for the preparation thereof, to pharmaceutical compositions that comprise those peptide analogues, and to the use thereof as medicaments or for the preparation of pharmaceutical compositions for contaalling virus-dependent diseases, and to novel intermediates for the preparation of those compounds.
The immune deficiency syndrome AIDS ("Acquired Immunodeficiency Syndrome") is a fatal disease. The disease is becoming increasingly widespread throughout the world primarily within certain risk groups, but it is also spreading beyond those risk groups. The disease already affects millions of people and the conx~ol of its causes is one of the most important aims of modern medicine. Hitherto the retrovimses HI:V-1 and HIV-2 (HIV
representing "Human Immunodeficiency Virus") have been identified as a cause of the disease and they have been characterised by moleculaz~ biology. From the point of view of treatment, in addition to previous ways of mitigating the symptoms of AIDS and certain preventive measures, there is particular interest in the search for compositions that inter-fere with the reproduction of the virus itself but do not damage the intact cells and tissues of the patient.
Compounds that appear especially promising are those which suppress the ,processing of the protein building blocks of the virus that are biosynthesised in human cells, and thus suppress the correct assembly of those building blocks to form complete, infectious virions.
HIV-1 and HIV-2 each have in their genome a region that codes for a "gag-protease". That "gag-protease" is responsible fox the correct proteolytic cleavage of the precursor proteins that are produced from the genome regions coding for the "Group Specific Antigens"
(gag). During the cleavage, the structural proteins of the virus core are liberated. The "gag-protease" itself is a component of a precursor protein encoded by the pal-genome region of HIV-1 and HIV-2, which protein also contains the regions for the "reverse transcriptase" and the "integrase" and is thought to be cleaved by autoproteolysis.
The "gag-protease" cleaves the major core protein p24 of HIV-1 and HIV-2 preferentially h1-terminally of proline residues, for example in the divalent residues Phe-Pro, Leu-Pro or Tyr-Pro. It is a protease having a catalytically active aspartate residue in the active centre>
a so-called aspartate protease.
If the action of the "gag-protease" could be suppressed, the proteins necessary for the assembly of the virus core would no longer be available to the virus. This would result in the limitation or even the suppression of the reproduction of the virus. There is therefore a need for inhibitory substances for the "gag-protease" for use as antiviral compositions against AmS and other retroviral diseases.
A number of "gag-protease" inhibitors containing central groups that axe not proteo-lytically cleavable peptide isosters have already been synthesised. Despite intensive research, however, it has not been possible hitherto for aspartate protease inhibitors suitable for use in humans to be used for the control of A>DS in a majority of infected patients, pharmacodynamic problems being the main determining factor in this regard. In addition, most of the "gag-protease" inhibitors known hitherto have more than two asymmetric carbon atoms in the said central building block, and this necessitates relatively expensive stereospecific syntheses or isomer separation methods. The object of this patent application is, therefore, to provide a novel class of inhibitory substances fox viral aspartate proteases having a novel central building block. Furthermore, it should be possible to synthesise that central building block in a sterically simple manner. In addition, the novel central building blacks have amino groups at both ends, so that if suitable substituents are selected, then, far example, structures analogous to retro-inverso-peptides are present.
The compounds according to the invention are compounds of formula R~
R Ra N ~/
R~ \~~~~N\N/~

Ra wherein Rl and R9 are each independently of the other hydrogen; acyl; unsubstituted or substituted alkyl., alkenyl o:r alkynyl; heterocyclyl; sulfo; sulfon~vl substituted by unsubstituted or substituted alkyl, aryl., t.eterocyclyl, alkoxy, which is unsubst.ituted or substituted, or by a:ryloxy; sulfamoyl that :is un substitut;ed or substitui~ed at the nitrogen atom; or phosphoryl substituted by or.~e or two radicals, which may be identical or different, selecl~ed from unsubstituted or substituted alkyl, frorr~ unsubstit.utE~d or substituted cycloalkyl, :from aryl, from hydroxy, from unsubstituted or substituted alkoxy, from cycloalkoxy and from aryloxy; with the proviso that not more than one of the radicals R1 and R9 is hydrogen; and Rx and R~ are each independently of the other hydrogen or crone of the radicals mentioned above for R1 and R9; or the pairs of substituents R1 and RZ, and RB and R9, each independently of the other, may form together with the nitrogen atom t:o which they are bonded a heterocyclic ring consisting of the bonding nitrogen atom together with a radical selected from ethylene, trimethylene, tetramet.hylene and pentamethylene in which a carbon atom may :have been replaced by nitz:ogen, oxygen, sulfur or by sulfur mono- or di--substituted by oxygen and which may beunsaturated, or one of those radicals with an oxo substituent at each of the two carbon atoms linked to the bonding carbon atom and with or without a fused-on benzene or naphthalene ring; R3 a.nd R~ are each independently of the other hydrogen, unsubstituted or substituted alkyl or cycloalkyl; aryl;: heterocyclyl; or unsubstituted or substituted alkenyl; or R3 and R~ together form unsubstituted or substituted alkylene, alkylidene or benzo-fused alkylene; RS is hydroxy; R6 is hydrogen;
or RS and R6 together are oxo;

3 ~.r and R~ is unsukast.itr.~t~ed or subst:,.tuted alkyl or cycloalkyl; aryl; hetero~~ycly:L; or un:-xux_:~st:.i.t..uted or substituted alkenyl;
and salts of -t:~e rnecr~.ianed c:cac~~rpouzuds where salt-farming groups are pr_ese~t.
According to ore as~JC::ct of t:he: i n~~~~ention, there is provided a compound of formul<~
R~ Rs ,Rs R7 I ,, , R1~N~,~: ,~ t. ,N_,,,N,...Rg (z), R3, .F~a I
R~
wherein R1 and R~ are each independent_Ly ~.~t the ot:..her hydrogen; C1-Czsacyl; subst:ituteci alkana~,;~l, a:~l.kaxy carbonyl, carbamoyl, or an acyl_ radi.c:al ~.:at- an arninc, a<,.id;
unsubstituted or substituted ,--C;,salky:zp ~.,,-~:::zsalk:e:rlyl or Cl-Czsalkynyl; Cz-C:zsheterac:ycly::l.; sulfc:a; .ult:onyl :>ubstituted by unsubstituted ar substi.t~utec: r:x:Lky:L, F.:r-~:~r aryl, Cz-Czsheterocyclyl, C~-Czsalkoxy, whi.c:ln ~> unsubstit:uted or substituted, or by Cf;-Czzarylo.xy; sul. f<r.rn~:}y1 ~:shat is unsubstituted or substituted at the rnit.ac>gecn atom;; a monovalent residue of (L) -~;ral ire=. :bond~:3c.~ W a the carbaxy group and acylated benzyl oxy~~,arborfyl. ~~.r:
thiomorpholinocarbonyl at r_he ~:~rnino nitrr_>gerl atom; or phosphory:l substituted by one ~:~.r twc> :rar~:a_c:ats, which may be identical or different, selected from r~c~ru.bstitu.tE=_d or substituted C~_-Czsalkyl, from unsubsti-tur~r>~~~ ar su.b~stituted C3-Czscycloalkyl, from C~-Cizary~..., fr:am P~z~~.~xo~y, from u.nsubstituted or substituted C:~--Gz,alko;~~~, f:ram C'n-Czsc~yclaal.koxy and fram cJ~;-~;_».~~ry:l..oxy; w ~ th the proviso that not more than one c~f thc: r:adi.a~_s R., sa~~::a Ry .LS hydrogen;
a.nd R~. and R~ are each indeper~dentl y of th~a c>the r hydrogen or 3b one of the radicals mentioned above for R1 and Ra,; or the pairs of R,, and Rz, and R8 and Rg, each independently of the other, may form together with the nitrogen. atom to which they are bonded a saturated or unsaturated Lxeterocyc:Lic ring consisting of the bonding nitrogen atom together with a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene in which a carbon atom may be rep:Laced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen or naphthalene-1,8-dicarbonylimido; R3 and R4 are each independently of the other hydrogen;
unsubstituted or substituted Cl-Czsalkyl or c~:3-C25cycloalkyl;
Ch-Czzaryl; Cz-Czsheterocyclyl; or unsubstituted or substituted C1-Czsalkenyl; or R~ arid R~ together form unsubstituted or substituted ~~~-Czsalkylene, C2-C~,Salky:lidene or benzo-fused C,,-Czsalkylene; RS is hydroxy; R~ i.s hydrogen;
or RS and R6 together are oxo; and R~ is u.nsubstituted or substituted C1-Czsalkyl o:r C3-Czscycloalkyl; c~'~-Czzax:yl;
Cz-Czsheterocyclyl; or unsubstituted or substituted C~-Czsalkenyl; or a salt of the compound where salt:-forming groups are present; with the exception ~:~f tLie compound of formula T wherein R1, Rz , R3 , R,~ , R~ and R~k are eacYx hydrogen, Rs is hydroxyl, R~ is a radical of the formula -C'Hz- (C=0) -NH-(1~-CH3) -CHz-C'.OOH, and R9 is tent-butoxycarbonyl.
In the description of this invention, the term "lower" used in the definition of groups or radicals, for example lower alkyl, lower alkoxy, lower alkanoyl etc., means that, unless expressly otherwise cLefined, the groups or radicals so defined contain up to and including 7, and preferably up to and including 4, carbon atoms.
Unless indicated to the contrary, the radicals R1, Rz, R3, R4, R~, RB and/'or R9 may be mono- to 'poly-substituted, 3c especially mono- to tri-substituted, for example mono-substituted, by identical or different substituents.
The carbon atoms in compounds of formula T
substituted by R3 and R4 and by R~ and R~;

2~'~~~~a may, if they are asymmetric, be in the (R)-, (S)- or (R,S)-configuration, as may also any other asymmetric carbon atoms present. Accordingly, the present compounds may be in the form of isomeric mixtures or in the form of pure isomers, especially in the form of dia-stereoisomeric mixtures, pairs of enantiomers or pure enantiomers. Preferred compounds of formula I are those wherein the carbon atom substituted by R3 or by hydroxy RS has the (S)-configuration and any other asymmetric carbon atoms that may be present are, independently of one another, in the (R)-, (S)- or (R,S)-configuration.
The general terms and names used in the description of this invention preferably have the following meanings, and within the different levels of meanings of the radicals listed hereinbefore arid hereinbelow it is possible to use any combinations or individual radicals instead of the general definitions:
Acyl R1, R2, Rg or R~ has, for example, up to 25, preferably up to 19, carbon atoms and is especially the acyl group of a carboxylic acid, of a semiester of carbonic acid, of an un-substituted or N-substituted carbamic acid, of an unsubstituted or N-substituted oxalamide or of an unsubstituted or substituted amino acid, it being possible for there to be thio-carbonyl groups instead of carbonyl groups in each of the acyl radicals mentioned.
Preferably not more than one of the radicals R1 and R,2 and not more than one of the radicals Rg and R9 is acylated.
Preferred acyl groups R1, R2, Rg and R9 of a carboxylic acid are unsubstituted or substi-tuted allcanoyl having up to 19 carbon atoms, for example n-decanoyl, or preferably lower alkanoyl, such as formyl, acetyl, propionyl, butyryl or pivaloyl, or substituted lower alkanoyl, especially in the form of cycloalkyl-lower alkanoyl wherein cycloalkyl has, for example, fram 3 to 7 carbon atoms and lower alkanoyl is as defined above, for example cycloalkylcarbonyl, especially having a total of from 4 to 8 carbon atoms, such as cyclopropyl-, cyclobutyl-, cyclopentyl-or cyclohexyl-carbonyl, or 2-cyclohexyl- or 2-cyclopentyl-acetyl, cycloalkenyl-lower alkanoyl wherein cycloalkenyl has, for example, from 3 to 7 carbon atoms, such as cycloalkenylcarbonyl, preferably having from 4 to 8 carbon atoms, such as 1-cyclohexenylcarbonyl, 1,4-cyclohexadienylcarbonyl or 1-cyclohexenylacetyl or 1,4-cyclohexadienylacetyl, bicycloalkyl-lower alkanoyl wherein bicycloalkyi contains, for example, from 5 to 10 carbon atoms, for example bicycloalkylcarbonyl, preferably having from 8 to 11 carbon atoms, such as decahydronaphthyl-2-carbonyl, endo- or exo-norbornyl-2-carbonyl, bicyclo[2.2.2]oct-2-ylcarbonyl or bicyclo[3.3.1]non-9-ylcarbonyl, and also bicyclo-hexyl-, -heptyl-, -octyl-, -nonyl- or -decyl-acetyl or -3-propionyl, such as bicyclo[3.1.0]hex-1-, -2-or -3-yl-, bicyclo[4.1.0]hept-1- or -7-yl-, bicyclo[2.2.1]kept-2-yl-, such as endo- or exo-norbornyl-, bicyclo[3.2.1]oct-2-yl-, bicyclo[3.3.0]oct-3-yl- or bicyclo[3.3.1]non-9-yl-, and also a- or ~i-decahydronaphthyl-acetyl or -3-propionyl, bicycloalkenylcarbonyl, preferably having from 8 to 12 carbon atoms, such as 5-norbornen-2-ylcarbonyl or bicyclo[2.2.2]octen-2-ylcarbonyl, tricycloalkyl-lower alkanoyl wherein tricycloalkyl contains, for example, from 8 to 10 carbon atoms, fox example tricycloalkylcarbonyl, preferably having from 8 to 11 carbon atoms, such as 1- or 2-adamantylcarbonyl, and also tricyclo[5.2.1.02~]dec-8-yl-or adamantyl-acetyl, such as 1-adamantyl-acetyl, aryl-lower alkanoyl wherein aryl has from 6 to 14 carbon atoms, such as in phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, and may be unsubstituted or especially mono- to tri-substituted by lower alkyl, for example methyl, ethyl or propyl, halo-lower alkyl, for example trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, for example methoxy, carbamoyl-lower alkoxy, N-lower alkyl-carbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, fox example fluorine, chlorine or bromine, carboxy, .lower alkoxycarbonyl, such as tert-butoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, such as benzyloxy-carbonyl, lower alkanoyl, sulfo, lower allcylsulfonyl, for example rnethylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylaminosulfonyl, nitro and/or by cyano, wherein phenyl may be present up to three times, for example in Biphenyl-, dibenzyl- or triphenyl-lower alkanoyl, such as Biphenyl-, dibenzyl-or tri-phenyl-acetyl, and wherein lower allcanoyl may be unsubstituted or substituted, for example by lower alkyl, far example methyl, heterocyclyl selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclo-hexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, hydroxy, lower alkoxy, lower alkanoyloxy, for example acetoxy, propionyloxy, butyroxy, isobutyroxy or pivaloyloxy, acetoacetoxy, amino- or benzyloxycarbonylamino-lower alkanoyloxy, for example 2-amina- or 2-benzyloxycarbonylamino-2-methyl-propionyloxy, aryl-lower alkanoyloxy when°ein aryl has from 6 to 10 carbon atoms, for example in benzoyloxy, phenylacetoxy, 1- or 2-naphthoyloxy, lower alkoxycarbonyloxy, for example methoxy-, ethoxy-, n-propoxy-, isopropoxy-, n-butoxy-, isobutoxy-, sec--s-butoxy-, tart-butoxy-, n-pentyloxy-, isopentyloxy-, neopentyloxy-, tart-pentyloxy-, n-hexyloxy-, isohexyloxy- or n-heptyloxy-carbonyloxy, mono- or di-lower aLkylamino-carbonyloxy, for example ethylaminocarbonyloxy or diethylaminocarbonyloxy, aryloxy-carbonyloxy wherein aryl has from 6 to 10 carbon atoms, for example phenoxycarbonyl-oxy or 1- or 2-naphthyloxycarbonyloxy, aryl-lower alkoxycarbonyloxy wherein aryl has from 6 to 14 carbon atoms, especially phenyl-lower alkoxycarbonyloxy, for example benzyloxycarbonyloxy, and also 1- or 2-naphthylmethoxycarbonyloxy or 9-fluorenyl-methoxycarbonyloxy, sulfonyloxy, lower allcylsulfonyloxy, for example methyl-, ethyl-, propyl-, isopropyl-, n-butyl-, isobutyl-, sec-butyl-, tart-butyl-, n-pentyl-, isopentyl-, neopentyl-, tart-pentyl-, n-hexyl-, isohexyl- or n-heptyl-sulfonyloxy, phenylsulfonyloxy, 2- or 4-toluenesulfonyloxy, 1- or 2-naphthylsulfonyloxy, carboxy, esterified carboxy selected from lower alkoxycarbonyl, for example methoxy-, ethoxy-, n-propoxy-, isopropoxy-, n-butoxy-, isobutoxy-, sec-butoxy-, tart-butoxy-, n-pentyloxy-, isopentyloxy-, neopentyloxy-, tart-pentyloxy-, n-hexyloxy-, isohexyloxy- or n-heptyloxy-carbonyl, aryl-oxycarbonyl wherein aryl has from 6 to 10 carbon atoms, for example phenoxycarbonyl or 1- or 2-naphthyloxycarbonyl, aryl-lower alkoxycarbonyl wherein aryl has from 6 to 12 carbon atoms, for example benzyloxycarbonyl, 1- or 2-naphthylmethoxycarbonyl or 2-fluorenylmethoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, for example methyl- or tart-butyl-sulfonyl, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbarnoyl, carbamoyl substituted by one or two radicals selected from lower alkyl, such as methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, spec-butyl, ten-butyl, n-pentyl, isopentyl, neopentyl, tart-pentyl, n-hexyl, isohexyl or n-heptyl, for example in N-methyl-carbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, from carboxy-lower alkyl or lower alkoxycarbonyl-lower alkyl, for example in the form of carboxymethylcarbamoyl (glyci~tylcarbonyl) or in the form of tart-butoxycarbonylmethylcarbamoyl, from di-lower alkylamino-lower alkyl, for example 2-dimethylaminoethyl, aminacarboxy-lower alkyl, for example 5-amino-5-carboxypentyl, from hydroxy-lower alkyl, for example hydroxy-methyl or hydroxyethyl, and from di-lower alkoxy-lower allcyl, for example 2-(2,2-dimethoxyethyl), or carbamoyl substituted by one radical selected from ethylene, tri-methylene, tetramethylene and pentamethylene in which a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which may be unsaturated, such as piperidin-1-yl-, pyrazin-1-yl-, piperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomarpholino- or S,~-dioxothio-morpholino-carbonyl; sulfamoyl, phosphono, benzofuranyl, oxo and/or by cyano and is unbranched or branched, for example selected from benzoyl that is unsubstituted or mono-or poly-substituted by lower alkyl, for example methyl, phenyl, halogen, for example fluorine or chlorine, hydroxy, lower alkoxy, for example methoxy, and/or by vitro, such as 4-chloro-, 4-methoxy- or 4-vitro-benzoyl, naphthylcarbonyl, such as a- or ~i-naphthyl-carbonyl or 1,8-naphthalenedicarbonyl bonded to the amino group via both carbonyl groups, indenylcarbonyl, such as'1-, 2- or 3-indenylcarbonyl, indanylcarbanyl, such as f-or 2-indanylcarbonyl, phenanthrenylcarbonyl, such as 9-phenanthrenylcarbonyl, phenyl-acetyl, a-naphthylacetyl, (3-naphthylacetyl, lower alkylphenylacetyl, such as 4-methyl-phenylacetyl, lower alkoxyphenylacetyl, such as 4-methoxyphenylacetyl, 3-phenyl-propionyl, 3-(p-hydroxyphenyl)-propionyl, diphenylacetyl, di-(4-methoxyphenyl)-acetyl, triphenylacetyl, 2,2-dibenzylacetyl, anilinophenylacetyl substituted in the phenyl radical by one or two radicals selected from lower alkyl, for example methyl or ethyl, hydroxy, lower alkoxy, for example methoxy, amino, mono- or di-lower alkylamino, for example ethylamino or dimethylamino, halogen, for example fluorine or chlorine, carboxy, sulfo, carbamoyl, sulfamoyl and cyano and/or at the amino group by one or two radicals selected from lower alkyl and benzyl, such as 2-(o,o-dichloroanilino)-phenylacetyl or 2-(0,0-dichloro-N-benzylanilino)-phenylacetyl, 3-a- or 3-~3-naphthylpropionyl, 2-benzyl-3-(1-pyrazolyl)-propionyl, 3-phenyl- or 3-a-naphthyl-2-hydroxypropionyl, 3-phenyl-or 3-a-naphthyl-2-lower alkoxypropionyl, such as 3-phenyl- or 3-a-naphthyl-2-neopentyloxy-propionyl, 3-phenyl- or 3-a-naphthyl-2-lower alkanoyloxypropionyl, such as 3-phenyl-2-pivaloyloxy- or -2-acetoxy-propionyl, 2-benzyl- or 1- or 2-naphthyl-3-(N-methoxy-N-methylamino)-propionyl, 3-a-naphthyl-2-acetoacetoxypropionyl, 3-a-naphthyl-2-ethyl-aminocarbonyloxy-propionyl or 3-a-naphthyl-2-(2-amino- or 2-benzyloxycarbonyl-amino-2-methylpropionyloxy)-propionyl, 3-phenyl- or 3-a-naphthyl-2-carboxymethyl-propionyl, 3-phenyl- or 3-a-naphthyl-2-lower alkoxycarbonyl-propionyl, such as 3-a-naphthyl-2-ethoxycarbonyl-propionyl, 3-phenyl- or 3-a-naphthyl-2-benzyloxycarbonyl-methyl-propionyl, 2-(S)benzyl-3-tert-butylsulfonyipropionyl, 3-phenyl-2-phosphono- or -phosphonomethylpropionyl, 3-phenyl-2-dimethoxyphosphoryl- or -dimethoxy-phosphorylmethyl-propionyl, 3-phenyl-2-diethoxyphosphoryl- or -diethoxyphosphoryl-methyl-propionyl, 3-phenyl-2-ethoxy- or -methoxy-hydroxyphosphorylpropionyl, phenyl-lower alkanoyl wherein the lower alkanoyi radical is substituted by carbamoyl, such as 2(R,S)-carbamoyl-3-phenylpropionyl, 3-phenyl- or 3-a-naphthyl-2-carbamoylpropionyl, 3-phenyl- or 3-a-naphthyl-2-tert-butylcarbamoyl-propionyl, 3-phenyl- or 3-a-naphthyl-2-(2-dimethylaminoethyl)carbarnoylpropionyl, 3-a-naphthyl-2-(carboxy- ar ten-butoxy-carbonyl)methylcarbamoyl-propionyl, 3-phenyl- or 3-a-naphthyl-2-(3-hydroxy-2-propyl)-carbamoyl-prapionyl, 3-phenyl- or 3-a-naphthyl-2-(2,2-dimethoxyethyl)carbamoyl-propionyl, 3-phenyl- or 3-a-naphthyl-2-(5-amino-5-carboxypentyl)-carbamoylpropionyl, 3-phenyl- or 3-a-naphthyl-2-cyanopropionyl, 3-phenyl- or 3-a-naphthyl-2-cyanomethyl-5.

~~~~F~r~~~
_g_ propionyl, 3-phenyl- or 3-a-naphthyl-2-acetonyl-prapionyl, 4-hydroxyphenylbutyryl, 4-phenyl- or 4-a-naphthyl-3-carboxybutyryl, 4-phenyl- or 4-a-naphthyl-3-benzyloxy-carbonyl-butyryl, 2-benzyl- or 2-a-naphthylmethyl-4-cyanobutyryl, 2-benzyl-4-(2-benzo-furanyl)-4-oxobutyryl, 2-benzyl- br 2-a-naphthylmethyl-5-dimethylamino-pentanoyl, 2-benzyl- or 2-a-naphthylmethyl-4-oxapentanoyl, 2-benzyl- or 2-a-naphthylmethyl-4,4-dimethyl-3-oxo-pentanoyl, 2-benzyl- or 2-a-naphthylmethyl-5-dimethylamino-4-oxo-pentanoyl, and 2-benzyl- or 2-a-naphthylmethyl-5,5-dimethyl-4-oxo-hexanoyl, especially phenyl-lower alkanoyl, such as phenylacetyl, or phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carbamoyl, such as 2(R,S)-carbamoyl-3-phenyl-propionyl, phenyl-lower alkenoyl, such as (3-phenylacryloyl or (3-phenylvinylacetyl, heterocyclyl-lower alkanoyl wherein lower alkanoyl is unsubstituted or substituted as defined above under aryl-lower alkanoyl Rt, R2, R8 and R9 and wherein heterocyclyl is preferably a single or double ring system having from 3 to 1D ring atoms, is bonded via a carbon atom or, especially, via a nitrogen atom and contains up to 3 further hetero atoms selected from oxygen, nitrogen, sulfur, selenium, and sulfur linked to 1 or 2 oxygen atoms, the mentioned ring system may also be fused with 1 or 2 phenyl or naphthyl radicals, it being possible for naphthyl also to be fused-on on both sides, or with 1 or 2 cycloalkyl z~adicals, cycloalkyl preferably having from 5 to 7 ring atoms; and may be unsaturated or partially or fully saturated, for example thienyl-, furyl-, pyranyl-, pyrrolyl-, imidazolyl-, pyrazolyl-, oxazolyl-, isoxazolyl-, thiazolyl-, furazanyl-, tetrazolyl-, pyridyl-, pyrazinyi-, pyrimidinyl-, pyridazinyl-, azepinyl-, indolyl-, benzimidazolyl-, 1H-indazolyl-, quinolyl-, isoquinolyl-, quinoxalinyl-, quinazolinyl-, cinnolyl-, purinyl-, pteridinyl-, naphthyridinyl-, 4H-quinolizinyl-, 3,1-benzofuranyl-, benz[e]indolyl-, 4,1-benzoxazinyl-, 4,1-benzo-thiazinyl-, carbazolyl-, (3-carbolinyl-, phenazinyl-, phenanthridyl-, acridinyl-, phen-oxazinyl-, phenothiazinyl-, 1-azaacenaphthenyl-, cyclohexa[b]pyrrolyl-, cyclohepta[b]-pyrrolyl-, cyclohexa[d]pyrazolyl-, cyclohexa[b]pyridyl-, cyclohexa[b]pyrazinyl-, cyclo-hexa[b]pyrimidinyl-, cyclohexa[b]-1,4-oxazinyl-, cyclohexa[b]-1,4-thiazinyl-, pyrrolidinyl-, pyrrolinyl-, imidazolidyl-, 2-imidazolinyl-, 2,3-dihydropyridyl-, piperidyl-, piperazinyl-, 2,3,5,6-tetrahydropyrazinyl-, morpholinyl-, thiomorpholinyl-, S,S-dioxo-thio-morpholinyl-, indolinyl-, isoindolinyl-, 4,5,6,7-tetrahydroindolyl-, 1,2,3,4-tetrahydro-quinolyl-, 1,2,3,4-tetrahydroisoquinolyl-, chromanyl-, thiochromanyl-, 1,2,3,4-tetrahydro-3,1-benzodiazinyl-, 3,4-dihydro-3H-4,1-benzoxazinyl-, 3,4-dihydra-3H-4,1-benzo-thiazinyl-, 2,3,4,5-tetrahydro-1H-5,1-benzazepinyl- or 5,6-dihydrophenanthridinyl-lower alkanoyl, the mentioned heterocyclyl radicals being unsubstituted or substituted by lower alkyl, fax example methyl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, for example benzyl, hydroxy-Iower alkyl, for example hydroxymethyl or 2-hydroxyethyl, lower alkoxy-lower alkyl, for example methoxymethyl or 2-methoxyethyl, phenoxy- or naphthyloxy-Iower alkyl, for example 2-phenoxyethyl, 1- or 2-naphthyloxymethyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, for example benzyloxy-lower alkyl, lower allcanoyloxy-lower alkyl, for example acetoxymethyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, for example benzoyloxy-, phenylacetoxy- or 1-or 2-naphthoyloxy-methyl, -2-ethyl or -2-(2,2-dimethylethyl), lower alkoxycarbonyloxy-lower alkyl, for example tent-butoxycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyloxy-lower alkyl, for example 2-benzyloxycarbonyloxy-ethyl or 9-fluorenylmethoxycarbonyloxyethyl, amino-lower alkyl, for example aminomethyl, 2-aminoethyl or 2-aminopropyl, carboxy-lower alkyl, for example carboxymethyl or 2-carboxyethyl, hydroxy, lower alkoxy, for example methoxy or ethoxy, phenyl- or naphthyl-lower alkoxy, for example benzyloxy or 1- or 2-naphthyloxy, amino, lower alkylamino, for example methyl-, ethyl- or tert-butyl-amino, di-Iower alkylamino, for example dimethyl- or diethyl-amino, carboxy, lower alkoxycarbonyl, for example methoxy-, isopropoxy-, sec-butoxy- or ten-butoxy-carbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, for example benzyloxycarbonyl, halogen, for example fluorine, chlorine, bromine or iodine, especially chlorine or bromine, lower alkanoyl, for example acetyl or pivaloyl, lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or dialkoxyphosphoryl, for example dimethoxy-or diethoxy-phosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, for example N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, hydroxy- or carboxy-lower alkylcarbamoyl, for example hydroxy- or carboxy-methylcarbamoyl or hydroxy- or carboxy-ethylcarbamoyl, sulfamoyl, vitro, oxo andlor by cyano, with hetero-cyclyl-lower alkanoyl being selected especially from pyrrolylcarbonyl that is unsubstituted or substituted by lower alkyl or by phenyl, for example 2- or 3-pyrrolylcarbonyl, ~- or 5-methylpyrrolylcarbonyl or 4- or 5-phenylpyrrolyl-2-carbonyl, thienylcarbonyl, such as 2-thienylcarbonyl, furylcarbonyl, such as 2-furylcarbonyl, pyridylcarbonyl, such as 2-, 3-or 4-pyridylcarbonyl, pyrimidin-1-ylcarbonyl, indolylcarbonyl that is unsubstituted or substituted by lower alkyl, such as methyl, phenyl-lower alkyl, such as benzyl, lower alkoxy, such as methoxy, phenyl-lower alkoxy, such as benzyloxy, or by halogen, such as chlorine, such as 2-, 3~ or 5-indolylcarbonyl, 1-methyl-, 5-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4.,5-dimethyl-indolyl-2-carbonyl, 1-benzylindolyl-2-or -3-carbonyl, 4,5,6,7-tetrahydroindolyl-2-carbonyl, unsubstituted or hydroxy-substituted quinolyl-lower alkanoyl, for example quinolylcarbonyl, such as 2-, 3- or ~-quinolyl-carbonyl or 4-hydroxyquinolyl-2-carbonyl, unsubstituted or hydroxy-substituted iso-quinolylcarbonyl, such as 1-, 3- or 4-isoquinolylcarbonyl or 1-oxo-1,2-dihydroiso-quinolyl-3-carbonyl, 2-quinoxalinylcarbonyl, 2-(3,1-benzofuranyl)-carbonyl, Benz[e]indolyl-2-carbonyl, (3-carbolinyl-3-carbonyl, cyclohepta[b]pyrrolyl-5-carbonyl, ' 3-chromanylcarbonyl, 3-thiochromanylcarbonyl, pyrrolidinyl-3-carbanyl, hydroxy-pyrrolidinylcarbonyl, such as 3- or 4-hydroxypyrrolidinyl-2-carbonyl, oxopyrrolidinyl-carbonyl, such as 5-oxopyrrolidinyl-2-carbonyl, piperidylcarbonyl, such as piperidino-carbonyl or 2-, 3- or 4-piperidylcarbonyl, pyrazinylcarbonyl, such as pyrazin-1-ylcarbonyl, piperazinylcarbonyl, such as piperazin-1-ylcarbonyl, morpholinyl-lower alkanoyl, for example morpholinylcarbonyl, such as morpholinocarbonyl, thiomoapholinyl-lower alkanoyl, for example thiomorpholinylcarbonyl, such as thiomorpholinocarbonyl, S,S-dioxothiomorpholinylcarbonyl, such as S,S-dioxothiomorpholinocarbonyl, indolinylcarbonyl, such as 2- or 3-indolinylcarbonyl, 1,2,3,4-tetrahydroquinolylcarbonyl, such as 1,2,3,4-tetrahydroquinolyl-2-, -3- or -4-carbonyl, 1,2,3,4-tetrahydroisoquinolyl-carbonyl, such as 1,2,3,4-tetrahydroisoquinolyl-1-, -3- or -4-carbonyl or 1-oxo-1,2,3,4-tetrahydroisoquinolyl-3-carbonyl, tetrazolyl-lower alkanoyl, such as 3-(tetrazol-1-yl)-propionyl, and pyridyl-lower alkanoyl, for example pyridylacetyl, such as 2-, 3- or 4-pyridylacetyl, heterocyclyl-lower alkanoyl being selected more especially from rnorpholinocarbonyl, thiomorpholinocarbonyl, S,S-dloxothiomorpholinocarbonyl, pyridyl-acetyl, indolylacetyl, benzofuranylacetyl, 4-pyrrolidinylacetyl, 1-imidazolylacetyl, quinolin-2-ylacetyl, indol-2-ylacetyl, 2-morpholino-2-isopropylacetyl and 2-(S,S-dioxo-thiomorpholino)-2-isopropylacetyl, most especially morpholinocarbonyl, thiomorpholino-carbonyl, quinolin-2-ylcarbonyl, 3-(tetrazol-1-yl)-propionyl or 2- or 3-pyridylacetyl, heterocyclyl-lower alkenoyl wherein heterocyclyl is selected especially from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, ~i-caxbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, for example pyrrolidyl-lower alkenoyl, such as IV-pyrrolidylacryloyl, hydroxy-lower alkanoyl, such as 3-hydroxypropionyl or 2-hydroxy-2-methylpentanoyl, hydroxy-lower alkoxy-lower alkanoyl, such as 3-hydroxy-n-propoxycarbonyl, lower allcoxy-lower alkanoyl, for example lower alkoxyacetyl or lower alkoxypropionyl, such as methoxyacetyl, ethoxyacetyl or 3-methoxypropionyl, lower alkoxy-lower alkoxy-lower alkanoyl, such as 2-methoxymethoxy-3-methyl-pentanoyl, phenoxy-Iower alkanoyl or nitrophenoxy-lower alkanoyl, such as phenoxyacetyl or 4-nitrophenoxyacetyl, naphthyloxy-lower alkanoyl, such as cx- or Li-naphthyloxyacetyl, 2~'~~'~3 lower alkanoyloxy-lower alkanoyl wherein lower alkanoyloxy is, far example, ~acetoxy, propionyloxy, butyroxy, isobutyroxy or pivaloyloxy, such as acetoxyacetyl or 3-acetoxy propionyl, ' ' acetoacetoxy-lower alkanoyl, such as 3-acetoacetoxy-propionyl amino- or benzyloxycarbonylamino-lower alkanoyloxy-lower alkanoyl, for example amino- or 2-benzyloxycarbonylamino-2-methylpropionyloxy-lower alkanoyl, such as -acetyl or -3-propionyl, .
aryl-lower alkanoyloxy-lower alkanoyl wherein aryl has from 6 to 10 carbon atoms, such as in benzoyloxy-, phenylacetoxy- or 1- or 2-naphthoyloxy-lower alkanoyl, lower alkoxycarbonyloxy-lower alkanoyl, for example methoxy-, ethoxy-, n-propoxy-, isopropoxy-, n-butoxy-, isobutoxy-, sec-butoxy-, tent-butoxy-, n-pentyloxy-, isopentyloxy-, neopentyloxy-, tart-pentyloxy-, n-hexyloxy-, isohexyloxy- or n-heptyloxy-carbonyloxy--lower alkanoyl, such as -acetyl or -3-propionyl, mono- or di-lower alkyl-aminocarbonyloxy-lower alkanoyl, for example ethylamino-carbonyloxy-lower alkanoyl or diethylaminocarbonyloxy-lower alkanoy.l, such as -acetyl or -3-propionyl, aryloxycarbonyloxy-lower alkanoyl wherein aryl has from 6 to 10 carbon atoms, for example phenoxycarbonyloxy- or 1- or 2-naphthyloxycarbonyloxy-lower alkanoyl, such as -acetyl or -3-propionyl, aryl-lower alkoxycarbonyloxy-lower alkanoyl wherein aryl has from 6 to 12 carbon atoms, for example phenyl-lower alkoxycarbonyloxy-lower alkanoyl, such as benzyloxy-carbonyloxy-acetyl or -3-propionyl, and also 1- or 2-naphthylmethoxycarbonyloxy-lower alkanoyl or 9-fluorenylmethoxycarbonyloxy-lower allcanoyl, such as -acetyl or -3-propionyl, sulfonyloxy-lower alkanoyl, such as -acetyl or -3-propionyl, lower alkylsulfonyloxy-lower alkanoyl, for example methyl-, ethyl-, propyl-, isopropyl-, n-butyl-, isobutyl-, sec-butyl-, tart-butyl-, n-pentyl-, isopentyl-, neopentyl-, tart-pentyl-, n-hexyl-, isohexyl- or n-heptyl-sulfonyloxy-lower alkanoyl, such as -acetyl or -3-propionyl, phenylsulfonyloxy-, 2- or 4-toluenesulfonyloxy- or 1- or 2-naphthylsulfonyloxy-lower alkanoyl, arylmercapto-lower alkanoyl wherein aryl has from 6 to 10 carbon atoms and is preferably phenyl or naphthyl, for example phenylmercapto-lower alkanoyl, such as -acetyl or -3-propionyl, amino-lower alkanoyl wherein the amino group is not in the in a- or (3-position, such as 5-aminopentanoyl, ~"~r~'~~

lower alkanoylamino-lower alkanoyl wherein the amino group is not in the a- or (3-position of the lower alkanoyl radical, such as 5-amino-pentanoyl, lower alkoxycarbonylamino-lower alkanoyl wherein the amino group is not in the a- of (3-position of the lower alkanoyl radical, such as 5-(tert-butoxycarbonylamino)-pentanayl, phenyl-lower alkoxycarbonylamino-lower alkanoyl wherein the amino group is not in the a- or (3-position of the lower alkanoyl radical, such as 5-benzyloxycarbonylamino-pentanoyl or 6-benzyloxycarbonylaminohexanoyl, amino-lower alkanoyl substituted at the amino nitrogen atom by heterocyclyl-lower alkanoyl as defined above for heterocyclyl-lower alkanayl Rl, R2, Rg or Rg, especially by N-morpholino- or N-thiomorpholino-carbonyl, for example N-morpholino- or N-thio-rnorpholino-carbonylamino-lower alkanoyl, such as N-morpholino- or N-thiornorpholino-carbonylamino-acetyl, halo-lower alkanoyl preferably containing up to 3 halogen atoms, for example a-halo-acetyl, such as a-fluoro-, a-chloro-, a-bromo-, a-iodo-, a,a,a-trifluoro- or a,a,a-tri-chloro-acetyl, or halopropionyl, such as B-chloro- or );-bromo-propionyl, caxboxy-lower alkanoyl, for example cwboxyacetyl or 13-carboxypropionyl, lower alkoxycarbonyl-lower alkanoyl, for example lower alkoxycarbonylacetyl or lower alkoxycarbonylpropionyl, such as methoxycarbonylacetyl, 3-methoxycarbonylpropionyl, ethoxycarbonylacetyl, 3-ethoxycarbonylpropionyl or ;3-tent-butoxycarbonylpropionyl, ' lower alkylcarbonyl-halo-lower alkanoyl, such as 3-ethoxycarbonyl-2-difluoramethyl-propionyl, 2-halo-lower alkoxycarbonyl-lower alkanoyl, such as 2-chloro-, 2-bramo-, 2-iodo- or 2,2,2-trichloro-ethoxycarbanyl-acetyl or -3-propionyl, phenyl- or naphthyl-lower alkoxycarbonyl-lower alkanayl, for example benzyloxy-carbonyl-lower alkanoyl, such as 3-benzyloxycarbonyl-2,2-dimethylpropionyl, heterocyclyl-lower alkoxycarbonyl-lower alkanoyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl and 13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, it also being possible for the mentioned radicals to be fully or partially saturated, such as in 4-pyridylmefhoxycarbonyl-acetyl or -3-propionyl or 2-morpholinocarbonyloxy-4-methyl-pentanoyl, sulfonyl-lower alkanoyl, such as 3-sulfonylpropionyl, lower alkylsulfonyl-lower alkanoyl, such as 2-ethylsulfonyl- or 2-tert-butylsulfanyl-acetyl, arylsulfonyl-lower alkanoyl wherein aryl preferably has from 6 to 10 carbon atoms, for example phenyl or naphthyl, such as phenylsulfoacetyl, carbamoyl-lower alkanoyl, such as carbamoylacetyl or 3-carbamoylpropionyl, lower alkylcarbamoyl-lower allcanoyl, for example lower alkylcarbamoylacetyl or methylcarbamoyl-lower alkanoyl, such as methylcarbamoylacetyl, di-lower alkylcarbamoyl-lower alkanoyl, for example di-lower alkylcarbamoylacetyl or dimethylcarbamoyl-lower alkanoyl, such as dirnethylcarbamoylacetyl, hydroxy-lower alkylcarbamoyl- or di(hydroxy-lower alkyl)carbamoyl-lower alkanoyl, such as hydroxyrnethylcarbamoyl- or di(hydroxymethyl)carbamoyl-acetyl or -propionyl, N-lower alkoxy-lower alkoxy-lower alkylcarbamoyl-lower alkanoyl, such as 2-isobutyl-3-(2-(2-methoxyethoxy)ethylaminocarbonyl)-propionyl, carboxy-lower alkylcarbamoyl- or di(carboxy-lower alkyl)carbamoyl-lower alkanoyl, such as carboxymethyl- or di(carboxymethyl)carbamoyl-acetyl or -propionyl, carbamoyl-lower alkanoyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, it also being possible for the radical so formed to be fully or partially unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomorpholino-carbonyl-lower alkanoyl, such as in morpholinocarbonyl-acetyl, 3-(morpholino-carbanyl)-propionyl or 3-(morpholinocarbonyl)-2-isobutyl-propionyl, N-heterocyclyl-lower alkylcarbamoyl-lower alkanoyl or N-lower alkyl-N-heterocyclyl-lower alkylcarbamoyl-lower alkanoyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxatinyl, f3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, from morpholinyl and thiomorpholinyl, such as N-methyl-2-(N-2-pyridylmethyl)-carbamoylacetyl, 2-(N-morpholino-lower alkylcarbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(2-morpholinoethyl)-carbamoyl-3-methyl-butyryl or 2-(N-(pyridyl-lower alkyl)-carbamoyl)-lower alkanoyl, such as (2(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-3-methyl)-butyryl, sulfamoyl-lower alkanoyl, such as 2-sulfamoylacetyl, N-(phenyl- or naphthyl-lower alkyl)sulfamoyl-lower alkanoyl, such as 3-benzylamino-sulfonyl-2-isopropyl-propionyl, sulfarnoyl-lower alkanoyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom may have been replaced by nitrogen, lower alkyl-substituted, such as methyl-substituted, nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, it also being possible for the radical so formed to be fully ar partially unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, 4-methylpiperazin-1-yl, pyrimi-din-1-yl-, pyridazin-1-yl-, mozpholino-, thiomorpholino- or S,S-dioxothiomoapholino-sulfonyl-lower alkanoyl, such as 3-(4-methylpiperazinylsulfonyl)-2-isopropylpropionyl or 3-(morpholinosulfonyl)-2-isopropyl-propionyl, oxo-lower alkanoyl, such as acetoacetyl or propionylacetyl, cyano-lower alkanoyl, such as cyanoacetyl, 2- or 3-cyanopropionyl or 2-, 3- or 4-cyano-butyryl, hydroxy-carboxy-lower alkanoyl, such as 2-hydroxy-2-carboxy-acetyl or 2-hydroxy-3-carboxypropionyl, a-naphthyloxy-carboxy-lower alkanoyl, such as 2-a-naphthyloxy-4-carboxy-butyryl, hydroxy-lower alkoxycarbonyl-lower allcanoyl, for example hydroxy-lower alkoxy-carbonyl-acetyl or -propionyl or hydroxy-ethoxy- or hydroxy-methoxy-caxbonyl-lower alkanoyl, such as 2-hydroxy-2-ethaxy- or -methoxy-carbanylacetyl or 2-hydroxy-3-eth-oxy- or -methoxy-carbonyl-propionyl, a-naphthyloxy-lower alkoxycarbonyl-lower alkanoyl, for example a-naphthyloxy-lower alkoxycarbonyl-acetyl, -propionyl or -butyryl or a-naphthyloxy-ethoxycarbonyl-lower allcanoyl, such as a-naphthyloxy-ethoxycarbonylacetyl, 2-a-naphthyloxy-3-ethoxy-carbonylpropionyl or 2-a-naphthyloxy-4-tert-butoxycaxbanylbutyryl, a-naphthyloxy-benzyloxycarbonyl-lower alkanoyl, such as 2-a-naphthyloxy-3-benzyloxycarbonyl-propionyl, esterified hydroxy-lower alkoxycarbonyl-lower alkanoyl wherein the hydroxy group is esterified by lower alkanoyl, for example acetyl, propionyl or pivaloyl; by cycloalkyl-lower alkanoyl wherein cycloalkyl has from 3 to 7 carbon atoms and lower alkanoyl is preferably as last defined, for example cyclohexylcarbonyl or 2-eyclohexyl- or 2-cyclo-pentyl-acetyl; by bicycloalkyl-lower alkanoyl wherein bicycloalkyl has, for example, fi~ozn to 10, especially from 6 to 9, carbon atoms, such as in bicyclohexyl-, -heptyl-, -octyl-, -nonyl- or -decyl-acetyl or -3-propionyl, for example bicyclo[3.1.0]hex-1-, -2-or -3-yl-, bicyclo[4.1.0]hept-1- or -7-yl-, bicyclo[2.2.1]hept-2-yl-, such as endo- or exo-norbornyl-, bicyclo[3.2.1]oct-2-yl-, bicyclo[3.3.0]oct-3-yl- or bicyclo[3.3.1]non-9-yl-, and also a- or 13-decahydronaphthyl-acetyl or -3-propionyl; by tricycloalkyl-lower alkanoyl wherein tricycloalkyl has, far example, from 8 to 10 carbon atoms, for example in tricyclo-[5.2.1.02~6]dec-8-yl- or adamantyl-, such as i-adamantyl-acetyl; by aryl-lower alkanoyl wherein aryl has from 6 to 14 carbon atoms, for example phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, which may be unsubstituted or mono- to tri-substituted by lower alkyl, such as isopropyl, halo-lower alkyl, such~as tri-fluaromethyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower allcoxy or N,N-di-lower alkylcarbaznoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such as fluorine, chlorine or bromine, carboxy, lower alkoxy-carbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, for example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano; by lower alkoxy-carbonyl, for example tert-butoxycarbonyl; by 2-halo-lower alkoxycarbonyl as defined above; or by phenyl- or fluorenyl-lower alkoxycarbonyl, for example benzyloxycarbonyl or 9-fluorenylmethoxycarbonyl, such as a-acetoxy-a-methoxycarbonyl-acetyl, a-benzoyl-oxy-, a-(1- or 2-naphthoyloxy)-, a-(phenyl-2-acetoxy)-, a-(1- or 2-naphthyl-2-acetoxy)-, a-(4-methylphenyl-2-acetoxy)-, a-(4-methoxyphenyl-2-acetoxy)- or a-(2-(o,o-dichloro-phenyl)-2-acetoxy)-a-methoxycarbonyl-acetyl, dihydroxy-carboxy-lower alkanoyl, such as 2,3-dihydroxy-3-carboxy-propionyl, dihydroxy-lower alkoxycarbonyl-lower alkanoyl, such as 2,3-dihydroxy-3-ethoxy-or -methoxy-carbonyl-propionyl, dihydroxy-lower alkoxycarbonyl-lower alkanoyl esterified by lower alkanoyl, such as acetyl, pxopionyl or butyryl, lower alkoxycarbonyl, far example tert-butoxycarbonyl, phenyl- or fluorenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl or 9-fluorenyl-methoxycarbonyl, lower alkylsulfonyl or by toluenesulfonyl, for example di-lower alkanoyloxy-lower alkoxy-propionyl, such as 2,3-diacetoxy-3-methoxycarbonyl-propionyl, a-naphthyloxy-di-lower alkylamino-lower alkanoyl, such as 2-a-naphthyloxy-5-dimethylamino-pentanoyl;
a-naphthyioxy-carbamoyl-lower alkanoyl, such as 2-a-naphthyloxy-4-carbamoyl-butyryl, a-naphthyloxy-oxo-lower alkanoyl, such as 2-a-naphthyloxy-4-oxo-pentanoyl, a-naphthyloxy-cyano-lower alkanoyl, such as a-naphthyloxy-cyano-acetyl or 2-a-naphthyloxy-4-cyanabutyryl, lower alkenoyl having from 3 to 7 carbon atoms, preferably having 3 or 4 carbon atoms, lower alkenoyl being unsubstituted or substituted by the same substituents as lower alkanoyl, especially by phenyl, hydroxy, lower alkoxy, such as methoxy, phenyl-lower alkoxy, such as benzyloxy, lower alkanoyloxy, such as acetoxy, lower alkanoylamino, such as acetylamino, lower allcoxycarbonyloxy, such as tent-butoxycarbonyloxy, phenyl-or naphthyl-lower alkoxycarbonyloxy, such as benzyloxycarbonyloxy, carboxy, lower ~~~r~/w~~~

alkoxycarbonyl, such as tart-butoxycarbonyl, phenyl- or naphthyl-lower alkoxycarbonyi, halogen, such as chlorine or bromine, carbamoyl and/or by mono- or di-lower alkyl-carbamoyl, such as in acryloyl, vinylacetyl, crotonoyl or 3- or 4-pentenoyl, 3-phenyl-acryioyl, 3-phenylvinyiacetyl or 5-phenyl-4-acetylaminopenten-2-oyl, cycloalkyl-lower alkenoyl wherein cycloallcyl preferably has from 3 to 7 carbon atoms, for example cyclohexylacryloyl, or lower allcynoyl having. from 3 to 7, preferably 3 or 4, carbon atoms, for example propioloyl or 2- or 3-butynoyl.
Prefezred acyl groups R1, R2, Rg and R9 of a semiester of carbonic acid are lower alkoxycarbonyl, for example methoxy-, ethoxy-, isopropoxy-, isobutoxy-or tart-lower alkoxy-carbonyl, such as tart-butoxycarbonyl or isobutoxycarbonyl, 2-halo-lower alkoxycarbonyl, such as 2-chloro-, 2-bromo-, 2-iodo- or 2,2,2-trichloro-ethoxycarbonyl, aryloxycarbonyl wherein aryl has from 6 to 14 carbon atoms and is, for example, phenyl, biphenylyl, 1- or 2-naphthyl, fluorenyl, or phenyl mono- or poly-substituted by lower alkyl, for example methyl or tart-butyl, hydroxy, lower alkoxy, for example methoxy, ethoxy or tart-butoxy, halogen, fox example chlorine or bromine, and/or by nitro, such as phenoxycarbonyl, aryl-lower allcoxycarbonyl, for example arylmethoxy-carbonyl, wherein aryl has from 6 to 14 carbon atoms and is, for example, phenyl, biphenylyl, 1- or 2-naphthyl, fluorenyl, or phenyl mono- or poly-substituted by lower alkyl, for example methyl or tent-butyl, hydroxy, lower alkoxy, for example methoxy, ethoxy or tent-butoxy, halogen, for example chlorine or bromine, and/or by nitro, for example phenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 4-nitrobenzyloxycarbonyl, diphenyl-lower alkoxycarbonyl, such as diphenylmethoxycarbonyl, di-(4-methoxyphenyl)-methoxy-carbonyl, trityloxycarbonyl or fluorenyl-lower alkoxycarbonyl, such as 9-fluorenyl-methoxycarbonyl, especially benzyloxycarbonyl, heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyri-midinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl,13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, from morpholinyl and from thiomorpholinyl and may be unsubstituted or substituted, especially by lower alkyl, such as methyl, such as 1-methyl-pyrrolidin-2-yl-methoxycarbonyl, 2-furylmethoxycarbonyl, 2-tetrahydrofuranyl-lower alkoxycarbonyl, such as 2-tetrahydrofuranyl-methoxycarbonyl, 1-methyl-2-piperidyl-i J

methoxycarbonyl or 2-morpholino-ethoxycarbonyl, or 2-, 3- or 4-pyridylmethoxycarbonyl, 2-tri-lower alkylsilyl-lower alkoxycarbonyl, such as 2-trimethylsilyloxyearbonyl, or 2-triarylsilyl-lower alkoxycarbonyl wherein aryl is phenyl or 1- or 2-naphthyl, such as triphenylsiiylethoxycarbonyl.
Preferred acyl groups Rl, R2, Rg and Rg of an unsubstituted or substituted carbamic acid, in addition to suitable radicals already mentioned as preferred aryl groups R1, R2, Rg and R9, are carbamoyl or unsubstituted or substituted N-alkyl- or N,N-dialkylcarbamoyl wherein the alkyl radical has up to 12 carbon atoms, preferably unsubstituted or substituted lower alkyl-or di-lower alkyl-carbamoyl, such as methyl-, ethyl-, propyl-, tent-butyl-, dimethyl-, diethyl- or di-n-propyl-carbamoyl, the substituents being selected from phenyl, for example in benzyl-carbamoyl, N-phenyl-lower alkyl-N-lower alkylcarbamoyl, such as N-benzyl-N-methyl-carbamoyl, or dibenzylcarbamoyl, heterocyclyl as defined under heterocyclyl-lower alkanoyl R1, R2, Rg and R9, preferably selected from thienyl, furyl, pyranyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, azepinyl, indolyl, benzimida;aolyl, 1H-indazolyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolinyl, cinnolyl, purinyl, pteridinyl, naphthyridinyl, 4H-quinolizinyl, 3,1-benzofuranyl, bent[e]indolyl, 4,1-benzoxazinyl, 4,1-benzothiazinyl, carbazolyl, (3-carbolinyl, phenazinyl, phenanthridyl, ac:ridyl, phenoxazinyl, phenothiazinyl, 1-azaacenaphthenyl, cyclohexa[b]pyrrolyl, cyclohepta[b]pyrrolyl, cyclohexa[d]pyrazolyl, cyclohexa[b]pyridyl, cyclohexa[b]pyrazinyl, cyclohexa[b]pyrimidinyl, cyclohexa[b]-1,4-oxazinyi, cyclohexa[b]-1,4-thiazinyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, 2-imidazolinyl, 2,3-dihydropyridyl, piperidyl, piperazinyl, 2,3,5,6-tetrahydropyrazinyl, morpholinyl, thiomorpholinyl, S,S-dioxothiomorpholinyl, indolinyl, isoindolinyl, 4,5,6,7-tetrahydroindolyl, 1,2,3,4-tetrahydroquinolyl, 1,2,3,4-tetrahydroisoquinolyl, chromanyl, thiochromanyl, 1,2,3,4-tetrahydro-3,1-benzodiazinyl, 3,4-dihydro-3H-4,1-benzoxazinyl, 3,4-dihydro-3H-4,1-benzothiazinyl, 2,3,4,~-tetrahydro--1H-5,1-benzazepinyl and 5,6-dihydrophenanthridinyl, the mentioned radicals being unsubstituted or substituted by lower alkyl, for example methyl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, for example benzyl, hydroxy-lower alkyl, far example hydroxymethyl or 2-hydroxyethyl, lower alkoxy-lower alkyl, for example methoxymethyl or 2-methoxyethyl, phenoxy-or naphthyloxy-lower alkyl, for example 2-phenoxyethyl, 1- or 2-naphthyloxymethyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, for example benzyloxy-lower alkyl, lower alkanoyloxy-lower alkyl, for example acetoxyrnethyl, phenyl- or naphthyl-~~ ~~~~a lower alkanoyloxy-lower alkyl, for example benzoyloxy-, phenylacetoxy- or 1-or 2-naphthoyloxy-metbyl, -2-ethyl or -2-(2,2-dimethylethyl), lower alkoxycarbonyloxy-lower alkyl, for example tert-butoxycarbo~nyloxy-lower alkyl, phenyl-, naphthyl- or ' fluorenyl-lower alkoxycarbonyloxy-lower alkyl, for example 2-benzyloxycarbonyl-oxyethyl or 9-fluorenylmethoxycarbonyloxyethyl, amino-lower alkyl, for example aminomethyl, 2-aminoethyl or 2-aminopropyl, carboxy-lower alkyl, for example carboxymethyl or 2-carboxyethyl, hydroxy, lower alkoxy, for example methoxy or etboxy, phenyl- or naphthyl-lower alkoxy, for example benzyloxy or 1- or 2-naphthylmethoxy, amino, lower alkylamino, for example methyl-, ethyl- or tert-butyl-amino, di-lower allcyl-amino, for example dimetbyl- or diethyl-amino, carboxy, lower alkoxycarbonyl, for example methoxy-, isopropoxy-, sec-butoxy- or tent-butoxy-carbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, for example benzyloxycarbonyl, halogen, for example fluorine, chlorine, bromine or iodine, especially chlorine or bromine, lower alkanoyl, for example acetyl or pivalayl, lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or dialkoxy-phosphoryl, for example dimethoxy- or diethoxy-phosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, for example N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, hydroxy-or carboxy-lower alkylcarbamoyl, for example hydroxy- or carboxy-methylcarbamayl or hydroxy- or carboxy-ethylcarbamoyl, sulfamoyl, nitro, oxo and/or by cyana, especially pyridyl, such as 2-, 3- or 4-pyridyl, more especially in N-heterocyclyl-lower alkyl-N-lower alkylcarbamoyl, for example N-pyridyl-lower alkyl-N-lower alkylcarbamoyl, such as N-(2-, 3- or 4-pyridylmethyl)-N-methyl-carbamoyl, or in N-heterocyclyl-lower alkyl-carbamoyl, for example 2- or 3-pyridyl-lower alkylaminocarbonyl, such as 2- or 3-pyridylmethylaminocarbonyl, hydroxy, for example in hydroxymethyl, 2-hydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl, N-dihydroxy-lower alkyl, such as 2,3-dihydroxy-n-propyl or 2-hydroxy-2,2-dimethylethyl, lower allcoxy, preferably in lower alkoxy-lower alkyl, for example methoxymethyl or 2-methoxyethyl, lower alkanoyloxy, preferably in lower alkanoyloxy-lawer alkyl, for example lower alkanoyloxymethyl or lower alkanoyloxyethyl, such as acetoxymethyl, 2-acetoxyethyl, 3-propionyloxymethyl, 2-propionyloxyethyl, 4-butyroxymethyl or 2-butyroxyethyl, aryloxy or aryloxy and hydroxy wherein aryl has from 6 to 14 carbon atoms, such as phenyl, naphthyl or fluorenyl, preferably in aryloxy-lower alkyl or aryloxyhydroxy-lower alkyl, such as phenoxymethyl, 2-phenoxyethyl, 1- or 2-naphthyloxymethyl or 1- or 2-naphthyloxyethyl, or 2-phenyl-2-hydroxyethyl, aryl being unsubstituted or mono- or di-substituted, for example by lower alkyl, for example methyl, ethyl, propyl, isopropyl, butyl, sec-butyl or tert-butyl, by hydroxy, by lower alkoxy, for example methoxy, ethoxy, propoxy, isopropoxy, butoxy, sec-butoxy or tert-butaxy, by carboxy, by lower alkoxycarbonyl, for example isopropoxycarbonyl, sec-trutoxycarb~>nyl or tert-butoxycarbonyl, or by carbamoyl, lower alkyl- or di-lower alkyl=carbamoyl andjcar by mono- or di-(hydroxy- or~
carboxy-lower alkyl)carbamoyl and it being possible for the rr~entioned substituents to be present in different ring positions, for example in the faun of 4-rnethylphenoxy, 2,4,x-tri-methylphenoxy, 4-hydroxyphenoxy, 4-methoxyphenaxy, 3,~-ciimethoxyphenoxy, 2.-carboxyphenoxy, 2-tert-butaxycarbanylphenoxy, 2- or 4-carbamoylphenaxy, carbamoyl, carboxy-lower allkylcarbamoyl or hydroxy-lower alkylcarbamcayl, such as in 4-carbamoyl-n-butyl, 7-carbamoyl-:n-heptyl, :.~-hydroxyethylcarbamoyl-n-butyl or 4-(tris[hydroxymethyl]methyl)-carbamoyl-n-butyl, and also ar~nino, for example in 2-aminoethyl or 3-aminoprapyl, lav~er alkylamino, fo~° example in methyl- or ethyl-aminomethyl, di-lower alkylamino, fc~r example in dimethylanair~omethyl, halogen, especially fluorine, chlorine or bromine, for example in 2,~,~;-tric~hloroethyl, sulfo, for example in sulfomethyl or 4-sulfobutylarnina, and sulfamoyl, for example in ~-sulfamoyl-ethyl.
Preferred acyl groups R1, R2, Rg and Rg of an unsubstituted or substituted N-substituted oxalamide are oxamoyl or lower alkyloxamovl, such as methyt- or ethyl-oxamoyl.
Preferred acyl groups R1, R2, Rg and Rg of an unsubstituted or substituted amino acid are farmed by the amino acid residues of an a- or (i-amine acid, especially a natural a-amino acid having the h-configuration, such as those normally occurring in proteins, or an epimer of such an amino acid, that is to say having the unnatura D-configuration, or a D,L-isomeric mi;cture thereof, a homologue of such an amino acid, far example wherein the amino acid side chain has been lengthened or shortened by one or two methylene groups, wherein the amino group is in the (3-position and/or wherein a methyl group has been replaced by hydrogen, a substituted aromatic amino acid wherein the aromatic radical has from 6 to 14 carbon atoms, for example a substituted phenyl-alanine ar phenylglycine wherein the phenyl may be mono- or poly-substituted by lower alkyl, for example methyl, hydroxy, lower alkuxy, far example methoxy, lower alkanoyl-oxy, for example acetoxy, amine, lower alkylamina, far ex;~mple methylamino, di-lower alkylamino, for example dimethylamino, lower alkanoylamino, fc~r example acetylamino or pivaloylamino, lower alkoxycarbonylamina, for example. teat-lautoxycarbonylamino, arylmethoxycarbonylamino wherein aryl preferably has from 6 to 14 carbon atoms, for example benzyloxycarbonylamino or 9-lluorenylmethoxycarbanylamina, halogen, for example fluorine, chlorine, bromine or iodine, carboxy and/or by nitro, a benzo-fused _2p~.
phenylalanine or phenylglycine, such as a-naphthylalanine, or a hydrogenated phenyl-alanine or phenylglycine, such as cyclohexylalanine or cyclohexylglycine.
7.'hose amino acids can be substituted at free amino or hydroxy functions, preferably at a free amino function, by one of the radicals mentioned abo~re under aryl R.I as the acyl.
group of a carboxylic acid, a semiester of carbonic acid, art unsubstituted or N-substituted carbamic acid or an unsubstituted or N-substituted oxalamide or by one of the radicals mentioned below under unsubstituted or substituted alkyl; aryl-lower alkyl;
heterocyclyl;
heterocyclyl-lower alkyl; sulfa; sulfonyl substituted by alkyl, w r I, aryl-lower alkyl, heterocyclyl-lower alkyl, alkoxy, aryloxy, aryl-lower alkoxy or by heteroc:yclyl-lower alkoxy; phosphoryl R 1, R2, Rg or Rc~ substituted by one or two identical or different radicals selected from alkyl, cycloal.kyl, cyc:lraalkyl-lower alkyd, ~~r°yl, aryl-lower alkyl, h:ydroxy, alkoxy, cycloalkaxy, uyclaalkyl-Iower alkaxy, ~~ryloxy and aryl-lower alkoxy;
and sulfamoyl R1, R2, Rg or R9, which is unsubstituted or substituted at the nitrogen atom; or by one of the radicals mentioned as protecting groups in the section relating to processes.
Especially preferred is the radical, bonded via a carboxy group, of an amino acid selected from glycine (H-Crly-OH), alarrine (;l;I-Ala-()I-l), saline (1-i-"'Val-OI-I), norvaline: (a-amino-vaeric acid), leucine (H-Leu-OH), isoleucine (H-Ile-OH), r~orleucine (a-aminohexanoic arid, H-Nle-OH), serine (H-Ser-OH), hamoserine (a-aminC>-y-hydroxybutyric acid), threonine (H-Thr-OH), methionine (1-1-Met-OH), cysteine (kI-(:'ys-OH), praline.
(I-1-Pro-OH), trans-3- and trans-4-hydroxyproline, phenylalanig~e (H-Phe-OH), tyrosine (H-Tyr-OH), 4-aminophenylalanine, 4-chlorophenylalan ine, 4-~,arboxyphenylalanine, I3-phenylserine (B-hydroxyphenylala:nine), phenylglycirte:, cx,-naphthylalanine (H-Nal-OH), cyclohexylalanine (H-Cha-OH), cyclohexylglycine, tryptophan (1-i-Trp-OI-i), indoline-2-carboxylic acid, 1,2,3,4-tetrahydroisoduinoline-3-carboxylic acid, aspartic acid (H-Asp-OH), asparagine (H-Asn-Ol-1), aminornalonic acid, aminornalonic acid mono-arnide, glutamic acid (H-Glu-OI-I), glutamine (lv-Gln-Ol-l), hiistwdine (H-His-OH), arginine (H-Arg-OH), lysine (H-Lys-OH), 8-hydroxylysine, arnithine (a,8-diaminovaleric acid)"
3-a.minopropanoic acid, a,y-diaminobutyric acid and a,li-diaminopropionic acid, especially preferably the radical of an aliphatic amino acid selecaed from valine, alanine, leucine and isoleucine, or an amino acid selected from glycine, glutamic acid and asparagine, it being possible for each of the mentioned amino acids (with the exception of gly~cine) to be in the D-, L- or (D,L)-form, preferably in the L-fc~rr~n (with the exception of Val which may also be in the (D)- or (U,L)-form), and wherein ~~~r~~~a the a-amino group may be unsubstituted or mono- or di-N-alkylated, far example by lower alkyl, such as methyl or n-propyl, by amino-lower alkyl, such as 3-aminopropyl, by phenyl- or naphthyl-amino-lower alkyl, such as 3-phenylaminopropyl, or by piperazinyl-' carbonyl-lower alkyl substituted at the nitrogen atom by lower alkyl, such as methyl, such as 4-methylpiperazinylcarbonylmethyl, or may be N-acylated, for example by lower alkanoyl, such as acetyl; by aryl-lower alkanoyl wherein aryl is selected from phenyl, indenyl, indanyi, naphthyl, anthryl, phenanthryl, acenaphthyl and fluorenyl and may be unsubstituted or especially mono- to tri-substituted by lower alkyl, for example methyl, ethyl or propyl, halo-lower alkyl, for example trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, for example methoxy, carbamoyl-lower alkoxy, N-lower alkyl-carbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine, chlorine or bromine, carbaxy, lower alkoxycarbonyl, such as tert-butoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, such as benzyloxy-carbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, for example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, caxbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylaminosulfonyl, vitro and/or by cyano, wherein phenyl may be present up to three times, for example in diphenyl-, dibenzyl- or triphenyl-lower alkanoyl, such as diphenyl-, dibenzyl-or triphenyl-acetyl, and wherein lower alkanoyl may be unsubstituted or substituted, for example by lower alkyl, for example methyl, heterocyclyl selected from pyrrolyl, furyl>
thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyndyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoguinolyl, quinoxalinyl, f3-carbolinyl and a benzo-, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, hydroxy, lower alkoxy, lower alkanoyloxy, for example acetoxy, propionyloxy, butyroxy, isobutyroxy or pivaloyloxy, acetoacetoxy, amino- or benzyloxycarbonylamino-lower alkanoyloxy, for example 2-amino- or 2-benzyloxycarbonylamino-2-methylpro-pionyloxy, aryl-lower alkanoyloxy wherein aryl has from 6 to 10 carbon atoms, for example in benzoyloxy, phenylacetoxy, 1- or 2-naphthoyloxy, lower alkoxycarbonyloxy, for example methoxy-, ethoxy-, n-propoxy-, isopropoxy-, n-butoxy-, isobutoxy-, sec-butoxy-, tent-butoxy-, n-pentyloxy-, isopentyloxy-, neopentyloxy-, tert-pentyloxy-, n-hexyloxy-, isohexyloxy- or n-heptyloxy-carbonyloxy, mono- or di-lower alkyl-amino-carbonyloxy, for example ethylaminocarbonyloxy or diethylaminocarbonyloxy, aryloxy-carbonyloxy wherein aryl has from 6 to 10 carbon atoms, for example phenoxycarbonyl-oxy or 1- or 2-naphthyloxycarbonyloxy, aryl-lower alkoxycarbonyloxy wherein aryl has from 6 to 14 carbon atoms, especially phenyl-lower alkoxycarbonyloxy, for example benzyloxycarbonyloxy, and also 1- or 2-naphthylmethoxycarbonyloxy or 9-fluorenyl-methoxycarbonyloxy, sulfonyloxy, lower allcylsulfonyloxy, for example methyl-, ethyl-, propyl-, isopropyl-, n-butyl-, isobutyl-, sec-butyl-, tert-butyl-, n-pentyl-, isopentyl-, neopentyl-, tent-pentyl-, n-hexyl-, isohexyl- or n-heptyl-sulfonyloxy, or phenylsulfonyl- , oxy, 2- or 4-toluenesulfonyloxy or 1- or 2-naphthylsnlfonyloxy, carboxy, esterified carboxy selected from lower alkoxycarbonyl, for example methoxy-, ethoxy-, n-propoxy-, isopropoxy-, n-butoxy-, isobutoxy-, sec-butoxy-, tert-butoxy-, n-pentyloxy-, isopentyloxy-, neopentyloxy-, tent-pentyloxy-, n-hexyloxy-, isohexyloxy- or n-heptyloxy-carbonyl, aryloxycarbonyl wherein aryl has from 6 to 10 carbon atoms, for example phenoxy-carbonyl or 1- or 2-naphthyloxycarbonyl, aryl-lower alkoxycarbonyl wherein aryl has from 6 to 12 carbon atoms, for example benzyloxycarbonyl, 1- or 2-naphthylmethoxy-carbonyl or 9-fluorenylmethoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, for example methyl- or tent-butyl-sulfonyl, hydroxy-lower alkoxyphosphoryl and di-lower alkoxy-phosphoryl, carbamoyl, carbamoyl substituted by one or two radicals selected from lower alkyl, such as methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tent-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, n-hexyl, isohexyl or n-heptyl, for example in N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, from carboxy-lower alkyl or lower alkoxycarbonyl-lower alkyl, for example in the form of carboxymethyl-carbamoyl (glycinylcarbonyl) or tert-butoxycarbonylrnethylcarbamoyl, from di-lower alkylamino-lower alkyl, for example 2-dimethylaminoethyl, aminocarboxy-lower alkyl, for example 5-amino-5-carboxypentyl, from hydroxy-lower alkyl, for example hydroxy-methyl or hydroxyethyl, and from di-lower alkoxy-lower alkyl, for example 2-(2,2-dimethoxyethyl), or carbamoyl substituted by one radical selected from ethylene, tri-methylene, tetramethylene and pentamethylene in which a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which may be unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piper-azin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, marpholino-, thiomorpholino- or S,S-dioxo-thiomorpholino-carbonyl; sulfamoyl, phosphono, benzofuranyl, oxo and/or by cyano and is unbranched or branched, preferably by aryl-lower alkanoyl wherein aryl has from 6 to 14 carbon atoms and is unsubstituted or substituted, for example by lower alkanoyl, such as in 2-benzyl-3-pivaloylpropionyl, or by lower alkylsulfonyl, such as in 2-benzyl-3-tert-butylsulfonylpropionyl, with phenyl-lower alkanoyl, for example phenylacetyl, being especially preferred; by heterocyclyl-lower alkanoyl selected from thienyl-y furyl-, pyranyl-, pyaolyl-, imidazolyl-, pyrazolyl-, oxazolyl-, isoxazolyl-, thiazolyl-, furazanyl-, tetrazolyl-, pyridyl-, pyrazinyl-, pyrimidinyl-, pyridazinyl-, azepinyl-, indolyl-, benz-imidazolyl-, 1H-indazolyl-, quinolyl-, isoquinolyl-, quinoxalinyl-, quinazolinyl-, cinnolyl-, 2fl~1?~~

purinyl-, pteridinyl-, naphthyridinyl-, 4H-quinolizinyl-, 3,1-benzofuranyl-, benz[e]-indolyl-, 4,1-benzoxazinyl-, 4,1-benzothiazinyl-, carbazolyl-, (3-carbolinyl-, phenazinyl-, phenanthridyl-, acridyl-, phenoxazinyl-, phenothiazinyl-, 1-azaacenaphthenyl-, cyclohexa-[b]pyrrolyl-, cyclohepta(b]pyrrolyl-, cyclohexa[d]pyrazolyi-, cyclohexa(b]pyridyl-, cyclo-hexa[b]pyrazinyl-, cyclohexa[b]pyrimidinyl-, cyclohexa[b]-1,4-oxazinyl-, cyclohexa[b]-1,4-thiazinyl-, pyrrolidinyl-, pyrrolinyl-, imidazolidinyl-, 2-imidazolinyl-, 2,3-dihydro-pyridyl-, piperidyl-, piperazinyl-, 2,3,5,6-tetrahydropyrazinyl-, morpholinyl-, thio-morpholinyl-, S,S-dioxothiomorpholinyl-, indolinyl-, isoindolinyl-, 4,5,6,7-tetrahydro-indolyl-, 1,2,3,4-tetrahydroquinolyl-, 1,2,3,4-tetrahydroisoquinolyl-, chromanyl-, thio-chromanyl-, 1,2,3,4-tetrahydro-3,1-benzodiazinyl-, 3,4-dihydro-3H-4,1-benzoxazinyl-, 3,4-dihydro-3H-4,1-benzothiazinyl-, 2,3,4,5-tetrahydro-1H-S,1-benzazepinyl-and S,6-dihydrophenanthridinyl-lower alkanoyl, the mentioned heterocyclyl radicals being unsubstituted or substituted by lower alkyl, for example methyl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, for example benzyl, hydroxy-lower alkyl, for example hydroxymethyl or 2-hydroxyethyl, lower alkoxy-lower alkyl, for example methoxymethyl or 2-methoxy-ethyl, phenoxy- or naphthyloxy-lower alkyl, for example 2-phenoxyethyl, 1- or 2-naphthyloxymethyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lowex alkyl, for example benzyloxy-lower alkyl, lower alkanoyloxy-lower alkyl, for example acetoxy-methyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, fox example benzoyloxy-, phenylacetoxy- or 1- or 2-naphthoyloxy-methyl, -2-ethyl or -2-(2,2-dimethylethyl), lower alkoxycarbonyloxy-lower alkyl, for example tert-buto:Kycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyloxy-lower alkyl, for example 2-benzyloxy-carbonyloxyethyl or 9-fluorenylmethoxycarbonyloxyethyl, amino-lower alkyl, for example aminomethyl, 2-aminoethyl or 2-aminopropyl, carboxy-lower alkyl, for example carboxymethyl or 2-carboxyethyl, hydroxy, lower alkoxy, for example methoxy or ethoxy, phenyl- or naphthyl-lower alkoxy, for example benzyloxy or 1- or 2-naphthylmethoxy, amino, lower alkylarnino, for example methyl-, ethyl- or tert-butyl-amino, di-lower alkyl-amino, for example dimethyl- or diethyl-amino, carboxy, lower alkoxycarbonyl, for example methoxy-, isopropoxy-, sec-butoxy- or tent-butoxy-carbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, for example benzyloxycarbonyl, halogen, for example fluorine, chlorine, bromine or iodine, especially chlorine or bromine, lower alkanoyl, for example acetyl or pivaloyl, lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or dialkoxy-phosphoryl, for example dimethoxy- or diethoxy-phosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, for example N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, hydroxy-or carboxy-lower alkylcarbamoyl, for example hydroxy- or carboxy-methylcarbamoyl or hydroxy- or carboxy-ethylcarbamoyl, sulfamoyl, nitro, axo and/or by cyano, for example pyridylcarbonyl, such as 2-, 3- or 4-pyridylcarbonyl, 3,4-dihydroxypyrrolidinylcarbonyl, N-benzyloxycaxbonyl-piperidin-4-ylcarbonyl, 1-methylpiperazin-4-ylcarbonyl, morpholinocarbonyl, thiomorpholinocarbonyl, S,S-dioxothiomorphalinocarbonyl, indol-2-ylcarbonyl, quinol-2-ylcarbonyl, pyridyiacetyl, such as 2- or 3-pyridylacetyl, imidazolylacetyl, such as imidazol-1-ylacetyl, morpholinylacetyl, such as morpholino-acetyl, pyridylpropionyl, such as 3-(2- or 3-pyridyl)propionyl, pyrrolidinylpropionyl, such as 3-(4-pyrrolidinyl)propionyl, morpholinylpropionyl, such as 3-morpholinopropionyl, or tetrazolylpropionyl, such as 3-(tetrazol-1-yl)-propionyl; by heterocyclyl-lower alkenoyl wherein heterocyclyl is selected especially from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, iso-quinolyl, quinoxalinyl,13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa-or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, for example pyrrolidyl-lower alkenoyl, such as N-pyrrolidyl-acryloyl, halo-lower alkanoyl containing up to 3 halogen atoms, for example a-haloacetyl, such as a-fluoro-, a-chloro-, a-bromo-, a-iodo-, a,a,a-trifluoro- or a,a,a-trichloro-acetyl, or halopropionyl, such as f3-chloro- or 13-bromo-propionyl; by lower alkoxycarbonyl, such as tert-butoxycarbonyl; by aryl-lower alkoxycarbonyl whexein aryl has from 6 to 14 carbon atoms and is selected, for example, from phenyl, naphthyl and fluorenyl, far example phenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl, or 9-fluorenylmethoxy-carbonyl; by heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is selected especially from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, axazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, !3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated and unsubstituted or substituted especially by lower alkyl, such as methyl, for example 1-methylpyrrolidin-2-yl-methoxycarbonyl, 2-furylmethoxycarbonyl, tetrahydrofuranyl-lower alkoxycarbonyl, such as 2-tetrahydro-furanyl-methoxycarbonyl, 1-methyl-2-piperidyl-methoxycarbonyl or 2-morpholino-ethoxycarbonyl; by carboxy-lower alkanoyl, such as 3-carboxypropionyl, 5-carboxy-pentanoyl or 6-carboxyhexanoyl; by lower alkoxycarbonyl-lower alkanoyl, such as 5-methoxycarbonylpentanoyl or 6-methoxycarbonylhexanoyl; by hydroxy-lower alkoxy-lower alkanoyl, such as 3-hydroxy-n-propoxycarbonyl; by amino-lower alkanoyl wherein the amino group is not in the a- or (3-position of the lower alkanayl radical, such as 5-aminopentanoyl; by phenyl-lower alkoxycarbonylamino-lower alkanoyl wherein the amino group is not in the a- or (3-position of the lower alkanoyl radical, such as 5-benzyi-oxycarbonylaminopentanoyl or 6-benzyloxycarbonylaminohexanoyl;

_25_ by amino-lower alkanoyl substituted at the amino nitrogen atom by heteracyclyl-lower alkanoyl, preferably as defined above for heterocyclyl-lower alkanoyl Rl, R2, Rg or Rg, especially by N-morpholino- or N-thiomorpholino-carbonyl, for example N-morpholino-or N-thiomorpholino-carbonylamino-lower alkanoyl, such as N-morpholino- or N-thio-morpholino-carbonylamino-acetyl;
by carbamoyl; by phenyl-lower alkylaminocarbonyl, such as benzylaminocarbonyl;
by N-di-lower alkylamino-lower alkyl-N-lower alkylaminocarbonyl, such as N-(2-dimethyl-amino)ethyl-N-methylaminocarbonyl; by N-dihydroxy-lower alkyl-N-lower alkylamino-carbonyl, such as N-(2,3-dihydroxy-n-propyl)-N-methylaminocarbonyl; by N-hetero-cyclyl-lower alkyl-N-lower alkylcarbamoyl wherein heterocyclyl is selected from thienyl, furyl, pyranyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, azepinyl, indolyl, benzimidazolyl, 1H-indazolyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolinyl, cinnolyl, purinyl, pteridinyl, naphthyridinyl, 4H-quinolizinyl, 3,1-benzofuranyl, benz[e]indolyl, 4,1-benz-oxazinyl, 4,1-benzothiazinyl, carbazolyl, [i-carbolinyl, phenazinyl, phenanthridyl, acridyl, phenoxazinyl, phenothiazinyl, 1-azaacenaphthenyl, cyclohexa[b]pyrrolyl, cyclohepta[b]-pyrrolyl, cyclohexa[d]pyrazolyl, cyclohexa[b]pyridyl, cyclohexa[b]pyrazinyl, cyclohexa-[b]pyrimidinyl, cyclohexa[b]-1,4-oxazinyl, cyclohexa[b]-1,4-thiazinyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, 2-imidazolinyl, 2,3-dihydropyridyl, piperidyl, piperazinyl, 2,3,5,6-tetrahydxopyrazinyl, morpholinyl, thiomorpholinyl, S,S-dioxothiomorpholinyl, indolinyl, isoindolinyl, 4,5,6,7-tetrahydroindolyl, 1,2"3,4-tetrahydroquinolyl, 1,2,3,4-tetra-hydroisoquinolyl, chromanyl, thiochromanyl, 1,2,3,4-tetrahydro-3,1-benzodiazinyl, 3>4-dihydro-3H-4,1-benzoxazinyl, 3,4-dihydro-3H-4,1-benzothiazinyl, 2,3,4,5-tetrahydro-1H-5,1-benzazepinyl and 5,6-dihydrophenanthridinyl, the mentioned radicals being nnsubsti-tuted or substituted by lower alkyl, for example methyl, phenyl, 1- or 2-naphthyl, phenyl--lower alkyl, for example benzyl, hydroxy-lower alkyl, for example hydroxyrnethyl or 2-hydroxyethyl, lower alkoxy-lower alkyl, fox example methoxymethyl or 2-methoxy-ethyl, phenoxy- or naphthyloxy-lower alkyl, for example 2-phenoxyethyl, 1- or 2-naphthyloxymethyl, phenyl-lower alkoxy- or naphthyl-lower aikoxy-lower alkyl, for example benzyloxy-lower alkyl, lower alkanoyloxy-lower alkyl, for example acetoxy-methyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, for example benzoyloxy-, phenylacetoxy- or 1- or 2-naphthoyloxy-methyl, -2-ethyl or -2-(2,2-dimethylethyl), lower alkoxycarbonyloxy-lower alkyl, for example tent-butoxycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyloxy-lower alkyl, for example 2-benzyloxy-carbonyloxyethyl or 9-fluorenylmethoxycarbonyloxyethyl, amino-lower alkyl, for example aminomethyl, 2-aminoethyl or 2-aminopropyl, carboxy-lower alkyl, for example ~~'~~'~8~~

carboxymethyl or 2-carboxyethyl, hydroxy, lower allcoxy, for example methoxy or ethoxy, phenyl- or naphthyl-lower alkoxy, for example benzyloxy or 1- or 2-naphthylmethoxy, amino, lower alkylamino, for example methyl-, ethyl- or tent-butyl-amino, di-lower alkyl=
amino, for example dimethyl- or diethyl-amino, carboxy, lower alkoxycarbonyl, for example methoxy-, isopropoxy-, sec-butoxy- or tent-butoxy-carbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, for example benzyloxycarbonyl, halogen, for example fluorine, chlorine, bromine or iodine, especially chlorine or bromine, lower alkanoyl, for example acetyl or pivaloyl, lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or dialkoxy-phosphoryl, for example di-methoxy- or diethoxy-phosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, for example N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, hydroxy-or carboxy-lower alkylcarbamoyl, for example hydroxy- or carboxy-methylcarbamoyl or hydroxy- or carboxy-ethylcarbarnoyl, sulfamoyl, nitro, oxo and/or by cyano, especially pyridyl, such as 2-, 3- or 4-pyridyl, for example 2- or 3-pyridyl-lower alkylaminocarbonyl, such as 2- or 3-pyridylmethylaminocarbonyl; by N-2-, N-3- or N-~1-pyridyl-lower alkyl-N-lower alkylaminocarbonyl, such as N-2-, N-3- or N-4-pyridylmethyl-N-methyl-aminocarbonyl;
by heterocyclyl-lower alkylcarbamoyl-lower alkanoyl, such as defined above for hetero-cyclyl-lower alkylcarbamoyl-lower alkanoyl Rl, R2, Rg or R~, for example 2-(N-morpholino-lower alkylcarbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(2-morpholino-ethyl)-carbaznoyl)-3-methyl-butyryl, or 2-(N-(pyridyl-lower alkyl)-carbamoyl)-lower alkanoyl, such as (2(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-3-methyl)-butyryl;
by sulfonyl; by lower alkylsulfonyl, such as methyl- or ethyl-sulfonyl; by arylsulfonyl wherein aryl has from 6 to 10 carbon atoms and, for example, is selected from phenyl and naphthyl and is unsubstituted or especially substituted by lower alkyl, such as methyl, or by lower alkoxy, such as methoxy, such as p-toluenesulfonyl; by heterocyclylsulfonyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, iso-quinolyl, quinoxalinyl,13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa-or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, from morpholinyl and from thiomorpholinyl and may be unsubstituted or substi-tuted, especially by lower alkyl, such as methyl, such as morpholinosulfonyl, thio-morpholinosulfonyl, piperidinosulfonyl, 4-methylpiperazinylsulfonyl or piperazino-sulfonyl (heterocyclylsulfonyl not being a substituent in preferred forms); by sulfamoyl or by sulfamoyl substituted by heterocyclyl-lower alkyl, wherein heterocyclyl is as last defined, and/or by lower alkyl, such as N-2-pyridylmethyl-N-methylaminosulfonyl, a carboxy group of the side chain is present in esterified or amidated form, for example in the form of a lower alkyl ester group, such as methoxycarbonyl or tart-butoxycarbonyl, an aryl ester group or an aryl-lower alkyl 'ester group, aryl being phenyl, 4-nitrophenyl, ' naphthyl or biphenylyl, for example in the form of a 4-nitrophenoxycarbonyl, benzyloxy-carbonyl or 9-fluorenylmethoxycarbonyl group, or in the form of a carbamoyl, a lower alkylcarbamoyl, such as methylcarbamoyl, a di-lower alkylaminocarbamoyl, such as dimethylcarbamoyl, a mono- or di-(hydroxy-lower alkyl)carbamoyl, such as hydroxy-methylcarbamoyl ar di(hydroxymethyl)carbamoyl, or mono- or di-(carboxy-lower alkyl)-carbamoyl group, such as a carboxymethylcarbamoyl or di-(carboxymethyl)carbamoyl group, an amino group of the side chain is present in alkylated form, for example in the form of mono- or di-lower alkylamino, such as n-butylamino or dimethylamino, or in acylated form, for example in the form of lower allcanoylamino, such as acetylamino or pivaloyl-amino, amino-lower alkanoylamino, such as 3-amino-3,3-dimethylpropionylamino, aryl-lower alkanoylamino wherein aryl has from 6 to 14 carbon atoms, for example phenyl, naphthyl or fluorenyl, and is unsubstituted or substituted by lower alkyl, hydroxy, lower alkoxy, carboxy, carbamoyl or by sulfamoyl, such as 4-hydroxyphenylbutyryl, lower alkoxycarbonylamino, such as tent-butoxycarbonylamino, arylmethoxycarbonylamino wherein aryl has from 6 to 14 carbon atoms, such as benzyloxycarbonylamino or 9-fluorenylmethoxycarbonylamino, piperidyl-1-carbonyl, morpholinocarbonyl, thio-morpholinocarbonyl or S,S-dioxothiomotpholinocarbonyl, and/or a hydroxy group of the side chain is present in etheiified or esterified form, for example in the form of a lower alkoxy, such as methoxy or tart-butoxy, aryl-lower alkoxy, such as benzyloxy, lower alkanoyioxy, such as acetoxy, or lower alkoxycarbonyloxy group, for example a tent-butoxycarbonyloxy group.
Special preference is given to acyl groups Rl, R2, Rg and R9 of an unsubstituted or substituted amino acid selected from phenylalanine, N-(benzyloxycarbonyl)-phenyl-alanine, N-(2(R,S)-benzyl-3-pivaloyl-propionyl)-phenylalanine, N-(9-fluorenylmethoxy-carbonyl)-phenylalanine, tyrosine, N-propyltyrosine, tyrosine-O-methyl ether, N-(3-amino-3,3-dimethylpropionyl)-tyrosine-O-methyl ether, N-(2(S)-benzyl-3-tart-butyl-sulfonylpropionyl)-tyrosine-O-tart-butyl ether, N-(9-fluorenylmethoxycarbonyl)-tyrosine-O-methyl ether, N-(9-fluorenylmethoxycarbonyl)-tyrosine-O-tart-butyl ether, N-morpholinocarbonyl-glycine, N-(N-(2-, 3- or 4-pyridyl)methyl-N-methylaminocarbonyl)-glycine, valine, N-(3-phenylaminopropyl)-valine, N-(4-methylpiperazinylcarbonyl-methyl)-valine, N-(trilluoroacetyl)-valine, N-phenylacetyl-valine, N-acetyl-valine, N-(3-phenylpropionyl)-valine, N-(2(R;S)- or -(~S)-benzyl-3-pivaloyl-propianyl)-valine, N-(2-carbamoyl-3-phenyl-propionyl)-valine, N-(2(S)-benzyl-3-tert-butylsulfonylpropionyl)-valine, N-(2(R,S)-carbamoyl-3-phenyl-propionyl)-valine, N-(2-, 3- or 4-pyridylcarbonyl)-valine, N-(1-imidazolylacetyl)-valine, N-(2- or 3-pyridylacetyl)-valine, N-(morpholino-acetyl)-valine, N-(3-(2- or 3-pyridyl)-propionyl)-valine, N-(3-(4-pyrrolidinyl)-propionyl)-valine, N-(3-(morpholino)-propionyl)-valine, N-(N-benzyloxycarbonylpiperidin-4-yl-carbonyl)-valine, N-tetrahydrofurylmethoxycarbonyl-valine, N-3-(tetrazol-1-yl)-propionyl-valine, N-(indol-2-ylcarbonyl)-valine, N-(quinoline-2-carbonyl)-valine, N-(1-methylpiperazin-4-ylcarbonyl)-valine, N-(3,4-dihydroxypyrrolidinylcarbonyl)-valine, N-methoxycarbonyl-valine, N-isobutoxycarbonyl-valine, N-tert-butoxycarbonyl-valine, N-benzyloxycarbonyl-valine, N-(2-furylmethoxycarbonyl)-valine, N-(1-methyl-pyrrolidin-2-yl-methoxycarbonyl)-valine, N-(1-methyl-2-piperidylmethoxycaxbonyl)-valine, N-(1-methyl-3-piperidyl-methoxycarbonyl)-valine, N-(2-(morpholino)ethoxy-carbonyl)-valine, N-(3-carboxypropionyl)-valine, N-(5-carboxypentanoyl)-valine, N-(6-carboxyhexanoyl)-valine, N-(5-methoxycarbonylpentanoyl)-valine, N-(6-methoxy-carbonylhexanoyl)-valine, N-(3-aminopropionyl)-valine, N-(4-aminobutyryl)-valine, N-(5-benzyloxycarbonylaminopentanoyl)-valine, N-(6-benzyloxycarbonylamino-hexanoyl)-valine, N-(morpholinocarbonyl)-valine, N-(thiomorpholinocarbonyl)-valine, N-(S,S-dioxothiomorpholinocarbonyl)-valine, N-(N-benzylaminocaxbonyl)-valine, N-(N-2-pyridylmethyl-N-methylaminocarbonyl)-valine, N-(N-3-pyridylmethyl-amino-carbonyl)-valine, N-(N-2-pyridylmethyl-aminocarbonyl)-valine, N-morpholino-carbonyl-amino-acetyl-vzline, N-(2-pyrrolidylacryloyl)-valine, N-methylsulfonyl-valine, N-morpholinosulfonyl-valine, N-(p-toluenesulfonyl)-valine, N-(4-methylpiperazinyl-sulfonyl)-valine, N-(N-(2-pyridylmethyl)-N-methyl-sulfamoyl)-valine, N-(N-2-pyridyl-methyl-N-methyl-aminocarbonyl)-valine, N-(3-aminopropyl)-leucine, N-acetyl-leucine, N-(3-aminopropionyl)-leucine, N-(2(R,S)- or N-(2S)-benzyl-3-pivaloyl-propionyl)-leucine, N-(2(S)-benzyl-3-tert-butylsulfonylpropionyl)-leucine, N-(2-, 3- or 4-pyridyl-carbonyl)-leucine, N-(4-thiomorpholinocarbonyl)-leucine, N-(4-(S,S-dioxothio-morpholino)carbonyl)-leucine, N-(4-aminobutyryl)-leucine, N-(3-hydroxy-n-propoxy-carbonyl)-leucine, N-(benzyloxycarbonyl)-leucine, N-(N-(2-(dimethylamino)ethyl)-N-methyl-aminocarbonyl)-leucine, N-(N-(2,3-dihydroxy-n-propyl)-N-methyl-amino-carbonyl)-leucine, N-acetyl-isoleucine, N-propionyl-isoleucine, N-(benzyloxycarbonyl)-isoleucine, N-(2(R,S)-benzyl-3-pivaloyi-propionyl)-norleucine, N-(2(S)-benzyl-3-tert-butylsulfonylpropionyl)-norleucine, N-(tert-butoxycarbonyl)-norleucine, N-(tert-butoxy-carbonyl)-serine, N-(benzyloxycarbonyl)-serine, N-acetyl-serine O-methyl ether, N-(benzyloxycarbonyl)-serine O-methyl ether, N-(2(R,S)-benzyl-3-pivaloyl-propionyl)-~~"~~'~

serine, N-benzyloxycarbonyl-glutamic acid, asparagine, N-benzyloxycarbonyl-asparagine, quinoline-2-carbonyl-asparagine, and N-(rnorpholinocarbonyl)-asparagine, the amino acid residues preferably being in the (L)- or (D,L)-form, and in the case of valine also in the (D)-form. ~ .-Unsubstituted or substituted alkyl R1, R2, Rg or R9 contains an alkyl radical having from 1 to 20, preferably up to.10, carbon atoms, is branched or unbranched, may contain instead of a methylene group a hetero atom selected from thia, aza and selena and is, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tart-pentyl, n-hexyl, isohexyl, n-heptyl, n-octyl, n-nonyl or n-decyl.
Preference is given to lower alkyl, for example methyl, ethyi, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tent-butyl, n-pentyl, isopentyl, neopentyl, tent-pentyl, n-hexyl, isohexyl or n-heptyl, which is unsubstituted or substituted.
Radicals suitable as substituents in substituted alkyl, preferably substituted lower alkyl, are the radicals mentioned for lower alkanoyl R1, R2, Rg and R9.
Substituted lower alkyl is preferably cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms and lower alkyl is as defined above, fox example cycloalkyl-methyl or -ethyl, preferably having a total of from 4 to 13 caxbon atoms, for example cyclopropyl-, cyclobutyl-, cyclopentyl-or cyclo-hexyl-lower alkyl, such as -methyl or -ethyl, cycloalkenyl-lower alkyl, for example cycloalkenylmethyl, wherein cycloalkyl preferably has from 4 to 8 carbon atoms, such as 1-cyclohexenylmethyl, 1,4-cyclohexa-dienylmethyl or 1-cyclohexenylethyl or 1,4-cyclohexadienylethyl, bicycloalkyl-lower alkyl wherein bicycloalkyl has, fox example, from 5 to 10 carbon atoms, for example bicycloalkyl-methyl or -ethyl, preferably having from 8 to 11 carbon atoms, such as decahydronaphthyl-2-methyl, endo- or exo-norbornyl-2-methyl, bicyclo-[2.2.2]oct-2-ylmethyl or bicycla[3.3.1]non-9-ylmethyl, and also bicyclo-hexyl-, -heptyl-, -octyl-, -nonyl- or -decyl-ethyl or -3-propyl, for example bicyclo[3.1.0]hex-1-, -2- or -3-yl-, bicyclo[4.1.0]kept-1- or -7-yl-, bicyclo[2.2.1]kept-2-yl-, for example endo- or -exo-norbornyl-, bicyclo[3.2.1]oct-2-yl-, bicyclo[3.3.0]oct-3-yl- or bicyclo[3.3.1]-non-9-yl-, and also a- or 13-decahydronaphthyl-ethyl or -3-propyl, tricycloallcyl-lower alkyl wherein tricycloallcyl contains, for example, from 8 to 10 carbon atoms, for example tricycloalkyl-methyl or -ethyl, preferably having from 8 to I 1 carbon atoms, such as I- or 2-adamantylmethyl, and also tricyclo[5.2.1.02~6Jdec-8-yl- or adamantyl-, such as 1-adarnantyl-ethyl, , aryl-lower alkyl wherein especially - aryl has from 6 to 14 carbon atoms, such as in phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, which may be unsubstituted or especially mono- to tri-substituted by lower allcyl, for example methyl, ethyl or isopropyl, halo-lower alkyl, such as trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, for example methoxy, carbamoyl-lower alkoxy, N-lower alkyicarbamoyl-lower allcoxy or N,N-di-lower alkylcaxbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine or chlorine, carboxy, lower alkoxycarbonyl, benzyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanayl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxy-phosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylearbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano, wherein phenyl may be present up to three times, such as in diphenyl-, dibenzyl- or triphenyl-lower alkyl, for example Biphenyl-, dibenzyl- or triphenyl-2-ethyl, and wherein lower alkyl is unsubstituted or substituted, for example by lower alkyl, such as methyl, heterocyclyl selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, 13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, hydroxy, lower alkoxy, lower alkanoyloxy, such as acetoxy, propionyloxy, ba~tyroxy, isobutyroxy or pivaloyloxy, acetoacetoxy, amino- or benzyloxycarbonylamino-louver alkanoyloxy, such as Z-amino- or 2-benzyloxycarbonylamino-2-methylpropionyloxy> aryl-lower alkanoyloxy wherein aryl has from 6 to 10 carbon atoms, such as in benzoyloxy, phenylacetoxy, 1- or 2-naphthoyl-oxy, lower alkoxycarbonyloxy, for example methoxy-, ethoxy-, n-propoxy-, isopropoxy-, n-butoxy-, isobutoxy-, sec-butoxy-, tert-butoxy-, n-pentyloxy-, isopentyloxy-, neopentyl-oxy-, tent-pentyloxy-, n-hexyloxy-, isohexyloxy- or n-heptyloxy-carbonyloxy, mono- or di-lower alkyl-aminocarbonyloxy, such as ethylaminocarbonyloxy or diethylamino-carbonyloxy, aryloxycarbonyloxy wherein aryl has from 6 to 10 carbon atoms, for example phenoxycarbonyloxy or 1- or 2-naphthyloxycarbonyloxy, aryl-lower alkoxy-carbonyloxy wherein aryl has from 6 to 12 carbon atoms, for example phenyl-lower alkoxycarbonyloxy, such as benzyloxycarbonyloxy, and also 1- or 2-naphthylmethoxy-carbonyloxy or 9-fluorenylmethoxycarbonyloxy, sulfonyloxy, lower alkylsulfonyloxy, for example methyl-, ethyl-, propyl-, isopropyl-, n-butyl-, isobutyl-, sec-butyl-, tert-butyl-, n-pentyl-, isopentyl-, neopentyl-, tert-pentyl-, n-hexyl-, isohexyl- or n-heptyl-sulfonyloxy, phenylsulfonyloxy, 2- or 4-toluenesulfonyloxy, 1- or 2-naphthylsulfonyloxy, amino, ~'~ ~f~a mono- or di-lower alkylamino, N-lower alkoxy-N-lower alkylamino, such as N-methoxy-N-methylamino, mono- or di-(phenyl- or -naphthyl-lower alkyl)amino, such as benzyl-amino, lower alkanoylamino, such as pivaloylamino, carboxy, esterified carboxy selected from lower alkoxycarbonyl, for example methoxy-, ethoxy-, n-propoxy-, isopropoxy-, n-butoxy-, isobutoxy-, sec-butoxy-, tert-butoxy-, n-pentyloxy-, isopentyloxy-, neo-pentyloxy-, tent-pentyloxy-, n-hexyloxy-, isohexyloxy- or n-heptyloxy-carbonyl, aiyloxy-carbonyl wherein aryl has from 6 to 10 carbon atoms, for example phenoxycarbonyl or f-or 2-naphthyloxycarbonyl, aryl-lower alkoxycarbonyl wherein aryl has from 6 to carbon atoms, for example benzyloxycarbonyl, 1- or 2-naphthylmethoxycarbonyl or 9-fluorenylmethoxycarbonyl, lower alkanoyl, such as pivaloyl or acetyl, lower alkyl-sulfonyl, such as tert-butylsulfonyl, hydroxy-lower alkoxyphosphoryl and di-lower alkoxyphosphoryl, carbamoyl, carbamoyl substituted by one or two radicals selected from lower alkyl, for example methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, n-hexyl, isohexyl or n-heptyl, such as in N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, from carboxy-lower alkyl or lower alkoxycarbonyl-lower alkyl, for f;xample in the form of carboxy-methylcarbamoyl (glycinylcarbonyl) or tent-butoxycarbonylmethylcarbamoyl, from di-lower alkylamino-lower alkyl, for example 2-dimethylaminoethyl, from aminocarboxy-lower alkyl, such as 5-amino-5-carboxypentyl, from hydroxy-lower alkyl, far example hydroxymethyl or hydroxyethyl, and from di-lower al;koxy-lower alkyl, for example 2-(2,2-dimethoxyethyl), or carbamoyl substituted by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene in which a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which may be unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino-or S,S-di-oxothiomorpholino-carbonyl; sulfamoyl, phosphono, benzfuranyl, oxo (which is not present at the carbon atom bonded to the amino nitrogen atom linked to Rl, R2, Rg or R~) and/or by cyano and is unbranched or branched, is especially selected from phenyl-lower alkyl, such as benzyl that is unsubstituted or mono- or poly-substituted in the benzyl radical by lower alkyl, for example methyl, phenyl, hydroxy, lower alkoxy, for example methoxy, halogen, for example chlorine, vitro, and/or by cyano, such as 4-methoxy-, 4-fluoro-, 4-chloro-, 4-vitro- or 4-cyano-benzyl, naphthylmethyl, such as a-or 1i-naphthyl-methyl, indenylmethyl, for example 1-, 2- or 3-indenylmethyl, indanylmethyl, such as f-or 2-indanylmethyl, and phenanthrenylmethyl, such as 9-phenanthrenylmethyl, 2-phenyl-ethyl, 2-a-naphthylethyl, 2-13-naphthylethyl, 2-lower alkylphenyl-ethyl, such as 2-(4-methylphenyl)ethyl, 2-lower alkoxyphenylethyl, such as 2-(4-methoxyphenyl)ethyl, 2,2-diphenylethyl, 2,2-di(4-methoxyphenyl)ethyl, 2,2,2-triphenylethyl and 2,2-dibenzylethyl, from phenyl-lower alkyl substituted in the 2- and p-positions by two radicals selected from phenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl, and lower alkanoylamino, such as pivaloylamino, such as 2,p-dibenzyloxycarbonylamino-phenylethyl or 2-pivaloyl-amino-p-benzyloxycarbonylamino-phenylethyl, 2,p-diamino-phenylethyl, 3-phenylpropyl, 3-(p-hydroxyphenyl)-propyl, 3-a- or 3-~i-naphthylpropyl, 2-benzyl-3-(1-pyrazolyl)-propyl, 3-phenyl- or 3-a-naphthyl-2-hydroxy-propyl, 3-phenyl- or 3-a-naphthyl-2-lower alkoxy-propyl, such as 3-phenyl- or 3-a-naphthyl-2-neopentyloxy-propyl, 3-phenyl- or 3-a-naphthyl-2-lower alkanoyloxy-propyl, such as 3-phenyl-2-pivaloyloxy- or -2-acetoxy-propyl, 2-benzyl- or 1- or 2-naphthyl-3-(N-methoxyl-N-methylamino)-propyl, 3-phenyl-or 3-a-naphthyl-2-dimethylaminomethyl-propyl, 3-a-naphthyl-2-pivaloyloxy- or -2-acetoxy-propyl, 3-a-naphthyl-2-acetoacetoxy-propyl, 3-a-naphthyl-2-ethylamino-carbonyloxy-propyl or 3-a-naphthyl-2-((2-amino- or 2-benzyloxycarbonylamino)-2-methylpropionyloxy)-propyl, 3-phenyl- or 3-a-naphthyl-2-carboxymethylpropyl, 3-phenyl- or 3-a-naphthyl-2-lower alkoxycarbonyl-propyl, such as 3-a-naphthyl-ethoxycarbonyl-propyl, 3-phenyl- or 3-a-naphthyl-2-benzyloxycaxbonylmethyl-propyl, 2-(S)-benzyl-3-tert-butylsulfonyl-propyl, 3-phenyl-2-phosphono- or -phosphonomethyl-propyl, 3-phenyl-2-dimethoxyphosphoryl- or -dimethoxyphosphorylmethyl-propyl, 3-phenyl-2-diethoxyphosphoryl- or -diethoxyphosphorylmethyl-propyl, 3-phenyl-2-ethoxy- or -methoxyhydroxyphosphoryl-propyl, 3-phenyl- or 3-a-naphthyl-2-carbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-tert-butylcarbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-(2-dimethylaminoethyl)carbamoyl-propyl, 3-a-naphthyl-2-(carboxy-or tent-butoxycarbonyl)methylcarbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-(3-hydroxy-2-propyl)carbarnoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-(2,2-dimethoxyethyl)-carbamoylpropyl, 3-phenyl- or 3-a-naphthyl-2-(5-amino-5-carboxypentyl)-carbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-cyano-propyl, 3-phenyl- or 3-a-naphthyl-2-cyano-methyl-propyl, 3-phenyl- or 3-a-naphthyl-2-acetonyl-propyl, 4-hydroxyphenylbutyl, 4-phenyl- or 4-a-naphthyl-3-carboxy-butyl, 4-phenyl- or 4-a-naphthyl-3-benzyloxy-carbonyl-butyl, 2-benzyl-4-(2-benzofuranyl)-4-oxobutyl, 2-benzyl- or 2-a-naphthyl-methyl-4-cyano-butyl, 2-benzyl- or 2-a-naphthylmethyl-5-dimethylamino-pentyl, 2-benzyl- or 2-a-naphthylmethyl-4-oxo-pentyl, 2-benzyl- or 2-a-naphthylmethyl-4,4-dimethyl-3-oxo-pentyl, 2-benzyl- or 2-a-naphthyimethyl-5-dimethylamino-4-oxo-pentyl or 2-benzyl- or 2-a-naphthylmethyl-5,5-dimethyl-4-oxo-hexyl, preferably phenyl-lower alkyl, such as benzyl, 2-phenylethyl or 3-phenylpxopyl, 4-hydroxybenzyl, 1- or 2-naphthyimethyl or 1- or 2-naphthyl-2-ethyl, especially phenyl-lower alkyl as last defined, heterocyclyl-lower alkyl containing especially unsubstituted or substituted heterocyclyl as mentioned under heterocyclyl-lower alkanoyl Rly R2, Rg and R9 and lower alkyl that is unsubstituted or substituted in the same manner as lower alkanoyl in heterocyclyl-lower alkanoyl R1, R2, Rg and R9 (oxo not being present at the carbon atom bonded to the nitrogen atom carrying the .radical R1, R2, Rg or R9), for example methyl, 2-ethyl or 3-propyl bonded to unsubstituted or lower alkyl- or phenyl-substituted pyrrolyl, such as 2-or 3-pyrrolyl, 4- or 5-methylpyrrolyl or 4- or 5-phenylpyrrolyl, thienyl, such as 2-thienyl, furyl, such as 2-furyl, pyrazolyl, such as 1-pyrazolyl, tetrazolyl, such as tetrazol-1-yl, pyridyl, such as 2-, 3- or 4-pyridyl, indolyl that is unsubstituted or substituted by lower alkyl, for example methyl, phenyl-lower alkyl, for example benzyl, lower alkoxy, for example methoxy, phenyl-lower alkoxy, for example benzyloxy, or by halogen, for example by chlorine, such as 2-, 3- or 5-indolyl, 1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl, 1-benzylindol-2-yl or -3-yl, 4,5,6,7-tetrahydroindol-2-yl, cyclohepta[b]pyrrol-5-yl, unsubstituted or hydroxy-substituted quinolyl, such as 2-, 3- or 4-quinolyl or 4-hydroxyquinol-2-yl, unsubstituted or hydroxy-substituted isoquinolyl, such as 1-, 3- or 4-isoquinolyl or 1-oxo-1,2-dihydroisoquinol-3-yl, 2-quinoxalinyl, 3,1-benzfuran-2-yl, benz[e]indol-2-yl, (3-casbolin-3-yl, 3-chromanyl, 3-thiochromanyl, 3-pyrrolidinyl, hydroxypyrrolidinyl, such as 3- or 4-hydroxypyrrolidin-2-yl, oxopyrrolidinyl, such as 5-oxopyrrolidin-2-yl, piperidinyl, such as 2-, 3- or 4-piperi-dinyl, morpholinyl, such as 2- or 3-morpholinyl, thiomorpholinyl, such as 2-or 3-thio-morpholinyl, S,S-dioxothiomorpholinyl, such as S,S-dioxothiomorpholin-2- or -3-yl, indolinyl, such as 2- or 3-indolinyl, 1,2,3,4-tetrahydroquinolyl, such as 1,2,3,4-tetrahydro-quinol-2-, -3- or -4-yl, 1,2,3,4-tetrahydroisoquinolyl, such as 1,2,3,4-tetrahydroiso-quinol-1-, -2- or -3-yl, or 1-oxo-1,2,3,4-tetrahydroisoquinol-3-yl, or 4-pyrrolidinylmethyl or 1-imidazolylmethyl, hydroxy-lower alkyl, such as 3-hydroxypropyl or 2-hydroxy-3-methylpentyl, lower alkoxy-lower alkyl, for example lower alkoxyethyl or lower alkoxypropyl, such as 2-methoxyethyl, 2-ethoxyethyl or 3-methoxypropyl, lower alkoxy-lower alkoxy-lower alkyl, such as 2-methoxymethoxy-3-methyl-pentyl, phenoxy-lower alkyl or nitrophenoxy-lower alkyl, such as phenoxyrnethyl, phenoxyethyl or 4-nitrophenoxymethyl, naphthyloxy-lower alkyl, for example a- or 13-naphthyloxyethyl, lower alkanoyloxy-lower alkyl, for example lower alkanoyloxyethyl or lower alkanoyl-oxypropyl, such as acetoxyethyl or 3-acetoxypropyl, acetoacetoxy-lower alkyl, arylmercapto-lower alkyl wherein aryl has from 6 to 10 carbon atoms, for example ~~'~~'~~

phenyl or naphthyl, such as phenylmercaptomethyl, amino-lower alkyl, such as 3-aminopropyl or 5-aminopentyl, mono- or di-lower alkylamino-lower alkyl, such as dimethylaminoethyl or 2-dimethyl-' amino-2-isopropylethyl, phenyl- or naphthyl-amino-lower alkyl, such as 3-phenylaminopropyl, lower alkanoylamino-lower alkyl, such as 4-acetylaminopentyl, piperazinylcarbonyl-lower alkyl substituted at the nitrogen atom by lower alkyl, such as methyl, such as 4-methylpiperazinylcarbonylmethyl, lower alkoxycarbonylamino-lower alkyl, such as 5-(tent-butoxycarbonylamino)-pentyl or 3-ethoxycarbonylamino-2-isobutyl-propyl, phenyl-lower alkoxycarbonylamino-lower alkyl, such as 5-(benzyloxycarbonylamino)-pentyl, aminocarbonylamino-lower alkyl, such as aminocarbonylamino-ethyl, N-phenyl-lower alkyl-N-lower allcylaminocarbonylamino-lower alkyl, for example isobutyl-3-(N-benzyl-N-methylaminocarbonylamino)propyl, halo-lower alkyl, for example 2-haloethyl, such as 2-fluoro-, 2-chloro-, 2-bromo-, 2-iodo-, 2,2,2-trifluoro- or 2,2,2-trichloro-ethyl, trifluoro-lower alkyl, such as trifluoro-methyl, or halopropyl, such as 3-chloro- or 3-bromopropyl, carboxy-lower alkyl, for example carboxyethyl or 3-carboxypropyl, lower alkoxycarbonyl-lower alkyl, for example lower alkoxycarbonylethyl or lower alkoxycarbonylpropyl, such as methoxycarbonylethyl, 3-methoxycarbonylpropyl, ethoxy-carbonylethyl or 3-ethoxycarbonylpropyl, 2-halo-lower alkoxycarbonyl-lower alkyl, such as 2-chloro-, 2-bromo-, 2-iodo-or 2,2,2-trichloro-ethoxycarbonyl-2-ethyl or -3-propyl, phenyl- or naphthyl-lower alkoxycarbonyl-lower alkyl, for example benzyloxy-carbonyl-lower alkyl, such as 3-benzyloxycarbonyl-2,2-dimethylpropyl, heterocyclyl-lower alkoxycarbonyl-lower alkyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl,13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, it also being possible for the mentioned radicals to be fully or partially saturated, such as in 4-pyridylmethoxycarbonyl-2-ethyl or -3-propyl or 2-rnorpholinocarbonyloxy-4-methyl-pentyl, lower alkylsulfonyl-lower alkyl, such as 2-ethylsulfonyl- or 2-tert-butylsulfonyl-methyl, arylsulfonyl-lower alkyl wherein aryl preferably has from 6 to 10 carbon atoms, for example phenyl or naphthyl, such as phenylsulfonylmethyl, 2~~'~ ~"~~~

carbamoyl-lower alkyl, such as carbamoylethyl or 3-carbamoylpropyi, lower alkylcarbamoyl-lower alkyl, for example lower alkylcarbamoylethyl or methyl-carbamoyl-lower alkyl, such as 2-methylcarbamoylethyl, di-lower alkylcarbamoyl-lower'alkyl, for example 2-di-lower alkylcarbamoylethyl or dimethylcarbamoyl-lower alkyl, such as 2-dimethylcarbamoylethyl, hydroxy-lower alkylcarbamoyl- or di(hydroxy-lower alkyl)carbamoyl-lower alkyl, such as 2-hydroxymethylcarbamoyl- or di(hydroxymethyl)carbamoyl-2-ethyl or -3-propyl, N-lower alkoxy-lower alkoxy-lower alkylcarbamoyl-lower alkyl, such as 2-isobutyl-3-(2-(2-methoxyethoxy)ethylaminocarbonyl)-propyl, carboxy-lower alkylcarbamoyl- or di(carboxy-lower alkyl)carbamoyl-lower alkyl, such as carboxymethyl- or di(carboxymethyl)carbamoyl-2-ethyl or -3-propyl, carbamoyl-lower alkyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom may have been replaced by nitrogen, oxygen, sulfi~r or by sulfur mono- or di-substituted by oxygen, it being possible for the radical so formed also to be fully or partially unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomozpholino-carbonyl-lower alkyl, such as in 2-morpholinocarbonyl-ethyl, 3-(morpholinocarbonyl)-propyl or 3-(morpholinocarbonyl)-2-isobutyl-propyl, N-lower alkyl-N-heterocyclyl-lower alkylcarbamoya-lower alkyl wherein heterocyclyl is preferably selected from pyrrolyl, furyi, thienyl, imidazolyi, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoduinolyl, quinoxalinyl, Ci-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be .fully or partially saturated, such as 2-(N-2-pyridylmethyl)-N-methylcarbamoyl-ethyl, suifamoyl-lower alkyl, such as 2-sulfamoylethyl, N-(phenyl- or naphthyl-lower alkyl)sulfamoyl-lower alkyl, such as 3-benzylamino-sulfonyl-2-isopropyl-propyl, or sulfamoyl-lower allcyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene and pentameihylene wherein a carbon atom may have been replaced by nitrogen, lower alkyl-substituted, such as methyl-substituted, nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, it being possible for the radical so formed also to be fully or partially unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, 4-methylpiperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomorpholino-sulfonyl-lower alkyl, such as 3-(4-methylpiperazinylsulfonyl)-2-isopropyl-propyl or 3-(4-morpholiny-sulfonyl)-2-isopropyl-propyl, oxo-lower alkyl (wherein oxo is not present at the carbon atom bonded to the nitrogen atom carrying the radical R1, R2, Rg or Rg), such as 3-oxo-n-butyl or 3-oxo-n-pentyl, cyano-lower alkanoyl, such as cyanomethyl, 2-cyanoethyl, 2- or 3-cyano-n-propyl or 2-, 3- or 4-cyano-n-butyl, hydroxy-carboxy-lower alkyl, such as 2-hydroxy-2-carboxy-ethyl or 2-hydroxy-3-carboxypropyl, a-naphthyloxy-carboxy-lower alkyl, such as 2-a-naphthyloxy-4-carboxy-n-butyl, hydroxy-lower alkoxycarbonyl-lower alkyl, for example 2-hydroxy-2-lower alkoxy-carbonyl-ethyl or -propyl or hydroxy-ethoxy- or hydroxy-methoxy-carbonyl-lower alkyl, such as 2-hydroxy-2-ethoxy- or -methoxy-carbonylethyl or 2-hydroxy-3-ethoxy-or -methoxy-carbonylpropyl, a-naphthyloxy-lower alkoxycarbonyl-lower alkyl, for example a-naphthyloxy-lower alkoxycarbonyl-2-ethyl, -2-propyl or -2-butyryl or a-naphthyloxyethoxycarbonyl-lower allcyl, such as a-naphthyloxy-ethoxycarbonyl-2-ethyl, 2-a-naphthyloxy-3-ethoxycarbonyl-propyl or 2-a-naphthyloxy-4-tent-butoxycarbonylbutyl, a-naphthyloxy-benzyloxycarbonyl-lower alkyl, such as 2-a-naphthyloxy-3-benzyloxy-carbonyl-propyl, esterified hydroxy-lower alkoxycarbonyl-lower alkyl wherein the hydroxy group is esterified by lower alkanoyl, for example acetyl, prop:ionyl or pivaloyl, cycloalkyl-lower alkanoyl wherein cyclo~dkyl has from 3 to 7 carbon atoms and lower alkanoyl is as last defined, for example cyclohexylcarbonyl or 2-cyclohexyl- or 2-cyclopentyl-acetyl, bicycloalkyl-lower alkanoyl wherein bicycloalkyl has, for example from 5 to 10, especially from 6 to 9, carbon atoms, such as in bicyclo-hexyl-, -heptyl-, -octyl-, -nonyl-or -decyl-acetyl or -3-propionyl, fox example bicyclo[3.1.0]hex-1-, -2- or -3-yl-, bicyclo-[4.1.0]hept-1- or -7-yl-, bicyclo[2.2.1]kept-2-yl-, for example endo- or exo-norbornyl-, bicyclo[3.2.1]oct-2-yl-, bicyclo[3.3.0]oct-3-yl- or bicyclo[3.3.1]non-9-yl-, and also a- or 13-decahydronaphthyl-acetyl or -3-propianyl, tricycloalkyl-lower alkanoyl wherein tri-cycloalkyl contains, for example, from 8 to 10 carbon atoms, for example m tricyclo-[5.2.1.02~6]dec-8-yl- or adamantyl-, such as 1-adamantyl-acetyl, aryl-lower alkanoyl wherein aryl has from 6 to 14 carbon atoms, for example phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, which may be unsubstituted or mono- to tri-substituted by lower alkyl, hydroxy, lower alkoxy, carbamoyl-lower allcoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such as fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, for example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, sx~lfamoyl, nitro and/or by cyano, lower alkoxycarbonyl, for example tent-butoxycarbonyl, 2-halo-lower alkoxy-carbonyl as defined above, or by phenyl- or fluorenyl-lower alkoxycarbonyl, far example benzyloxycarbonyl or 9-fluorenylmethoxycarbonyl, such as 2-acetoxy-2-methoxy-carbonyl-ethyl, 2-benzoyloxy-, 2-(1- or 2-naphthoyloxy)-, 2-(phenyl-2-acetoxy)-, 2-(1- or 2-naphthyl-2-acetoxy)-, 2-(4-methylphenyl-2-acetoxy)-, 2-(4-methoxyphenyl-2-acetoxy)-or 2-(2-(o,o-dichlorophenyl)2-acetoxy)-2-methoxycarbonyl-ethyl or -3-propyl, dihydroxy-carboxy-lower alkyl, such as 2,3-dihydroxy-3-carboxy-propyl, dihydroxy-lower alkoxycarbonyl-lower alkyl, such as 2,3-dihydroxy-3-ethoxy- or -methoxy-carbonyl-propyl, dihydroxy-lower alkoxycarbonyl-lower alkyl esterified by lower alkanoyl, such as acetyl, propionyl or butyryl, lower alkoxycarbonyl, for example tert-butoxycarbonyl, phenyl- or fluorenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl or 9-fluorenyl-methoxycarbonyl, lower alkylsulfonyl or by toluenesulfonyl, for example di-lower alkanoyloxy-lower alkoxy-propyl, such as 2,3-diacetoxy-3-methoxycarbonyl-propyl, a-naphthyloxy-di-lower alkylamino-lower alkyl, such as 2-a-naphthyloxy-5-dimethyl-aminopentyl, a-naphthyloxy-carbamoyl-lower alkyl, such as 2-a-naphthyloxy-4-carbamoyl-butyl, a-naphthyloxy-oxo-lower alkyl (wherein oxo is nol: present at the carbon atom bonded to the nitrogen atom carrying the radical R1, R2, Rg or 1(t9), such as 2-a-naphthyloxy-4-oxo-pentyl, or a-naphthyloxy-cyano-lower alkyl, such as 2-a-naphthyloxy-cyano-ethyl or 2-a-naphthyloxy-4-cyanobutyl.
Lower alkyl, such as methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl or tert-butyl, is especially preferred.
Alkenyl Rt, R2, Rg or Ry preferably contains from 2 to 10 carbon atoms, is preferably lower alkenyl having from 2 to 7, especially from 2 to 4, carbon atoms and is, for example, vinyl, allyl or 2- or 3-butenyl. Lower alkenyl Rt, R2, R8 or R9 may be substituted by the same substituents as may lower alkyl, for example by cycloalkyl, as defined in the case of cycloalkyl-lower alkanoyl Rt, R.,, R8 or R9, that is unsubstituted or mono- to tri-substi-tuted by lower alkyl, such as isopropyl, halo-lower alkyl, such as trifluoromethyl, hydroxy, lower alkoxy, earbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such 2~"~~"~~~

as fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, for example methyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkyl-sulfamoyl, nitro and/or by cyano and is bonded, especially at the terminal carbon atom, to lower alkenyl, such as in cyclobutyl-, cyclopentyl-, cyclohexyl- or cycloheptyl-methyl-2-vinyl, -2- or -3-allyl or -2-, -3- or -4-but-2-enyl; aryl, as defined under aryl-lower alkanoyl Rl, R2, R8 or R9, that is unsubstituted or substituted and is bonded, preferably terminally, to lower alkenyl, such as in styryl, 3-phenylallyl (cinnamyl), 2-(a-naphthyl)-vinyl or 2-((3-naphthyl)-vinyl; unsubstituted or substituted heterocyclyl, as defined under hetero-cyclyl-lower alkanoyl Rt, R2, Rg or R9, preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, ~-carbolinyl and a benzo-, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated and are unsubstituted or substituted as indicated above and are bonded via a nitrogen or carbon atom to lower alkenyl, preferably to the terminal carbon atom of the lower alkenyl radical, which is selected, for example, from vinyl, allyl and 2-or 3-butenyl, for example in the form of pyrimidin-1-yl-, piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-~dioxothiomorphalino-lower alkenyl, such as in 2-morpholino-vinyl, 3-mozvpholino-allyl or 4-morpholino-2- or -3-butenyl, pyrrolyl-lower alkenyl that is unsubstituted or substituted by lower alkyl or by phenyl, such as 2- or 3-pyrrolyl-vinyl or -allyl, 4- or 5-methylpyrrolyl-vinyl or -allyl or 4- or 5-phenylpyrrolyl-vinyl or -allyl, thienyl-lower alkenyl, such as 2-thienyl-vinyl or -allyl, furyl-lower alkenyl, such as 2-furyl-vinyl or -allyl, pyridyl-lower alkenyl, such as 2-, 3- or 4.-pyridyl-vinyl or -allyl, indolyl-lower alkenyl that is unsubstituted or substituted by lower alkyl, for example methyl, phenyl-lower alkyl, for example benzyl, lower alkoxy, for example methoxy, phenyl-lower alkoxy, for example benzyloxy, or by halogen, for example chlorine, such as 2-, 3- or 5-indolyl-vinyl or -allyl, 1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl-, 1-benzylindol-2-yl- or -3-yl-vinyl or -allyl, 4,5,6,7-tetrahydroindol-2-yl-methyl, -ethyl or -n-propyl, cyclohepta-[b]pyrrol-5-yl-vinyl or -allyl, unsubstituted or hydroxy-substituted quinolyl-lower alkenyl, for example 2-, 3- or 4-quinolyl- or 4-hydroxyquinol-2-yl-vinyl or -allyl, unsubstituted or hydroxy-substituted isoquinolyl-lower alkenyl, such as 1-, 3- or 4-isoquinolyl-or 1-oxo-1,2-dihydroisoquinol-3-yl-vinyl or -allyi, 2-quinoxalinyl-vinyl or -allyl, 3,1-benzo-furan-2-yl-vinyl or -allyl, bent[e]indol-2-yl-vinyl or -allyl, (3-carbolin-3-yl-vinyl or -allyl, 3-chromanyl-vinyl or -allyl, 3-thiochromanyl-vinyl or -allyl, 3-pyrrolidinyl-vinyl or -allyl, hydroxypyrrolidinyl-lower alkenyl, such as 3- or 4-hydroxypyrrolidin-2-yl-vinyl or -allyl, oxopyrrolidinyl-lower alkenyl, such as 5-oxopyrrolidin-2-yl-vinyl or.-allyl, piperidinyl-lower alkenyl, such as 2-, 3- or 4-piperidinyl-vinyl- or -allyl, morpholinyl-lower alkenyl, such as 2- or 3-morpholinyl-vinyl or -allyi, thiomorpholinyl-lower alkenyl, such as 2- or 3-thiomorpholinyl-vinyl or -allyl, S,S-dioxothiomorpholinyl-lower alkenyl, such as S,S-dioxothiornorpholin-2- or -3-yl-vinyl or -allyl, indolinyl-lower alkenyl, such as 2- or 3-indolinyl-vinyl or -allyl, 1,2,3,4-tetrahydroquinolyl-lower alkenyl, such as 1,2,3,4-tetra-hydroquinol-2-, -3- or -4-yl-vinyl or -allyl, 1,2,3,4-tetrahydroisoquinolyl-lower alkenyl, such as 1,2,3,4-tetrahydroisoquinol-1-, -2- or -3-yl-vinyl or -allyl, or 1-oxo-1,2,3,4-tetra-hydroisoquinol-3-yl-vinyl or -allyl; also hydroxy; etherified hydroxy selected from lower alkoxy, such as methoxy or ethoxy, phenoxy or naphthyloxy, phenyl- or naphthyl-lower alkoxy, such as benzyloxy, and heterocyclyl-lower alkoxy wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, ø-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, for example 4-pyrrolidinyl-methoxy, 1-imidazolylmethoxy, 2-pyridylmethoxy, 3-pyridylmethoxy, quinolin-2-yl-methoxy or indol-2-ylmethoxy; esterifted hydroxy selected from lower alkanoyloxy, such as acetoxy, propionyloxy, butyroxy, isobutyroxy or pivaloyloxy, acetoacetoxy, amino- or benzyloxycarbonylamino-lower alkanoyloxy, such as 2-amino- or 2-benzyloxycarbonyl-amino-2-methylpropionyloxy, aryl-lower alkanoyloxy wherein aryl contains from 6 to 10 carbon atoms, such as in benzoyloxy, phenylacetoxy, 1- or 2-naphthoyloxy, lower alkoxy-carbonyloxy, for example methoxy-, ethoxy-, n-propoxy-, isopropoxy-, n-butoxy-, iso-butoxy-, sec-butoxy-, tert-butoxy-, n-pentyloxy-, isopentyloxy-, neopentyloxy-, tert-pentyloxy-, n-hexyloxy-, isohexyloxy- or n-heptyloxy-carbonyloxy, mono- or di-lower alkylaminocarbonyloxy, such as ethylaminocarbonyloxy or diethylaminocarbonyloxy, aryloxyearbonyloxy wherein aryl contains from 6 to 10 carbon atoms, for example phenoxycarbonyloxy or 1- or 2-naphthyloxycarbonyloxy, aryl-lower alkoxycarbonyloxy wherein aryl contains from 6 to 12 carbon atoms, for example phenyl-lower alkoxy-carbonyloxy, such as benzyloxycarbonyloxy, and also 1- or 2-naphthylmethoxycarbonyl-oxy or 9-fluorenylmethoxycarbonyloxy, sulfonyloxy, lower alkylsulfonyloxy, for example methyl-, ethyl-, propyl-, isopropyl-, n-butyl-, isobutyl-, sec-butyl-, tent-butyl-, n-pentyl-, isopentyl-, neopentyl-, tent-pentyl-, n-hexyl-, isohexyl- or n-heptyl-sulfonyloxy, phenyl-sulfonyloxy, 2- or 4-toluenesulfonyloxy and 1- or 2-naphthylsulfonyloxy;
halogen, for example chlorine or bromine; carboxy; esterified carboxy selected from lower alkoxy-carbonyl, such as methoxycarbonyl, ethoxycarbonyl and ten-butoxycarbonyl, 2-halo-~'~~~1 lower allcoxycarbonyl, for example 2-chloro-, 2-bromo-, 2-iodo- or 2,2,2-trichloro-ethoxy-carbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, for example benzyloxycarbonyl, and heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, it also being possible for the mentioned radicals to be fully or partially saturated, for example in 4-pyridylmethoxycarbonyl; or amidated carboxy selected from carbamoyl, lower alkyl-carbamoyl, such as methylcarbamoyl, di-lower allylcarbamoyl, such as dimethyl-carbamoyl, hydroxy-lower alkylcarbamoyl or di(hydroxy-lower alkyl)carbamoyl, such as hydroxymethylcarbamoyl or di(hydroxymethyl)carbamoyl, N-lower alkoxy-lower alkoxy-lower alkylcarbamoyl, such as 2-(2-methoxyethoxy)ethylaminocarbonyl, carboxy-lower alkylcarbamoyl or di(carboxy-lower alkyl)carbamoyl, for example carboxymethyl-or di(carboxymethyl)-carbamoyl, and from carbarnoyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, it also being possible for the radical so formed to be fully or partially unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, mot~pholino-, thiomorpholino- or S,S-dioxothiomorpholino-carbonyl, N-lower alkyl-N-heterocyclyl-lower alkylcarbamoyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrirnidinyl, indolyl, quinolyl, iso-quinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclo-hepta-fused derivative of those radicals, which may also be fully or partially saturated, for example N-2-pyridyhnethyl-N-methylcarbamoyl.
Alkynyl Rt, R2, Rg or R9 contains especially from 2 to 10, preferably, as lower alkynyl, from 2 to 7, especially from 2 to 4, carbon atoms, and is, for example, ethynyl, 1-.propynyl or 2-propynyl, it being possible for the mentioned radicals to be unsubsrituted or substi-tuted by the radicals menrioned for lower alkenyl Rl, Rz, Rg or Rg, ~Ieterocyclyl Rl, R2, R8 and R9 is bonded via a carbon atom and contains especially an unsubstituted or substituted heterocyclyl mentioned under heterocyclyl-lower alkanoyl Rt, R2, Rg and R9 and is preferably pyrrolyl that is unsubstituted or substituted by lower alkyl or by phenyl, such as 2- or 3-pyrrolyl, 4- or 5-methylpyrrolyl or 4- or 5-phenylpyrrolyl, thienyl, such as 2-thienyl, furyl, such as 2-furyl, pyridyl, such as 2-, 3- or ~4-pyridyi, 2"d?'~~3 indolyl that is unsubstituted or substituted by lawer alkyl, for example methyl, phenyl-lower alkyl, for example benzyl, lower alkoxy, for example methoxy" phenyl-lower alkoxy, for example benzyloxy, or by halogen, for example chlorine, such as 2-, 3- or 5-indolyl, 1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl, 1-benzylindol-2-yl or -3-yl, 4,5,6,7-tetrahydroindol-2-yl, unsubstituted or hydroxy-substituted quinolyl, such as 2-, 3- or 4-quinolyl or 4-hydroxyquinol-2-yl, unsubstituted or hydroxy-substituted isoquinolyl, such as 1-, 3- or 4-isoquinolyl or 1-oxo-1,2-dihydroisoquinol-3-yl, 2-quinoxalinyl, 3,1-benzofuran-2-yl, benz[e]indol-2-yl, (3-carbolin-3-yl, cyclohepta[b]pyrrol-5-yl, 3-chromanyl, 3-thiochromanyl, 3-pyrrolidinyl, hydroxypyrrolidinyl, such as 3- or 4-hydroxypyrrolidin-2-yl, oxopyrrolidinyl, such as 5-oxopyrrolidin-2-yl, piperidyl, such as 2-, 3- or 4-piperidyl, mozpholinyl, such as 2- or 3-morpholinyl, thiomorpholinyl, such as 2- or 3-thiomorpholinyl, S,S-dioxothio-morpholinyl, such as S,S-dioxothiomorpholin-2- or -3-yl, indolinyl, such as 2-or 3-indolinyl, 1,2,3,4-tetrahydroquinolyl, such as 1,2,3,4-tetrahydroquinol-2-, -3- or -4-yl, 1,2,3,4-tetrahydroisoquinolyl, such as 1,2,3,4-tetxahydroisoquinol-1-, -2- or -3-yl, or 1-oxo-1,2,3,4-tetrahydroisoquinol-3-yl.
Alkyl-substituted sulfonyl Rt, R2, Rg and R9 preferably contains an unsubstituted or substituted alkyl radical mentioned under alkyl Rt, R,;, R8 and R9 and is especially lower alkylsulfonyl, such as methylsulfonyl, ethylsu:lfonyl, n-propylsulfonyl or tert-butyl-sulfonyl, aryl-lower alkyl-substituted sulfonyl that contains, for example, an unsubstituted or substituted radical mentioned under aryl-lower alkyl Rl, R2, R$ and R9 and is selected especially from the radicals benzyl-, 4-chloro-, 4-methoxy- or 4-nitro-benzyl-, naphthyl-methyl-, for example a- or (3-naphthylmethyl-, 2-phenylethyl-, 2-a-naphthylethyl-, 2-(3-naphthylethyl-, 2-(4-methylphenyl)ethyl-, 2-(4-methoxyphenyl)ethyl-, 3-phenylpropyl-, 3-(p-hydroxyphenyl)-propyl-, 2,2-diphenylethyl- and 2,2-di(4-methoxyphenyl)-ethyl-sulfonyl, or heterocyclyl-lower alkyl-substituted sulfonyl that contains, for example, an unsubsdtuted or substituted radical mentioned under heterocyclyl-lower alkyl Rz, R2, Rg and R9 and is selected especially from radicals such as 2- or 3-pyrrolyl-, 2-thienyl-, 2-furyl-, 1-pyrazolyl-, 2-, 3- or 4-pyridyl-, 2-, 3- or 5-indolyl-, (1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl)-, (1-benzylindol-2-yl or -3-yl)-, 4,5,6,?-tetrahydroindol-2-yl-, (2-, 3- or 4-quinolyl or 4-hydroxyquinol-2-yl)-, (1-, 3- or 4-isoquinolyl or 1-oxo-1,2-dihydroisoquinol-3-yl)-, 3-pyrrolidinyl-, (3- or 4-hydroxy-pyrrolidin-2-yl)-, S-oxopyrrolidin-2-yl-, (2- or 3-morpholinyl)-, (2- or 3-thiomorphalinyl)-, ~~~~~'~~3 (S,S-dioxothiomorpholin-2- or -3-yl)-, (2- or 3-indolinyl)-, (1,2,3,4-tetrahydroquinol-2-, -3- or -4-yl)- and (1,2,3,4-tetrahydroisoquinol-1-, -2- or -3-yl)-methyl-sulfonyl.
Aryl-substituted sulfonyl Rl, R2,'Rg and Rg preferably contains an unsubstituted or substi-tuted aryl radical mentioned under aryl-lower alkanoyl Rt, R2, Rs and Rg and is especially phenyl- or 1- or 2-naphthyl-sulfonyl that is unsubstituted or mono- or di-substituted by lower alkyl, such as phenylsulfonyl, 2- or 4-toluenesulfonyl or 1- or 2-naphthylsulfonyl.
Heterocyclyl-substituted sulfonyl Rt, R2, Rs and Rg preferably contains heterocyclyl that is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, from morpholinyl and from thiomorpho-linyl and may be unsubstituted or substituted, especially by lower alkyl, such as methyl, such as morpholinosulfonyl, thiomorpholinosulfonyl, piperidinosulfonyl, 4-methyl-piperazinylsulfonyl or piperazinosulfonyl. In especially preferred forms of the invention, heterocyclylsulfonyl as substituent may be absent.
Alkoxy-substituted sulfonyl Rt, R2, R8 and Rg preferably contains an unsubstituted or substituted alkyl radical mentioned under alkyl Rt, R,Z, R$ and Rg and is selected especially from lower alkoxy-, such as methoxy-, ethoxy- or tert-butoxy-sulfonyl, heterocyclyl-lower alkoxysulfonyl that contains, for example, an unsubstituted or substi-tuted heterocyclyl-lower alkyl radical mentioned under heterocyclyl-lower alkyl Ri, R2, R8 and Rg and is selected especially from 2- or 3-pyrrolyl-, 2-thienyi-, 2-furyl-, 1-pyrazolyl-, 2-, 3- or 4-pyridyl-, 2-, 3- or 5-indolyl-, (1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl)-, (1-benzylindol-2-yl or -3-yl)-, 4,5,6,7-tetrahydroindol-2-yl-, (2-, 3- or 4-quinolyl or 4-hydroxyquinol-2-yl)-, (1-, 3- or 4-isoquinolyl or 1-oxo-1,2-dihydroisoquinol-3-yl)-, 3-pyrrolidinyl-, (3- or 4-hydroxy-pyrrolidin-2-yl)-, 5-oxopyrrolidin-2-yl-, (2- or 3-morpholinyl)-, (2- or 3-thiomorpholinyl)-, (S,S-dioxothiomorpholin-2- or -3-yl)-, (2- or 3-indolinyl)-, (1,2,3,4-tetrahydroquinol-2-, -3- or -4-yl)- and (1,2,3,4-tetrahydroisoquinol-1-, -2- or -3-yl)-methoxysulfonyl or -ethoxysulfonyl, aryl-lower alkoxysulfonyl that contains, for example, an unsubstituted or substituted aryl-lower alkyl radical mentioned under aryl-lower alkyl Rl, Rz, R8 and Rg, such as benzyloxysulfonyl, ~~~~~t~.7~

hydroxy-lower alkoxy-, such as 3-hydroxypropoxy- or 2-hydroxy-3-methylpentyloxy-sulfonyl, , lower alkoxy-lower alkoxy-, for example lower alkoxyethoxy- or lower alkoxypropoxy-, such as methoxyethoxy- or 3-mechoxypropoxy-sulfonyl, lower alkoxy-lower alkoxy-lower alkoxy-, such as 2-methoxymethoxy-3-methylpentyl-oxy-sulfonyl, phenoxy-lower alkoxy- or nitrophenoxy-lower alkoxy-, such as phenoxymethoxy-, phenoxyethoxy- or 4-nitrophenoxymethoxy-sulfonyl, naphthyloxy-lower alkoxy-, such as a- or ~3-naphthyloxyethoxy-sulfonyl, lower alkanoyloxy-lower alkoxy-, for example lower alkanoyloxyethoxy- or lower alkanoyloxypropoxy-, such as acetoxyethoxy- or 3-acetoxypropoxy-sulfonyl, amino-lower alkoxy-, such as 5-aminopentyloxy-sulfonyl, mono- or di-lower alkylamino-lower allcoxy-, such as dimethylaminoethoxy- or 2-dirnethylamino-2-isopropylethoxy-sulfonyl, lower alkanoylamino-lower alkoxy-, such as 4-acetylaminopentyloxy-sulfonyl, lower alkoxycarbonylainino-lower alkoxy-, such as 5-(tert-butoxycarbonylamino)-pentyloxy- or 3-ethoxycarbonylamino-2-isobutyl-pro;poxy-sulfonyl, phenyl-lower alkoxycarbonylamino-lower alkoxy-, such as 5-(benzyloxycarbonyl-amino)-pentyloxy-sulfonyl, acetoacetoxy-sulfonyl, aminocarbonylamino-lower alkoxy-, such as aminocarbonylamino-ethoxy-sulfonyl, N-phenyl-lower alkyl-N-lower alkyl-aminocarbonylamino-lower alkoxy-, for example 2-isobutyl-3-(N-benzyl-N-methylaminocarbonylamino)propoxy-sulfony1, halo-lower alkoxy-, for example 2-haloethoxy-, such as (2-chloro-, 2-bromo-, 2-iodo- or 2,2,2-trichloro-ethoxy)-, or halopropoxy-, such as (3-chloro- or 3-bromo-propoxy)-sulfonyl, carboxy-lower alkoxy-, such as carboxyethoxy- or 3-carboxypropoxy-sulfonyl, lower alkoxycarbonyl-lower alkoxy-, for example lower alkoxycarbonylethoxy- or lower alkoxycarbonylpropoxy-, such as methoxycarbonylethoxy-, 3-methoxycarbonylpropoxy-, ethoxycarbonylethoxy- or 3-ethoxycarbonylpropoxy-sulfonyl, 2-halo-lower alkoxycarbonyl-lower alkoxy-, such as (2-chloro-, 2-bromo-, 2-iodo- or 2,2,2-trichloro-ethoxycarbonyl-2-ethoxy or 3-propoxy)-sulfonyl, lower alkylsulfonyl-lower alkoxy-, such as (2-ethylsulfonyl- or 2-tert-butylsulfonyl-methoxy)-sulfonyl, carbamoyl-lower alkoxy-, such as carbamoylethoxy- or 3-carbamoylpropoxy-sulfonyl, and carbamoyl-lower alkoxysulfonyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene whe~°ein a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, it also being possible for the radical so formed to be fully or partially unsatur-ated, for example in the form of (piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomorpholino-carbonyl-lower alkoxy)-, such as in 2-morpholinocarbonyl-ethoxy-, 3-(morpholino-carbonyl)-propoxy- ar 3-(morpholinocarbonyl)-2-isobutyl-propoxy-sulfonyl.
Aryloxy-substituted sulfonyl Rt, R2, R8 and R9 preferably contains an unsubstituted or substituted aryl radical mentioned under aryl-lower alkanoyl Rt, R2, Rs and R9 and is selected especially from benzylaxysulfonyl and 1- or 2-naphthyloxysulfonyh Sulfamoyl Rt, R2, R8 and R9 substituted at the nitrogen atom may be substituted preferably by the same radicals as may carbamoyl in carbamoyl-lower al.kanoyl Rt, R2, R8 and R9 and is selected especially from mono- or di-lower alkylsulfamoyl, such as N,N-dimethylsulfamoyl, N-(phenyl- or naphthyl-lower alkyl)sulfamoyl, such as 3-benzyl-sulfamoyl, and sulfamoyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene or pentamethylene wherein a carbon atom may have been replaced by nitrogen, lower alkyl-substituted, such as methyl-substituted, nitrogen, oxygen, sulfur or by sulfiu mono- or di-substituted by oxygen, it also being possible for the radical so formed to be fully or partially unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, methylpiperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomorpholino-sulfonyl, such as 4-methylpiperazinylsulfonyl or morpholinosulfonyl-2-isopropyl-propyl.
Phosphoryl Rt, R2, Rg and R9 substituted by one or two identical or different radicals selected from alkyl, cycloalkyl, cycloalkyl-lower alkyl, aryl, aryl-lower alkyl, hydroxy, alkoxy, cycloalkoxy, cycloalkyl-lower alkoxy, aryloxy and aryl-lower alkoxy preferably contains as unsubstituted ar substituted alkyl one or two of the unsubstituted or substituted radicals mentioned under alkyl, especially lower alkyl Rt, R2, Rg and R9, for example lower alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl and tent-butyl, - cycloalkyl-lower alkyl that is a lower alkyl radical substituted especially terminally by one of the cycloalkyl radicals mentioned under cycloalkyl-lower alkanoyl Rt, R2, R8 and R9, such as cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, 2-cyclopentylethyl, - ~5 -3-cyclopentylpropyl, cyclohexylrnethyl, 2-cyclohexylethyl or 3-cyclohexylpropyl, - aryl-lower alkyl, as defined under aryl-lower allcyl Rl, R2, R8 or R9, especially benzyl, unsubstituted, mono- or poly-substituted preferably by lower alkyl, for example methyl, phenyl, hydroxy, lower alkoxy, for example methoxy, halogen, for example chlorine, and/or by nitro, such as 4-methoxy-, 4-chloro- or 4-nitro-benzyl, naphthylmethyl, such as a- or (3-naphthylmethyl, 2-phenylethyl, 2-a-naphthylethyl, 2-(3-naphthylethyl, 2-lower alkylphenylethyl, such as 2-(4-methylphenyl)ethyl, 2-lower alkoxyphenylethyl, such as 2-(4-methoxyphenyl)ethyl, 2,2-diphenylethyl, 2,2-di(4-methoxyphenyl)-ethyl, 2,2,2-tri-phenylethyl, 2,2-dibenzylethyl, 2,p-diamino-phenylethyl, or phenyl-lower alkyl substi-tuted in the 2- and p-positions by two radicals selected from phenyl-lower alkoxycarbonyl, for example benzyloxycarbonyl, and lower alkanoylamino, for example pivaloylamino, such as Z,p-dibenzyloxycarbonylamino-phenylethyl or 2-pivaloylamino-p-benzyloxy-carbonylamino-phenylethyl, 3-phenylpropyl, 3-(p-hydroxyphenyl)-propyl, 3-a- or 3-(3-naphthylpropyl, 2-benzyl-3-(1-pyrazolyl)-propyl, 3-phenyl- or 3-a-naphthyl-2-hydroxy-propyl, 3-phenyl- or 3-a-naphthyl-2-lower alkoxy-propyl, such as 3-phenyl- or 3-a-naphthyl-2-neopentyloxy-propyl, 3-phenyl- or 3-a-naphthyl-2-lower alkanoyloxy-propyl, such as 3-phenyl- or 3-a-naphthyl-2-pivaloyloxy- or -2-acetoxy-propyl, 2-benzyl- or 1- or 2-naphthyl-3-(N-methoxy-N-methylamino)-propyl, 3-phenyl- or 3-a-naphthyl-2-dimethyl-aminomethyl-propyl, 3-a-naphthyl-2-acetoacetoxy-propyl, 3-a-naphthyl-2-ethylamino-carbonyloxy-propyl or 3-a-naphthyl-2-(2-amino- or 2-benzyloxycarbonylamino-2-methyl-propionyloxy)-propyl, 3-phenyl- or 3-a-naphthyl-2-carboxymethyl-propyl, 3-phenyl- or 3-a-naphthyl-2-lower alkoxycarbonyl-propyl, such as 3-a-naphthyl-2-ethoxycarbonyl-propyl, ~-phenyl- or 3-a-naphthyl-2-benzyloxycarbonylmethyl-propyl, 2-(S)-benzyl-3-tent-butylsulfonyl-propyl, 3-phenyl-2-phosphono- or -phosphonomethyl-propyl, 3-phenyl-2-dimethoxyphosphoryl- or -dimethoxyphosphorylmethyl-propyl, 3-phenyl-diethoxyphosphoryl- or -diethoxyphosphorylmethyl-propyl, 3-phenyl-2-ethoxy- or -methoxy-hydroxyphosphorylpropyl, 3-phenyl- or 3-a-naphthyl-2-carbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-tert-butylcarbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-(2-dimethylaminoethyl)carbamoyl-propyl, 3-a-naphthyl-2-(carboxy- or tent-butoxycarbonyl)-methylcarbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-(3-hydroxy-2-propyl)-carbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-(2,2-dimethoxyethyl)-carbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-(5-amino-5-carboxypentyl)-carbamoyl-propyl, 3-phenyl- or 3-a-naphthyl-2-cyano-propyl, 3-phenyl- or 3-a-naphthyl-2-cyanomethyl-propyl, 3-phenyl- or 3-a-naphthyl-2-acetonyl-propyl, 4-hydroxyphenylbutyl, 4-phenyl- or 4-a-naphthyl-3-carboxy-butyl, 4-phenyl- or 4-a-naphthyl-3-benzyloxycarbonyl-butyl, 2-benzyl- or 2-a-naphthyl-methyl-4-cyano-butyl, 2-benzyl-4-(2-benzofuranyl)-4-oxobutyl, 2-benzyl- or 2-a-naphthylmethyl-5-dimethylamino-pentyl, 2-benzyl- or 2-a-naphthylmethyl-4-oxo-pentyl, 2-benzyl- or 2-a-naphthylmethyl-4,4-dimethyl-3-oxa-pentyl, 2-benzyl- or 2-a-naphthyl-methyl-5-dimethylamino-4-oxo-pentyl, or 2-benzyl- or 2-a-naphthylmethyl-5,5-dimethyl-4-oxo-hexyl, as cycloalkyl one of the radicals mentioned under cycloalkyl-lower allcanoyl Rt, RZ, Rg and Rg, especially cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, as aryl one of the unsubstituted or substituted radicals mentioned under aryl-lower alkanoyl Rl, R2, R8 and Rg, preferably phenyl, unsubstituted, mono- or poly-substituted by lower alkyl, for example methyl, halo-lower alkyl, for example trifluoromethyl, phenyl, hydroxy, lower alkoxy, for example methoxy, halogen, for example fluorine or chlorine, and/or by nitro, such as 4-methyl-, 3-hydroxy-, 4-methoxy-, 4-chloro- or 4-nitro-phenyl, naphthyl, such as a- or (3-naphthyl, or anilinophenyl substituted in the phenyl radical by one or two radicals selected from lower alkyl, such as methyl or ethyl, hydroxy, lower alkoxy, such as methoxy, amino, mono- or di-lower alkylamino, such as ethylamino or dimethylamino, halogen, such as fluorine or chlorine, carboxy, sulfo, carbarnoyl, sulfamoyl and cyano, and/or at the amino group by one or two radicals selected from lower alkyl and benzyl, such as 2-(o,o-dichloroanilino)-phenyl or 2-(o,o-dichloro-N-benzylanilino)-phenyl, as alkoxy one of the unsubstituted or substituted radicals mentioned in the case of alkoxy-substituted sulfonyl Rt, R2, R8 and Rg, especially lower alkoxy, such as methoxy, ethoxy or tent-butoxy, cycloalkyl-lower alkoxy with one of the radicals mentioned under phosphoryl Rl, R2, Rg and R9 substituted by cycloalkyl-lower alkyl, bonded via oxygen, such as cyclapropylmethoxy, cyclobutylmethoxy, cyclopentylmethoxy, 2-cyclopentyl-ethoxy, 3-cyclopentylpropoxy, cyclohexylmethoxy, 2-cyclohexylethoxy or 3-cyclohexyl-propoxy, aryl-lower allcoxy with one of the radicals mentioned under sulfonyl Rl, R2, R8 and Rg substituted by aryl-lower alkoxy, bonded via oxygen, especially benzyloxy, hydroxy-lower alkoxy, such as 3-hydroxypropoxy or 2-hydroxy-3-methylpentyloxy, lower alkoxy-lower alkoxy, for example lower alkoxyethoxy or lower alkoxypropoxy, such as methoxyethoxy or 3-methoxypropoxy, lower alkaxy-lower alkoxy-lower alkoxy, such as 2-methoxymethoxy-3-methylpentyloxy, phenoxy-lower alkoxy or nitrophenoxy-lower alkoxy, such as phenoxymethoxy, phenaxyethoxy or 4-nitrophenoxymethoxy, naphthyl-oxy-lower alkoxy, such as a- or (3-naphthyloxyethoxy, lower alkanoyloxy-lower alkoxy, such as lower alkanoyloxyethoxy or lower alkanoyloxyprapoxy, such as acetoxyethoxy or 3-acetoxypropoxy, amino-lower alkoxy, such as 5-aminopentyloxy, mono- or di-lower alkylamino-lower alkoxy, such as dimethylaminoethoxy or 2-dimethylamino-2-isopropyl-ethoxy, lower all:anoylamino-lower alkoxy, such as 4-acetylaminopentyloxy, lower 2~~~ ~~'~

alkoxycarbonylamino-lower alkoxy, such as 5-(tent-butoxycarbonylamino)-pentyloxy or 3-ethoxycarbonylamino-2-isobutyl-propoxy, phenyl-lower alkoxycarbonylamino-lower alkoxy, such as 5-(benzyloxycarbonylamino)-pentyloxy, aminocarbonylamino-lower alkoxy, such as aminocarbonylamino-ethoxy, N-phenyl-lawer alkyl-N-lower alkyl-amino-caxbonylamino-lower alkoxy, such as 2-isobutyl-3-(N-benzyl-N-methylaminocarbonyl-amino)propoxy, hula-lower alkoxy, for example 2-haloethoxy, such as 2-chloro-, 2-bromo-, 2-iodo- or 2,2,2-trichloro-ethoxy, or halopropoxy, such as 3-chloro-or 3-bromo-propoxy, carboxy-lower alkoxy, such as carboxyethoxy or 3-carboxypropoxy, lower alkoxycarbonyl-lower alkoxy, for example lower alkoxycarbonylethoxy or lower alkoxycarbonylpropoxy, such as methoxycarbonylethoxy, 3-methoxycarbonylpropoxy, ethoxycarbonylethoxy or 3-ethoxycarbonylpropoxy, 2-halo-lower alkoxycarbonyl-lower alkoxy, such as 2-chloro-, 2-bromo-, 2-iodo- or 2,2,2-trichloro-ethoxycarbonyl-2-ethoxy or -3-propoxy, lower alkylsulfonyl-lower alkoxy, such as 2-ethylsulfonyl- or 2-tent-butyl-sulfonyl-methoxy, carbamoyl-lower alkoxy, such as carbamoylethoxy or 3-carbamoyl-propoxy, or carbamoyl-lower alkoxy substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom may have been replaced by nitrogen, oxygen, sulfur ox by sulfur mono- or di-substituted by oxygen, it also being possible for the ring formed to be fully or partially unsaturated, for example in the form of (piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomorpholino-carbonyl)-lower alkoxy, such as in 2-morpholinocarbonyl-ethox;y, 3-(morpholinocarbonyl)-propoxy or 3~(morpholinocarbonyl)-2-isobutyl-propoxy, as cycloalkoxy one of the cycloalkyl radicals mentioned under cycloalkyl-lower alkanoyl Rl, R2, R8 and R9, bonded via oxygen, such as cyclobutoxy, cyclopentyloxy or cyclo-hexyloxy, or as aryloxy one of the radicals mentioned under aryloxy-substituted sulfonyl Rl, R2, R8 and R9, especially benzyloxy or 1- or 2-naphthyloxy, and is especially preferably lower alkylphosphoryl, such as tert-butylphosphoryl, hydroxy-lower alkoxyphosphoryl, such as hydroxy-methoxy-phosphoryl ox hydroxy-ethoxy-phosphoryl, or di-lower alkoxyphosphoryl, such as dimethoxy-phosphoryl or diethoxy-phosphoryl.
The phosphono radicals and the individual definitions of the radicals Rt, R2, R8 and R9 mentioned for substituted phosphoryl may also, independently of one another, be omitted from the definition of the radicals Rt, R2, Rs and R9 in the compounds of formula I.

_~s-Preferably not more than one of the radicals Rt and R2 and of the radicals R$
and R9 is defined by the radicals mentioned under acyl, sulfo, substituted sulfo, phosphono or substituted phosphoryl, while the other radical is selected from the remaining substituents mentioned.
A heterocyclic ring formed by the pairs of substituents Rt and R2, and Rg and R9, independently of one another, together with the nitrogen atom to which they are bonded, and comprising the bonding nitrogen atom together with a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene in which a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which may be unsaturated, or one of those radicals with an oxo substituent at each of the two carbon atoms linked to the bonding carbon atom and with or without a fused-on benzene or naphthalene ring, is preferably piperidino, pyrazin-1-yl, piperazin-1-yl, pyrimidin-1-yl, pyridazin-1-yl, morpholino, thiomorpholino, S,S-dioxothiomorpholino, succinimido, malimido, oxalimido, maleimido, phthalimido or naphthalene-1,8-dicarbonylimido, preferably only one of the pairs of substituents Rt and R2 or R8 and R~
forming one of the said heterocyclic rings.
Unsubstituted or substituted alkyl R~, Rq, or R~ is preferably one of the unsubstituted or substituted radicals mentioned under alkyl Rl y R2, R8 and R9 and is selected especially from lower alkyl, for example methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl or tent-butyl, cycloalkyl-lower alkyl that contains, for example, the cycloalkyl radicals mentioned under cycloalkyl-lower alkanoyl Rl, R2, Rg or R~, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl, cycloalkyl being unsubstituted or mono-to tri-substituted by lower alkyl, such as isopropyl, halo-lower alkyl, such as trifluoromethyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower allcoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such as fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, far example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mano-or di-lower alkylsulfamoyl, nitro and/or by cyano and being bonded, preferably terminally, to lower alkyl, especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or tert-butyl, such as cyclobutyl-, cyclopentyl-, cyclohexyl- or cycloheptyl-lower alkyl, such as -methyl 2~~ ~'~

or -ethyl, especially preferably cyclohexyl-lower alkyl, such as cyclohexylmethyl, bicycloalkyl-lower alkyl wherein bicycloalkyl contains, for example, from 5 to 10, especially from 6 to 9, carbon atoms, for example bicycloalkyl-methyl or -ethyl, preferably having from 8 to 11 carbon atoms, such as decahydronaphthyl-2-methyl, endo-or exo-norbornyl-2-methyl, bicyclo[2.2.2]oct-2-ylmethyl or bicyclo[3.3.1]non-9-ylmethyl, and also bicyclo-hexyl-, -heptyl-, -octyl-, -nonyl- or -decyl-ethyl or -3-propyl, for example bicyclo[3.1.0]hex-1-, -2- or -3-yl-, bicyclo[4.1.0]hept-1- or -7-yl-, bicyclo[2.2.1]hept-2-yl-, for example endo- or exo-norbornyl-, bicyclo[3.2.1]oct-2-yl-, bicyclo[3.3.0]oct-3-yl- or bicyclo[3.3.1]non-9-yl-, and also a- or (3-decahydronaphthyl-ethyl or -3-propyl, tricycloalkyl-lower allcyl, wherein tricycloalkyl contains, for example, from 8 to 10 carbon atoms, for example tricycloalkyl-methyl or -ethyl, preferably having from 8 to 11 carbon atoms, such as 1- or 2-adamantylmethyl, and also tricyclo[5.2.1.02>b]dec-8-yl- or adamantyl-, such as 1-adamantyl-ethyl, aryl-lower alkyl, for example as defined under aryl-lower alkyl R1, R2, Rg or Rc~, that is unsubstituted or substituted as defined there, for example phenyl-lower alkyl, such as benzyl, 2-phenylethyl, 3-phenylpropyl, 4-fluoro-, 4-cyano-, 4-methoxy- or 4-hydroxy-benzyl, or 1- or 2-naphthyl-methyl or -2-ethyl, especially phenyl-lower alkyl, as last defined, heterocyclyl-lower alkyl, for example as defined under heterocyclyl-lower alkyl R1, R2, Rg or R9, that is unsubstituted or substituted as defined there and is selected especially from pyrimidin-1-yl-, piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyridazin-1-yl-, morpho-lino-, thiomorpholino- or S,S-dioxothiomorpholino-lower alkyl, such as in 2-morpholino-ethyl, 3-morpholino-propyl or 3-morpholino-2-isobutyl-propyl, unsubstituted or lower alkyl- or phenyl-substituted pyrrolyl-lower alkyl, such as 2- or 3-pyrrolyl-methyl, -ethyl or -n-propyl, 4- or 5-methylpyrrolyl-methyl, -ethyl or -n-propyl or 4- or 5-phenylpyrrolyl-methyl, -ethyl or -n-propyl, thienyl-lower alkyl, such as 2-thienyl-methyl, -ethyl or -n-propyl, 1-imidazolylmethyl, furyl-lower alkyl, such as 2-furyl-methyl, -ethyl or -n-propyl, pyridyl-lower alkyl, such as 2-, 3- or 4-pyridyl-methyl, -ethyl or -n-propyl,' indolyl-lower alkyl that is unsubstituted or substituted by lower alkyl, for example methyl, phenyl-lawer alkyl, for example benzyl, lower alkoxy, for example methoxy, phenyl-lower alkoxy, for example benzyloxy, or by halogen, for example chlorine, such as 2-, 3-or 5-indolyl-methyl, -ethyl or -n-propyl, 1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl-, 1-benzylindol-2-yl- or -3-yl-methyl, -ethyl or -n-propyl, 4,5,6,7-tetrahydroindol-2-yl-methyl, -ethyl or -n-propyl, cyclohepta[b]pyrrol-5-yl-methyl, -ethyl or -n-propyl, unsubstituted or hydroxy-substituted quinolyl-lower alkyl, for example 2-, 3- or 4-quinolyl- or 4-hydroxyquinol-2-yl-methyl, -ethyl or -s~--n-propyl, unsubstituted or hydroxy-substituted isoquinolyl-lower alkyl, such as 1-, 3- or 4-isoquinolyl- or 1-oxo-1,2-dihydroisoquinol-3-yl-methyl, -ethyl or -n-propyl, 2-quinoxa-linyl-methyl, -ethyl or -n-propyl, 3,1-benzofuran-2-yl-methyl, -ethyl or -n-propyl, bent[e~-indol-2-yl-methyl, -ethyl or -n-propyl, (3-carbolin-3-yl-methyl, -ethyl or -n-propyl, 3-chromanyl-methyl, -ethyl or -n-propyl, 3-thiachromanyl-methyl, -ethyl or -n-propyl, 3- or 4-pyrrolidinyl-methyl, -ethyl or -n-propyl, hydroxypyrrolidinyl-lower alkyl, such as 3- or 4-hydroxypyrrolidin-2-yl-methyl, -ethyl or -n-propyl, oxopyrrolidinyl-lower alkyl, such as 5-oxopyrrolidin-2-yl-methyl, -ethyl or -n-propyl, piperidinyl-lower alkyl, such as 2-, 3- or 4-piperidinyl-methyl, -ethyl or -n-propyl, morpholinyl-lower alkyl, such as 2-or 3-morpholinyl-methyl, -ethyl or -n-propyl, thiomorpholinyl-lower alkyl, such as 2- ar 3-thiomorpholinyl-methyl, -ethyl or -n-propyl, S,S-dioxothiomorpholinyl-lower alkyl, such as S,S-dioxothiomorpholin-2- or -3-yl-methyl, -ethyl or -n-propyl, indolinyl-lower alkyl, such as 2- or 3-indolinyl-methyl, -ethyl or -n-propyl, 1,2,3,4-tetrahydroquinolyl-lower alkyl, such as 1,2,3,4-tetrahydroquinol-2-, -3- or -4-yl-methyl, -ethyl or -n-propyl, 1,2,3,4-tetrahydroisoquinolyl-lower alkyl, such as 1,2,3,4-tetrahydroisoquinol-1-, -2- or -3-yl-methyl, -ethyl ox -n-propyl, and 1-oxo-1,2,3,4-tetrahydroisoquinol-3-yl-methyl, -ethyl or -n-propyl, hydroxy-lower alkyl, such as 3-hydroxypropyl or 2-hydroxy-3-methylpentyl, lower alkoxy-lower alkyl, for example lower alkoxyethyl or lower alkoxypropyl, such as 2-methoxyethyl, 2-ethoxyethyl or 3-methoxypropyl, phenoxy-lower alkyl or nitxophertoxy-lower alkyl, such as phenoxymethyl, phenoxyethyl or 4-nitrophenoxymethyl, naphthyloxy-lower alkyl, such as a- or (3-naphthyloxyethyl, lower alkanoyloxy-lower alkyl, for example lower alkanoyloxyethyi or lower alkanoyl-oxypropyl, such as acetoxyethyl or 3-acetoxypropyl, acetoacetoxy-lower alkanoyl, arylmercapto-lower alkyl wherein aryl contains from 6 to 10 carbon atoms, for example phenyl or naphthyl, such as phenylmercaptomethyl, amino-lower alkyl, such as 5-aminopentyl, mono- or di-lower alkylamino-lower alkyl, such as dimethylaminoethyl or 2-dimethyl-amino-2-isopropylethyl, phenyl- or naphthyl-amino-lower alkyl, such as 3-phenylaminopropyl, lower alkanoylamino-lower alkyl, such as 4-acetylaminopentyl, piperazinylcarbamoyl-lower alkyl substituted at the nitrogen atom by lower alkyl, such as methyl, such as 4-methylpiperazinylcarbonylmethyl, lower alkoxycarbonylamino-lower alkyl, such as 5-(tert-butoxycarbonylamino)-pentyl or 3-ethoxycarbonylamino-2-isobutyl-propyl, phenyl-lower alkoxycarbonylamino-lower alkyl, such as 5-(benzyloxycarbonylamino)-pentyl, aminocarbonylamino-lower alkyl, such as 2-aminocarbonylamino-ethyl, N-phenyl-lower alkyl-N-lower alkylaminocarbonylamino-lower alkyl, such as 2-isobutyl-3-(N-benzyl-N-methylaminocarbonylamino)propyl, halo-lower alkyl wherein halogen is selected from fluorine, chlorine, bromine and iodine, for example 2-haloethyl, such as 2-fluoro-, 2-chloro-, 2-bromo-, 2-iodo-, 2,2,2-trifluoro- or 2,2,2-trichloro-ethyl, trifluoro-lower alkyl, such as trifluoromethyl, or halopropyl, such as 3-fluoro-, 3-chloro- or 3-bromo-propyl, carboxy-lower alkyl, such as carboxyethyl or 3-carboxypropyl, lower alkoxycarbonyl-lower alkyl, for example lower alkoxycarbonylethyl or lower alkoxycarbonylpropyl, such as methoxycarbonylethyl, 3-methoxycarbonylpropyl, ethoxy-carbonylethyl or 3-ethoxycarbonylpropyl, 2-halo-lower alkoxycarbonyl-lower alkyl, such as 2-chloro-, 2-bromo-, 2-iodo-or 2,2,2-trichloro-ethoxycarbonyl-2-ethyl or -3-propyl, phenyl- or naphthyl-lower alkoxycarbonyl-lower alkyl, for example benzyloxycarbonyl-lower alkyl, such as 3-benzyloxycarbonyl-2,2-dimethylpropyl, heterocyclyl-lower alkoxycarbonyl-lower alkyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicais, it also being possible for the mentioned radicals to be fully or partially saturated, such as in 4-pyridylmethyloxycarbonyl-2-ethyl or -3-propyl or 2-morpholinocarbonyloxy-4-methyl-pentyi, lower alkylsulfonyl-lower alkyl, for example 2-ethylsulfonyl- or 2-tent-butylsulfonyl-methyl, arylsulfonyl-lower alkyl wherein aryl preferably contains from 6 to 10 carbon atoms, for example phenyl or naphthyl, such as phenylsulfomethyl, carbamoyl-lower alkyl, such as carbamoylethyl or 3-carbamoylpropyl, lower alkylcarbamoyl-lower alkyl, for example lower alkylcarbamoylethyl or methyl-carbamoyl-lower alkyl, such as 2-methylcarbamoylethyl, di-lower alkylcarbamoyl-lower alkyl, for example 2-di-lower alkylcarbamoylethyl or di-methylcarbamoyl-lower alkyl, such as 2-dimethylcarbamoylethyl, hydroxy-lower alkylcarbamoyl- or di(hydroxy-lower alkyl)carbamoyl-lower alkyl, Sllch as 2-hydroxymethylcarbamoyl- or di(hydroxymethyl)carbamoyl-2-ethyl or -3-propyl, N-lower alkoxy-lower alkoxy-lower alkylcarbamoyl-lower alkyl, such as 2-isobutyl-3-(2-(2-rnethoxyethoxy)ethylaminocarbonyl)-propyl, carboxy-lower alkylcarbamoyl- or di(carboxy-lower alkyl)carbamoyl-lower alkyl, for ' example carboxymethyl- or di(carboxymethyl)-carbamoyl-2-ethyl or -3-propyl, carbamoyl-lower alkyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, terramethylene and pentamethylene wherein a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, it also being possible for the radical so formed to be fully or partially unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomorpholino-carbonyl-lower alkyl, such as in 2-morpholinocarbonyl-ethyl, 3-(morpholinocarbonyl)-propyl or 3-(morpholinocarbonyl)-2-isobutyl-propyl, N-lower alkyl-N-heterocyclyl-lower alkylcarbamoyl-lower alkyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, such as 2-(N-2-pyridylrnethyl)-N-methylcarbamoyl-ethyl, sulfamoyl-lower alkyl, such as 2-sulfamoylethyl, N-(phenyl- or naphthyl-lower alkyl)sulfamoyl-lower alkyl, such as 3-benzylamino-sulfonyl-2-isopropyl-propyl, or sulfamoyl-lower alkyl substituted at the nitrogen atom by a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom may have been xepiaced by nitrogen, nitrogen substituted by lower alkyl, such as methyl, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, it also being possible for the radical so formed to be fully or partially unsaturated, for example in the form of piperidino-, pyrazin-1-yl-, piperazin-1-yl-, 4-methylpiperazin-1-yl-, pyrimidin-1-yl-, pyridazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomorpholino-sulfonyl-lower alkyl, for example 3-(4-methylpiperazinylsulfonyl)-2-isopropyl-propyl or 3-(morpholino-sulfonyl)-2-isopropyl-propyl, oxo-lower alkyl (wherein oxo is not present at the carbon atom that is bonded to the nitrogen atam carrying the radical R~), such as 3-oxo-n-butyl or 3-oxo-n-pentyl, cyano-lower alkyl, such as cyanomethyl, 2-cyanoethyl, 2- or 3-cyano-n-propyl or 2-, 3-or 4-cyano-n-butyl, hydroxy-carboxy-lower alkyl, such as 2-hydroxy-2-carboxyethyl or 2-hydroxy-3-carboxypropyl, ~~~~~?'~~

a-naphthyloxy-carboxy-lower alkyl, such as 2-a-naphthyloxy-4-carboxy-n-butyl, hydroxy-lower alkoxycarbonyl-lower alkyl, for example 2-hydroxy-2-lower alkoxy-carbonyl-ethyl or -propyl or hydroxy-ethoxy- or hydroxy-methoxy-carbonyl-lower alkyl,' such as 2-hydroxy-2-ethoxy- or -methoxy-carbonylethyl or 2-hydroxy-3-ethoxy-or -methoxy-carbonyl-propyl, a-naphthyloxy-lower alkoxycarbonyl-lower alkyl, for example a-naphthyloxy-lawer alkoxycarbonyl-2-ethyl,,-2-propyl or -2-butyryl or a-naphthyloxyethoxycarbonyl-lower alkyl, such as a-naphthyloxyethoxycarbonyl-2-ethyl, 2-a-naphthyloxy-3-ethoxycarbonyl-propyl or 2-a-naphthyloxy-4-tent-butoxycarbonylbutyl, lower alkylcarbonylhalo-lower alkyl, such as 3-ethoxycarbonyl-2-difluoromethyl, a-naphthyloxy-benzyloxycarbonyl-lower alkyl, such as 2-a-naphthyloxy-3-benzyloxy-carbonyl-propyl, esterified hydroxy-lower alkoxycarbonyl-lower alkyl wherein the hydroxy group is esterified by lower allcanoyl, for example acetyl, propionyl or pivaloyl, cycloalkyl-lower alkanoyl wherein cycloallcyl contains from 3 to 7 carbon atoms and lower alkanoyl is as last defined, for example cyclohexylcarbonyl or 2-cyclohexyl- or 2-cyclopentyl-acetyl, bicycloalkyl-lower alkanoyl wherein bicycloallcyl contains, for example, from S to 10, especially from 6 to 9, carbon atoms, such as in bicyclo-hexyl-, -heptyl-, -octyl-, -nonyl-or -decyl-acetyl or -3-propionyl, for example bicyclo[3.1.0]hex-1-, -2- or -3-yl-, bicyclo-[4.1.0]hept-1- or -7-yl-, bicyclo[2.2.1]hept-2-yl-, for example endo- or exo-norbornyl-, bicyclo[3.2.1]oct-2-yl-, bicyclo[3.3.0]oct-3-yl- or bicyclo[3.3.1]non-9-yl-, and also a- or (~-decahydronaphthyl-acetyl or -3-propionyl, tricycloalkyl-lower alkanoyl wherein tricycloalkyl contains, for example, from 8 to 10 carbon atoms, for example in tricyclo-[5.2.1.02~6]dec-8-yl- or adamantyl-, such as 1-adamantyl-acetyl, aryl-Iower allcanoyl wherein aryl contains from 6 to 14 carbon atoms, for example phenyl, indenyl, indanyl, naphihyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, and may be unsubstituted or mono- to tri-substituted by lower alkyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lawer alkylamino, halogen, such as fluorine, chlorine ox bromine, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, for example methylsulfonyl, phosphono, hydroxy-lower alkoxyphospharyl, di-lower alkoxyphosphoryl, carbamoyl, sulfamoyl, nitro and/or by cyano, lower alkoxycarbonyl, for example ten-butoxycarbonyl, 2-halo-lower alkoxy-carbonyl, as defined above, or by phenyl- or fluorenyl-lower alkoxycarbonyl, for example benzyloxycarbonyl or 9-fluorenylmethoxycarbonyl, such as 2-acetoxy-2-methoxy-carbonyl-ethyl, 2-benzoyloxy-, 2-(1- or 2-naphthoyloxy)-, 2-(phenyl-2-acetoxy)-, 2-(1- or 2~~~'l?p~~
-s~-2-naphthyl-2-acetoxy)-, 2-(4-methylphenyl-2-acetoxy)-, 2-(4-methoxyphenyl-2-acetoxy)-or 2-(2-(o,o-dichlorophenyl)-2-acetoxy)-2-methoxycarbonyl-ethyl or,-3-propyl, dihydroxy-carboxy-lower alkyl, such as 2,3-dihydroxy-3-carboxy-propyl, dihydroxy-lower alkoxycarbonyl-lower alkyl, such as 2,3-dihydroxy-3-ethoxy- or -methoxy-carbonyl-propyl, dihydroxy-lower alkaxycarbonyl-lower alkyl esterified by lower alkanoyl, such as acetyl, propionyl or butyryl, lower alkoxycarbonyl, for example tert-butoxycarbonyl, phenyl- or fluorenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl or 9-fluorenylmethoxy-carbonyl, lower alkylsulfonyl or by toluenesulfonyl, for example di-lower alkanoyloxy-lower alkoxy-propyl, such as 2,3-diacetoxy-3-meihoxycarbonyl-propyl, a-naphthyloxy-di-lower alkylamino-lower alkyl, such as 2-a-naphthyloxy-s-dimethyl-amino-pentyl, a-naphthyloxy-caxbamoyl-lower alkyl, such as 2-a-naphthyloxy-4-carbamoyl-butyl, a-naphthyloxy-oxo-lower alkyl (wherein oxo is not present at the carbon atom that is bonded to the nitrogen atom carrying the radical R~), such as 2-a-naphthyloxy-oxo-pentyl, or a-naphthyloxy-cyano-lower alkyl, such as 2-a-naphthyloxy-cyano-ethyl or 2-a-naphthyl-oxy-4-cyano-butyl.
Lower alkyl that is unsubstituted or mono- or poly-substituted by hydroxy, lower alkoxy, amino, mono- or di-lower alkylamino, fluorine, chlorine or by cyano is preferred, and lower alkyl, such as methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl or tent-butyl, is very especially preferred.
Cycloalkyl R3, R4 or R7 is preferably as defined under cyeloalkyl-lower alkanoyl Rl, R2, Rg or Rg, for example cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cyclo-heptyl, cycloallcyl being unsubstituted or mono- to tri-substituted by lower alkyl, such as isopropyl, halo-lower alkyl, such as trifluoromethyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy ~r N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such as fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxy-carbanyl, lower alkanoyl, lower alkylsulfonyl, for example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono-or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, vitro and/or by cyano, such as cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl, especially cyclohexyl.

~~~~s~"'~~
-ss-Aryl R3, R4 or R7 is preferably one of the unsubstituted or substituted aryl radicals mentioned under aryl-lawer alkanoyl R1, R2, Rg or R~ and is especially phenyl, naphthyl or fluorenyl that is unsubstituted or mono- to tri-substituted by lower alkyl, such as isopropyl, halo-lower alkyl, such ~as trifluoromethyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such as fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxy-carbonyl, lower alkanoyl, lower alkylsulfonyl, for example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono-or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, vitro and/or by cyano, such as phenyl, 4-methoxyphenyl, 4-fluorophenyl, 4-nitrophenyl, 4-cyanophenyl or 1- or 2-naphthyl.
lHeterocyclyl R3, R4 or R7 is preferably as defined under heterocyclyl Rl, R2, Rg or R9, which is unsubstituted or substituted as defined there, and is selected especially from 2- or 3-pyrrolyl, 4- or 5-methylpyrrolyl or 4- or 5-phenylpyrrolyl, 2-thienyl, 2-furyl, 2-, 3- or 4-pyridyl, 2-, 3- or 5-indolyl, 1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro-or 4,5-dimethyl-indol-2-yl, 1-benzylindol-2- or -3-yl, 4,5,6,7-tetrahydroindol-2-yl, cyclo-hepta[b]pyrrol-5-yl, 2-, 3- or 4-quinolyl or 4-hydroxyquinol-2-yl, 1-, 3- or 4-isoquinolyl, 1-oxo-1,2-dihydroisoquinol-3-yl, 2-quinoxalinyl, 3,1-benzofuran-2-yl, benz[e]indol-2-yl, (3-carbolin-3-yl, 3-chromanyl, 3-thiochromanyl, 3-pyrrolidinyl, 3- or 4-hydroxypyrrolidin-2-yl, such as 5-oxopyrrolidin-2-yl, 2-, 3- or 4-piperidinyl, 2- or 3-morpholinyl, 2- or 3-thiomorpholinyl, S,S-dioxothiomorpholin-2- or -3-y.l, 2- or 3-indolinyl, 1,2,3,4-tetra-hydroquinol-2-, -3- or -4-yl, 1,2,3,4-tetrahydroisoquinol-1-, -2- or -3-yl, or 1-oxo-1,2,3,4-tetrahydroisoquinol-3-yl.
Unsubstituted or substituted alkenyl R3, R4 or R7 is preferably as defined under alkenyl R1, R2, Rg or R9, especially lower alkenyl that is unsubstituted or substituted as defined there, for example lower alkenyl, such as vinyl, allyl or 2- or 3-butenyl, cycloalkyl-lower alkenyl wherein cycloalkyl is as defined in the case of cycloalkyl-lower alkanoyl Rl, R2, Rg or R9 and is unsubstituted or mono- to tri-substituted by lower alkyl, such as isopropyl, halo-lower alkyl, such as trifluoromethyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lawer alkyl-carbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such as fluorine, chlorine or bromine, cttrboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, for example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl ar di-lower aikoxypho~phoryi, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano and is banded especially to the terminal carbon atom of lower alkenyl, such as cyclobutyl-, cyclopentyl-, cyclohexyl- or cycloheptyl-methyl-2-vinyl, -2-or -3-allyl or -2-, -3- or -4-but-2-enyl, aryl-lower alkenyl having an unsubstituted or substituted aryl radical defined under aryl R3 or Rq. that is banded, preferably terminally, to lower alkenyl, and having a lower alkenyl radical defined under lower allcenyl R1, R2, Rg or R9, such as styryl, 3-phenyl-allyl (cinnamyl), 2-(a-naphthyl)-vinyl or 2-((i-naphthyl)-vinyl, or unsubstituted ar substituted heteracyclyl-lower alkenyl that contains, for example, an unsubstituted or substituted lower alkenyl radical mentioned under alkenyl Rl, R2, Rg or Rc~, for example vinyl, allyl or 2- or 3-butenyl, that is substituted, preferably at the terminal carbon atom, by an unsubstituted or substituted heterocyclyl radical mentioned under heterocyclyl R1, R2, Rg or R9, for example in the form of pyrimidin-1-yl-, piper-idino-, pyrazin-1-yl-, piperazin-1-yl-, pyri.dazin-1-yl-, morpholino-, thiomorpholino- or S,S-dioxothiomorpholino-lower alkenyl, such as in 2-morpholino-vinyl, 3-morpholino-allyl or ~-morpholino-2- or -3-butenyl, unsubstituted or lower alkyl- or phenyl-substituted pyrrolyl-lower alkenyl, such as 2- or 3-pyrrolyl-vinyl or -allyl, ~.- or 5-methylpyrrolyl-vinyl or -allyl or 4- or 5-phenylpyrrolyl-vinyl or -allyl, thienyl-lower alkenyl, such as 2-thienyl-vinyl or -allyl, furyl-lower alkenyl, such as 2-furyl-vinyl or -allyl, pyridyl-lower alkenyl, such as 2-, 3- or 4-pyridyl-vinyl ar -aiiyl, indalyl-lower alkenyi that is unsubsti-tuted or substituted by lower alkyl, for example methyl, phenyl-lower alkyl, for example benzyl, lower alkoxy, for example methoxy, phenyl-lower allcoxy, far example benzyloxy, or by halogen, for example chlorine, such as 2-, 3- or 5-indolyl-vinyl or -allyl, 1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl-, 1-benzyl-indol-2-yl- or -3-yl-vinyl or -allyl, 4,5,6,7-tetrahydroindol-2-yl-methyl, -ethyl or -n-propyl, cycloheptajb]pyrrol-5-yl-vinyl or -allyl, unsubstituted or hydroxy-substituted quinolyl-lower alkenyl, for example 2-, 3- or 4-quinolyl- or 4-hydroxyquinol-2-yl-vinyl or -allyl, unsubstituted or hydroxy-substituted isoquinolyl-lower alkenyl, such as 1-, 3-or 4-isoquinolyl- or 1-oxo-1,2-dihydroisoquinol-3-yl-vinyl or -allyl, 2-quinoxalinyl-vinyl or -allyl, 3,1-benzofuran-2-yl-vinyl or -allyl, benz[e]indol2-yl-vinyl or -allyl, ~i-carbolin-3-yl-vinyl or -allyl, 3-chromanyl-vinyl or -allyl, 3-thiochromanyl-vinyl or -allyl, 3-pyrrol-idinyl-vinyl or -allyl, hydroxypyrrolidinyl-lower alkenyl, such as 3- or 4-hydroxy-pyrrolidin-2-yl-vinyl or -allyl, oxopyrrolidinyl-lower alkenyl, such as 5-oxopyrrolidin-2-yl-vinyl or -allyl, piperidinyl-lower alkenyl, such as 2-, 3- or 4-piperidinyl-vinyl or c -allyl, morpholinyl-lower alkenyl, such as 2- or 3-morpholinyl-vinyl or -allyl, thiomorpho-linyl-lower alkenyl, such as 2- or 3-thiomorphalinyl-vinyl or -allyl, S,S-dioxothio-morpholinyl-lower alkenyl, such as S,S-dioxothiomorpholin-2- or -3-yl-vinyl or -allyl, indolinyl-lower alkenyl, such as 2- or 3-indolinyl-vinyl or -allyl, 1,2,3,4-tetrahydro-quinolyl-lower alkenyl, such as 1,2,3,4-tetrahydroquinol-2-, -3- or -4-yl-vinyl or -allyl, 1,2,3,4-tetrahydroisoquinolyl-lower alkenyl, such as 1,2,3,4-tetrahydroisoquinol-1-, -2- or -3-yl-vinyl or -allyl, or 1-oxo-1,2,3,4-tetrahydroisoquinol-3-yl-vinyl or -allyl.
Unsubstituted or substituted alkylene formed by R3 and R4 together contains especially an alkylene radical having up to 20 carbon atoms, it also being possible for the mentioned radicals to contain one or more double bonds, preferably lower alkylene, for example ethylene, trimethylene, tetramethylene, pentamethylene, hexamethylene or hepta-methylene, that is unsubstituted or substituted, especially by unsubstituted or substituted aryl, as defined under aryl-lower alkanoyl R1, R2, Rg or Rc~, preferably by phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, which are unsubstituted or mono- to tri-substituted by radicals such as lower alkyl, for example methyl, ethyl or propyl, halo-lower alkyl, for example trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, for example methoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower allcylcarbamoyl-lower alkoxy, amino, mano- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine, chlorine or bromine, cauboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkyl-sulfonyl, for example methylsulfonyl, phosphono> hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono-or di-lower alkylaminosulfonyl, nitro and/or cyano, and/or is substituted in the same manner as lower alkanoyl in aryl-lower alkanoyl R1, R2, Rg or R9, especially by lower alkyl, for example methyl, hydroxy, lower alkoxy, for example methoxy or ethoxy, lower alkanoyloxy, for example acetoxy or propionyloxy, benzoyloxy, phenylacetoxy or 1- or 2-naphthoyloxy, lower alkoxycarbonyloxy, for example isopropoxycarbonyloxy or tert-butoxycarbonyloxy, phenyl-lower alkoxycarbonyloxy, for example benzyloxy-carbonyloxy, 9-fluorenylmethoxycarbonyloxy, sulfonyloxy, lower alkylsulfonyloxy, for example methyl- or ethyl-sulfonyloxy, phenylsulfonyloxy, 2- or 4-toluenesulfonyloxy, amino, mono- or di-lower alkylamino, for example mono- or di-methylamino or -ethyl-amino, lower alkanoylamino, for example acetylamino or pivaloylamino, carboxy, lower alkoxycarbonyl, for example isopropoxy- or tert-butoxy-carbonyl, benzyloxycarbonyl, 9-fluorenylmethoxycarbonyl, lower alkanoyl, for example acetyl or propionyl, lower alkylsulfonyl, such as methylsulfanyl or tent-butylsulfonyl, phosphono, carbamoyl, mono-or di-lower alkylcarbamoyl, for example N-methylcarbamoyl or N,N;dimethylcarbamoyl, piperidino, pyrazin-1-yl, pyrimidin-1-yl, pyridazin-1-yl, morpholino, thiomorpholino or S,S-dioxothiomorpholino, sulfambyl, oxo and/or by cyano, such as ethylene, ethyl-ethylene, trimethylene, propylene or tetramethylene.
Unsubstituted or substituted alkylidene formed by R3 and R4 together contains up to 20 carbon atoms and no double bonds or one or more double bonds in addition to the linking double bond, and is preferably lower alkylidene, for example methylene, ethylidene, propylidene, butylidene or pentylidene, that is unsubstituted or substituted especially by cycloalkyl, such as mentioned under cycloalkyl-lower alkanoyl Rl, R2, Rg or R~, for example cyclopropyl, cyclobutyl, cyclopenryl or cyclohexyl, cycloalkenyl, such as mentioned under cycloalkenyl-lower alkanoyl Rl, R2, Rg or R9, for example cyclo-hexen-1-yl or 1,4-cyclohexadienyl, unsubstituted or substituted aryl, such as defined under aryl-lower alkanoyl Rl, R2, Rg or R9, preferably by phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, which are unsubstituted or mono- to tri-substituted by radicals such as lower alkyl, for example methyl, ethyl or propyl, halo-lower alkyl, for example trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, far example methoxy, cwbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, phenyl-, na;phthyl- or fluorenyl-lower alkoxy-carbonyl, lower alkanoyl, sulfo, lower aL~Cylsulfonyl, :fox example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower aLkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylaminosulfonyl, nitro and/or cyano, and/or is substituted in the same manner as lower alkanoyl in aryl-lower alkanoyl R1, R2, Rg or R9, especially by lower alkyl, for example methyl, hydroxy, lower alkoxy, for example methoxy or ethoxy, lower alkanoyloxy, for example acetoxy or prapionyloxy, benzoyloxy, phenylacetoxy or 1- or 2-naphthoyloxy, lower alkoxycarbonyl-oxy, for example isopropoxycarbonyloxy or tert-butoxycarbonyloxy, phenyl-lower alkoxy-carbonyloxy, for example benzylaxycarbonyloxy, 9-fluorenylmethoxycarbonyloxy, sulfonyloxy, lower alkylsulfonyloxy, for example methyl- or ethyl-sulfonyloxy, phenyl-sulfonyloxy, 2- or 4-toluenesulfonyloxy, amino, mono- or di-lower alkylamino, for example mono- or di-methyl-amino or -ethyl-amino, lower alkanoylamino, for example acetylamino or pivaloylamino, carboxy, lower alkoxycarbonyl, for example isopropoxy-or tert-butoxy-carbonyl, benzyloxycarbonyl, 9-fluorenylmethoxycarbonyl, lower alkanoyl, X07 ~~

for example acetyl or propionyl, lower alkylsulfonyl, such as methylsulfonyl or tent-butyl-sulfonyl, phosphono, carbamoyl, mono- or di-lower alkylcarbamoyl, for example N-methylcarbamoyl or N,N-dimethylcarbamoyl, piperidino, pyrazin-1-yl, pyrimidin-1-yl;
pyridazin-1-yl, morpholino, thiomorpholino or S,S-dioxothiomorpholino, sulfamoyl, oxo and/or by cyano, such as ethylidene, propylidene, butylidene, benzylidene or cinnamylidene.
Unsubstituted or substituted benzo-fused alkylene formed by R3 and Rq.
together contains up to 20 carbon atoms and is preferably lower alkylene, for example ethylene, trimethyl-ene, tetramethylene, pentamethylene, hexamethylene or heptamethylene, anto which a benzene ring has been fused, and is unsubstituted or substituted especially by unsubsti-tuted or substituted aryl, as deFtned under aryl-lower alkanoyl Rl, R2, Rg or R9, preferably by phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, which are unsubstituted or mono- to tri-substituted by radicals such as lower alkyl, for example methyl, ethyl or propyl, halo-lower alkyl, for example trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, for example methoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine, chlorine or bromine, carboxy, lower alkoxy-carbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, fox example methylsulfonyl, phosphono, hydroxy-lower alkoxy-phosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylaminosulfonyl, nitro and/or cyano, and may also be substituted by lower alkyl, for example methyl, hydroxy, lower alkoxy, for example methoxy or ethoxy, lower alkanoyloxy, for example acetoxy or propionyloxy, benzoyloxy, phenylacetoxy or 1- or 2-naphthoyloxy, lower alkoxycarbonyloxy> for example iso-propoxycarbonyloxy or tart-butoxycarbonyloxy, phenyl-lower alkoxycaxbonyloxy, for example benzyloxycarbonyloxy, 9-fluorenylmethoxycarbonyloxy, sulfonyloxy, lower alkylsulfonyloxy, for example methyl- or ethyl-sulfonyloxy, phenylsulfonyloxy, 2- or 4-toluenesulfonyloxy, amino, mono- or di-lower alkylamino, for example mono- or di-methyl-amino or -ethyl-amino, lower alkanoylamino, for example acetylamino or pivaloylamino, carboxy> lower alkoxycarbonyl, for example isopropoxy- or tent-butoxy-carbonyl, benzyloxycarbonyl, 9-fluorenylmethoxycarbonyl, lower alkanoyl, for example acetyl or propionyl, lower alkylsulfonyl, such as methylsulfonyl or tert-butylsulfotryl, phosphono, carbamoyl, mono- or di-lower alkylcarbamoyl, for example N-methyl-carbamoyl or N,N-dimethylcarbamoyl, piperidino, pyrazin-1-yl, pyrimidin-1-yl, pyrid-~?~~

azin-1-yl, moaphoiino, thiomorpholino or S,S-dioxothiomorpholino, sulfamoyl, oxo and/or by cyano, such as ortho-phenylene. , When, in the compounds of formula I substituted by the mentioned radicals, nitrogen atoms having free hydrogen and/or hydroxy groups are vicinal with respect to double or triple bonds (as in the case of unsubstituted or substituted alkenyl or alkynyl R1, R2, Rg or R9), the corresponding tautomeric imino and oxo compounds are always also included.
Salts of compounds of formula I are especially acid addition salts, salts with bases or, where several salt-forming groups are present, can also be mixed salts or internal salts.
Salts are especially the pharmaceutically acceptable, non-toxic salts of compounds of formula I.
Such salts are formed, for example, from compounds of formula I having an acid group, for example a carboxy group, a sulfo group, or a phosphoryl group substituted by one or two hydroxy groups, and are, for example, salts thereof with suitable bases, such as non-toxic metal salts derived from metals of groups Ia, Ib, lIa and IIb of the Periodic Table of the Elements, especially suitable alkali metal salts, for example lithium, sodium or potassium salts, or alkaline earth metal salts, for example magnesium or calcium salts, also zinc salts or ammonium salts, as well as salts fozrned with organic amines, such as unsubstituted or hydroxy-substituted mono-, dl- or tri-alkylamines, especially mono-, di-or tri-lower alkylamines, or with quaternary ammonium compounds, for example with N-methyl-N-ethylamine, diethylamine, triethylamine, mono-, bis- or tris-(2-hydroxy-lower alkyl)amines, such as mono-, bis- or tris-(2-hydroxyethyl)amine, 2-hydroxy-tert-butyl-amine or tris(hydroxymethyl)methylamine, N,N-di-lower alkyl-N-(hydroxy-lower alkyi)-amines, such as N,N-dimethyl-N-(2-hydroxyethyl)-amine or tri-(2-hydroxyethyl)-amine, N-methyl-D-glucamine, or quaternary ammonium salts, such as tetrabutyiammonium salts. The compounds of formula I having a basic group, for example an amino group, can form acid addition salts, for example with inorganic acids, for example hydrohalic acids, such as hydrochloric acid, sulfuric acid or phosphoric acid, or with organic carboxylic, sulfonic, sulfo or phospho acids or N-substituted sulfamic acids, for example acetic acid, propionic acid, giycolic acid, succinic acid, malefic acid, hydroxymaleic acid, methyl-maleic acid, fumaric acid, malic acid, tartaric acid, gluconic acid, glucaric acid, glucuronic acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, salicylic acid, 4-aminosali-cyiic acid, 2-phenoxybenzoic acid, 2-acetoxybenzoic acid, embonic acid, nicotinic acid or a isonicotinic acid, as well as with amino acids, for example the a-amino acids mentioned hereinbefore, especially glutamic acid and aspartic acid, and with methanesulfonic acid, ethanesulfonic acid, 2-hydroxyethanesulfonic acid, ethane-1,2-disulfonic acid, benzene-sulfonic acid, 4-methylbenzenesuJfonic acid, naphthalene-2-sulfonic acid, 2-or 3-phosphoglycerate, glucose-6-phosphate, N-cyciohexylsulfamic acid (forming cycla-mates) or with other acidic organic compounds, such as ascorbic acid.
Compounds of formula I having acid and basic groups can also form internal salts.
For isolation or purification purposes, it is also possible to use pharmaceutically unaccept-able salts.
The compounds of the present invention have an inhibiting effect on viral aspartate proteases, especially a gag-protease-inhibiting effect. In the tests described below, at concentrations of 10-6 to 10-9 mol/1 they inhibit especially the action of the gag-protease of HIV-1 and HIV-2 and are therefore suitable as agents against diseases caused by those viruses or by related retroviruses, fox example against EI.mS.
The ability of the compounds of formula I to inhibit the proteolytic activity of, fox example, HIV-1 protease can be demonstrated, for example, by the method described by J.
I-Iansen et al., The EMBO Journal 7, 1785-1791 (1988). In that method, the inhibition of the action of the gag-protease is measured on a substrate that is a fusion protein of the gag-precursor protein and MS-2, expressed in E. coli. The substrate and its cleavage products are separated by polyacrylamide gel electrophoresis and made visible by immunoblotting using monoclonal antibodies to MS-2.
In a test that is even simpler to carry out and that gives precise quantitative results, there is used as substrate for the gag-protease a synthetic peptide that corresponds to the cleavage site of the gag-precursor protein. That substrate and its cleavage products can be analysed by high-pressure liquid chromatography (HPLC).
For example, there is used as substrate for a recombinant HIV-1 protease (preparation in accordance with Billich, S. et al., J. Biol. Chem. 263(34), 17905 - 17908 (1990)) a synthetic chromophoric peptide (for example HT~ARVL[N02]FEANleS (Sachem, Switz-erland) or an icosapeptide such as RRSNQVSQNYPIVQNIQGRR (prepared by peptide synthesis using known methods) that corresponds to one of the cleavage sites of the gag-precursor protein. That substrate and its cleavage products can be analysed by high-0~

pressure liquid chromatography (HPLC).
For that purpose an inhibitor of formula I to be tested is dissolved in dimethyl sulfoxide;
the enzyme assay is carried out by adding suitable dilutions of the inhibitor in 20 mM
~i-morpholinoethanesulfonic acid (MES) buffer, pH 6.0, to the assay mix of 67.2 ~.M of the above-mentioned chromophoric peptide in 0.3M sodium acetate, 0.1M NaCI, pH
7.4, or 122 ~.M of the above-mentioned icosapeptide in 20 mM MES buffer, pH 6Ø
The size of the batches is 100 ~1. The reaction is started by the addition of, in the first case, 2 ~.1 and, in the second case, 10 ~.1 of HIV-1 protease and is stopped in the first case after 15 min by the addition of 100 ~1 of 0.3M HC104 and in the second case after incubation for one hour at 37°C by the addition of 10 ~.1 of 0.3M HC104. After centrifugation of the sample for 5 min at 10 000 x g in 100 ~.1 (batch with chromophoric peptide) or 20 ~.1 (icosapeptide batch) of the resulting supernatant and application to a 125 x 4.6 mm Nucleosil~ C18-5~, I-IPLC column (Macherey & Nagel, Diiren) and elution, the reaction products are quantified by reference to the peak height of the cleavage product at 280 (batch with chromophoric peptide) or at 215 nm (batch with icosapeptide), gradient:
100 % eluant 1-> 50 % eluant 1/50 % eluant 2 (eluant 1: 75 % acetonitrile, 90 % H20, 0.1 % trifluoroacetic acid (TFA); eluant 2: 75 % acetonitrile, 25 % H20, 0.08 % TFA) in the course of 15 min; throughput rate 1 ml/min.
In this test, there are preferably obtained ICSp values (ICSp = the concentration that reduces the activity of HIV-1 protease by 50 % compared with a control without an inhibitor) of approximately from 10-6 to 10-9M, especially from approximately 10-7 to approximately 10-8M, for compounds of formula I.
In a further test it can be shown that the compounds of the present invention protect cells that normally become infected by HIV from such infection or at least slow down such infection. In that test the human T-cell leukaemia cell line MT-2 (Science 229, 563 (1985)), which is extremely sensitive to the cytopathogenic effect of HIV, is incubated with HIV alone or with HIV in the presence of the compounds of the invention and after a few days the viability of the cells thus treated is assessed.
For that purpose the MT-2 cells are kept at 37°C in humid air with 5 %
C02 in RPMI
1640 medium (Gibco, Switzerland; RPMI 1640 comprises an amino acid mixture without L-Gln) supplemented with 10 % heat-inactivated foetal calf serum, L-glutamine, hepes (2-(4-(2-hydroxyethyl)-1-piperazino]-ethanesulfonic acid) and standard antibiotics. 50 ~.1 fy~ ..
of the particular test compound in culture medium and 10(9 p.1 of HIV-1 in culture medium (800 TCID50/ml) (TCID50 = Tisscre Culture Infectious Dose '_i0 = dose drat infects 50 %
of the MT-2 cells) axe added to 4x103 exponentially growing MT-2 cells in 50 wl of culture medium per well on 9fi-well microtitre, plates. Parallel batches on a further micro-titxe plate with cells and test compound receive 1t~0 ~.l of culture medium without virus.
After incubation for 4 days, the reverse transcriptase (RT) activity is determined in 10 p.l of cell supernatant. The RT activity is determined in 50 mM of Iris (a,a,a-izis(hydroxy-rnethyl)methylamine, ultra pure, Merck, Federal Republic of Clermany) pH 7.8;
75 mM of KCI, 2 mM of dithiothreitol, 5 mM of MgCl2; 0.05 % Nonidet P-40 (detergent;
Sigma, Switzerland); 50 ~.g/ml of polyaderaylic acid (F'harmacia, Sweden); 1.6 p.g/ml of dT(12-18) TM
(Sigma, Switzerland). The mixture is filtered through a 0.45 a Acrodisc filter (Gellman Science Inc, Ann Arbor) and stored at -20°C. 0. I % (;v/v) [alpha-32P]dTTP is added to aliquots of that solution in order to achieve a final radioactive activity of 10 p.Ci/ml. 10 ltl of the culture supernatant are transferred to a new 96-well microtitre plate and. 30 ~1 of the mentioned RT cocktail are added thereto. After mixing, the plate is incubated for from 1.5 TM
to 3 hours at 37°C. 5 p.l of that reaction mixture are transferred to Whatman DE81 paper (Whatman). The dried filters are washed three times for 5 minutes with 300 mM
of NaCI/25 mM of trisodium citrate and once with 95 °lo ethanol and again air-dried. Eval-r nation is effected in a Matrix packard 9b-well counter (Packard). The ED90 values are calculated and defined as the lowest concentration of the p~.rticular test compound that reduces the RT activity by 90 %'o in comparison with cell batches not treated with the test compound. The RT activity is a measure of the reproduction c~f HIV-1.
In that test, the campounds of the invention exhibit an ED90 of approximately from 10-5 to 10-8M, preferably approximately from 5 x 10-7 to 5 x 10-BM.
In the groups of compounds of formula I mentioned below" it may be advantageous, for example in order to replace rather general definitions with more specific definitions, to use definitions of radicals from the above-mentioned general defrrritions or t:o insert or omit definitions from the other groups.
Preference is given to a corrrpcaund of formula 1 according tc~ claim 1 wherein R 1 and R9 are each independently of the other hydrogen; lower alkanoyl" such as formyl, acetyl, propionyi, butyryl or pivaloyl, especially acetyl; aryl-tower alkarroyl wherein aryl is preferably as defined above under the general clef"initiorzs c~f ~ary~l-lower alkanoyl and is unsubstituted or substituted as defined them:, i.e. aryl k~as from ~ to 14 carbon atoms, as in _6q_ phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, and may be unsubstituted or especially mono- to tri-substituted by lower alkyl, for example methyl, ethyl or propyl, halo-lower alkyl, for example trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkox~y, for example methoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower allcoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, such as tent-butoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl, lower aLkanoyl, sulfo, lower alkylsulfonyl, for example methyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylamino-sulfonyl, nitro and/or by cyano, wherein phenyl may be present up to three times, for example in diphenyl-, dibenzyl- or triphenyl-lower alkanoyl, such as diphenyl-, dibenzyl-or triphenyl-acetyl, and wherein lower alkanoyl is unsubstituted or substituted by carba-rnoyl or by carbamoyl substituted at the nitrogen atom by one or two xadicals selected from lower alkyl, carboxy-lower alkyl, lower alkoxycarbonyl-lower alkyl, di-lower alkyl-amino-lower alkyl, aminocarboxy-lower alkyl, hydroxy-lower alkyl and di-lower alkoxy-lower alkyl, preferably as described under aryl-lower alkanoyl above in the general defini-tions, for example 4-chloro-, 4-methoxy- or 4-nitro-bt:nzoyl, naphthylcarbonyl, such as a-or 13-naphthylcarbonyl, or 1,8-naphthalene-dicarbonyl bonded to the amino group via both carbonyl groups, indenylcarbonyl, such as I-, 2- or 3-indenylcarbonyl, indanylcarbonyl, such as 1- or 2-indanylcarbonyl, phenanthrenylcarbonyl, such as 9-phenanthrenylcarbonyl, phenyl-lower alkanoyl, such as phenylacetyl or 3-phenylpropionyl, a-naphthylacetyl, 13-naphthylacetyl, lower alkylphenylacetyl, such as 4-methylphenylacetyl, lower alkoxy-phenylacetyl, such as 4-methoxyphenylacetyl, 3-phenylpropionyl, 3-(p-hydroxyphenyl)-pxopionyl, diphenylacetyl, di(4-methoxyphenyl)acetyl, triphenylacetyl, 2,2-dibenzylacetyl, 3-a- or 3-~i-naphthylpropionyl, phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carbamoyl, such as 2(R,S)-carbamoyl-3-phenylpropionyl, 3-phenyl- or 3-a-naphthyl-2-carbamoylpropionyl, 3-phenyl- or 3-a-naphthyl-2-tert-butylcarbamoyl-propionyl, 3-phenyl- or 3-a-naphthyl-2-(2-dimethylaminoethyl)carbamoylpropionyl, 3-a-naphthyl-2-(carboxy- or tert-butoxycarbonyl)methylcarbamoylpropionyl, 3-phenyl- or 3-a-naphthyl-2-(3-hydroxy-2-propyl)carbamoylpropionyl, 3-phenyl- or 3-a-naphthyl-2-(2,2-dimethoxyethyl)-carbamoylpropionyl, 3-phenyl- or 3-a-naphthyl-2-(5-amino-5-carboxypentyl)-carbamoylpropionyl, especially phenyl-lower alkanayl, such as phenyl-acetyl, or phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carb-amoyl, such as 2(R,S)-carbamoyl-3-phenylpropionyl; heterocyclyl-lower alkanoyl that is preferably as defined above for heteroaryl-lower alkanoyl R1, R2, Rg and R9, especially heterocyclyl-lower alkanoyl wherein lower alkanoyl is unsubstituted and wherein hetero-cyclyl is preferably a single or a double ring system having from 3 to 10 ring atoms, is bonded via a carbon atom or, especially, via a nitrogen atom, contains up to three further hetero atoms selected from oxygen, nitrogen, sulfur, selenium, and sulfur linked to 1 or 2 oxygen atoms, and may be unsaturated or partially or fully saturated, for example thienyl-, furyl-, pyranyl-, pyrrolyl-, imidazolyl-, pyrazolyl-, oxazolyl-, isoxazolyl-, thiazolyl-, furazanyl-, tetrazolyl-, pyridyl-, pyrazinyl-, pyrimidinyl-, pyridazinyl-, azepinyl-, indolyl-, benzimidazolyl-, 1H-indazolyl-, quinolyl-, isoquinolyl-, quinoxalinyl-, quinazolinyl-, cinnolyl-, purinyl-, pteridinyl-, naphthyridinyl-, 4H-quinolizinyl-, 3,1-benzofuranyl-, 4,1-benzoxazinyl-, 4,1-benzothiazinyl-, cyclohexa[b]pyrrolyl-, cyclohepta[b]pyrrolyl-, cyclohexa[d]pyrazolyl-, cyclohexa[b]pyzidyl-, cyclohexa[b]pyrazinyl-, cyclohexa[b]~-pyrimidinyl-, cyclohexa[b]-1,4-oxazinyl-, cyclohexa[b]-1,4-thiazinyl-, pyrrolidinyl-, pyrrolinyl-, irnidazolidyl-, 2-imidazolinyl-, 2,3-dihydropyridyl-, piperidyl-, piperazinyl-, 2,3,5,6-tetrahydropyrazinyl-, morpholinyl-, thiomorpholinyl-, S,S-dioxo-thiomorpholinyl-, indolinyl-, isoindolinyl-, 4,5,6,7-tetrahydroindolyl-, 1,2,3,4-tetrahydroquinolyl-, 1,2,3,4-te-trahydroisoquinolyl-, chromanyl-, thiochromanyl-, 1,2,3,4-tetrahydro-3,1-benzodiazinyl-, 3,4-dihydro-3H-4,1-benzoxazinyl- or 3,4-dihydro-3H-4,1-benzothiazinyl-lower alkanoyl, the mentioned heterocyclyl radicals being unsubstitutf;d or substituted by lower alkyl, for example rnetlryl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, for example benzyl, hydroxy-lower alkyl, for example hydroxymethyl or 2-hydroxyethyl, lower alkoxy-lower alkyl, for example methoxymethyl or 2-methoxyethyl, phenoxy- or naphthyloxy-lower alkyl, for example 2-phenoxyethyl, 1- or 2-naphthyloxymethyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, for example benzyloxy-lower alkyl, lower alkanoyl-oxy-lower alkyl, for example acetoxymethyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, for example benzoyloxy-, phenylacetoxy- or 1- or 2-naphthoyloxy-methyl, -2-ethyl or -2-(2,2-dimethylethyl), lower alkoxycarbonyloxy-lower alkyl, for example tent-butoxycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxy-carbonyloxy-lower alkyl, for example 2-benzyloxycarbonyiaxyethyl or 9-fluorenyl-methoxycarbonyloxyethyl, amino-lower alkyl, for example aminomethyl, 2-aminoethyl or 2-aminopropyl, carboxy-lower alkyl, for example carboxymethyl or 2-caxboxyethyl, hydroxy, lower alkoxy, for example methoxy or ethaxy, phenyl- or naphthyl-lower atkoxy, for example benzyloxy or 1- or 2-naphthyloxy, amino, lower alkylamino, for example methyl-, ethyl- or tent-butyl-amino, di-lower alkylamino, for example dimethyl-or diethyl-amino, carboxy, lower alkoxycarbonyl, for example methoxy-, isopropoxy-, sec-butoxy- or tert-butoxy-carbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, for zz7~

example benzyloxycarbonyl, halogen, for example fluorine, chlorine, bromine or.iodine, especially chlorine or bromine, lower alkanoyl, for example acetyl or pivaloyl, lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, phosphono, hydroxy-lower alkoxy-' phosphoryl or dialkoxyphosphoryl, for example dimethoxy- or diethoxy-phosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, for example N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, hydroxy- or carboxy-lower alkyl-carbamoyl, for example.hydroxy- or carboxy-methylcarbamoyl or hydroxy- or carboxy-ethylcarbamoyl, sulfamoyl, nitro, oxo and/or by cyano, with heterocyclyl-lower alkanoyl being selected especially from pyrrolylcarbonyl that is unsubstituted or substituted by lower alkyl or by phenyl, for example 2- or 3-pyrrolylcarbonyl, 4- or 5-methylpyrrolylcarbonyl or 4- or 5-phenylpyrrolyl-2-carbonyl, thienylcarbonyl, such as 2-thienylcarbonyl, furylcarbonyl, such as 2-furylcarbonyl, pyridylcarbonyl, such as 2-, 3-or 4-pyridylcarbonyl, pyrimidin-1-ylcarbonyl, indolylcarbonyl that is unsubstituted or substituted by lower allcyl, such as methyl, phenyl-lower alkyl, such as benzyl, lower alkoxy, such as methoxy, phenyl-lower alkoxy, such as benzyloxy, or by halogen, such as chlorine, such as 2-, 3- or 5-indolylcarbonyl, 1-methyl-, 5-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indolyl-2-carbonyl, 1-benzyl-indolyl-2-or -3-carbonyl, 4,5,6,7-tetrahydroindolyl-2-carbonyl, unsubstituted or hydroxy-substituted quinolyl-lower alkanoyl, for example quinolylcarbonyl, such as 2-, 3- or 4-quinolyl-carbonyl or 4-hydroxyquinolyl-2-carbonyl, unsubstituted or hydroxy-substituted isoquin-olylcarbonyl, such as 1-, 3- or 4-isoquinolylcarbonyl or 1-oxo-1,2-dihydroisoquinolyl-3-carbonyl, 2-quinoxalinylcarbonyl, 2-(3,1-benzofuranyl)carbonyl, cyclohepta[b]-pyrrolyl-5-carbonyl, 3-chromanylcarbonyl, 3-thiochrornanylcarbonyl, pyrrolidinyl-3-carb-onyl, hydroxypyrrolidinylcarbonyl, such as 3- or 4-hydroxypyrrolidinyl-2-carbonyl, oxo-pyrrolidinylcarbonyl, such as 5-oxopyrrolidinyl-2-carbonyl, piperidylcarbonyl, such as piperidinocarbonyl or 2-, 3- or 4-piperidylcarbonyl, pyrazinylcarbonyl, such as pyrazin-1-ylcarbonyl, piperazinylcarbonyl, such as piperazin-1-ylcarbonyl, morpholinyl-lower alkanayl, for example morpholinylcarbonyl, such as morpholinocarbonyl, thiomorpho-linyl-lower alkanoyl, for example thiomorpholinylcarbonyl, such as thiomorpholino-carbonyl, S,S-dioxothiomorpholinylcarbonyl, such as S,S-dioxothiomorpholinocarbonyl, indolinylcarbonyl, such as 2- or 3-indolinylcarbonyl, 1,2,3,4-tetrahydroquinolylcarbonyl, such as 1,2,3,4-tetrahydroquinolyl-2-, -3- or -4-carbonyl, 1,2,3,4-tetrahydroisoquinolyl-carbonyl, such as 1,2,3,4-tetrahydroisoquinolyl-1-, -3- or -4-carbonyl or 1-oxo-1,2,3,4-tetrahydroisoquinolyl-3-carbonyl, tetrazolyl-lower alkanoyl, such as 3-(tetrazol-1-yl)-propionyl, and pyridyl-lower alkanoyl, for example pyridylacetyl, such as 2-, 3- or 4-pyridylacetyl, heterocyclyl-lower alkanoyl being selected more especially from rnorpho-lino-lower alkanoyl, such as morpholinocarbonyl, thiomorpholino-lower alkanoyl, such as thiomorpholinocarbonyl, pyridyl-lower alkanoyl, such as 2-, 3- or 4-pyridylacetyl, quino-linyl-lower alkanoyl, such as quinoline-2_carbonyl, and tetrazolyl-lower alkanoyl, such a's 3-tetrazol-1-ylpropionyl; amino-lower alkanoyl substituted at the amino nitrogen atom by .
heterocyclyl-lower alkanoyl wherein heterocyclyl-lower alkanoyl is as defined above for heterocyclyl-lower alkanoyl Rl, R2, Rg or R9, preferably as defined for heterocyclyl-lower alkanoyl R1 and R9, especially amino-lower alkanoyl substituted at the amino nitrogen atom by N-morpholino- or by N-thiomorpholino-carbonyl, more especially N-morpholino- or N-thiomorpholino-carbonylamino-lower alkanoyl, such as N-morpho-lino- or N-thiomorpholino-carbonylamino-acetyl; halo-lower alkanoyl containing up to three halogen atoms, especially a-haloacetyl, such as a-fluoro-, a-chloro-, a-bromo-, a-iodo-, a,a,a-trifluoro- or a,a,a-trichloro-acetyl, or halopropionyl, such as B-chloro- or Li-bromo-propionyl, especially trifluoroacetyl; (N-heterocyclyl-lower alkylcarbamoyl)-lower alkanoyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, b-carbolinyl and a benzo-fused, cyclopenta-, cyclo-hexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, from morpholinyl and from thiomorpholinyl, especially 2-(N-morpholino-lower alkylcarbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(~;-morpholinoethyl)-carbamoyl)-3-methylbutyryl, or 2-(N-(pyridyl-lower alkyl)-carbaraoyl)-lower alkanoyl, such as ~(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-3-methylbutyryl; lower alkoxycarbonyl, especially methoxy-, ethoxy-, isopropoxy-, isobutoxy- or tent-lower alkoxy-caxbonyl, for example methoxycarbonyl, tert-butoxycarbonyl or isobutoxycarbonyl; aryl-lower alkoxy-carbonyl wherein aryl preferably has from 6 to 14 carbon atoms and is, for example, phenyl, biphenylyl, 1- or 2-naphthyl, fluorenyl, or phenyl that is mono- or poly-substituted by lower alkyl, for example methyl or tert-butyl, hydroxy, lower allcoxy, for example methoxy, ethoxy or tert-butoxy, halogen, for example chlorine or bromine, and/or by vitro, for example phenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl, 4-methoxybenzyl-oxycarbonyl, 4-nitrobenzyloxycarbonyl or fluorenyl-lower alkoxycarbonyl, such as 9-fluorenylmethoxycarbonyl, especially phenyl-lower alkoxycarbonyl, such as benzyloxy- .
carbonyl; heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isaquinolyl, quinoxalinyl,13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, and from morpholinyl and from thiomorpholinyl and is unsubstituted or substituted, especially by lower alkyl, such as by methyl, for example _68_ 1-methylpyrrolidin-2-ylmethoxycarbonyl, 2-furylmethoxycarbonyl, 2-tetrahydrofuranyl-lower alkoxycarbonyl, such as 2-tetrahydrofurylmethoxycarbonyl, 1-methyl-2-piperidyl-methoxycarbonyl or 2-morpholinoethoxycarbonyl, or 2-, 3- or 4-pyridylmethoxycaxbony~, especially tetrahydrofuranyl-lower alkoxycarbonyl, such as 2(R,S)-tetrahydrofuranyl-methoxycarbonyl; lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, such as methylsulfonyl; heterocyclylsulfonyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyri-midinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl,13-carbolinyl and a benzo-fused, cyclopenta-, cyclahexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially satuxated, from morpholinyl and from thiomorpholinyl and may be unsubstituted or substituted, especially by lower alkyl, such as methyl, such as morpho-linosulfonyl, thiomorpholinosulfonyl, piperidinosulfonyl, 4-methylpiperazinylsulfonyl or piperazinosulfonyl; N-heterocyclyl-lower alkyl-N-lower alkylcarbamoyl that is as defined above under unsubstituted or substituted N-alkyl- or N,N-dialkyl-carbamoyl Rl, R2, Rg or R~, wherein heterocyclyl is preferably selected from thienyl, furyl, pyranyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, azepinyl, indolyl, benzimidazolyl, 1H-indazolyl, quinolyl, iso-quinolyl, quinoxalinyl, quinazolinyl, cinnolyl, purinyl, pteridinyl, naphthyridinyl, 4H-quinolizinyl, 3,1-benzofuranyl, benz[e]indolyl, 4,1-benzoxazinyl, 4,1-benzothiazinyl, carbazolyl, (3-carbolinyl, phenazinyl, phenanthridyl, acridyl, phenoxazinyl, phenothiazinyl, 1-azaacenaphthenyl, cyclohexa[b]pyrrolyl, cyclohept<i[b]pyrrolyl, cyclohexa[d]pyrazolyl, cyclohexa[b]pyridyl, cyclohexa[b]pyrazinyl, cyclohexa[b]pyrimidinyl, cyclohexa[b]-1,4-oxazinyl, cyclohexa[b]-1,4-thiazinyl, pyrrolidinyl, pysrolinyl, imidazolidinyl, 2-imidazo-linyl, 2,3-dihydropyridyl, piperidyl, piperazinyl, 2,3,5,6-tetrahydropyrazinyl, morpholinyl, thiomorpholinyl, S,S-dioxothiomorpholinyl, indolinyl, isoindolinyl, 4,5,6,7-tetrahydro-indolyl, 1,2,3,4-tetrahydroquinolyl, 1,2,3,4-tetrahydroisoquinolyl, chromanyl, thiochrom-anyl, 1,2,3,4-tetrahydro-3,1-benzodiazinyl, 3,4-dihydro-3H-4,1-benzoxazinyl, 3,4-di-hydro-3H-4,1-benzothiazinyl, 2,3,4,5-tetrahydro-1H-5,1-benzazepinyl and 5,6-dihydro-phenanthridinyl, the mentioned radicals being unsubstituted or substituted by lower alkyl, for example methyl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, for example benzyl, hydroxy-lower alkyl, for example hydroxymethyl or 2-hydroxyethyl, lower allcoxy-lower alkyl, for example methoxymethyl or 2-methoxyethyl, phenoxy- or naphthyloxy-lower alkyl, for example 2-phenoxyethyl, 1- or 2-naphthyloxymethyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, for example benzyloxy-lower alkyl, lower alkanoyl-oxy-lower alkyl, for example acetoxymethyl, phenyl- or naphthyl-lower allcanoyloxy-lower alkyl, for example benzoyloxy-, phenylacetoxy- or 1- or 2-naphthoyloxy-methyl, -2-ethyl or -2-(2,2-dimethylethyl), lower alkoxycarbonyloxy-lawer alkyl, for exarrtple tert-butoxycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxy-carbonyloxy-lower alkyl, for example 2-benzyloxycarbonyloxyethyl or 9-fluorenyl-methoxycarbonyloxyethyl, amino-lower alkyl, for example aminomethyl, 2-aminoethyl or 2-aminopropyl, carboxy-lower alkyl, for example carboxymethyl or 2-carboxyethyl, hydroxy, lower alkoxy, for example methoxy or ethoxy, phenyl- or naphthyl-lower alkoxy, for example benzyloxy or 1- or 2-naphthylmethoxy, amino, lower alkylamino, for example methyl-, ethyl- or tert-butyl-amino, di-lower alkylamino, for example dimethyl-or diethyl-amino, carboxy, lower alkoxycarbonyl, for example methoxy-, isopropoxy-, sec-butoxy- or tert-butoxy-carbonyl, phenyl- or naphthyl-lower alkaxycarbonyl, for example benzyloxycarbonyl, halogen, for example fluorine, chlorine, bromine or iodine, especially Chlorine or bromine, lower alkanoyl, for example acetyl or pivalayl, lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, phosphono, hydroxy-lower alkoxy-phosphoryl or dialkoxyphosphoryl, for example dimethoxy- or diethoxy-phosphoryl, carbatnoyl, mono- or di-lowex alkylcarbamoyl, for example N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, hydroxy- or carboxy-lower alkyl-carbamoyl, for example hydroxy- or carboxy-methylcarbamoyl or hydroxy- or carboxy-ethylcarbamoyl, sulfamoyl, vitro, oxo and/or by cyano, and is especially pyridyl, such as 2-, 3- or 4-pyridyl, more especially N-pyridyl-lower alkyl-N-lower alkylcarbamoyl, such as N-(2-,3- or 4-pyridylmethyl)-N-methylcarbamoyl; or an acyl radical of an amino acid the amino function of which is free or acylated by one: of the other radicals mentioned hitherto for R1 and Rg, the amino acid radicals, each ;independently of the athers, preferably being as defined fox unsubstituted or substituted amino acids as acyl R1, R2, Rg and Rg, especially the radical of a natural a-amino acid having the L-configuration, such as those normally occurring in proteins, or an epimer of such an amino acid, i.e. having the unnatural D-configuration, or the D,L-isomeric mixture thereof, a homologue of such an amino acid, for example wherein the amino acid side Chain has bean lengthened or shortened by one or two methylene groups, wherein the amino group is in the (3-position and/or wherein a methyl group has been replaced by hydrogen, a substituted aromatic amino acid wherein the aromatic radical has from 6 to 14 carbon atoms, for example a substituted phenylalanine or phenylglycine wherein phenyl may be mono- or poly-substituted by lower alkyl, for example methyl, hydroxy, lower alkoxy, for example methoxy, lower alkanoyloxy, for example acetoxy, amino, lower alkylamino, for example methylamino, di-lower alkylamino, for example dimethylamino, lower alkanoylamino, for example acetylamino or pivaloylamino, lower alkoxycarbonylamino, for example tert-butoxycarbonylamino, arylmethoxycarbonylamino wherein aryl preferably has from 6 _7p_ to 14 carbon atoms, for example benzyloxycarbonylamino or 9-fluorenylmethoxy-carbonylamino, halogen, for example fluorine, chlorine, bromine or iodine, carboxy and/or by nitro, a benzo-fused phenylalanine or phenylglycine, such as a-naphthylalanine, or a hydrogenated phenylalanine or phenylglycine, such as a cyclohexylalanine or cyclohexyl-glycine, especially the radical, bonded via a carboxy group, of an amino acid selected from glycine (H-Gly-OH), alanine (H-Ala-OH), valine (H-Val-OH), norvaline (a-amino-valer~ic acid), leucine (I~-Leu-OH), isoleucine (H-Ile-OH), norleucine (a-aminohexanoic acid, H-Nle-OH), serine (H-Ser-OH), homosezine (a-amino-y-hydroxybutyric acid), threonine (H-Thr-OH), methionine (I-I-lVfet-OH), cysteine (H-Cys-OH), proline (H-Pro-OH), trans-3- and trans-4-hydroxyproline, phenylalanine (H-Phe-OH), tyrosine (H-Tyr-OH), 4-aminophenylalanine, 4-chlorophenylalanine, 4-carboxyphenylalanine, B-phenylserine (B-hydroxyphenylalanine), phenylglycine, a-naphthylalanine (H-Nal-OH), cyclohexylalanine (H-Cha-OH), cyclohexylglycine, tryptophan (H-Trp-OH), indoline-2-caxboxylic acid, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, aspartic acid (I3-Asp-OH), asparagine (H-Asn-OI-I), aminomalonic acid, aminomalonic acid monoamide, glutarnic acid (H-Glu-OH), glutamine (I-I-Gln-OH), histidine (I-I-His-OH), arginine (H-Arg-OI-I), lysine (H-Lys-OH), b-hydroxylysine, ornithine (a,b-diaminovaleric acid), 3-aminopropanoic acid, a,y-diaminobutyric acid and a,B-diaminopropionic acid, more especially the radical of an amino acid selected from valine, alanine, leucine, isoleucine, glycine, glutamic acid and asparagine, whf;rein each of the mentioned amino acids (with the exception of glycine) may be in the I~-, L- or (D,L)-form, preferably (with the exception of Val, which may also be in the (D)- or (D,L)-form) in the L-form, the a-amino group is unsubstituted or N-acylated by one of the radicals mentioned above fox R~ and R9, especially by lower alkanoyl, phenyl-lower alkanoyl, such as phenylacetyl, phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carbamoyl, such as 2(R,S)-carbamoyl-3-phenylpropionyl, morpholino-lower allcanoyl, such as morpholinocarbonyl, thiomorpholino-lower allcanoyl, such as thiomorpholinacarbonyl, pyridyl-lower alkanoyl, such as 2-, 3- or 4-pyridylacetyl, quinolinyl-lower alkanoyl, such as quinoline-2-carbonyl, tetrazolyl-lower alkanoyl, such as 3-tetrazol-1-ylpropionyl, amino-lower alkanoyl substituted at the amino nitrogen atom by N-morpholino-or N-thiomorpholino-carbonyl, for example N-morpholino- or N-thiomozpholino-carbonyl-amino-lower alkanoyl, such as N-morpholino- or N-thiomorpholino-carbonylaminoacetyl, halo-lower alkanoyl containing up to three halogen atoms, for example a-haloacetyl, such as a-fluoro-, a-chloro-, a-bromo- a-iodo-, a,a,a-trifluoro- or a,a,a-trichloro-acetyl, or halopropionyl, such as ~-chloro- or (3-bramo-propionyl, especially tr-ifluoroacetyl, 2-(N-morpholino-lower alkylcarbamoyl)-lower alkanoyl, such as 0'~
-2(R,S)-(N-(2-morpholinoethyl)-carbamoyl-3-methylbutyryl, 2-(N-(pyridyl-lower alkyl)-carbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-lower alkanoyl, lower alkoxycarbonyl, phenyl-lower alkoxycarbonyl, tetrahydrofmanyl-lower alkoxycarbonyl, such as 2(R,S)-tetrahydrofuranylmethoxycarbonyl, lower alkylsulfonyl, morpholinosulfonyl, thiomorpholinosulfonyl, piperidinosulfonyl, 4-methylpiperazinylsulfonyl or piperazinosulfonyl or N-pyridyl-lower alkyl-N-lower alkylcarbamoyl, such as. N-(2-, 3- or 4-pyridylmethyl)-N-methylcarbamoyl, special prefer-ence being given to N-morpholinocarbonyl-glycine, N-(N-(2-, ~- or 4-pyridyl)methyl-N-methylaminocarbonyl)-glycine, valine, N-(trifluoroacetyl)-valine, N-phenylacetyl-valine, N-(2- or 3-pyridyl)-acetyl-valine, N-acetyl-valine, N-(2-carbamoyl-3-phenyl-propionyl)-valine, N-(2(R,S)-carbamoyl-3-phenylpropionyl)-valine, N-(~- or 3-pyridyl-acetyl)-valine, N-2-tetrahydrofurylmethoxycarbonyl-valine, N-(3-(tetrazol-1-yl)-propionyl)-valine, N-(quinoline-2-carbonyl)-valine, N-methoxycarbonyl-valine, N-isobutoxycarbonyl-valine, N-tert-butoxycarbonyl-valine, N-benzyloxycarbonyl-valine, N-(mozpholinocarbonyl)-valine, N-(thiomorpholinocarbonyl)-valine, N-(S,S-dioxothio-morpholinocarbonyl)-valine, N-(N-2-pyridylmethyl-N-methylaminocarbonyl)-valine, N-morpholinocarbonylaminoacetyl-valine, N-methylsulfonyl-valine, N-acetyl-isoleucine, N-,propionyl-isoleucine, N-(benzyloxycarbonyl)-isoleucine, N-benzyloxycarbonyl-glutamic acid, asparagine, N-benzyloxycarbonyl-asparagine or quinoline-2-carbonyl-asparagine, the mentioned amino acid radicals preferably being in the (L)- or (D,L)-form, and in the case of valine also in the (D)-form, with the proviso that not more than one of the two radicals Rl and R9 rnay be hydrogen, R2, R~, R6 and Rs are hydrogen, R~ is lower alkyl, such as isobutyl or n-butyl; cycloalkyl-lower alkyl as defined above for cycloalkyl-lower alkyl R3, R4 and R~, wherein, preferably, cycloalkyl has from 3 to 7 carbon atoms and is unsubstituted or mono- to tri-substituted by lower alkyl, such as isopropyl, halo-lower alkyl, such as trifluoromethyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such as fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxy-carbonyl, lower alkanoyl, lower alkylsulfonyl, for example methylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono-or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano and is bonded, preferably terminally, to lower alkyl, especially methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or tert-butyl, such as cyclobutyl-, cyclopentyl-, cyclohexyl- or cycloheptyl-lower alkyl, such as -methyl or -ethyl, especially cyclohexyl-o~z~~

lower alkyl, most especially cyclohexylmethyl; or is aryl-lower alkyl that is preferably as defined under aryl-lower alkyl R3, R4 and R~, wherein aryl contains especially from 6 to 14 carbon atoms, such as in phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl, and is unsubstituted or substituted, and may be, especially, mono- to tri-substituted by lower alkyl, for example methyl, ethyl or isopropyl, halo-lower alkyl, such as trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, for example methoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine or chlorine, carboxy, lower alkoxycarbonyl, benzyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, vitro and/or by cyano, wherein phenyl may be present up to three times, such as in diphenyl-, dibenzyl- or triphenyl-lower alkyl, for example diphenyl-, dibenzyl- or triphenyl-2-ethyl, especially phenyl-lower alkyl that is unsubstituted or substituted by the mentioned substituents, especially benzyl, 2-phenylethyl, 3-phenylpropyl, 4-fluoro-, 4-cyano-, 4-methoxy- ar 4-hydroxy-benzyl, RS is hydroxy, and R~ is unsubstituted or substituted lower alkyl, preferably unsubstituted or substituted as described above for unsubstituted or substituted alkyl R3, R~ or R~, especially lawer alkyl, more especially isobutyl or n-butyl, cycloalkyl-lower alkyl, as last described for cyclo-alkyl-lower alkyl R3, especially cyclohexyl-lower alkyl, such as cyclohexylmethyl, or aryl-lower alkyl, as last described for aryl-lower alkyl R3, especially phenyl-lower alkyl that is unsubstituted or substituted by the mentioned substituents, such as benzyl, 2-phenylethyl, 3-phenylpropyl, 4-fluoro-, 4-cyano-, 4-methoxy- or 4-hydroxy-benzyl, or a salt thereof where a salt-forming group is present.
Of the last-mentioned compounds of formula I, special preference is given to those wherein Rt and R9 are each independently of the other hydrogen; lower alkanoyl; aryl-lower alkanoyl wherein the lower alkanoyl radical is unsubstituted or substituted by carbamoyl or by carbamoyl substituted at the nitrogen atom by one or two radicals selected from lover alkyl, carboxy-lower alkyl, lower allcoxycarbonyl-lower alkyl, di-lower alkyl-amino-lower alkyl, aminocarboxy-lower alkyl, hydroxy-lower alkyl or by di-lower alkoxy-lower alkyl, and wherein azyl contains from 6 to 14 carbon atoms;
heterocyclyl-lower alkanoyl wherein heterocyclyl contains from 3 to 10 ring atoms and up to 4 hetero atoms selected from O, N, S, Se, and S linked to I or 2 oxygen atoms (S=O, O=S=O);
halo-lower alkanoyl having from 1 to 3 halogen atoms; N-heterocyclyl-lower alkyl-carbamoyl-lower alkanoyl; lower alkoxycarbonyl; aryl-lower alkoxycarbonyl wherein aryl contains from 6 to I4 carbon atoms; heterocyclyl-lower alkoxycarbonyl wherein hetero-cyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyelopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated;
lower alkylsulfonyl; N-(heterocyclyl-lower alkyl)-carbamoyl-N-lower alkylcarbamoyl; or the radical, bonded via the carboxy group, of an amino acid selected from glycine, alanine, valine, norvaline, leucine, isoleucine, norleucine, serine, homoserine, threonine, methionine, cysteine, proline, trans-3- and trans-4-hydroxyproline, phenylalanine, tyrosine, 4-aminophenylalanine, 4-chlorophenylalanine, 4-carboxyphenylalanine, (3-hydroxyphenylalanine, phenylglycine, a-naphthylalanine, cyclohexylalanine, cyclo-hexylglycine, tryptophan, aspartic acid, asparagine, aminomalonic acid, aminomalonic acid monoamide, glutamic acid, glutamine, histidine, arginine, lysine, 8-hydroxylysine, ornithine, a,y-diaminobutyric acid or a,~3-diaminopropionic acid, the amino acid radicals being unsubstituted or substituted by one of the mentioned radicals Rt or R9 with the exception of the radical of one of the amino acids itself;
R2, R4, R6 and R9 are hydrogen, R3 is cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms, or is aryl-lower alkyl wherein aryl has from 6 to 14 carbon atoms, RS is hydroxy, and R~ is lower alkyl, cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms, or is aryl-lower alkyl wherein aryl has from 6 to I4 carbon atoms, and salts of such compounds having salt-forming groups, the general expressions and definitions preferably having the meanings mentioned as preferred in the previous para-graph.
Preference is likewise given to the compounds mentioned in the penultimate section above in which the substituents have all the meanings mentioned with the exception of morpho-linosulfonyl, thiomorpholinosulfonyl, piperidinosulfonyl, 4-methylpiperazinylsulfonyl or piperazinosulfonyl as Rl and/or R9.
Preference is given also to the compounds of formula I wherein Rt and R9 are each independently of the other .
- hydrogen, - lower alkoxycarbonyl, - 2-halo-lower alkoxycarbonyl, - aryloxycarbonyl wherein aryl has from 6 to 14 carbon atoms, - aryl-lower alkoxycarbonyl wherein aryl has from 6 to 14 carbon atoms, - heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclo-hexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, - 2-tri-lower alkylsilyl-lower alkoxycarbonyl, - 2-triarylsilyl-lower alkoxycarbonyl wherein aryl is phenyl or 1- or 2-naphthyl, - the radical, bonded via the carboxy group, of an amino acid selected from glycine, alanine, valine, norvaline, leucine, isoleucine, norleucine, serine, homoserine, threonine, methionine, cysteine, proline, trans-3- and trans-4-hydroxyproline, phenylalanine, tyrosine, 4-aminophenylalanine, 4-chlorophenylalanine, 4-carboxyphenylalanine, (3-phenylserine, phenylglycine, a-naphthylalanine, cyclohexylalanine, cyclohexylglycine, tryptophan, indoline-2-carboxylic acid, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, aspartic acid, asparagine, aminomalonic acid, aminornalonic acid monoamide, glut<lmic acid, glutamine, histidine, arginine, lysine, S-hydroxy'.lysine, ornithine, a,y-diaminobutyric acid and a,~i-diaminopropionic acid, it being possible for each of those amino acids to be in the D-, L- or (D,L)-form, preferably in the L-form, and wherein the a-amino group may be unsubstituted or mono- or di-N-alkylated by lower alkyl, by amino-lower alkyl, by phenyl- or naphthyl-amino-lower alkyl, or by piperazinylcarbonyl-lower alkyl substituted at the nitrogen atom by lower alkyl, or may be N-acylated by lower alkanoyl; by aryl-lower alkanoyl wherein aryl is selected from phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl and fluorenyl and may be unsubstituted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylaminosulfonyl, nitro and/or by cyano, wherein phenyl may be present up to three times, and wherein lower alkanoyl may be 2~°~~~

unsubstituted or substituted by lower alkyl, heterocyclyl selected from pyrrolyl, furyl, thienyl, imidazolyl, pyxazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-, cyclopenta-, Cyclohexa- oz cyclohepta-fused derivative of those radicals, which may also be fully or partially sari~rated, hydroxy, lower allcoxy, lower alkanoyloxy, acetoacetoxy, amino- or benzyloxy-carbonylamino-lower aikanoyloxy, aryl-lower alkanoyloxy wherein aryl has from 6 to 10 carbon atoms, lower alkoxycarbonyloxy, mono- or di-lower alkylaminocarbonyloxy, aryloxycarbonyloxy wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxy-carbonyloxy wherein aryl has from 6 to 14 carbon atoms, sulfonyloxy, lower alkyl-sulfonyloxy, phenylsulfonyloxy, 2- or 4-toluenesulfonyloxy or 1- or 2-naphthylsulfonyl-oxy, carboxy, esterified carboxy selected from lower alkoxycarbonyl, aryloxycarbonyl wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyl wherein aryl has from 6 to 12 carbon atoms, lower alkanoyl, lower alkylsulfonyl, hydroxy-lower alkoxy-phosphoryl and di-lower alkoxyphosphoryl, carbamoyl, carbamoyl substituted by one or two radicals selected from lower alkyl, carboxy-lower alkyl, lower alkoxycarbonyl-lower alkyl, di-lower alkylamino-lower alkyl, arninocarbox;y-lower alkyl, hydroxy-lower alkyl and di-lower alkoxy-lower alkyl or carbamoyl substituted by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene, in which a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which may be unsaturated, and also sulfa.moyl, phosphono, benzofuranyl, oxo and/or by cyano and is branched or unbranched; by heterocyclyl-lower alkanoyl selected from thienyl-, furyl-, pyranyl-, pyrrolyl-, imidazolyl-, pyrazolyl-, oxazolyl-, isoxazolyl-, thiazolyl-, furazanyl, pyridyl-, pyrazinyl-, pyrimidinyl-, pyridazinyl-, azepinyl-, indolyl-, benzirnidazolyl-, 1H-indazolyl-, quinolyl-, isoquinolyl-, quinoxalinyl-, quinazolinyl-cinnolyl-, purinyl-, pteridinyl-, naphthyridinyl-, 4H-quinolizinyl-, 3,I-benzofuranyl-, benz-[e]indolyl-, 4,1-benzoxazinyl-, 4,1-benzothiazinyl-, carbazolyl-, a-carbolinyl-, phen-azinyl-, phenanthridyl-, acridyl-, phenoxazinyl-, phenothiazinyl-, 1-azaacenaphthenyl-, cyclohexa[b]pyrrolyl-,cyclohepta[b]pyrrolyl-, cyclohexa[d]pyrazolyl-, cyclohexa[b]-pyridyl-, cyclohexa[b]pyrazinyl-, cyclohexa[b]pyrimidinyl-, cyclohexa[b]-1,4-oxazinyl-, cyclohexa[b]-1,4-thiazinyl-, pyrolidinyl-, pyrrolinyl-, imidazolidinyl-, 2-imidazolinyl-, 2,3-dihydropyridyl-, piperidyl-, piperazinyl-, 2,3,5,6-tetrahydropyrazinyl-, morpholinyl-, thiomorpholinyl-, S,S-dioxothiomorpholinyl-, indolinyl-, isoindolinyl-, 4,5,6,7-tetxahydro-indolyl-, 1,2,3,4-tetrahydroquinolyl-, 1,2,3,4-tetrahydroisoquinolyl-, chroman-, thio-chroman-, 1,2,3,4-tetrahydro-3,1-benzodiazinyl-, 3,4-dihydro-3H-4,1-benzoxazinyl-, 3,4-dihydro-3H-4,1-benzothiazinyl-, 2,3,4,5-tetrahydro-1H-5,1-benzazepinyl-and 5,6-dihydrophenanthridinyl-lower alkanoyl, the mentioned heterocyclyl radicals being 20~27~5 unsubstituted or substituted by lower alkyl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, hydroxy-lower alkyl, lower alkoxy-lower alkyl, phenoxy- or naphthyloxy-lower alkyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, lower alkanoyloxy-lower alkyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, lower alkoxycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower allcoxycarbonyloxy-lower alkyl, amino-lower alkyl, carboxy-lower alkyl, hydroxy, lower alkoxy, phenyl- or naphthyl-lower alkoxy, amino, lower alkylamino, di-lower alkylamino, carboxy, lower alkoxycarbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, halogen, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, dialkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, hydroxy- or carboxy-lower alkylcarbamoyl, sulfamoyl, nitro, oxo and/or by cyano; by heterocyclyl-lower alkenoyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated; by lower alkoxycarbonyl; by aryl-lower alkoxycarbonyl wherein aryl has from S to 14 carbon atoms; by heterocyclyl-lower alkoxycarbonyl wherein hetero-cyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, ~i-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated and unsubstituted or substituted by lower alkyl; by carboxy-lower alkanoyl; by lower alkoxycarbonyl-lower alkanoyl; by hydroxy-lower alkoxy-lower alkanoyl; by amino-lower alkanoyl; or by benzyloxy-carbonylamino-lower alkanoyl wherein the amino group is not bonded in the a-or (3-position; by carbamoyl; by phenyl-lower alkylaminocarbonyl; by N-di-lower alkyl-amino-lower alkyl-N-lower alkylaminocarbonyl; by N-dihydroxy-lower alkyl-N-lower alkylaminocarbonyl; by 2- or 3-pyridyl-lower alkylaminocarbonyl; by N-2-pyridyl-lower alkyl-N-lower alkylaminocarbonyl; by sulfonyl; by lower allcylsulfonyl; by arylsulfonyl wherein aryl has from 6 to 10 carbon atoms and is unsubstituted or substituted by lower alkyl or by lower alkoxy; by heterocyclylsulfonyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, (3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated; by sulfamoyl; or by sulfamoyl substituted by heterocyclyl-lower alkyl wherein heteracyclyl is as last defined, and/or by lower alkyl;
a carboxy group of the side chain is present in free form or in esterifted form as a lower alkyl ester group, as an aryl ester group or as an aryl-lower alkyl ester group, wherein aryl ~~~~
is phenyl, 4-nitrophenyl, naphthyl or biphenylyl, or in amidated form as a carbamoyl, lower alkylcarbamoyl, di-lower alkylaminocarbamoyl, mono- or di-(hydroxy-lower alkyl)-carbamoyl or mono- or di-(carboxy-lower alkyl)-carbamoyl group, an amino group of the side chain is present in free form or in alkylated form as mono- or di-lower alkylamino or in acylated form as lower alkanoylamino, as amino-lower alkanoylarnino, as aryl-lower alkanoylamino wherein aryl has from 6 to 14 carbon atoms and is unsubstituted or substituted by lower alkyl, hydroxy, lower alkoxy, carboxy, carbamoyl or by sulfamoyl, as a lower alkoxycarbonylamino group, an arylmethoxy-carbonylamino group wherein aryl has from 6 to 14 carbon atoms, as piperidyl-1-carbonyl, morpholinocarbonyl, thiomorpholinocarbonyl or as S,S-dioxothiomorpholinocarbonyl and/or a hydroxy group of the side chain is present in free form or in etherified or esterified form as a lower alkoxy, aryl-lower alkoxy, lower alkanoyloxy or lower alkoxycarbonyloxy group, - lower alkylsulfonyl, - 2- or 3-pyrrolyl-, 2-thienyl-, 2-furyl-, 1-pyrazolyl-, 2-, 3- or 4-pyridyl-, 2-, 3- or 5-indolyl-, (1-methyl-, 2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl)-, (1-benzylindol-2-yl or -3-yl)-, 4,5,6,7-ted-ahydroindol-2-yl-, (2-, 3- or 4-quinolyl or 4-hydroxyquinol-2-yl)-, (1-, 3- or 4-isoquinolyl or 1-oxo-1,2-dihydroiso-quinol-3-yl)-, 3-pyrrolidinyl-, (3- or 4-hydroxypyrrolidin-2-yl)-, 5-oxopyrrolidin-2-yl-, (2-or 3-morpholinyl)-, (2- or 3-thiomorpholinyl)-, (S,S-dioxothiomorpholin-2- or -3-yl)-, (2-or 3-indolinyl)-, 1,2,3,4-tetrahydroquinol-2-, -3- or -4-yl)- or (1,2,3,4-tetrahydroiso-quinol-1-, -2- or -3-yl)-methylsulfonyl, - phenyl- or 1- or 2-naphthyl-sulfonyl that is unsubstituted or mono- or di-substituted by lower alkyl, - lower alkoxysulfonyl, or benzyloxysulfonyl or 1- or 2-naphthyloxysulfonyl, with the result that not more than one of the radicals Rt and R9 may be hydrogen, and R2 and R$ are each independently of the other hydrogen or the same radicals as Rt and Rg, or the pairs of substituents Rl and R9, and R2 and Rs, each independently of the other, together with the bonding nitrogen atom and a radical selected from ethylene, trimethyl-ene, tetrarnethylene and pentamethylene in which a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which may be unsaturated, form a heterocyclic ring, R3 is - cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms and is unsubsti-20~2~~
tuted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkyl-carbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, carboxy, lowei allcoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxy-phosphoryl, carbamayl, mono- or di-lower alkylaminacarbamoyl, sulfamayl, mono-or di-lower alkylsulfamoyl, nitro and/or by cyano and is bonded to lower alkyl, or - aryl-lower alkyl wherein aryl is selected from phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl and fluorenyl, which may be unsubstituted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, phenyl, 1- ar 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoyl-amino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkaxycarbonyl, lower alkanoyl, sulfo, lower alkylsuLfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkyl-carbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano, wherein phenyl may be present up to three times, and wherein lower alkyl is unsubstituted or substituted by lower alkyl, heterocyclyl selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazalyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquin-olyl, quinoxalinyl, ~3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa-or cyclo-hepta-fused derivative of those radicals, which may also be fully or partially saturated, hydroxy, lower alkoxy, lower alkanoyloxy, acetoacetoxy, amino- or benzyloxycarbonyl-amina-Iower alkanoyloxy> aryl-lower alkanoyloxy wherein aryl has from 6 to 10 carbon atoms, lower alkoxycarbonyloxy, mono- or di-lower alkylaminocarbonyloxy, aryloxy-carbonyloxy wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyloxy wherein aryl has from 6 to 12 carbon atoms, sulfonyloxy, lower alkylsulfonyloxy, phenyl-sulfonyloxy, 2- or 4-toluenesulfonylaxy or 1- or 2-naphthylsulfonyloxy, amino, mono- or di-lower alkylamino, N-lower alkoxy-N-lower alkylamino, mono- or di-(phenyl-or naphthyl-lower alkyl)-amino, lowex alkanoylamino, carboxy, esterified carboxy selected from lower alkoxycarbonyl, aryloxycarbanyl wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyl wherein aryl has from 6 to 12 carbon atoms, lower alkanoyl, lower alkylsulfonyl, hydroxy-lower alkoxyphosphoryl and di-lower alkoxyphosphoryl, carbamoyl, carbamayl substituted by one or two radicals selected from lower alkyl, from carboxy-lower alkyl or lower alkoxycarbonyl-lower alkyl, from di-lower alkylamino-lower alkyl, from aminocarboxy-lower alkyl, from hydroxy-lower alkyl and from di-lower alkoxy-lower alkyl, or carbamoyl substituted by one radical selected from ethylene, 20'~~5 trimethylene, tetramethylene and pentamethylene in which a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which may be unsaturated, and also sulfamoyl, phosphono, benzofuranyl, oxo and/or by cyano and is unbranched or branched, R4 is hydrogen, RS is hydroxy and R6 is hydrogen, or RS and R6 together are oxo and R~ is - lower alkyl, - cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms and is unsubsti-tuted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, hydroxy, lower allcoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkyl-carbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxy-phosphoryl, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mono-or di-lower alkylsulfamoyl, vitro and/or by cyano and is 'bonded to lower alkyl, - bicycloalkyl-lower alkyl wherein bicycloalkyl contains from 5 to 10 carbon atoms, - tricycloalkyl-lower alkyl wherein tricycloalkyl contains from 8 to 10 carbon atoms, - aryl-lower alkyl wherein aryl is selected from phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl and fluorenyl, which may be unsubstituted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy, N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoyl-amino, halogen, carboxy, lower aikoxycarbonyl, benzyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkyl-carbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, vitro and/or by cyano, wherein phenyl may be present up to three times, and wherein lower alkyl is unsubsdtuted or substituted by lower alkyl, heterocyclyl selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquin-olyl, quinoxalinyl, J3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa-or cyclo-hepta-fused derivative of those radicals, which may also be fully or partially saturated, hydroxy, lower alkoxy, lower alkanoyloxy, acetoacetoxy, amino- or benzyloxycarbonyl-amino-lower alkanoyloxy, aryl-lower alkanoyloxy wherein aryl has from 6 to 10 carbon ~o~~
g0 -atoms, lower alkoxycarbonyloxy, mono- or di-lower alkylaminocarbonyloxy, aryloxy-carbonyloxy wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyloxy wherein aryl has from 6 to 12 carbon atoms, sulfonyloxy, lower alkylsulfonyloxy, phenyl-sulfonyloxy, 2- or 4-toluenesulfonyloxy, 1- or 2-naphthylsulfonyloxy, amino, mono- or di-lower alkylamino, N-lower alkoxy-N-lower alkylamino, mono- or di-(phenyl-or naph-thyl-lower alkyl)amino, lower alkanoylamino, carboxy, esterified carboxy selected from lower alkoxycarbonyl, aryloxycarbonyl wherein aryl has from 6 to 10 carbon atoms, aryl-lower allcoxycarbonyl wherein aryl has from 6 to 12 carbon atoms, lower alkanoyl, lower alkylsulfonyl, hydroxy-lower alkoxyphosphoryl and di-lower alkoxyphosphoryl, carbamoyl, carbamoyl substituted by one or two radicals selected from lower alkyl, from carboxy-lower alkyl, from lower alkoxycarbonyl-lower alkyl, from di-lower alkylamino-lower alkyl, from aminocarboxy-lower alkyl, from hydroxy-lower alkyl and from di-lower alkoxy-lower alkyl, or carbamoyl substituted by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene in which a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which may be unsaturated, and also sulfamoyl, phosphono, benzofuranyl, oxo (which is not bonded to the carbon atom that is linked to the nitrogen atom bonding the radical R~) and/or by cyano and is unbranched or branched, - heterocyclyl-lower alkyl wherein heterocyclyl is preferably selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, l3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, for example 4-pyrrolidinylmethyl, 1-imidazolylmethyl, 2-pyridyl-methyl, 3-pyridylmethyl, quinolin-2-ylmethyl or indol-2-ylmethyl, - hydroxy-lower alkyl, - lower alkoxy-lawer alkyl, - phenoxy-lower alkyl or nitrophenoxy-lower alkyl, - naphthyloxy-lower alkyl, - lower alkanoyloxy-lower alkyl, - acetoacetoxy-lower alkyl, - arylmercapto-lower alkyl wherein aryl has from 6 to 10 carbon atoms, - amino-lower alkyl, - mono- or di-lower alkylamino-lower alkyl, - phenyl- or naphthyl-amino-lower alkyl, - lower alkanoylamino-lower alkyl, - piperazinylcarbonyl-lower alkyl substituted at the nitrogen atom by lower alkyl, 2~i2~~
- 8l _ - lower allcoxycarbonylamino-lower alkyl, .
- phenyl-lower alkoxycarbonylamino-lower alkyl, - aminocarbonylamino-lower alkyl, - N-phenyl-lower alkyl-N-lower alkylaminocarbonylamino-lower alkyl, - halo-lower alkyl, - carboxy-lower alkyl, - lower allcoxycarbonyl-lower alkyl, - 2-halo-lower alkoxycarbonyl-lower alkyl, - phenyl- or naphthyl-lower alkoxycarbonyl-lower alkyl, - heterocyclyl-lower alkoxycarbonyl-lower alkyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, l3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, it also being possible for the mentioned radicals to be fully or partially saturated, - lower alkylsulfonyl-lower alkyl, - arylsulfonyl-lower alkyl wherein aryl has from 6 to 10 carbon atoms, - carbamoyl-lower alkyl, - lower alkylcarbamoyl-lower alkyl, - di-lower alkylcarbamoyl-lower alkyl, - hydroxy-lower alkylcarbamoyl- or di(hydroxy-lower alkyl)carbamoyl-lower alkyl, - N-lower alkoxy-lower alkoxy-lower alkylcarbamoyl-lower alkyl, - carboxy-lower alkylcarbamoyl- or di(carboxy-lower alkyl)carbamoyl-lower alkyl, - carbamoyl-lower alkyl substituted at the nitrogen atom by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom may have been replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, it also being possible for the radical so formed to be fully or partially unsaturated, - N-lower alkyl-N-heterocyclyl-lower alkylcarbamoyl-lower alkyl wherein heterocyclyl is selected froze pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl,13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, - sulfamoyl-lower alkyl, - N-(phenyl- or naphthyl-lower alkyl)sulfamoyl-lower alkyl, - sulfamoyl-lower alkyl substituted at the nitrogen atom by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom may have been replaced by nitrogen, lower alkyl-substituted nitrogen, oxygen, sulfur or by ~~27~5 sulfiu' mono- or di-substituted by oxygen, it also being possible for the radical so.formed to be fully or partially unsaturated, - oxo-lower alkyl (wherein oxo is riot bonded to the carbon atom that is linked to the nitrogen atom that carries R~), - cyano-lower alkyl, - hydroxy-carboxy-lower alkyl, - a-naphthyloxy-carboxy-lower alkyl, - hydroxy-lower alkoxycarbonyl-lower alkyl, - a-naphthyloxy-lower alkoxycarbonyl-lower alkyl, - lower alkylcarbonyl-halo-lower alkyl, - a-naphthyloxyethoxycarbonyl-lower alkyl, - a-naphthyloxy-'oenzyloxycarbonyl-lower alkyl, - esterified hydroxy-lower alkoxycarbonyl-lower alkyl wherein the hydroxy group is esterified by lower alkanoyl, cycloalkyl-lower alkanoyl wherein cycloalkyl has from 3 to 7 carbon atoms, bicycloalkyl-lower alkanoyl wherein bicycloalkyl has from 5 to 10 carbon atoms, tricycloalkyl-lower alkanoyl wherein tricycloalkyl has from 8 to 10 carbon atoms, aryl-lower alkanoyl wherein aryl has from 6 to 14 carbon atoms and may be unsubstituted or mono- to tri-substituted by lower alkyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, di-lower aikoxyphosphoryl, carbamoyl, sulfamoyl, nitro and/or by cyano, lower alkoxycarbonyl, 2-halo-lower alkoxy-carbonyl or by phenyl- or fluorenyl-lower alkoxycarbonyl, - dihydroxy-carboxy-lower alkyl, - dihydroxy-lower alkoxycarbonyl-lower alkyl, dihydroxy-lower alkoxycarbonyl-lower alkyl esterified by lower alkanoyl, lower alkoxy-carbonyl, phenyl- or fluorenyl-lower alkoxycarbonyl, lower alkylsulfonyl or by toluene-sulfonyl, - a-naphthyloxy-di-lower alkylamino-lower alkyl, - a-naphthyloxy-carbamoyl-lower alkyl, - a-naphthyloxy-oxo-lower alkyl (wherein oxo is not bonded to the carbon atom that is linked to the nitrogen atom that carries R~), or - a-naphthyloxy-cyano-lower alkyl, and the salts of the mentioned compounds where salt-forming groups are present.

_83_ Special preference is given to the compounds of formula I wherein R1 and R9 are each independently of the other hydrogen; lower alkanoyl, such as formyl, acetyl, propionyl, butyryl or pivaloyl, especially acetyl; aryl-lower alkanoyl wherein aryl is phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl and may be unsubstituted or especially mono- to tri-substituted by lower alkyl, for example methyl, ethyl or propyl, halo-lower allcyl, for example trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, for example methoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy, N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkyl-amino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, such as tart-butoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl, lower alkanoyl, sulfo, lower allcylsulfonyl, far example methylsulfonyl, phosphono, hydroxy-lower alk-oxyphosphoryl, di-lower alkoxyphosphoryl, carbarnoyl, mono- or di-lower alkyl-carbamoyl, sulfamoyl, mono- or di-lower alkylaminosulfonyl, nitxo and/or by cyano>
wherein phenyl may be present up to three times, for example in diphenyl-, dibenzyl- or triphenyl-lower alkanoyl, such as diphenyl-, dibenzyl- or triphenyl-acetyl, and wherein lower alkanoyl is unsubsrituted or substituted by carbamoyl or by carbamoyl substituted at the nitrogen atom by one or two xadicals selected from lower alkyl, carboxy-lower alkyl, lower alkoxycarbonyl-lower alkyl, di-lower alkylamino-lower alkyl, aminocarboxy-lower alkyl, hydroxy-lower alkyl and di-lower alkoxy-lower alkyl, for example by carbamoyl, carbamoyl substituted by one or two radicals selected from methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tart-butyl, n-pentyl, isopentyl, neopentyl, tert-pentyl, n-hexyl, isohexyl and n-heptyl, for example in N-methylcarbarnoyl, N-n-butyl-carbamoyl or N,N-dimethylcarbamoyl, by carboxymethylcarbamoyl (glycinylcarbonyl), by tart-butoxycarbonylmethylcarbamoyl, by 2-dimethylaminoethyl, by 5-amino-5-carboxypentyl, by hydroxymethyl, by hydroxyethyl or by 2-(2,2-dimethoxyethyl)-carbamoyl, for example 4-chloro-, 4-methoxy- or 4-nitro-benzoyl, naphthylcarbonyl, such as a- or Li-naphthylcarbonyl, indenylcarbonyl, such as 1-, 2- or 3-indenylcarbonyl, indanylcarbonyl, such as 1- or 2-indanylcarbonyl, phenanthrenylcarbonyl, such as 9-phen-anthrenylcarbonyl, phenyl-lower alkanoyl, such as phenylacetyl or 3-phenylpropionyl, phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carbamoyl, such as 2(R,S)-carbamoyl-3-phenylpropionyl, a-naphthylacetyl, J3-naphthylacetyl, lower alkylphenylacetyl, such as 4-methylphenylacetyl, lower alkoxyphenylacetyl, such as 4-methoxyphenylacetyl, 3-(p-hydroxyphenyl)-propionyl, diphenylacetyl, di-(4-methoxy-phenyl)-acetyl, triphenylacetyl, 2,2-dibenzylacetyl, 3-a- or 3-(3-naphthylpropionyl, 3-phenyl- or 3-a-naphthyl-2-carbamoylpropionyl, 3-phenyl- or 3-a-naphthyl-2-tart-butyl-~o~~~~~

carbamoyl-propionyl, 3-phenyl- or 3-a-naphthyl-2-(2-dimethylaminoethyl)carbamoyl-propionyl, 3-a-naphthyl-2-(carboxy- or tert-butoxycarbonyl)methylcarbamoyl-propionyl, 3-phenyl- or 3-a-naphthyl-2-(3-hydroxy-2-propyl)carbamoyl-propionyl, 3-phenyl-or 3-a-naphthyl-2-(2,2-dimethoxyethyl)-carbamoylpropionyl, 3-phenyl- ar 3-a-naphthyl-2-(5-amino-5-carboxypentyl)-carbamoylpropionyl, especially phenyl-lower allcanoyl, such as phenylacetyl, or phenyl-lower alkanoyl wherein the lower alkanoyl radical is substi-tuted by carbamoyl, such as 2(R,S)-carbamoyl-3-phenyl-propionyl; heterocyclyl-lower alkanoyl wherein lower alkanoyl is unsubstituted and wherein heterocyclyl is selected from thienyl, furyl, pyranyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, tetrazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, azepinyl, indolyl, benzimidazolyl, 1H-indazolyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolinyl, cinnolyl, purinyl, pteridinyl, naphthyridinyl, 4H-quinolizinyl, 3,1-benzofuranyl, 4,1-benz-oxazinyl, 4,1-benzothiazinyl, cyclohexa[b]pyrrolyl, cyclohepta[b]pyrrolyl, cyclohexa-[d]pyrazolyl, cyclohexa[b]pyridyl, cyclohexa[b]pyrazinyl, cyclohexajb],pyrimidinyl, cyclohexa[b]-1,4-oxazinyl, cyclohexa[b]-1,4-thiaziny:l, pyrrolidinyl, pyrrolinyl, imidazol-idyl, 2-imidazolinyl, 2,3-dihydropyridyl, piperidyl, piperazinyl, 2,3,5,6-tetrahydro-pyrazinyl, morpholinyl, thiomorpholinyl, S,S-dioxo-thiomorpholinyl, indolinyl, isoindol-inyl, 4,5,6,7-tetrahydroindolyl, 1,2,3,4-tetrahydroquinolyl, 1,2,3,4-tetrahydroisoquinolyl, chromanyl, thiochxomanyl, 1,2,3,4-tetrahydro-3,1-ber~zodiazinyl, 3,4-dihydro-3H-4,1-benzoxazinyl and 3,4-dihydro-3H-4,1-benzothiazinyl, the mentioned heterocyclyl radicals being unsubstituted or substituted by lower alkyl, for example methyl, phenyl, 1- or 2.-naphthyl, phenyl-lower alkyl, for example benzyl, hydroxy-lower alkyl, for example hydroxymethyl or 2-hydroxyethyl, lower alkoxy-lower alkyl, for example methoxymethyl or 2-methoxyethyl, phenoxy- or naphthyloxy-lower alkyl, for example 2-phenoxyethyl, f-or 2-naphthyloxymethyl, phenyl-lower alkoxy- or naphthyl-lower allcoxy-lower alkyl, for example benzyloxy-lower alkyl, lower alkanoyloxy-lower alkyl, for example acetoxy-methyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, for example benzoyloxy-, phenylacetoxy- or 1- or 2-naphthoyloxy-methyl, -2-ethyl or -2-(2,2-dimethylethyl), lower alkoxycarbonyloxy-lower alkyl, for example tert-butoxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyloxy-lower alkyl, for example 2-benzyloxycarbonyloxy-ethyl or 9-fluorenylmethoxycarbonyloxyethyl, amino-lower alkyl, for example amino-methyl, 2-aminoethyi or 2-aminopropyl, carboxy-lower alkyl, for example carboxymethyl or 2-carboxyethyl, hydroxy, lower allcoxy, for example methoxy or ethoxy, phenyl- or naphthyl-lower alkoxy, for example benzyloxy or 1- or 2-naphthyloxy, amino, lower alkylamino, for example methyl-, ethyl- or tert-butyl-amino, di-lower alkylamino, for example dimethyl- or diethyl-amino, carboxy, lower alkoxycarbonyl, for example 20~27~.5 methoxy-, isoprapoxy-, sec-butoxy- or tert-butoxy-carbonyl, phenyl- or naphthyl lower alkoxycarbonyl, for example benzyloxycarbonyl, halogen, for example fluorine, chlorine, bromine or iodine, especially chlorine or bromine, lower alkanoyl, for example acetyl or pivaloyl, lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl ar dialkoxyphosphoryl, for example dimethoxy-or diethoxy-phosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, for example N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, hydroxy- or carboxy-lower alkylcarbamoyl, for example hydroxy- or carboxy-methylcarbamoyl or hydroxy- or carboxy-ethylcarbamoyl, sulfamoyl, nitro, oxo and/or by cyano, hetero-cyclyl-lower alkanoyl being selected especially from unsubstituted or lower alkyl- or phenyl-substituted pyrrolylcarbonyl, for example 2- or 3-pyrrolylcarbonyl, 4-or 5-methyl-pyrrolylcarbonyl or 4- or 5-phenylpyrrolyl-2-carbonyl, thienylcarbonyl, such as 2-thienyl-carbonyl, furylcarbonyl, such as 2-furylcarbonyl, pyridylcarbonyl, such as 2-, 3- or 4-pyridylcarbonyl, pyrimidin-1-ylcarbonyl, indolylcarbonyl that is unsubstituted or substituted by lower alkyl, such as methyl, phenyl-lower alkyl, such as benzyl, lower alkoxy, such as methoxy, phenyl-lower alkoxy, such as benzyloxy, or by halogen, such as chlorine, such as 2-, 3- or 5-indolylcarbonyl, 1-methyl-, 5-methyl-, S-methoxy-, 5-benzyloxy-, S-chloro- or 4,S-dimethyl-indolyl-2-carbonyl, 1-benzylindolyl-2-or -3-carbonyl, 4,5,6,7-tetrahydroindolyl-2-carbonyl, unsubstituted or hydroxy-substituted quinolyl-lower alkanoyl, for example quinolylcarbonyl, such as 2-, 3- or 4-quinolyl-carbonyl or 4-hydroxyquinolyl-2-carbonyl, unsubstituted or hydroxy-substituted isoquinolylcarbonyl, such as 1-, 3- or 4-isoquinolylcarbonyl or 1-oxo-1,2-dihydroiso-quinolyl-3-carbonyl, 2-quinoxalinylcarbonyl, 2-(3,1-benzofuranyl)-carbonyl, cyclohepta-[b]pyrrolyl-5-carbonyl, 3-cluomanylcarbonyl, 3-thiochromanylcarbonyl, pyrrolidinyl-3-carbonyl, hydroxypyrrolidinylcarbonyl, such as 3- or 4-hydroxypyrrolidinyl-2-carbonyl, oxopyrrolidinylcarbonyl, such as 5-oxopyrrolidinyl-2-carbonyl, piperidylcarbonyl, such as piperidinocarbonyl or 2-, 3- or 4-piperidylcarbonyl, pyrazinylcarbonyl, such as pyrazin-1-ylcarbonyl, piperazinylcarbonyl, such as piperazin-1-ylcarbonyl, morpholinyl-lower alkanoyl, for example morpholinylcarbonyl, such as morpholinocarbonyl, thiornorpho-linyl-lower alkanoyl, for example thiomorpholinylcarbonyl, such as thiomorpholino-carbonyl, S,S-dioxothiomorpholinylcarbonyl, such as S,S-dioxothiomorpholinocarbonyl, indolinylcarbonyl, such as 2- or 3-indolinylcarbonyl, 1,2,3,4-tetrahydroquinolylcarbonyl, such as 1,2,3,4-tetrahydroquinolyl-2-, -3- or -4-carbonyl, 1,2,3,4-tetrahydroisoquinolyl-carbonyl, such as 1,2,3,4-tetrahydroisoquinolyl-1-, -3- or -4-carbonyl or 1-oxo-1,2,3,4-tetrahydroisoquinolyl-3-carbonyl, tetrazolyl-lower alkanoyl, such as 3-(tetrazol-1-yl)-propionyl, and pyridyl-lower alkanoyl, for example pyridylacetyl, such as 2-, 3- or 20~2~~
4-pyridylacetyl, heterocyclyl-lower alkanoyl being selected more especially from morpholino-lower alkanoyl, such as morpholinocarbonyl, thiomorpholino-lower alkanoyl, such as thiomorpholinocarbonyl, pyridyl~lower alkanoyl, such as 2-, 3- or 4-pyridylacetyl, quinalinyl-lower alkanoyl, such as quinoline-2-carbonyl, and tetrazolyl-lower alkanoyl, such as 3-tetrazol-1-ylpropionyl; amino-lower alkanoyl substiriited at the amino nitrogen atom by heterocyclyl-lower alkanoyl wherein heterocyclyl-Lower alkanoyl is as defined for heterocyclyl-lower alkanoyl R1 and R9, especially amino-lower alkanoyl substituted at the amino nitrogen atom by N-morpholino- or N-thiomorpholino-carbonyl, especially N-morpholino- or N-thiomorpholino-carbonylamino-lower alkanoyl, such as N-morpho-lino- or N-thiomorpholino-carbonylamino-acetyl; halo-lower alkanoyl containing up to three halogen atoms, especially a-haloacetyl, such as a-fluoro-, a-chloro-, a-bromo-, a-iodo-, a,a,a-trifluoro- or a,a,a-trichloro-acetyl, or halopropionyl, such as 13-chloro- or 13-bromo-propionyl, for example trifluoroacetyl; (N-heterocyclyl-lower alkylcarbamoyl)-lower alkanoyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl,13-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which rnay also be fully or partially saturated, from morpholine and from thiomorpholine, especially 2-(N-morpholino-lower alkylcarbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(?-morpholinoethyl)-carbamoyl)-3-methyl-butyryl, or 2-(N-(pyridyl-lower alkyl)-carbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-3-methyl-butyryl; lower alkoxycarbonyl, especially methoxy-, ethoxy-, isopropoxy-, isobutoxy- or tent-lower alkoxy-carbonyl, for example methoxycarbonyl, tent-butoxycarbonyl or isobutoxycarbonyl; aryl-lower alkoxycarbonyl wherein aryl is phenyl, biphenylyl, 1- or 2-naphthyl, fluorenyl, or phenyl that is mono- or poly-substituted by lower alkyl, for example methyl or tert-butyl, hydroxy, lower alkoxy, for example methoxy, ethoxy or tert-butoxy, halogen, for example chlorine or bromine, and/or by nitro, for example phenyl-lower allcoxycarbonyl, such as benzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 4-nitrobenzyloxycarbonyl or fluor-enyl-lower alkoxycarbonyl, such as 9-fluorenylmethoxycarbonyl, especially phenyl-lower allcoxycarbonyl, such as benzyloxycarbonyl; heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, J3-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, and from morpholinyl and thiomorpholinyl and is unsubstituted or substituted by lower alkyl, for example methyl, such as 1-methylpyrrolidin-2-yl-methoxycarbonyl, 2-furylmethoxycarbonyl, 2-tetrahydro-za727~
_g7_ furyl-methoxycarbonyl, 1-methyl-2-piperidyl-methoxycarbonyl or 2-morpholino-ethoxy-carbonyl, or 2-, 3- or 4-pyridylmethoxycarbonyl, especially tetrahydrofuranyl-lower alkoxycarbonyl, such as 2(1~,5)-tetrahydrofuranylmethoxycarbonyl; lower alkylsulfonyl,' for example methyl- or ethyl-sulfonyl, such as rnethylsulfonyl;
morpholinosulfonyl, thio-morpholinosulfonyl, piperidinosulfonyl, 4-methylpiperazinylsulfonyl or piperazino-sulfonyl; N-heterocyclyl-lower alkyl-N-lower alkylcarbamoyl wherein heterocyclyl is selected from thienyl, furyl, pyranyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, azepinyl, indolyl, benzimidazolyl, 1H-indazolyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolinyl, cinnolyl, purinyl, pteridinyl, naphthyridinyl, 4H-quinolizinyl, 3,1-benzofuranyl, benzje]indolyl, 4,1-benzoxazinyl, 4,1-benzothiazinyl, carbazolyl, ~-carbolinyl, phenazinyl, phenanthridyl, acridyl, phenoxazinyl, phenothiazinyl, 1-azaacenaphthenyl, cyclohexa[b]gyrrolyl, cyclo-hepta[b]pyrrolyl, cyclohexa[d]pyrazolyl, cyclohexa[b]pyridyl, cyclohexa[b]pyrazinyl, cyclohexa[b]pyrimidinyl, cyclohexa[b]-1,4-oxazinyl, cyclohexa[b]-1,4-thiazinyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, 2-irnidazolinyl, 2,3-dihydropyridyl, piperidyl, piperazinyl, 2,3,5,6-tetrahydropyrazinyl, morpholinyl, thiomorpholinyl, S,S-dioxothio-morpholinyl, indolinyl, isoindolinyl, 4,5,6,7-tetrahydroindolyl, 1,2,3,4-tetrahydroquinolyl, 1,2,3,4-tetrahydroisoquinolyl, chxomanyl, thiochrommyl, 1,2,3,4-tetrahydro-3,1-benzodiazinyl, 3,4-dihydro-3H-4,1-benzoxazinyl, 3,4-dihydro-3H-4,1-benzothiazinyl, 2,3,4,5-tetrahydro-lI-I-5,1-benzazepinyl and 5,6-dihydrophenanthridinyl, the mentioned radicals being unsubstituted or substituted by lower alkyl, for example methyl, phenyl, f-or 2-naphthyl, phenyl-lower alkyl, for example benzyl, hydroxy-lower allcyl, for example hydroxymethyl or 2-hydroxyethyl, lower alkoxy-lower alkyl, for example methoxymethyl or 2-rnethoxyethyl, phenoxy- or naphthyloxy-lower alkyl, for example 2-phenoxyethyl, f-or 2-naphthyloxymethyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, for example benzyloxy-lower alkyl, lower alkanoyloxy-lower alkyl, for example acetoxy-methyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, for example benzoyloxy-, phenylacetoxy- or 1- or 2-naphthoyloxy-methyl, -2-ethyl or -2-(2,2-dimethylethyl), lower alkoxycarbonyloxy-lower alkyl, for example tort-butoxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyloxy-lower alkyl, for example 2-benzyloxycarbonyloxy-ethyl or 9-fluorenylmethoxycarbonyloxyethyl, amino-lower alkyl, for example amino-methyl, 2-aminaethyl or 2-aminopropyl, carboxy-lower alkyl, for example carboxymethyl or 2-carboxyethyl, hydroxy, lower alkoxy, for example methoxy or ethoxy, phenyl- or naphthyl-lower alkoxy, for example benzyloxy or 1- or 2-naphthylmethoxy, amino, lower alkylamino, for example methyl-, ethyl- or tort-butyl-amino, di-lower alkylamino, for example dimethyl- or diethyl-amino, carboxy, lower alkoxycarbonyl, for example 20°~~~~5 -gg_ methoxy-, isopropoxy-, sec-butoxy- or tert-butoxy-carbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, for example benzyloxycarbonyl, halogen, for example fluorine, chlorine, bromine or iodine, especially chlorine or bromine, lower alkanoyl, for example acetyl or pivaloyl, Lower alkylsulfonyl, for example methyl- or ethyl-sulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or dialkoxyphosphoryl, for example dimethoxy-or diethoxy-phosphoryl, carbamoyl, mono- or di-lower aikylcarbamoyl, for example N-methylcarbamoyl, N-n-butylcarbamoyl or N,N-dimethylcarbamoyl, hydroxy- or carboxy-lower alkylcarbamoyl, for example hydroxy- or carboxy-methylcarbamoyl or hydroxy- or carboxy-ethylcarbamoyl, sulfamoyl, nitro, oxo and/or by cyano, and is especially pyridyl, such as 2-, 3- or 4-pyridyl, especially N-pyridyl-lower alkyl-N-lower alkylcarbamoyl, such as N-(2-, 3- or 4-pyridylmethyl)-N-methylcarbamoyl; or an acyl radical of an amino acid the amino function of which is free or acylated by one of the other radicals mentioned hitherto for Rt and R9, the amino acids being selected from glycine (H-Gly-OH), alanine (H-Ala-OH), valine (H-Val-OH), nozvaline (a-aminovaleric acid), Ieucine (H-Leu-OI-I), isoleucine (H-Ile-OH), norleucine (a-aminohexanoic acid, H-Nle-OH), serine (H-Ser-OI-I), homoserine (a-amino-y-hydroxybutyric acid), threonine (H-Thr-OH), methionine (H-Met-OH), cysteine (H-C;ys-OH), proline (H-Pro-OH), txans-3- and trans-4-hydroxyproline, phenylalanine (FI-Phe-OH), tyrosine (H-Tyr-OH), 4-aminophenylalanine, 4-chlorophenylalanine, 4-carboxyphenylalanine,13-phenylserine (f3-hydroxyphenylalanine), phenylglycine, a-naphthylalanine (I-I-Nal-OH), cyclohexyl-alanine (H-Cha-OI-i), cyclohexylglycine, tryptophan (H-Trp-OH), indoline-2-carboxylic acid, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, aspartic acid (H-Asp-OH), aspa-ragine (FI-Asn-OH), aminomalonic acid, aminomalonic acid monoamide, glutamic acid (H-Glu-OH), glutamine (H-Gln-OH), histidine (H-His-OH), arginine (H-Arg-OH), lysine (H-Lys-OH), 8-hydroxylysine, ornithine (a,8-diaminovaleric acid), 3-aminopropanoic acid, a,~y-diaminobutyric acid and a,(3-diaminopropionic acid, more especially the radical of an amino acid selected from valine, alanine, leucine, isoleucine, glycine, glutamic acid and asparagine, it being possible for each of the mentioned amino acids (with the exception of glycine) to be in the D-, L- or (D,L)-form, preferably (with the exception of Val, which may also be in the (D)- or (D,L)-form) in the L-form, and the a-amino group being unsubstituted or N-acylated by one of the radicals mentioned above for R1 and R9, especially by lower alkanoyl, phenyl-lower alkanoyl, such as phenylacetyl, phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carbamoyl, such as 2(R,S)-carbamoyl-3-phenylpropionyl, morpholino-lower alkanoyl, such as morpholino-carbonyl, thiomorpholino-lower alkanoyl, such as thiomorpholinocarbonyl, pyridyl-lower alkanoyl, such as 2-, 3- or 4-pyridylacetyl, quinolinyl-lower alkanoyl, such as quinoline-2-carbonyl, tetrazolyl-lower alkanoyl, such as 3-tetrazol-1-ylpropionyl; amino-lower aLkanoyl substituted at the amino nitrogen atom by N-morphoiino- or N-thiomorpholino-caxbonyl, for example'N-morpholino- or N-thiomorpholino-carbonyl-' amino-lower alkanoyl, such as N-rnorpholino- or N-thiomorpholino-carbonylaminoacetyl, halo-lower alkanoyl containing up to three halogen atoms, for example a-haloacetyl, such as a-fluoro-, a-chloro-, a-bromo-, a-iodo-, a,a,a-trifluoro- or a,a,a-trichlozo-acetyl, or halopropionyl, such as B-chloro- or 13-bromo-propionyl, especially trifluoroacetyl, 2-(N-morpholino-lower alkyicarbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(~-mozpho-linoethyl)-carbamoyl)-3-methyl-butyryl, 2-(N-(pyridyl-lower alkyl)-carbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-lower alkanoyl, lower alkoxy-carbonyl, phenyl-lower alkoxycarbonyl, tetrahydrofuranyl-lower alkoxycarbonyl, such as 2(R,S)-tetrahydrofuranylmethoxycarbonyl, lower alkylsulfonyl or N-pyridyl-lower alkyl-N-lower alkylcarbamoyl, such as N-(2-, 3- or 4-pyridylmethyl)-N-methylcarbamoyl, greatest preference being given to N-morpholinocarbonyl-glycine, N-(N-(2-, 3-or 4-pyridyl)methyl-N-methylaminocarbonyl)-glycine, valine, N-(trifluoroacetyl)-valine, N-phenylacetyl-valine, N-(2- or 3-pyridyl)-acetyl-valine, N-acetyl-valine, N-(2-carbam-oyl-3-phenylpropionyl)-valine, N-(2(R,S)-carbamoyl-3-phenylpropionyl)-valine, N-(2- or 3-pyridylacetyl)-valine, N-2-tetrahydrofurylmethoxycarbonyl-valine, N-(3-(tetrazol-1-yl)-propionyl)-valine, N-(quinoline-2-carbonyl)-val:ine, N-methoxycarbonyl-valine, N-isobutoxycarbonyl-valine, N-tert-butoxycarbonyl-valine, N-benzyloxycarbonyl-valine, N-(morpholinocarbonyl)-valine, N-(thiomorpholinocaxbonyl)valine, N-{S,S-dioxothio-morpholinocarbonyl)-valine, N-(N-2-pyridylmethyl-I'f-methylaminocarbonyl)-valine, N-morpholinocarbonylaminoacetyl-valine, N-methylsulfonyl-valine, morpholino-sulfonyl-valine, N-acetyl-isoleucine, N-propionyl-isoleucine, N-(benzyloxycarbonyl)-isoleucine, N-benzyloxycarbonyl-glutamic acid, asparagine, N-benzyloxycarbonyl-asparagine and quinoline-2-carbonyl-asparagine, wherein each of the amino acid radicals is preferably in the (L)- or (D,L)-form, and in the case of valine also in the (D)-form; with the proviso that not more than one of the radicals R1 and R9 is hydrogen, R2, R4, R6 and Rg are hydrogen, R3 is lower alkyl, such as isobutyl or n-butyl; cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms and is unsubstituted or mono- to tri-substituted by lower alkyl, such as isopropyl, halo-lower alkyl, such as trifluoromethyl, hydraxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkyl-carbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, such as fluorine, chlorine or bromine, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, for example methylsulfonyl, 20~27~5 phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano and is bonded, preferably terminally, to lower alkyl, especially ' methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl or tert-butyl, such as cyclobutyl-, cyclopentyl-, cyclohexyl- or cycloheptyl-lower alkyl, such as -methyl or -ethyl, especially cyclohexyl-lower alkyl, more especially cyclohexylmethyl; or aryl-lower alkyl wherein aryl is phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl and is unsubstituted ar substituted by lower alkyl, for example methyl, ethyl or isopropyl, halo-lower alkyl, such as trifluoromethyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, far example methoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, for example pivaloylamino, halogen, for example fluorine or chlorine, carbaxy, lower alkoxycarbonyl, benzyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitxo and/or by cyano, wherein phenyl may be present up to three times, such as in diphenyl-, dibenzyl- or triphenyl-lower alkyl, for example diphenyl-, dibenzyl- or triphenyl-2-ethyl, especially phenyl-lower alkyl that is unsubsti-tuted or substituted by the mentioned substituents, especially benzyl, 4-fluoro- or ~-cyano-benzyl, R~ is hydroxy, and R~ is unsubstituted lower alkyl, especially isobutyl or n-butyl; or cycloalkyl-lower alkyl, for example as last described for cycloalkyl-lower alkyl R3, especially cyclohexyl-lower alkyl, more especially cyclahexylmethyl; or aryl-lower alkyl as last described for aryl-lower alkyl R3, especially phenyl-lower alkyl that is unsubstituted or substituted by the mentioned substituents, more especially benzyl, 4-fluoro- or 4-cyano-benzyl, or a salt thereof where at least one salt-forming group is present.
Special preference is given also to the compounds of formula I wherein Rl is lower alkoxycarbonyl, phenyl-lower alkoxycarbonyl, the monovalent radical, bonded via the carboxy group, of an aliphatic amino acid selected from valine, alanine, leucine and isoleucine, or the radical, bonded via the carboxy group, of an aliphatic amino acid as defined above that is acylated at the amino nitrogen atom by one of the radicals phenyl-lower alkanoyl, morpholinyl-lower alkanoyl, thiomorpholinyl-lower alkanoyl, S,S-dioxo-thiomorpholinyl-lower alkanoyl, pyridyl-lower alkanoyl, lower alkoxycarbanyl and phenyl-lower alkoxycarbonyl, all the mentioned amino acids being in the D-, D,L- or L-form, preferably in the L-form, R~, is hydrogen, R3 is phenyl-lower alkyl, Rq. is hydrogen, R5 is hydroxy, R6 is hydrogen, R~ is lower alkyl, cyclohexyl-lower alkyl or phenyl-lower alkyl, Rg is hydrogen and R9 is one of the radicals mentioned for R1 and the asymmetric carbon atoms carrying the radicals R~ and RS are in the S-configuration, and the pharmacologically acceptable salts of such compounds.
Very special preference is given to the compounds of formula I wherein R1 is tert-butoxy-carbonyl, benzyloxycarbonyl, the monovalent radical, bonded via the carboxy group, of the amino acid valine or the radical, bonded via the carboxy group, of alanine acylated at the amino nitrogen atom by one of the radicals phenylacetyl, 3-pyridylacetyl, morpholino-carbonyl, thiomorpholinocarbonyl, tent-butoxycarbonyl and benzyloxycarbonyl, R2 is hydrogen, R3 is benzyl, Rq. is hydrogen, RS is hydroxy, R6 is hydrogen, R7 is isobutyl, cyclohexylmethyl or benzyl, Rg is hydrogen and R9 is one of the radicals mentioned for R1 and the asymmetric carbon atoms carrying the radicals R3 and R5 are in the S-configuration, and the pharmacologically acceptable salts of such compounds.
Great preference is given to the compounds of formula I wherein R1 and R9 are each independently of the other hydrogen, lower alkanoyl, such as acetyl, phenyl-lower alkanoyl, such as phenylacetyl, phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carbamoyl, such as 2(R,S)-carbamoyl-3-phenyl-propionyl, morpholino-lower alkanoyl, such as morpholinocarbonyl, thiomotpholino-lower alkanoyl, such as thiomorpholino-Carbonyl, pyridyl-lower alkanoyl, such as 2-, 3- or 4-pyridylacetyl, quinolyl-lower alkanoyl, such as quinoline-2-carbonyl, tetrazolyl-lower alkanoyl, such as 3-tetrazol-1-yl-propionyl, amino-lower alkanoyl substituted at the amino nitrogen atom by N-morpholino- or N-thiomorpholino-carbonyl, for example N-morpholino- or N-thia-morpholino-carbonylamino-lower alkanoyl, such as N-morpholino- or N-thiomorpholino-carbonylamino-acetyl, halo-lower alkanoyl containing up to three halogen atoms, such as trifluoroacetyl, 2-(N-morpholino-lower alkylcarbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(2-morpholinoethyl)-carbamoyl-3-methyl-butyryl, 2-(N-pyridyl-lower alkyl-carbamoyl)-lower alkanoyl, such as 2(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-3-methyl-butyryl, lower alkoxycarbonyl, such as methoxy-, isobutoxy- or tent-lower alkoxy-carbonyl, phenyl-lower alkoxycarbonyl, such as benzyloxycarbonyl, tetrahydrofuranyl-lower alkoxycarbonyl, such as 2(R,S)-tetrahydrofuranyl-methoxycarbonyl, Lower alkyl-sulfonyl, for example methyl- or ethyl-sulfonyl, morpholinosulfonyl, thiomorpholino-sulfonyl, N-pyridyl-lower alkyl-N-lower alkylcarbamoyl, or an acyl radical of an amino 0~~7v5 acid selected from glycine, alanine, valine, leucine, isoleucine, glutamic acid and.
asparagine in the (D)-, (L)- or (D,L)-form, wherein the a-amino group is unsubstituted or acylated by one of the other radicals Ri or R2 mentioned hitherto, greatest preference being given to N-morpholinocarbonyl-glycine, N-(N-(2-, 3- or 4-pyridyl)methyl-N-methylaminocarbonyl)-glycine, valine, N-(trifluoroacetyl)-valine, N-phenylacetyl-valine, N-(2- or 3-pyridyl)-acetyl-valine, N-acetyl-valine, N-(2-carbamoyl-3-phenyl-propionyl)-valine, N-(2(R,S)-carbamoyl-3-phenyl-propionyl)-valine, N-(2- or 3-pyridyl-acetyl)-valine, N-2-tetxahydrofurylmethoxycarbonyl-valine, N-(3-(tetrazol-1-yl)-propionyl)-valine, N-(quinoline-2-carbonyl)-valine, N-methoxycarbonyl-valine, N-iso-butoxycarbonyl-valine, N-tent-butoxycarbonyl-valine, N-benzyloxycarbonyl-valine, N-(morpholinocarbonyl)-valine, N-(thiomorpholinocarbonyl)-valine, N-(S,S-dioxothio-morpholinocarbonyl)-valine, N-(N-2-pyridylmethyl-N-methylaminocarbonyl)-valine, N-morpholinocarbonylaminoacetyl-valine, N-methylsulfonyl-valine, morpholinosulfonyl-valine, N-acetyl-isoleucine, N-propionyl-isoleucine, N-(benzyloxycarbonyl)-isoleucine, N-benzyloxycarbonyl-glutamic acid, asparagine, N-benzyloxycarbonyl-asparagine and quinoline-2-carbonyl-asparagine, wherein the amino acid radicals are each preferably in the (L)- or (D,L)-form, and in the case of valine also in the (D)-Form; with the proviso that not more than one of the radicals Rl and R~ is hydroge:n, R2, Rq, R6 and Rg are hydrogen, Rg is lower alkyl, such as n-butyl or isobutyl, cycloh~exyl-lower alkyl, such as cyclo-hexylmethyl, or phenyl-lower alkyl that is unsubstitutf;d or substituted by halogen, such as fluorine, lower alkoxy, such as methoxy, or by cyano> especially benzyl, 4-fluorobenzyl or 4-cyanobenzyl, RS is hydroxy, and R~ is lower alkyl; cyclohexyl-lower alkyl; or phenyl-lower alkyl that is unsubstituted or substituted by halogen, such as fluorine, lower alkoxy, such as methoxy, or by cyano; as last defined for R3, or a salt thereof where salt-forming groups are present, still greater preference being given to those compounds in which Rt and/or R9 are not morpholinosulfonyl or thiomorpholino-sulfonyl.
Most preferred of all are the compounds mentioned in the Examples and their salts.

20'~2~~5 The compounds of formula I and salts of such compounds having at Least one salt-forming group are obtained by means of processes known her se, for example as follows:
a) a hydrazine derivative of the formula R~
I
HN ~N 'Ry (III)>

Rs wherein the radicals are as defined above, is added to an epoxide of the formula Rz Rs O
N (N)>
R~
R3 Ra wherein the radicals are as defined above, free functional groups, with the exception of those paz~ticipating in the reaction, being optionally in protected form, and any protecting groups present are removed, or b) for the preparation of compounds of formula I wherein R1 and R9 are acyl;
sulfo;
sulfonyl substituted by unsubstituted or substituted alkyl, aryl, heterocyclyl, alkoxy, which is unsubstituted or substituted, or by aryloxy; sulfamoyl that is unsubstituted or substituted at the nitrogen atom; or phosphoryl substituted by one or two identical or different radicals selected from substituted or unsubstituted alkyl, unsubstituted or substituted cycloalkyl, aryl, hydroxy, unsubstituted or substituted alkoxy, cycloalkoxy and aryloxy;
Rz and Rg are hydrogen, unsubstituted or substituted alkyl, alkenyl or alkynyl, or heterocyclyl, and the remaining radicals are as defined, an amino compound of the formula R~
R5 Rs N
R/'i ~~>K~N~N/H (V)>

Ra 20'2?~5 wherein the radicals are as defined immediately above, is condensed with an acid of the formula R~-OH (VI) or with a reactive acid derivative thereof, wherein R9 is as defined immediately above, free functional groups, with the exception of those participating in the reaction, being optionally in protected form, and any protecting groups present are removed, or c) for the preparation of compounds of formula I wherein R1 and R~ are aryl;
sulfo;
sulfonyl substituted by unsubstituted or substituted alkyl, aryl, heterocyclyl, alkoxy, which is unsubstituted or substituted, or by aryloxy; sulfamoyl that is unsubstituted or substituted at the nitrogen atom; or phosphoryl that is substituted by one or two identical or different radicals selected from substituted or unsubstituted alkyl, unsubstituted or substituted cycloalkyl, aryl, hydroxy, unsubstituted or substituted alkoxy, cycloalkoxy and aryloxy;
R2 and Rg are hydrogen, unsubstituted or substituted alkyl, alkenyl or alkynyl, or hetero-cyclyl, and the remaining radicals are as defined, an amino compound of the formula R RB
N/N'~~~N~N/R9 (VII).

wherein the radicals are as defined immediately above, is condensed with an acid of the formula Rl-OH (VIII) or with a reactive acid derivative thereof, wherein R1 is as defined immediately above, free functional groups, with the exception of those participating in the reaction, being optionally in protected form, and any protecting groups present are removed, or d) for the preparation of compounds of formula I wherein Rl and R9 are two identical radicals selected from aryl; sulfo; sulfonyl substituted by unsubstituted or substituted allcyl, aryl, heterocyclyl, alkoxy, which is unsubstituted or substituted, or by aryloxy;

~~~z sulfamoyl that is unsubstituted or substituted at the nitrogen atom; and phosphoryl that is substituted by one or two identical or different radicals selected from substituted or unsubstituted alkyl, unsubstituted or substituted cycloalkyl, aryl, hydroxy, unsubstituted or substituted alkoxy, cycloalkoxy and aryloxy; R2 and Rg are hydrogen, unsubstituted or substituted alkyl, alkenyl or alkynyl, or heterocyclyl, and the remaining radicals are as defined, a diamino compound of the formula R~
N Rs Rs Rs wherein the radicals are as defined immediately above, is condensed with an acid suitable for introducing the identical radicals Rt and R9, or with reactive acid derivatives thereof, wherein R1 and R9 are as defined immediately above, free functional groups, with the exception of those participating in the reaction, being optionally in protected form, and any protecting groups present are removed, or e) for the preparation of a compound of formula I wherein in place of the radical R~ there is a radical R7" which is unsubstituted or substituted alkyl or cycloalkyl, in a compound of the formula I' R
R Rs /N
R, i wN /.R9 Rs wherein R~' is hydrogen and the remaining radicals are as defined above, the radical R~"
is introduced by substitution with a compound of the formula XII, R~"-X (XII) wherein X is a leaving group and R~" is unsubstituted or substituted alkyl or cycloalkyl, free functional groups, with the exception of those participating in the reaction, being optionally in protected form, and any protecting groups present are removed, or 2p~2 f) in a compound of formula I wherein the substituents are as defined above, with the proviso that in the compound of formula I in question at least one functional group is protected by protecting groups, the protecting groups present are removed and, if desired, a compound of formula I obtainable in accordance with any one of processes a) to f) above having at least one salt-forming group is converted into its salt or an obtainable salt is converted into the free compound or into a different salt and/or any isomeric mixtures that are obtainable are separated and/or a compound of formula I
according to the invention is converted into a different compound of formula I
according to the invention.
The above processes are described in detail below:
I7rocess a) (Addition of an amine to an epoxide):
Depending on the meaning of R~, in the hydrazine derivative of formula III the amino group participating in the reaction preferably has at least one free hydrogen atom; it may, however, itself have been derivatised in order to increase the reactivity of the hydrazine derivative.
The epoxide of formula IV has especially a stn~cture l:hat allows the preferential terminal addition of the hydrazine derivative.
Functional groups in starting materials that are not to participate in the reaction, especially carboxy, amino, hydroxy, mercapto and sulfo groups, can be protected by suitable protect-ing groups (conventional protecting groups) which are customarily used in the synthesis of peptide compounds, but also in the synthesis of cephalosporins and penicillms as well as nucleic acid derivatives and sugars. Those protecting groups may already be present in the precursors and are intended to protect the relevant functional groups against undesired secondary reactions, such as acylation, etherification, esterification, oxidation, solvolysis, etc.. In certain cases the protecting groups can additionally cause the reactions to proceed selectively, for example stereoselectively. It is a characteristic of protecting groups that they can be removed easily, i.e. without undesired secondary reactions, for example by solvolysis, reduction, photolysis> and also enzymatically, for example also under physio-logical conditions. Radicals analogous to protecting groups may, however, also be present in the end products. Compounds of formula I having protected functional groups may ~~72~~~

have a higher degree of metabolic stability or otherwise better pharmacodynamic, charact-eristics than do the corresponding compounds having free functional groups. J-Ierein-before and hereinafter, it is protecting groups in the narrower sense that are referred to unless the relevant radicals are present in the end products.
The protection of functional groups by such protecting groups, the protecting groups them-selves and the reactions for their removal are described, for example, in standard works such as J. F. W. McOmie, "Protective Groups in Organic Chemistry", Plenum Press, London and New York 1973, in Th. W. Greene, "Protective Groups in Organic Synthesis", Wiley, New York 1981, in "The Peptides' ; Volume 3 (E. Gross and J.
Meienhofer, eds.), Academic Press, London and New York 1981, in "Methoden der organischen Chemie", Houben-Weyl, 4th edition, Volume 15/1, Georg Thieme Verlag, Stuttgart 1974, in H.-D.
Jakubke and H. Jescheit, "Aminosauren, Peptide, Proteine" ("Amino acids, peptides, proteins"), Verlag Chemie, Weinheim, Deerfield Beach and Basel 1982, and in Jochen Lehmann, "Chemie der Kohlenhydrate: Monosaccharide and Derivate" {"The Chemistry of Carbohydrates: monosaccharides and derivatives"), Georg Thieme Verlag, Stuttgart 1974.
A carboxy group is protected, for example, in the fornz of an ester group which can be removed selectively under mild conditions. A carboxy group protected in esterified form is esterifted especially by a lower alkyl group that is preferably branched in the 1-position of the lower alkyl group or substituted in the 1- or 2-position of the lower alkyl group by suitable substituents.
A protected carboxy group esterified by a lower alkyl group is, for example, methoxy-carbonyl or ethoxycarbonyl.
A protected carboxy group esterified by a lower alkyl group that is branched in the 1-position of the lower alkyl group is, for example, tert-lower alkoxycarbonyl, for example tent-butoxycarbonyl.
A protected carboxy group esterified by a lower alkyl group that is substituted in the 1- or 2-position of the lower alkyl group by suitable substituents is, for example, aryimethoxy-carbonyl having one or two aryl radicals, wherein aryl is phenyl that is unsubstituted or mono-, di- or tri-substituted, for example, by lower alkyl, for example tert-lower alkyl, such as tort-butyl, lower alkoxy, for example methoxy, hydroxy, halogen, for example chlorine, and/or by vitro, for example benzyloxycarbonyl, benzyloxycarbonyl substituted by the mentioned substituents, for example 4-nitrobenzyloxycarbonyl or 4-methoxy-benzyloxycarbonyl, diphenylmethoxycarbonyl or diphenylmethoxycarbonyl substituted liy the mentioned substituents, for example di(4-methoxyphenyl)methoxycarbonyl, and also carboxy esterified by a lower alkyl group, the lower alkyl group being substituted in the f-or 2-position by suitable substituents, such as 1-lower alkoxy-lower alkoxycarbonyl, for example methoxymethoxycarbonyl, 1-methoxyethoxycarbonyl or 1-ethoxyethoxy-carbonyl, 1-lower alkylthio-lower alkoxycarbonyl, for example 1-methylthiamethoxy-carbonyl ar 1-ethylthioethoxycarbonyl, aroylmethoxycarbonyl wherein the aroyl group is benzoyl that is unsubstituted or substituted, for example, by halogen, such as bromine, for example phenacyloxycarbonyl, 2-halo-lower alkoxycarbonyl, for example 2,2,2-trichlaro-ethoxycarbonyl, 2-bromaethoxycarbonyl or 2-iodaethoxycarbonyl, as well as 2-(tri-substi-tuted silyl)-lower alkoxycarbonyl wherein the substituents are each independently of the others an aliphatic, araliphatic, cycloaliphatic or aromatic hydrocarbon radical that is unsubstituted or substituted, for example, by lower alkyl, lower alkoxy, aryl, halogen and/or by vitro, for example lower alkyl, phenyl-lawe:r alkyl, cycloalkyl or phenyl each of which is unsubstituted or substituted as above, for example 2-tri-lower alkylsilyl-lower alkaxycarbonyl, such as 2-tri-lower alkylsilylethoxycarbonyl, for example 2-trimethyl-silylethoxycarbonyl or 2-(di-n-butyl-methyl-silyl)-ethoxycarbonyl, or 2-triarylsilylethoxy-carbonyl, such as triphenylsilylethoxycarbonyl.
A carboxy group can also be protected in the form of an organic silyloxycarbonyl group.
An organic silyloxycarbonyl group is, for example, a tri-lower alkylsilyloxycarbonyl group, for example trimethylsilyloxycarbonyl. The silicon atom of the silyloxycarbonyl-group can also be substituted by two lower alkyl groups, for example methyl groups, and the amino group or the carboxy group of a second molecule of formula I.
Compounds having such protecting groups can be prepared, for example, using dimethylchlorosilane as silylating agent.
A protected carboxy group is preferably tert-lower alkoxycarbonyl, for example tert-but-oxycarbonyl, benzyloxycarbonyl, 4-nitrobenzyloxycarbonyl, 9-fluorenylmethoxycarbanyl or diphenylmethoxycarbonyl.
A protected amino group can be protected by an amino-protecting group, for example in the form of an acylamino, arylmethylamino, etherified mercaptoamino, 2-acyl-lower alk-1-enylamino or silylamino group or in the form of an azido group.

~t~72~~5 In a corresponding acylamino group, acyl is, for example, the acyl radical of an organic carboxylic acid having, for example, up to 18 carbon atoms, especially an unsubstituted or substituted, for example halo- or aryl-substituted, lower alkanecarboxylic acid or an unsubstituted or substituted, for example halo-, lower alkoxy- or nitre-substituted, benzoic acid, or, preferably, of a carbonic acid semi-aster. Such acyl groups are, for example, lower allcanoyl, such as formyl, acetyl, propionyl or pivaloyl, halo-lower alkanoyl, for example 2-haloacetyl, such as 2-chloro- 2-bromo-, 2-iodo-, 2,2,2-trifluoro- or 2,2,2-tri-chloro-acetyl, unsubstituted or substituted, for example halo-, lower alkoxy-or nitro-substituted, benzoyl, such as benzoyl, 4-chlorobenzoyl, 4-methoxybenzoyl or 4-nitro-benzoyl, lower alkoxycarbonyl, preferably lower alkoxycarbonyl that is branched in the 1-position of the lower alkyl radical or suitably substituted in the 1- or 2-position, for example tert-lower alkoxycarbonyl, such as tert-butoxycarbonyl, arylmethoxycarbonyl having one, two or three aryl radicals which are phenyl that is unsubstituted or mono- or poly-substituted, for example, by lower alkyl, especially tert-lower alkyl, such as tert-butyl, lower alkoxy, such as methoxy, hydroxy, halogen, such as chlorine, and/or by nitre, for example benzyloxycarbonyl, 4-nitrobenzyloxycarbonyl, diphenylmethoxy-carbonyl, 9-fluorenylmethoxycarbonyl or di(4-methoxyphenyl)methoxycarbonyl, aroyl-methoxycarbonyl wherein the aroyl group is preferably benzoyl that is unsubstituted or substituted, for example, by halogen, such as bromine, for example phenacyloxycarbonyl, 2-halo-lower alkoxycarbonyl, for example 2,2,2-trich',loroethoxycarbonyl, 2-bromoethoxy-carbonyl or 2-iodoethoxycarbonyl, 2-(tri-substituted silyl)-lower alkoxycarbonyl, for example 2-tri-lower alkylsilyl-lower alkoxycarbonyl, such as 2-trimethylsilylethoxy-carbonyl or 2-(di-n-butyl-methyl-silyl)-ethoxycarbonyl, or triarylsilyl-lower alkoxy-carbonyl, for example 2-triphenylsilylethoxycarbonyl.
In an arylmethylamino group, which is, for example, a mono-, di- or especially tri-aryl-methylamino group, the aryl radicals are especially unsubstituted or substituted phenyl radicals. Such groups are, for example, benzyl-, diphenylmethyl- or especially trityl-amino.
In an etherified mercaptoamino group the mercapto group is especially in the form of substituted arylthio or aryl-lower alkylthio, wherein aryl is, for example, phenyl that is unsubstituted or substituted, for example, by lower alkyl, such as methyl or test-butyl, lower alkoxy, such as methoxy, halogen, such as chlorine, and/or by nitre, for example 4-nitrophenylthio.

20'~~~5 ioo In a 2-acyl-lower alk-1-enyl radical that can be used as an amino-protecting group, acyl is, for example, the corresponding radical of a lower alkanecarboxylic acid, of a benzoic acid that is unsubstituted or substituted, for example, by lower alkyl, such as methyl or tert-butyl, lower alkoxy, such as methoxy, halogen, such as chlorine, and/or by nitro, or especially of a carbonic acid semi-ester, such as a carbonic acid lower alkyl semi-ester.
Corresponding protecting groups are especially 1-lower alkanoyl-lower alk-1-en-2-yl, for example 1-lower alkanoyiprop-1-en-2-yl, such as 1-acetylprop-1-en-2-yl, or lower alkoxy-carbonyl-lower alk-1-en-2-yl, for example lower alkoxycarbonyl-prop-1-en-2-yl, such as 1-ethoxycarbonylprop-1-en-2-yl.
A silylamino group is, for example, a tri-lower alkylsilylamino group, for example trimethylsilylamino or tert-butyl-dimethylsilylamino. The silicon atom of the silylamino group can also be substituted by only two lower alkyl groups, for example methyl groups, and the amino group or carboxy group of a second molecule of formula I.
Compounds having such protecting groups can be prepared, for example, using the corresponding chlorosilanes, such as dimethylchlorosilane, as silylating agents.
An amino group can also be protected by conversion into the protonated form;
suitable corresponding anions are especially those of strong inorganic acids, such as sulfuric acid, phosphoric acid or hydrohalic acids, for example the chlorine or bromine anion, or of organic sulfonic acids, such as p-toluenesulfonic acid.
Preferred amino-protecting groups are lower alkoxycarbonyl, phenyl-lower alkoxycar-bonyl, fluorenyl-lower alkoxycarbonyl, 2-lower alkanoyl-lower alk-1-en-2-yl and lower alkoxycarbonyl-lower allc-1-en-2-yI.
A hydroxy group can be protected, fox example, by an acyl group, for example lower alkanoyl substituted by halogen, such as chlorine, such as 2,2-dichloroacetyl, or especially by an acyl radical of a carbonic acid semi-ester mentioned for protected amino groups. A
preferred hydroxy-protecting group is, for example, 2,2,2-trichloroethoxycarbonyl, 4-nitrobenzyloxycarbonyl, diphenylmethoxycarbonyl or trityl. A hydroxy group can also be protected by tri-lower alkylsilyl, for example trimethylsilyl, triisopropylsilyl or tert-butyl-dimethylsilyl, a readily removable etherifying group, for example an alkyl group, such as tert-lower alkyl, for example tert-butyl, an oxa- or a thia-aliphatic or -cyclo-aliphatic, especially 2-oxa- or 2-thia-aliphatic or -cycloaliphatic, hydrocarbon radical, for zo~z~~~

example 1-lower alkoxy-lower alkyl or 1-lower alkylthio-lower alkyl, such as methoxy-methyl, 1-methoxyethyl, 1-ethoxyethyl, methylthiomethyl, 1-methylthioethyl or 1-ethyl-thioethyl, or ~-oxa- or 2-thia-cycloalkyl having from 5 to 7 ring atoms, such as 2-tetra-hydrofuryl or 2-tetrahydropyranyl, or a corresponding thia analogue, as well as by 1-phenyl-lower allcyl, such as benzyl, diphenylmethyl or trityl, wherein the phenyl radicals can be substituted, for example, by halogen, for example chlorine, lower alkoxy, for example methoxy, and/or by nitro.
Two hydxoxy groups, especially adjacent hydroxy groups, occurring in a molecule, or a hydroxy group and an amino group that are adjacent to one another, can be protected, for example, by bivalent protecting groups, such as a methylene group that is preferably substituted, for example, by one or two lower alkyl radicals or by oxo, for example unsubstituted or substituted alkylidene, for example lower alkylidene, such as isopropyl-idene, cycloalkylidene, such as cyclohexylidene, a carbonyl group or benzylidene.
A mercapto group, for example in cysteine, can be protected especially by S-alkylation with unsubstituted or substituted alkyl radicals, by silylation, by thioacetal formation, by S-acylation or by the formation of asymmetric disulfide groupings. Preferred mercapto-protecting groups are, for example, benzyl that is unsubstituted or substituted in the phenyl radical, for example by methoxy or by vitro, such as ~l-methoxybenzyl, diphenylmethyl that is unsubstituted or substituted in the phenyl radical, fox example by methoxy, such as di-(4-methoxyphenyl)-methyl, triphenylmethyl, pyxidyldiphenylmethyl, trimethylsilyl, benzylthiomethyl, tetrahydropyranyl, acylaminomethyl, such as acetamidomethyl, iso-butyrylacetamidomethyl or 2-chloroacetamidomethyl, benzoyl, benzyloxycarbonyl or alkyl-, especially lower alkyl-aminocarbonyl, such as ethylaminocarbonyl, as well as lower alkylthio, such as S-ethylthio or S-tent-butylthio, ar S-sulfo.
A sulfo group can be protected, for example, by lower allcyl, for example methyl or ethyl, by phenyl or in the form of a sulfonamide, for example in the form of an imidazolide.
In the context of this Application, a protecting group, for example a carboxy-protecting group, is to be understood as being expressly also a polymeric carrier that is bonded in a readily removable manner to the functional group, for example the carboxy gxoup, to be protected, for example a earner suitable for the Merrifield synthesis. An example of such a suitable polymeric carrier is a polystyrene resin, weakly cross-linked by copolymerisa-tion with divinylbenzene, that carries bridge members suitable for reversible bonding.

~o~~~~

The addition of the compounds of formula III to the epoxides of fornaula IV is preferably effected under the reaction conditions customary for the addition of nucleophiles to epoxides.
The addition is effected especially in aqueous solution and/or in the presence of polar solvents, such as alcohols, for example methanol, ethanol or ethylene glycol, ethers, such as dioxane, amides, such as dimethylformamide, or phenols, such as phenol, and also under anhydrous conditions, in apolar solvents, such as benzene and toluene, or in benzene/water emulsions, where appropriate in the presence of acid or basic catalysts, for example hydroxide solutions, such as sodium hydroxide solution, or in the presence of solid phase catalysts doped with the hydrazine, such as aluminium oxide, in ethers, for example diethyl ether, in general at temperatures of approximately from 0°C to the boiling temperature of the reaction mixture in question, preferably from 20° to 130°C, where appropriate under reflux, under increased pressure, for example in a bomb tube, it being possible also to exceed the boiling temperature, and/or under inert gas, such as nitrogen or argon, it being possible for each of the two compounals of formula III and N
to be present in excess, for example in a molar ratio of from 1:1 to 1:100, preferably in a molar ratio of from 1:1 to 1:10, especially in a ratio of from 1:1 to 1:3.
The freeing of protected groups is effected as appropriate by the methods described under Process f) Removal of protecting groups).
Process b) (Formation of an amide bond) In starting materials of formulae V and VI, functional groups, with the exception of the groups that are intended to participate in the reaction or that do not react under the reaction conditions, are protected each independently of the others by one of the protecting groups mentioned under Process a).
The compounds of formula VI contain a free carboxy, sulfo or phosphoryl group or reactive acid derivatives thereof, for example the derived activated esters or reactive anhydrides, and also reactive cyclic amides. The reactive acid derivatives can also be formed fn citu.
Activated esters of compounds of formula VI having a terminal carboxy group are ~0~~7~5 especially esters unsaturated at the linking carbon atom of the esterifying radical, for example of the vinyl ester type, such as vinyl esters (obtainable, for example, by traps-esterification of a corresponding ester with vinyl acetate; activated vinyl ester method), carbamoyl esters (obtainable, for'example, by treatment of the corresponding acid with an isoxazolium reagent; 1,2-oxazolium or Woodward method), or 1-lower alkoxyvinyl esters (obtainable, for example, by treatment of the corresponding acid with a lower alkoxy-acetylene; ethoxyacetylene method), or esters of the amidino type, such as N,N'-disub-stituted amidino esters (obtainable, for example, by treatment of the corresponding acid with a suitable N,N'-disubstituted carbodiimide, for example N,N'-dicyclohexylcarbo-cliimide; carbodiimide method), or N,N-disubstituted amidino esters (obtainable, for example, by treatment of the corresponding acid with an N,N-disubstituted cyanamide;
cyanamide method), suitable aryl esters, especially phenyl esters suitably substituted by electron-attracting substituents (obtainable, for example, by treatment of the corres-ponding acid with a suitably substituted phenol, for example 4-nitrophenol, 4-methyl-sulfonylphenol, 2,4,5-trichlorophenol, 2,3,4,5,6-pentachlorophenol or 4-phenyldiazo-phenol, in the presence of a condensation agent, such as N,N'-dicyclohexylcarbodiimide;
activated aryl esters method), cyanomethyl esters (obtGunable, for example, by treatment of the corresponding acid with chloroacetonitrile in tht; presence of a base;
cyanomethyl esters method), thioesters, especially unsubstituted or substituted, for example nitro-substituted, phenylthio esters (obtainable, for example, by treatment of the corresponding acid with unsubstituted or substituted, for example nitro-substituted, thiophenols, inter adia by the anhydride or carbadiimide method; activated thiol esters method), or especially amino or amido esters (obtainable, for example, by treatment of the corresponding acid with an N-hydroxyamino or N-hydroxyamido compound, for example N-hydroxysuccin-imide, N-hydroxypiperidine, N-hydroxyphthalimide, N-hydroxy-5-norbornene-2,3-di-carboxylic acid imide, 1-hydroxybenzotriazole or 3-hydroxy-3,4-dihydro-1,2,3-benzo-triazin-4-one, for example by the anhydride or carbodiimide method; activated N-hydroxy esters method). Internal esters, for example y-lactones, can also be used.
Anhydrides of acids may be symmetric or preferably mixed anhydrides of those acids, for example anhydrides with inorganic acids, such as acid halides, especially acid chlorides (obtainable, for example, by treatment of the corresponding acid with thionyl chloride, phosphorus pentachloride, phosgene or oxalyl chloride; acid chloride method), azides (obtainable, for example, from a corresponding acid ester via the corresponding hydrazide by treatment thereof with nitrous acid; azide method), anhydrides with carbonic acid semi-esters, for example carbonic acid lower alkyl semi-esters (obtainable, for example, 20~2~~~

by treatment of the corresponding acid with chloroformic acid lower alkyl esters or with a 1-lower alkaxycarbonyl-2-lower alkoxy-1,2-dihydroquinoline; mixed (?-alkylcarbonic acid anhydrides method), or anhydrides with dihalogenated, especially dichlarinated, phosphoric acid (obtainable, for example, by treatment of the corresponding acid with phosphorus oxychloride; phosphorus oxychloride method), anhydrides with other phosphoric acid derivatives (for example those obtainable with phenyl-N-phenylphosphor-amidochloridate or by reaction of alkylphosphoric acid amides in the presence of sulfonic acid anhydrides and/or racemisation-reducing additives, such as N-hydroxybenzotriazole, or in the presence of cyanophosphonic acid diethyl ester) or with phosphorous acid deriv-atives, or anhydrides with organic acids, such as mixed anhydrides with organic acids, such as mixed anhydrides with organic carboxylic acids (obtainable, for example, by treat-ment of the corresponding acid with an unsubstituted or substituted lower alkane- or phenyl-lower alkane-carboxylic acid halide, for example phenylacetic acid chloride, pivalic acid chloride or trifluoroacetic acid chloride; mixed carboxylic acid anhydrides method) or with organic sulfonic acids (obtainable, fo:r example, by treatment of a salt, such as an alkali metal salt, of the corresponding acid with a suitable organic sulfonic acid halide, such as lower alkane- or aryl-, for example methane- or p-toluene-sulfonic acid chloride; mixed sulfonic acid anhydrides method) and symmetric anhydrides (obtainable, for example, by condensation of the corresponding acid in the presence of a carbodiimide or 1-diethylaminopropyne; symmetric anhydrides method).
Suitable cyclic amides are especially amides having five-membered diazacycles of aromatic character, such as amides with imidazoles, for example imidazole (obtainable, for example, by treatment of the corresponding acid with N,N'-carbonyldiimidazole;
imidazole method), or pyrazole, for example 3,5-dimethylpyrazole (obtainable, for example, via the acid hydrazide by treatment with acetylacetone; pyrazolide method).
As mentioned, derivatives of carboxylic acids that are used as acylating agents can also be formed in situ. For example, N,N'-disubstituted amidino esters can be fozmed in situ by reacting a mixture of the starting material of formula V and the acid used as acylating agent, in the presence of a suitable N,N'-disubstituted carbodiimide, for example N,N'-cyclohexylcarbodiimide. In addition, amino or amido esters of the acids used as acylating agents can be formed in the presence of the starting material of formula V to be acylated, by reacting a mixture of the corresponding acid and amino starting materials in the presence of an N,N'-disubstituted carbodiimide, for example N,N'-dicyclohexylcarbo-diimide, and of an N-hydroxyamine or N-hydroxyamide, for example N-hydroxysuccin-~o~~~~~

imide, where appropriate in the presence of a suitable base, for example 4-dimethyl-amino-pyridine. Moreover, activation in situ can be achieved by reaction with N,N,N',N'-tetraalkyluronium compounds, such as O-benzotriazol-1-yl-N,N,N',N'-tetra-methyluronium hexafluorophosphate, O-(1,2-dihydro-2-oxo-1-pyridyl)-N,N,N',N'-tetra-methyluronium tetrafluoroborate or O-(3,4-dihydro-4-oxo-1,2,3-benzotriazolin-3-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate. Finally, phosphoric acid anhydrides of the carboxylic acids of formula VI or VII can be prepared in situ by reacting an alkyl-phosphoric acid amide, such as hexamethylphosphoric acid triamide, in the presence of a sulfonic acid anhydride, such as 4-toluenesulfonic acid anhydride, with a salt> such as a tetrafluoroborate, for example sodium tetrafluoroborate, or with another derivative of hexamethylphosphoric acid triamide, such as benzotriazol-1-yloxy-tris(dimethylamino)-phosphonium hexafluoride, preferably in the presence of a racemisation-reducing additive, such as N-hydroxybenzotriazole.
In an analogous manner, many of the reaction types listed above for carboxylic acids of fornnula VI can also be carried out for compounds of formula III having a terminal sulfonyl or phosphoryl group in the condensation with compounds of formula V
to form sulfonamides.
For example, it is possible to use activated sulfonic acid esters, for example the corres-ponding aryl esters, especially those substituted by nitro groups, such as phenyl esters, it being possible far the amine component of formula V also to be used in the farm of an alkali metal amide, for example an alkali metal arylamide, such as sodium aniline amide, or an alkali metal salt of nitrogen-containing heterocycles, for example potassium pyrrolide.
In addition, reactive anhydrides, such as the corresponding symmetric acid anhydrides (which can be prepared, for example, by reaction of the alkylsulfonic acid silver salts with alkylsulfonyl chlorides) or, preferably, the corresponding asymmetric acid anhydrides, fox example anhydrides with inorganic acids, such as sulfonyl halides, especially sulfonyl chlorides (obtainable, for example, by reaction of the corresponding sulfonic acids with inorganic acid chlorides, for example thionyl chloride, phosphon~s pentachloride), with organic carboxylic acids (obtainable, for example, by treatment of a sulfonic acid halide with the salt of a carboxylic acid, such as an alkali metal salt, analogously to the above-mentioned mixed sulfonic acid anhydrides method), or azides (obtainable, for example, from a corresponding sulfonic acid chloride and sodium azide or via the corresponding k t _2~27~5 hydxazide and treatment thereof with nitrous acid analogously to the above-mentioned azide method).
The phosphoryl radicals IZ9 having the above-mentioned substituents can be fused to compounds of formula V by analogous processes, such as by means of activated phosphorus derivatives, for example correspondingly substituted phosphoryl halides having one or more halogen atoms, such as phosphorus oxychloride, in the absence or the presence of bases, such as sterically hindered amines, in aqueous or non-aqueous solvents, any excess halogen atoms subsequently being replaced by suitable substituents by hydrol-ysis or by reactian with the corresponding alcohols. .
The phosphoryl radicals substituted by hydroxy, alkoxy, cycloalkoxy, cycloalkyl-lower alkoxy, aryloxy or by aryl-lower alkoxy can be reacted with the compounds of formula V, for example by reaction of the correspondingly substituted phosphates, for example diaryl-oxyphosphite or dialkoxyphosphite, or the correspondingly substituted mono- or di-halo-, such as mono- or di-chloro-phosphates, in the presence of a base, such as 2,6-dimethyl-pyridine, triethylamine or imidazole, in aqueous or anhydrous solvents, such as alcohols, far example ethanol, corresponding esters or dichloromethane or tetrachlorometiiane, where appropriate under a protective gas, such as argon, at temperatures of from -50 to 100°C, preferably from -10 to 50°C, especially under the conditions described in European Patent .Application EP-A 0 376 040 published on 04.07.90.
The cozresponding phosphoryl radicals substituted symmetrically or, preferably, asymmetrically by the mentioned radicals bonded via oxy can be obtained by reaction of phosphorus trihalides, such as phosphorus trichloride, with the corresponding amines of formula V and in the presence of organic amines, such as triethylamine, the corresponding dichlorophosphoryl compounds being formed, reaction of those compounds with the first corresponding alcohol or with water which are preferably used in stoichiometric amounts, in the presence of a tertiary amine, and where appropriate subsequent reaction of the second halogen atom with a further alcohol ar water in the presence of a tertiary amine, to obtain the corresponding disubstituted phosphate compounds which are then oxidised; for example with halogens, such as iodine, peroxides, such as hydrogen peroxide, peracids, such as m-chloroperbenzoic acid, or with molecular oxygen.
The amino group of compounds of formula V that participates in the reaction preferably carnes at least one reactive hydrogen atom, especially when the carboxy, sulfonyl or phosphoryl group with which it reacts is present in reactive form; it may, however, itself have been derivatised, for example by reaction with a phosphite, such as diethylchloro-phosphite, 1,2-phenylenechlorophosphite; ethyl dichlorophosphite, ethylenechloro- ' phosphite or tetraethylpyrophosphite. A derivative of such a compound having an amino group is, for example, also a carbamic acid halide or an isocyanate, the amino group that participates in the reaction being substituted by halocarbonyl, for example chlorocarbonyl, or being modified in the form of an isocyanate group; in the latter case only compounds of formula I that carry a hydrogen atom at the nitrogen atom of the amide group formed by the reaction are obtainable.
If the compound of formula V is mono-substituted at the amino group by lower allyl or by aryl-lower alkyl, then a corresponding urea compound also constitutes a reactive derivative, For example, on hating equimolar amounts of that urea compound and the compound of formula VI or VIII having a free carboxy group, corresponding compounds of formula I are obtained.
Condensation for the preparation of an amide bond can be earned out in a manner.known per se, for example as described in standard works such as "Houben-Weyl, Methoden der organischen Chemie", 4th edition, Volume 15/II (1974), Volume 1X (1955) Volume (1985), Georg Thieme Verlag, Stuttgart, "The Peptidea" (E. Gross and J.
Meienhofer, eds.), Volumes 1 and 2, Academic Press, London and New York, 1979/1980, or M.
Bodansky, "Principles of Peptide Synthesis", Springer-Verlag, Berlin 1984.
The condensation of a free carboxylic acid with the corresponding amine can be carried out preferably in the presence of one of the customary condensation agents, or using carboxylic acid anhydrides or carboxylic acid halides, such as chlorides, or activated carboxylic acid esters, such as p-nitrophenyl esters. Customary condensation agents are, for example, carbodiimides, for example diethyl-, dipropyl-, N-ethyl-N'-(3-dimethyl-aminopropyl)-carbodiimide or especially dicyclohexylcarbodiimide, also suitable carbonyl compounds, for example carbonylimidazole, 1,2-oxazolium compounds, for example 2-ethyl-5-phenyl-1,2-oxazolium 3'-sulfonate and 2-tert-butyl-5-methylisoxazolium perchlorate, or a suitable acylaznino compound, for example 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline, N,N,N',N'-tetraalkyluronium compounds, such as O-benzotri-azol-1-yl-N,N,N',N'-tetramethyluroniurn hexafluorophosphate, also activated phosphoric acid derivatives, far example diphenylphosphoryl azide, diethylphosphoryl cyanide, phenyl-N-phenylphosphoroamidochloridate, bis(2-oxo-3-oxazolidinyl)phosphinic acid 20°~2~~5 chloride or 1-benzotriazolyloxy-tris(dimethylamino)phosphonium hexafluorophosphate.
If desired, an organic base is added, preferably a tertiary amine, for example a tri-lower alkylamine having bulky radicals, for example ethyl diisopropylamine or triethylamine, and/or a heterocyclic base, for example 4-dimethylaminopyridine or preferably N-methyl-morpholine or pyridine.
The condensation of activated esters, reactive anhydrides or reactive cyclic amides with the corresponding amines is customarily carried out in the presence of an organic base, for example simple tri-lower alkylamines, for example triethylamine or tributylamine, or one of the above-mentioned organic bases. If desired, a condensation agent is additionally used, for example as described for free carboxylic acids.
The condensation of acid anhydrides with amines can be effected, for example, in the presence of inorganic carbonates, for example ammonium or alkali metal carbonates or hydrogen carbonates, such as sodium or potassium carbonate or hydrogen carbonate (if desired together with a sulfate).
Carboxylic acid chlorides, for example the chlorocarbonic acid derivatives derived from the acid of formula VI, or sulfonic acid chlorides are Condensed with the corresponding amines preferably in the pxesence of an organic amine, for example the above-mentioned tri-lower alkylarnines or heterocyclic bases, where appropriate in the presence of a hydrogen sulfate.
The condensation is preferably carried out in an inert, aprotic, preferably anhydrous, solvent or solvent mixture, for example in a carboxylic acid amide, for example formamide or dimethylformamide, a halogenated hydrocarbon, for example methylene chloride, carbon tetrachloride or chlorobenzene, a ketone, for example acetone, a cyclic ether, for example tetrahydrofuran, an ester, for example ethyl acetate, or a nitrite, for example acetanitrile, or in a mixture thereof, as appropriate at reduced or elevated temperature, for example in a temperature range of from approximately -40°C to approx-imately +100°C, preferably from approximately -10°C to approximately +50°C, and in the case where arylsulfonyl esters are used also at approximately from +100°C to +200°C, and where appropriate under an inert gas atmosphere, for example a nitrogen or argon atmosphere.

2.0~2~~

Aqueous, for example alcoholic, solvents, for example ethanol, or aromatic solvepts, for example benzene or toluene, may also be used. When alkali metal hydroxides are present as bases, acetone can also be added where appropriate.
The condensation can also be carried out in accordance with the technique known as solid phase synthesis which originates from R. Merrifield and is described, far example, in Angew. Chem. 97, 801 - 812 (1985), Naturwissenschaften 71, 252 - 258 (1984) or in R. A.
Houghten, Proc. Natl. Aced. Sci. USA 82, 5131 - 5135 (1985).
Depending on the starting compounds used, the radicals Rt and R9 in the obtainable compounds of formula I can be identical or different from one another.
The freeing of protected groups is effected where appropriate by the methods described under Process f) (Removal of protecting groups).
Process c) (Formation of an amide bond) In starting materials of formulae VII and VIII, functional groups, with the exception of the groups that are intended to participate in the reaction or that do not react under the reaction conditions, are protected each independently of the others by one of the protecting groups mentioned under Process a).
The process is totally analogous to the process mentioned under Process b) except that instead of compounds of formula V those of formula VII are used, and instead of compounds of formula VI those of formula VITI are used, and, in the case of the acylation, Rt instead of R9 bonds to compounds of formula VII instead of the compounds of formula V.
Depending on the starting materials used, the radicals Rl and R9 in the obtainable compounds of fozxnula I can be identical or different from one another.
The freeing of protected groups is effected where appropriate by the methods described under Process f) (Removal of protecting groups).
Process d) (Formation of an amide bond) ~U~27~5 In starting materials of formula IX and in the acid suitable for introducing the identical radicals R1 and R9, or the reactive derivatives thereof, functional groups that are riot intended to participate in the reaction or that do not react under the reaction conditions are protected each independently of the others by one of the protecting groups mentioned under Process a).
The acid suitable for introducing the identical radicals Rl and R9 is preferably an acid of formula VI or VIII.
Preferred as starting materials of formula IX that may be protected by protecting groups are those of formula II which are described below in the section relating to starting materials.
The process is totally analogous to the process mentioned under Process b), except that instead of compounds of formula V those of formula IX are used, and instead of compounds of formula VI those of formula VI or VIII are used.
The freeing of protected groups is effected where appropriate by the methods described under Process f) (Removal of protecting groups).
Process e) (Alkylation of a secondary nitrogen atom) In starting materials of formula I' and in the compound of formula XII
suitable for intro-ducing the radical R~", or the reactive derivatives thereof, functional groups that are not intended to participate in the reaction or that do not react under the reaction conditions are protected each independently of the others by one of the protecting groups mentioned under Process a).
A leaving group X is especially a nucleofugal leaving group selected from hydroxy esteri-fied by a strong inorganic or organic acid, such as hydroxy esterified by a mineral acid, for example a hydrohalic acid, such as hydrochloric acid, hydrobromic acid or hydriodic acid, or by a strong organic sulfonic acid, such as a lower alkanesulfonic acid that is unsubsti-tuted or substituted, for example by halogen, such as fluorine, or an aromatic sulfonic acid, for example a benzenesulfonic acid that is unsubstituted or substituted by lower alkyl, such as methyl, halogen, such as bromine, and/or by nitro, for example a methanesulfonic acid, p-bromotoluenesulfonic acid or p-toluenesulfonic acid, or hydroxy esterified by hydrazoic acid.
The substitution can take place under the conditions of a first-order or second-order nucleophilic substitution. ' For example, the compound of formula XII wherein X is a leaving group having a high polarisability of the electron shell, for example iodine, can be reacted in a polar apzotic solvent, for example acetone, acetonitrile, nitromethane, dimethyl sulfoxide or dimethyl-formamide. The reactionmay also be carried out in water to which, where appropriate, an organic solvent, for example ethanol, tetrahydrofuran or acetone, has been added as solubiliser. The substitution reaction is carried out as appropriate at reduced or elevated temperature, for example in a temperature range of from approximately -40° to approximately 100°C, preferably from approximately -10° to approximately 50°C, and where appropriate under an inert gas, for example under a nitrogen or argon atmosphere.
The freeing of protected groups is effected where appropriate by the methods described under Process f) (Removal of protecting groups).
Process f) (Removal of protecting groups) The xemoval of protecting groups that are not constituents of the desired end product of formula I, for example the carboxy-, amino-, hydroxy-, mercapto- and/or sulfo-protecting groups, is effected in a manner known her se, for example by means of solvolysis, especially hydrolysis, alcoholysis or acidolysis, or by means of reduction, especially hydrogenolysis or chemical reduction, as well as by photolysis, as appropriate stepwise or simultaneously, it being possible also to use enzymatic methods. The removal of the protecting groups is described, for example, in the standard works mentioned above in the section relating to "Protecting groups".
For example, protected carboxy, for example tert-lower alkoxycarbonyl, lower alkoxy-carbonyl substituted in the 2-position by a trisubstituted silyl group or in the 1-position by lower alkoxy or lower alkylthio, or unsubstituted or substituted diphenylmethoxycarbonyl can be converted into free carboxy by treatment with a suitable acid, such as formic acid, hydrogen chloride or trifluoroacetic acid, where appropriate with the addition of a nucleo-philic compound, such as phenol or anisole. Carboxy can also be freed from lower alkoxycarbonyl by means of bases, such as hydroxides, for example alkali metal hydroxides, such as sodium hydroxide or potassium hydroxide. Unsubstituted or.
substituted benzyloxycarbonyl can be freed, for example, by means of hydrogenolysis, i.e.
by treatment with hydrogen in the presence of a metal hydrogenation catalyst, such as a ' palladium catalyst. In addition, suitably substituted benzyloxycarbonyl, such as 4-nitro-benzyloxycarbonyl, can also be converted into free carboxy by reduction, for example by treatment with an alkali metal dithionate, such as sodium dithionate, or with a reducing metal, for example zinc,, or a reducing metal salt, such as a chromium(II) salt, for example chromium(II) chloride, customarily in the presence of a hydrogen-yielding agent that, together with the metal, is capable of producing nascent hydrogen, such as an acid, especially a suitable carboxylic acid, such as an unsubstituted or substituted, for example hydroxy-substituted, lower alkanecarboxylic acid, for example acetic acid, formic acid, glycolic acid, diphenylglycolic acid, lactic acid, mandelic acid, 4-chloromandelic acid or tartaric acid, or in the presence of an alcohol or thiol, water preferably being added. By treatment with a reducing metal or metal salt, as described above, 2-halo-lower alkoxy-carbonyl (where appropriate after conversion of a 2-bromo-lower alkoxycarbonyl group into a corresponding 2-lode-lower alkoxycarbonyl group) or aroylmethoxycarbonyl can also be converted into free carboxy. Aroylmethoxycarbonyl can also be cleaved by treatment with a nucleophilic, preferably salt-forming, reagent, such as sodium thio-phenolate or sodium iodide. 2-(tri-substituted silyl)-It>wer alkoxycarbonyl, such as 2-tri-lower alkylsilyl-lower alkoxycarbonyl, can also be converted into free carboxy by treatment with a salt of hydrofluoric acid that yields the fluoride anion, such as an alkali metal fluoride, for example sodium or potassium fluoride, where appropriate in the presence of a macrocyclic polyether ("Crown ether"), or with a fluoride of an organic quaternary base, such as tetra-lower alkylammonium fluoride or tri-lower alkylaryl-lower alkylammonium fluoride, for example tetraethylammonium fluoride or tetrabutyl-amtnonium fluoride, in the presence of an aprotic, polar solvent, such as dimethyl sulfoxide or N,N-dimethylacetamide. Carboxy protected in the form of organic silyloxy-carbonyl, such as tri-lower alkylsilyloxycarbonyl, for example trimethylsilyloxycarbonyl, can be freed in customary manner by solvolysis, for example by treatment with water, an alcohol or an acid, or, furthermore, a fluoride, as described above.
Esterified carboxy can also be freed enzymatically, for example by means of esterases or suitable peptidases, for example esterified arginine or lysine, such as lysine methyl ester, using trypsin.
A protected amino group is freed in a manner known Qer se and, according to the nature of the protecting groups, in various ways, preferably by solvolysis or reduction.
Lower alkaxycarbonylamino, such as tent-butoxycarbonylamino, can be cleaved in the presence 2f~~2~'~~

of acids, for example mineral acids, far example a hydrogen halide, such as hydrogen chloride or hydrogen bromide, or sulfuric or phosphoric acids, preferably hydrogen chloride, or strong organic acids, such as trihaloacetic acid, far example trifluaxoacetic acid, or formic acid, in polar solvents, such as water, or ethers, preferably cyclic ethers, such as dioxane, 2-halo-lower alkoxycarbonylamino (where appropriate after conversion of a 2-bromo-lower alkoxycarbonylamino group into a 2-iodo-lower alkoxycarbonylamino group), or dissolved directly in a liquid organic carboxylic acid, such as formic acid and aroylmethoxycarbonylamino or 4-nitrobenzyloxycarbonylamino can be cleaved, for example, by treatment with a suitable reducing agent, such as zinc in the presence of a suitable carboxylic acid, such as aqueous acetic acid.
Aroylmethoxycarbonylamino can also be cleaved by treatment with a nucleophilic, preferably salt-forming, reagent, such as sodium thiophenolate, and 4-nitrobenzyloxycarbonylamino also by treatment with an alkali metal dithionate, for example sodium dithionate. Unsubstituted or substituted diphenylmethoxycarbonylamino, ten-lower alkoxycarbonylamino or 2-(tri-substituted silyl)-lower alkoxycarbonylamino, such as 2-tri-lower alkylsilyl-lower alkoxycarbonyl-amino, can be freed by treatment with a suitable acid, fox example formic acid or trifluoro-acetic acid; unsubstituted or substituted benzyloxycar'bonylamino can be freed, for example, by means of hydrogenolysis, i.e. by treatment with hydrogen in the presence of a suitable hydrogenation catalyst, such as a platinum or palladium catalyst;
unsubstituted or substituted triarylmethylamino or formylamino can be; freed, for example, by treatment with an acid, such as a mineral acid, for example hydrochloric acid, or an organic acid, for example formic, acetic or trifluoroacetic acid, where appropriate in the presence of water;
and an amino group protected in the form of silylamino can be freed, for example, by means of hydrolysis or alcoholysis. An amino group protected by 2-haloacetyl, for example 2-chloroacetyl, can be freed by treatment with thiourea in the presence of a base, or with a thiolate salt, such as an alkali metal thiolate of thiourea, and subsequent solvolysis, such as alcoholysis or hydrolysis, of the resulting substitution product; and amino is freed from trifluoroacetylamino, for example, by hydrogenolysis with bases, such as alkali metal hydroxides or carbonates, such as Na2C03 or K~C03, in polar solvents, for example alcohols, such as methanol, at temperatures of from 0 to 100°C, especially at from ~0 to 80°C. An amino group protected by 2-(tri-substituted silyl)-lower alkoxy-carbonyl, such as 2-tri-lower alkylsilyl-lower alkoxycarbonyl, can also be converted into the free amino group by treatment with a salt of hydrofluoric acid that yields fluoride anions as indicated above in connection with the freeing of a correspondingly protected carboxy group. Likewise, silyl bonded directly to a hetero atom, such as nitrogen, such as trimethylsilyl, can be removed using fluoride ions.

Amino protected iri the form of an azido group is converted into free amino, for example, 'by reduction, for example by catallrtic hydrogenation with hy~Irogen in the presence of a' .ra.r hydrogenation catalyst, such as platinum oxide, palladium or ltaney nickel, by reduction using mercapto compounds, such a.s dithiothreitoi or mercaptcaethanol, or by treatment with zinc in the presence of an acid, such as acetic acid. 'fhe catalytic hydrogenation is preferably carried out in an inert solvent, such as a halogenated hydrocarbon, for example methylene chloride, or in water or in a mixture of water and an organic salvent, such as an alcohol or dioxane, at approximately from 2U°C to 25°C, or with cooling or heating.
A hydroxy or mercapto group protected by a suitable aryl group, a tri-lower alkylsilyl grroup or by unsubstituted or substituted 1-phenyl-lower alkyl is freed analogously to a correspondingly protected amino group, A hydroxy or mercapto group protected by 2,2-dichloroacetyl is freed, for exarn,ple, by basic hydrolysis, and a hydroxy or mercapto L,~roup protected by tent-lower alkyl or by a 2-oxa- or 2-thin-aliphatic or -cycloaliphatic hydrocarbon radical is freed by acidolysis, for example by treatment with a mineral acid or a strong carboxylic acid, for example trifluoroacetic acid. Mercapto protected by pyridyl-diphenylmethyl can be freed, for example, using mercury(II) salts at pH 2-6 or by zinc/-acetic acid or by electrolytic reduction; acetamidomethyl and isabutyrylamidomethyl can be freed, for example, by reaction with mercury~Ii) salts at p1=1 2-6; 2-chloroacetamido-rnethyl can be freed, for example, using I-piperidirtothiocar~boxamide; and S-ethylthio, S-ten-butylthio and S-sulfa can be freed, for example, by t.ltiolysis with thiophenol, thio-glycolic acid, sodium thiophenolate: or l,~-dithiothreitol. "fwc~ hydroxy groups or an adjacent amino and hydroxy group which are protected togethc;r by means of a bivalent protecting group, preferably, for example, by a methylene grotap mono- or di-substituted by lower alkyl, such as lower alkylidene, for example isapropylidene, cycloalkylidene, for example cyclohexylidene, or benzylidene, can be freed by acid solvolysis, especially in the presence of a mineral acid or a strong organic acid, A tri-lower alkylsilyl group is Izkewise removed by acidolysis, for example by a mineral acid, preferably hydrofluoric acid, or a strong carboxylic acid. 2-halo-lower allCOxwcarbony~ is removed using the above-mentioned reducing agents, 1'or exancple a reducing; metal, such as zinc, reducing metal salts, such as chrorrciurn(II) s4~lts, or by sulfur ccampounds, for example sodium dithionate or preferably sodium sulfide and carbon cii:~ulfide.
A sulfa group protected in the for~rn of a sulfonic acid ester or ~.
sulfonarnicle is freed, for example, by acid hydrolysis, for example in the presence of a mineral acid, or preferably ~~~~7~5 l I5 -by basic hydrolysis, for example with alkali metal hydroxide or alkali metal carbonate, for example sodium carbonate.
When several protected functional groups are present, if desired the protecting groups can be so selected that more than one such group can be removed simultaneously, for example by acidolysis, such as by treatment with trifluoroacetic acid, or with hydrogen and a hydrogenation catalyst, such as a palladium-on-carbon catalyst. Conversely, the groups can also be so selected that they cannot all be removed simultaneously, but rather in a desired sequence, the corresponding intermediates being obtained.
Additional Process Steps In the additional process steps, which are optional, functional groups of the starting compounds that are not to take part in the reaction may be in unprotected or protected form, for example may be protected by one or mare of the protecting groups mentioned above under Pxocess a). The protecting groups may be retained in the end products or some or all of them may be removed according to one of the methods mentioned under Process f).
Salts of compounds of formula I having at least one salt-forming group may be prepared in a manner known per se. For example salts of compounds of formula I having acid groups may be formed, for example, by treating the compounds with metal compounds, such as alkali metal salts of suitable organic carboxylic acids, e.g. the sodium salt of 2-ethyl-hexanoic acid, with organic alkali metal or alkaline earth metal compounds, such as the corresponding hydroxides, carbonates or hydrogen carbonates, such as sodium or potassium hydroxide, carbonate or hydrogen carbonate, with corresponding calcium compounds or with ammonia or a suitable organic amine, stoichiometric amounts or only a small excess of the salt-forming agent preferably being used. Acid addition salts of compounds of formula I are obtained in customary manner, e.g. by treating the compounds with an acid or a suitable anion exchange reagent. Internal salts of compounds of formula I
comprising acid and basic salt-forming groups, e.g. a free carboxy group and a free amino group, may be formed, e.g. by the neutralisation of salts, such as acid addition salts, to the isoelectric point, e.g. with weak bases, or by treatment with ion exchangers.
Salts can be converted in customary manner into the free compounds; metal and ammonium salts can be converted,,for example, by treatment with suitable acids, and acid ~~~'2~~5 addition salts, for example, by treatment with a suitable basic agent.
Stereoisomeric mixtures, that is mixtures'of diastereoisomers and/or enantiomers, such as, for example, racemic mixtures, can be separated in a manner known Qer se by suitable separating processes into the corresponding isomers. For example mixtures of diastereo-isomers can be separated into the individual diastereoisomers by fractional crystallisation, chromatography, solvent partition etc. Racemates can be separated from one another, after conversion of the optical antipodes into diastereoisomers for example by reaction with optically active compounds, e.g. optically active acids or bases, by chromatography on column materials covered with optically active compounds or by enzymatic methods, e.g.
by selective reaction of only one of the two enantiomers. This separation can be carried out either at the stage of one of the starting products or with the compounds of formula I
themselves.
T'he configuration at individual chirality centres in a compound of formula I
can be select-ively revexsed. For example the configuration of asymmetric carbon atoms that carry nucleophilic substituents, such as amino or hydroxy, can be reversed by second-order nucleophilic substitution, optionally after conversion of the bonded nucleophilic substit-uent into a suitable nucleofugal leaving group and reaction with a reagent that introduces the original substituent, or the configuration at carbon atoms having hydroxy groups, such as the RS-carrying carbon atom of formula I, can be reversed by oxidation and reduction of compounds of formula I as described below.
The radicals hydroxy RS and hydrogen R6 in a compound of formula I can be oxidised to an oxo group, the oxidising agents used preferably being those that selectively convert the hydroxy group into a keto group, for example chromic acid or a derivative thereof, such as pyridinium chromate or tart-butyl chromate, dichromate/sulfuric acid, sulfur trioxide in the presence of heterocyclic bases, such as pyridine/S03, also nitric acid, pyrolusite or selenium dioxide, or dimethyl sulfoxide in the presence of oxalyl chloride, in water, aqueous or organic solvents, such as halogenated solvents, e.g. methylene chloride, car-boxylic acid amides, such as dimethylformamide, or di-lower alkyl sulfoxides, such as dimethyl sulfoxide, in the presence or absence of basic amines, e.g. tri-lower alkylamines, such as triethylamine, at temperatures of from -50 to 100°C, preferably from -10 to 50°C, for example as described in European Patent Application EP-A-0 236 734.
Conversely, in compounds of formula I obtained in that manner in which R5 and together form an oxo group, the oxo group cart be reduced to a hydroxy group.
Suitable reducing agents for reducing the o:xc> group in a compound of formula 1 are those that under the reaction conditions of the process reduce an isolated keto group selectively or more quickly than amide groups present irx compounds of formula 1.
There may be mentioned, especially, suitable borohydrides, such as alkali metal boro-hydrides, especially sodium borohydride, lithium borohydride or sodium cyanoboro-hydride, also zinc borahydride, or suitable aluminium hydrides, such a:~
alkali metal lower alkoxyaluminium hydrides having voluminous radicals, e.g. lithium tri-tart-butoxyalumin-ium hydride.
The reduction can also be carried out with hydrogen in the presence of suitable heavy ~r~t metal catalysts, e.g. Raney nickel or platinum or palladium catalysts, e.g.
platinum/- or palladium/activated carbon, or according to hrleerwein-Ponndorf-Verley with the aid of aluminium alkanolates, preferably aluminium-2-propanolate or ethanolate.
'The reduction can preferably be carried out with staichiometric amounts or an expediently measured excess of the reducing agent in an inert solvent at temperatures of from -80°C to the boiling point of the solvent, e.g. from -"~t~°C to tl~°C, if necessary under a protective gas, e.g. nitrogen or argon. An excess of the reducing agent is necessary especially when it reacts also with the solvent, e.g. the protons of a erotic solvent.
'JVhen sodium borohydride is used, polar erotic solvents are suitable, e.g.
methanol, ethanol or isopropanol; when the other reducing agents are used, polar aprotic solvents are suitable, e.g. tetrahydrofuran.
In a compound of formula I in which R1, R2, Rg and Rc~ contain no aryl radicals or arrrl radicals that are not very reactive, an arrrl radical present in R~, R3 and/or R4, especially a phenyl radical, can be hydrogenated for exarl~ple by catalytic lay~lrogenation, especiall!r in the presence of heavy metal oxides, such as rltcxliumiplatinum rn~xed oxides, e;.g. with the 1'Jishimura catalyst, preferably in a iaolar solvent, such ;as m alcohol, e.g.
methanol or ethanol, at temperatures of from 0 to 81~°C, especially frt>m 10 to 40°C, ,and at a hydrogen pressure of from 1 to 10 atm, preferably at approximately nc~~-mal pressure.
In an obtainable compound of formula I an amino or carboxamide group may be substi tuted, a carboxy group that is free or in reactive farm may be e;~t~rified or amidated, or an ~o~~~~~

esterified or aanidated carboxy group may be converted into a free carboxy group.
The substitution of a carboxamide group or of another primary ar secondary amino group, e.g. in order to introduce radicals~such as unsubstituted or substituted alkyl, alkenyl or alkynyl, aryl-lower alkyl, or heterocyciyl or heterocyclyl-lower alkyl bonded by carbon R1, R2, Rg or R9 into compounds of formula I in which one or more of the mentioned radicals are hydrogen, is effected e.g. by alkylation.
Suitable agents for alkylating a carboxamide group in a compound of formula I
are e.g.
diazo compounds, e.g. diazomethane. Diazomethane can be decomposed in an inert solvent, the free methylene formed reacting with the carboxamide group in the compound of formula I. The decomposition of diazomethane is carried out preferably by catalysis, e.g. in the presence of a noble metal in finely divided form, e.g. copper, or of a noble metal salt, e.g. copper(I) chloride or copper(II) sulfate.
Alkylating agents are also mentioned in German Offenlegungsschrift 2 331 133, e.g. alkyl halides, sulfonic acid esters, Meerwein salts or 1-substituted 3-aryltriazenes, which can be reacted under the conditions mentioned therein with a. compound of formula I
having a carboxamide group.
Further alkylating agents are selected from compounds of formulae R 1-X (X), R2-X (XI)9 Rg-X (XIII) and R9-X (XIV), wherein X is a leaving group and the remaining radicals are as defined, with the exception of acyl, sulfo unsubstituted or substituted as above, phosphono, and phosphoryl substituted as above. A leaving group is especially a nucleofugal leaving group selected from hydraxy esterified by a strong inorganic or organic acid, such as hydroxy esterified by a mineral acid, e.g. a hydrohalic acid, such as hydrochloric, hydrobromic or hydriodic acid, or by a strong organic sulfonic acid, such as an unsubstituted or substituted, for example halo-sub-stituted, such as fluoro-substituted, lower alkanesulfonic acid, or an aromatic sulfonic acid, e.g. a benzenesulfonic acid that is unsubstituted or substituted by lower alkyl, such as methyl, by halogen, such as bromine, and/or by nitro, e.g. a methanesulfonic, trimethane-sulfonic or p-toluenesulfonic acid, and hydroxy esterified by hydrazoic acid.

20°~2'~~5 The reaction can be carried out under the conditions of a first-order or second-order nucleophilic substitution.
For example, one of the compou~lds of formulae VIII to XIII wherein X is a leaving group with high polarisability of the electron shell, e.g. iodine, can be reacted in a polar aprotic solvent, e.g. acetone, acetonitrile, nitromethane, dimethyl sulfoxide or dimethylform-amide. The reaction may also becarried out in water to which, where appropriate, an organic solvent, e.g. ethanol, tetrahydrofuran or acetone, has been added as solubiliser.
The substitution reaction is tamed out if desired at reduced or elevated temperature, e.g.
in a temperature range of from approximately -40° to approximately 100°C, preferably from approximately -10° to approximately 50°C, and if desired under an inert gas, e.g.
under a nitrogen or argon atmosphere.
For the esterification or amidation of a carboxy group in a compound of formula I, if desired the free acid can be used or the free acid can be converted into one of the above-mentioned reactive derivatives and reacted with an alcohol, with ammonia, or with a primary or secondary amine, or, in the case of esterification, the free acid or a reactive salt, e.g. the caesium salt, can be reacted with a reactive derivative of an alcohol. For example the caesium salt of a carboxylic acid can be reacted with a halide or sulfonic acid ester corresponding to the alcohol. The esterification of the carboxy group can also be carried out with other customary alkylating agents, e.g. with diazomethane, alkyl halides, sulfonic acid esters, Meerwein salts or 1-substituted 3-aryltriazenes, etc..
One of the methods described above for the removal of the carboxy-protecting groups or, if desired, m alkaline hydrolysis in accordance with customary reaction conditions, such as those specified in Organikum, 17th edition, VEB Deutscher Verlag der Wissenschaften, Bexlin 1988, can be used to convert an esterified or amidated carboxy group into the free carboxy group.
An esterified carboxy group in a compound of formula I can be canverted by aminolysis with ammonia or with a primary or secondary amine into an unsubstituted or substituted carboxamide group. The aminolysis can be carried out according to customary reaction conditions, such as those specified for such reactions in Organikum, 15th edition, VEB
Deutscher Verlag der Wissenschaften, Berlin (East) 1976.
A free amino group present in a compound of formula I can be acylated, for example to 2o~z~~~

introduce one of the radicals acyl, sulfo, substituted sulfonyl, phosphono or substituted phosphoryl mentioned for R1, R2, Rg or R9 . The acylation is carried out according to one of the methods mentioned above under Process b), c) or d) for condensation or according to one of the methods mentioned'for protecting groups or, for example, according to one of the processes mentioned in flrganikum, 17th edition, VEB Deutscher Verlag der Wissenschaften, Berlin (East) 1988.
In an obtainable compound of formula I wherein the substituents are as defined and at least one free hydroxy group is present and the remaining functional groups are in pro-tected form, the free hydroxy group can be acylated or etherified.
The acylation can be carried out with acylating reagents according to one of the methods mentioned under Processes b) to d), according to one of the methods mentioned for protecting groups, or according to one of the processes mentioned in Organikum, 17th edition, VEB Deutscher Verlag der Wissenschaften, Berlin (East) 1988.
The etherification can be carried out with the above-mentioned alkylating agents and under the same reaction conditions, e.g. with diazomethane, alkyl halides, sulfonic acid esters, Meerwein salts, 1-substituted 3-aryltriazenes, etc., In an obtainable compound of formula I a sulfinyl or sulfonyl group can be produced from a thio gxoup, and the corresponding sulfoxide or sulfone from a sulfide, by oxidation.
The oxidation to the sulfonyl group or to the sulfone can be carried out with most of the customary oxidising agents. The oxidising agents used are especially preferably those that .
oxidise the thio group or the sulfide sulfur selectively in the presence of other functional groups of the compound of formula I in question, e.g. amino or hydroxy groups;
examples of SLICK oxidising agents are aromatic or aliphatic peroxycarboxylic acids, e.g. peroxy-benzoic acid, monoperphthalic acid, m-chloroperbenzoic acid, peracetic acid, performic acid or trifluoroperacetic acid. The oxidation with peroxycarboxylic acids is carried out in the customary solvents suitable therefor, for example chlorinated hydrocarbons, e.g.
methylene chloride or chloroform, ethers, such as diethyl ether, esters, such as ethyl acetate or the like, at temperatures of from -78°C to room temperature, e.g. from -20°C to +10°C, preferably about 0°C. The peroxycarboxylic acid can also be formed in situ, e.g.
with hydrogen peroxide in acetic acid or formic acid that may or may not contain acetic anhydride, e.g. with 30 % or 90 % hydrogen peroxide in acetic acid/acetic anhydride. Also suitable are other peroxo compounds, for example potassium peroxomonosulfate in lower alkanol/water mixtures, e.g. methanol/water or ethanol/water, or in aqueous acetic acid at temperatures of from -70°C to +30°C, e.g. from -20°C to room temperature, and also sodium metaperiodate in methanol or methanol/water mixtures at temperatures of from 0°C to 50°C, e.g. approximately room temperature. If stoichiometric amounts of the men-tioned oxidising agents are used it is also possible for the corresponding sulfuric acids or sulfoxides to be obtained. There are suitable for that purpose, for example, sodium mete-periodate in methanol or methanol/water mixtures at temperatures of from -15°C to room temperature, e.g. approximately 0°C, m-chloroperbenzoic acid in methylene chloride, chloroform or ethyl acetate at temperatures of from -78°C to 10°C, preferably from -30°C
to 0°C, also tert-butylhypochlorite in lower alkanols, e.g. methanol, or hydrogen peroxide in acetone or acetic acid at temperatures of approximately 0°C, or the above-mentioned potassium peroxomonosulfate at low temperatures.
If desired, the corresponding thio compound or the corresponding sulfide can be obtained by reducing a sulfonyl group or a sulfone radical in an obtainable compound of formula I, for example with diisobutylaluminium hydride in ether or tetrahydrofuxan.
In an obtainable compound of formula I having a sulfinyl group, that group can be reduced to a thio group. Selective reducing agents that leave other functional groups of the compound of formula I, e.g. the amide function, unchanged are preferred.
Examples of such selective reducing agents are dichloroborane, which is preferably used in tetrahydro-furan or dimethoxyethane at temperatures of from -30°C to +10°C, triphenylphosphine in boiling carbon tetrachloride, trichlorosilane or hexachlorodisilane, iron pentacarbonyl, also sodium hydrogen sulfite in aqueous/alcoholic solvents, e.g.
water/methanol, water/-ethanol or also water/tetrahydrofuran, at temperatures of from -10°C to +50°C, also sodium borohydride in the presence of cobalt(II) chloride or also hydrogen in the presence of catalytic amounts of palladium, e.g. palladium/carbon in boiling ethanol.
Protecting groups present in a compound of formula I or suitable radicals Rl, R2, R8 or R9, i.e. those representing aryl, sulfo, substituted sulfo, phosphono or substituted phos-phoryl, can be removed according to one of the processes mentioned under Process f), especially by hydrolysis, for example in the presence; of bases, such as alkali or alkaline earth metal hydroxides, e.g. sodium hydroxide, or acids, such as organic acids or mineral acids, e.g. hydrogen halide, such as hydrogen chloride. The hydrolysis is carried out under customary conditions, for example in aqueous solution or in anhydrous solvents, 2~'~27~5 especially in ethers, such as dioxane, at temperatures of from -50°C to the reflux temp-erature of the Corresponding reaction mixtures, e.g. from 0°C to 50°C, preferably in the presence of a protective gas, such as argon or nitrogen.
All of the process steps specified above can be carried out under reaction conditions that are known her se, preferably those specifically mentioned, in the absence or customarily in the presence of solvents or diluents, preferably those that are inert towards and dissolve the reagents used, in the absence or presence of catalysts, condensation agents or neutral-ising agents, e.g. ion exchangers, such as ration exchangers, e.g. in the H~
form, depend-ing on the nature of the reaction and/or the reactants at reduced, normal or elevated temp-erature, e.g. in a temperature range of from approximately -100°C to approximately 190°C, preferably from approximately -80°C to approximately 150°C, e.g. at from -80 to -50°C, at room temperature, at from -20 to 40°C or at the boiling point of the solvent used, under atmospheric pressure or in a closed vessel, if desired under pressure, and/or under an inert atmosphere, e.g. under an argon or nitrogen atmosphere.
In the case of all starting compounds and intermediates where there are salt~forming groups, salts may be present. Salts may also be present during the reaction of such compounds, provided they do not interfere in the reaction.
At all stages of the reaction, isomeric mixtures that are obtained can be sepazated into the individual isomers, e.g. diastereoisomers or enantiomers, or into any mixtures of isomers, e.g. racemates or diastereoisomeric mixtures, for example analogously to the methods described under "Additional I9rocess Steps".
In certain cases, for example in the case of hydrogenation, it is possible to achieve stereo-selective reactions, so that e.g. simplified production of individual isomers is possible.
The solvents from which those suitable for the reaction in question can be selected include, for example, water, esters, such as lower alkyl lower alkanoates, e.g. diethyl acetate, ethers, such as aliphatic ethers, e.g. diethyl ether, or cyclic ethers, e.g. tetrahydro-furan, liquid aromatic hydrocarbons, such as benzene or toluene, alcohols, such as methanol, ethanol or 1- or 2-propanol, nitrites, such as acetonitrile, halogenated hydro-carbons, such as methylene chloride, acid amides, such as dimethylformamide, bases, such as heterocyclic nitrogen bases, e.g. pyridine, carboxylic acid anhydrides, such as lower alkanoic acid anhydrides, e.g. acetic anhydride, cyclic, linear or branched hydrocarbons, such as cyclohexane, hexane or isopentane, or mixtures of those solvents, e.g.
aqueous solutions, provided nothing else is specified in the description of the process. Such solvent mixtures can also be used in working up, for example by chromatography or partitioning.
The invention relates also to those embodiments of the process in which a compound obtainable at any stage as intermediate is used as starting material and the remaining steps are carried out, or the process is discontinued at any stage, or a starting material is formed under the reaction conditions or is used in the foam of a reactive derivative or salt, or in which a compound obtainable according to the process of the invention is produced under the process conditions and further processed in situ. The starting materials used are pref erably those that result in the compounds referred to above as preferred, especially those referred to as especially preferred, more especially preferred and/or preferred above all.
Pharmaceutical Compositions:
The invention relates also to pharmaceutical compositions comprising compounds of formula I.
The pharmacologically acceptable compounds of the present invention may be used, e.g., for the preparation of pharmaceutical compositions that comprise an effective amount of the active ingredient together or in admixture with a significant amount of inorganic or organic, solid or liquid, pharmaceutically acceptable carriers.
The invention relates also to a pharmaceutical composition that is suitable for administra-tion to warm-blooded animals, especially humans, far the treatment or prevention of a disease that responds to inhibition of a retroviral protease, especially a retroviral aspartate protease, such as HIV-I- or HIV-II-gag protease, e.g. a retroviral disease such as AIDS, comprising an amount of a compound of formula I effective for the inhibition of retroviral protease, or a pharmaceutically acceptable salt thereof, together with at least one pharma-ceutically acceptable carrier.
The pharmaceutical compositions according to the invention are those for enteral, such as nasal, rectal or oral, or parenteral, such as intramuscular or intravenous, administration to warm-blooded animals (humans or animals), that comprise an effective dose of the pharmacological active ingredient, alone or together with a significant amount of a pharmaceutically acceptable carrier. The dace of the active ingredient depends on the 20~2~~5 species of warm-blooded animal, the body weight, the age and the individual condition, individual pharmacokinetic data, the disease to be treated and the mexhod of administra-tion.
The invention relates also to a method of treating diseases caused by viruses, especially by retroviruses, for example AIDS, which comprises administering a therapeutically effective amount of z compound of formula I according to the invention, especially to a warm-blooded animal, for example a human, who on account of one of the mentioned diseases, especially AIDS, requires such treatment. The dose to be administered to warm-blooded animals, for example humans of approximately 70 kg body weight, is from approximately 3 mg to approximately 3 g, preferably from approximately 10 mg to approximately 1.5 g, for example from approximately 300 mg to 1000 mg per person per day, divided prefer-ably into 1 to 3 single doses which may, for example, be of the same size.
Usually, children receive half of the adult dose.
The pharmaceutical compositions comprise from approximately 1 % to approximately 95 %, preferably from approximately 20 % to approximately 90 % active ingredient.
Pharmaceutical compositions according to the invention may be, for example, in unit dose form, such as in the form of ampoules, vials, suppositories, dragees, tablets or capsules.
The pharmaceutical compositions of the present invention are prepared in a manner known her se, for example by means of conventional dissolving, lyophilising, mixing, granulating or confectioning processes.
Solutions of the active ingredient, and also suspensions, and especially isotonic aqueous solutions or suspensions, are preferably used, it being possible, for example in the case of lyophilised compositions that comprise the active ingredient alone or together with a carnet, e.g. mannitol, for such solutions or suspensions to be produced prior to use. The pharmaceutical compositions may be sterilised and/or may comprise excipients, e.g.
preservatives, stabilisers, wetting and/or emulsifying agents, solubilisers, salts for regulat-ing the osmotic pressure and/or buffers, and are prepared in a manner known her se, e.g.
by means of canventional dissolving or lyophilising processes. The said solutions or suspensions may camprise viscosity-increasing substances, such as sodium carboxy-methylcellulose, carboxymethylcellulose, dextran, polyvinylpyrrolidone or gelatin.
Suspensions in oil comprise as the oil component the synthetic or semi-synthetic vegetable 2~'~2'~~~

oils customary for injection purposes. There may be mentioned as such especially liquid fatty acid esters that contain as the acid component a long-chained fatty acid having from 8 to 22, especially from 12 to 22, carban atoms, e.g. lauric acid, tridecylic acid, myristic acid, pentadecylic acid, palmitic acid, margaric acid, stearic acid, arachidic acid, behenic acid or corresponding unsaturated acids, e.g. oleic acid, elaidic acid, erucic acid, brasidic acid or linoleic acid, if desired with the addition of antioxidants, e.g.
vitamin E, ~-carotene or 3,S-di-tert-butyl-4-hydroxytoluene. The alcohol component of those fatty acid esters has a maximum of 6 carbon atoms and is a mono- or poly-hydric, e.g. a mono-, dl- or tri-hydric, alcohol, e.g. methanol, ethanol, propanol, butanol or pentanol or the isomers thereof, but especially glycol and glycerol. The following examples of fatty acid esters are therefore to be mentioned: ethyl oleate, isopropyl myristate, isopropyl palmitate, "Labrafil M 2375" (polyoxyethylene glycerol trioleate, Gattefosse, Paris), "Miglyol 812"
(tri-glyceride of saturated fatty acids with a chain length of Cg to C12, Hills AG, Germany), but especially vegetable oils, such as cottonseed oil, almond oil, olive oil, castor oil, sesame oil, soybean oil and more especially groundnut oil.
The injection compositions are prepared in customary manner under sterile conditions; the same applies also to introducing the compositions into ampoules or vials and sealing the containers.
Pharmaceutical compositions for oral administration can be obtained by combining the active ingredient with solid carriers, if desired granulating a resulting mixture, and processing the mixture, if desired or necessary, after the addition of appropriate excipients, into tablets, dragee cores or capsules. It is also possible for them to be incorporated into plastics carriers that permit the release or diffusion of the active ingredients in measured amounts.
Suitable carriers are especially fillers, such as sugars, e.g. lactose, saccharose, mannitol or sorbitol, cellulose preparations and/or calcium phosphates, e.g. tricalcium phosphate or calcium hydrogen phosphate, and binders, such as starch pastes using e.g.
corn, wheat, rice or potato starch, gelatin, tragacanth, methylcellulase, hydroxypropylmethylcellulose, sodium carboxymethylcellulose and/or polyvinylpyrrolidone, and/or, if desired, disinte-grators, such as the above-mentioned starches, also carboxymethyl starch, crosslinked polyvinylpyrrolidone, agar, alginic acid or a salt thereof, such as sodium alginate.
Excipients are especially flow conditioners and lubricants, e.g. silicic acid, talc, stearic acid or salts thereof, such as magnesium or calcium stearate, and/or polyethylene glycol.

~o~ ~~ ~~
- las-Dragee cores are provided with suitable, optionally enteric, coatings, there being used, inter alia, concentrated sugar solutions which may comprise gum arabic, talc, polyvinyl-pyrrolidone, polyethylene glycol and/or titanium dioxide, or coating solutions in suitable organic solvents, or, for the preparation of enteric coatings, solutions of suitable cellulose preparations, such as ethylcellulose phthalate or hydroxypropylmethylcellulose phthalate.
Capsules are dry-filled capsules made of gelatin and soft sealed capsules made of gelatin and a plasticises, such as glycerol or sorbitol. The dry-filled capsules may comprise the active ingredient in the form of granules, e.g. with fillers, such as lactose, binders, such as starches, and/or glidants, such as talc or magnesium stearate, and if desired with stabil-isers. In soft capsules the active ingredient is preferably dissolved or suspended in suitable oily excipients, such as fatty oils, paraffin oil or liquid polyethylene glycols, it being possible also for stabilisers and/or antibacterial agents to be added. Dyes or pigments may be added to the tablets or dragee coatings or the capsule casings, e.g. fox identification purposes or to indicate different doses of active ingredient.
Starting materials:
The present invention relates also to novel st~u-ting materials and/or intermediates and to processes for their preparation. Preferably the starting materials and reaction conditions are so selected that the compounds listed above as preferred are obtained.
In the preparation of all starting materials free functional groups that are not to participate in the reaction in question may be in unprotected or protected form, for example they may be protected by the protecting groups mentioned above under Process a). Those protecting groups may be removed at appropriate times by the reactions described under Process f).
The starting materials of Process a) are known or, if novel, can be prepared according to processes known her se, e.g. compounds of formula III can be prepared from hydrazine or suitable derivatives thereof and compounds of formula IV can be prepared from suitable amino acids or analogues thereof, for example those having one or two of the mentioned side chains 123 atld 124.
The compounds of formula III can be obtained, for example, from compounds of formula H2~-WRIl ~xV) 20~27~5 wherein Rt t is hydrogen or an amino-protecting group, as described above under .Process b), especially tart-lower alkoxycarbonyl, such as tart-butoxycarbonyl; aryl-lower alkoxy-carbonyl, such as benzyloxycarbonyl or 9-fluorenylmethoxycarbonyl, or one of the above-mentioned acylamino-protecting groups by, in order to prepare a compound of formula I wherein in place of R~ there is a xadical R~" which is unsubstituted or sub-stituted alkyl or cyclollkyl, alkylating with a compound of formula XII to introduce R~", as described above under Process e), or introducing the radical R~ by reaction of suitable carbonyl compounds with the free amino group of the compound of formula VIII
or an acylated derivative thereof and subsequent reduction of the resulting hydrazone to form hydrazine derivatives of formula R~-NT-I-NH-Ri i (XV I), wherein the radicals in all of the mentioned compounds are as defined hereinbefore and functional groups in participating reagents that are not to take pert in the reaction are, if desired, protected, where appropriate removing the protecting group Rtt, if it does not correspond to one of the radicals Rg or R9 in compounds of formula I, and/or removing other protecting groups, and reacting the radicals Rg and R9 other than hydrogen, by con-densation under the conditions mentioned in Process b), with acids of formula VI or of formula Rx-OI-I (XVII), wherein Rg is as defined, or by alkylation with a compound of formula XIII or XIV, as defined above, or both, in accordance with the conditions indicated above in the additional process steps.
The carbonyl compounds suitable for the introduction of R~ that are used for the prepara-tion of compounds of formula XVI are aldehydes or ketones of which the reactive carbonyl group is a component of one of the mentioned radicals R~ after the reaction with compounds of formula XV and the subsequent reduction, preferably aldehydes that are suitable for the introduction of lower alkyl, cyclohexyl-lower alkyl or phenyl-lower alkyl.
The reaction of the carbonyl compounds with the compounds of formula XVI to form the corresponding hydrazones is earned out under the conditions customary for the reaction of carbonyl compounds with amines, preferably in polar organic solvents, e.g.
ethers, such as :1489-8495 - 12f3 -tetrahydrofuran or diethyl ether, al.cohols, such as methanol or ethanol, carboxylic acid amides, such as ilimethylformamide, or esters, such as ethyl acetate, pr in aqueous solution, preferably in methanol, and also in the presence oz' absence of acid catalysts, e.g.
carboxylic acids, such as formic acrid or acetic acid, or sulfonic acids, such as p-toluene-sulfonic acid, at temperatures of from 0°C' tc> the reflex ternpcwrature of the reaction mixture, preferably at temperatures of from 20°C to the reflex temperate of the reaction mixture.
The reduction of the resulting hydrazones is carried out preferably by hydrogenation in the presence of a suitable catalyst. Suitable catalysts used for the hydrogenation include metals, such as nickel, iron, cobalt or ruthenium, and noble metals and their oxides, such as palladium or rhodium and their oxides, where appropriate ;applied e.g. to a suitable support, such as barium sulfate, aluminium oxide or activated carbon, or in the form of ~rM
skeleton catalysts, such as Raney nickel. Customary solvents far the catalytic hydrogen-ation are, for example, water, alcohols, such as methanol or ethanol, esters, such as etlayl acetate, ethers, such as dioxane, chlorinated hydrocarbons, such as dichlotromethane, car-boxylic acid amides, such as dimethylformamide, or carboxylic acids, such as glacial acetic acid, or mixtures of those solvents. The hydrogenation is carried out at temperatures of from 10 to 250°C, preferably from roam temperature to 101)°~, and at hydrogen pressures of from 1 to 200 bar, pref°erably tram 1 to 10 bar, in the customary apparatus.
Especially preferred for the preparation of c;ompaunds of formula XV are reaction condi-tions analogous to those described in Je Chern. Sac. Perkin l, 1712 (1975).
The compounds of formula IV can be obtained, for example, by the reduction of amino acids of formula R ~a- N %~ COOH
(XVIi:I), R3 Rp wherein Rl0 is hydrogen or one of the amino-protecting grr~ups mentioned under Process a), especially tert-lower alkoxycarbonyl, such :as tern-butoxycarbonyl, aryl-lower alkoxy-carbonyl, such as benzyloxycarbonyl or 9-flu~arenylmethox ycarbc~nyl, or one of the acyl-~o~~~~~

amino-protecting groups mentioned under that process, and R3 and R4 are as defined fox compounds of formula I, preferably of amino acids of formula ~
R~~-NH~COOH
Y (XVIII A), wherein the radicals are as defined, to aldehydes of formula Rio NH CHO
~ (X~)>
R3/ \Ra wherein the radicals are as defimed, preferably to the aldehydes of formula Rya--NH~CHO
(XIX A), R~
wherein the radicals are as defined (which are obtainable, for example, from compounds of foxmula XVIII A), by reaction of those aldehydes with an ylide compound, preferably a sulfur-glide compound, to form an epoxide of formula ' ~ o R~s N (~)>
R3 Ra wherein the radicals are as defined, preferably to compounds of formula 2 0'~ 2'~ ~ 5 H
O
R,.s NH ~ (XX A), (obtainable, for example, from compounds of formula XIX A), wherein the radicals are as defined, where appropriate removal of the protecting group Rrt, provided that does not correspond to one of the radicals R8 or R~ in compounds of formula I, and acylation of the amino group of the resulting compound with an acid of formula VIII or formula R2-OH (XXI), wherein the radicals are as defined, under the conditions described for Process b), and/or alkylation of the amino group of the resulting compound with reagents having nucleofugal leaving groups of formula X or XI, wherein the radicals are as defined, under the condi-tions described for additional process steps.
The reduction of amino acids of formula XVIII or XVIII A to the corresponding aldehydes XIX and XIX A is earned out, for example, by reduction to the corresponding alcohols and subsequent oxidation to the said aldehydes.
The reduction to the alcohols is carried out, for example, by hydrogenation of the acid halides or other activated carboxylic acid derivatives mentioned under Process b) under the conditions mentioned for the hydrogenation of hydxazones obtained from compounds of formula XVI, or with complex hydrides, such as sodium borohydride. The subsequent oxidation of the resulting alcohols is possible, for example, under the conditions for the oxidation of compounds of formula I in which RS is hydroxy and R6 is hydrogen to compounds of formula I in which R5 and R6 together are oxo, as described in the addi-tional process steps, or by oxidation of the hydroxy group with a sulfoxide, such as dimethyl sulfoxide, in the presence of a reagent that activates the hydroxy group, such as a carboxylic acid chloride; e.g. oxalyl chloride, in an inert solvent, e.g. a halogenated hydro-carbon, such as dichloromethane, and/or an acyclic or cyclic ether, such as tetrahydro-furan; at from -80 to 0°C, e.g. from -78 to -50°C.
Direct reduction of the amino acids to the aldehydes is also possible, for example by hydrogenation in the presence of a partially contaminated palladium catalyst or by reduc-tion of the corresponding amino acid ester, e.g. the lower alkyl ester, such as ethyl ester, with complex hydrides, e.g. borohydrides, such as sodium borohydride, or preferably aluminium hydrides, e.g. lithium aluminium hydride, lithium tri-(tert-butoxy)aluminium hydride or especially diisobutylall~minium hydride, in apolar solvents, e.g.
in hydro-carbons or aromatic solvents, such as toluene, at from -100 to 0°C, preferably from -70° to -30°C, and subsequent reaction to form the corresponding semicarbazones, e.g. with the corresponding acid salts of semicarbazones, such as semicarbazide hydrochloride, in aqueous solvent systems, such as alcohol/water, e.g. ethanol/water, at temperatures of from -20 to 60°C, preferably from 10 to 30°C, and reaction of the resulting semicarbazone with a reactive aldehyde, e.g. formaldehyde, in an inert solvent, for example a polar organic solvent, e.g. a carboxylic acid amide, such as dimethylformamide, at temperatures of from -30 to 60°C, preferably from 0 to 30°C, and then with an acid, for example a strong mineral acid, SllCh as hydrogen halide, in aqueous solution, if desired in the presence of the previously used solvent, at temperatures of from -40 to 50°C, preferably from -10 to 30°C. The corresponding esters are obtained by reaction of the amino acids with the corresponding carboxylic acids, for example ethanol, analogously to the condi-tions used in the condensation in Process b), for example by reaction with inorganic acid halides, such as thionyl chloride, in organic solvent rr~ixtures, such as mixtures of aromatic and alcoholic solvents, e.g. toluene and ethanol, at temperatures of from -50 to 50°C, preF
erably from -10 to 20°C.
The preparation of compounds of formulae XIX and XIX A is carried out especially pref erably under conditions analogous to the reaction conditions mentioned in J.
Org. Chem.
47, 3016 (1982) or 1. Org. Chem. 43, 3624 (1978).
A sulfur-ylide suitable for the reaction of compounds of formula XIX or XIX A
to form the epoxides of formula XX or XX A is, for example, a dialkylsulfonium methylide, e.g.
dimethylsulfonium methylide, an alkyl- or phenyl-dialkylaminosulfoxonium methylide, e.g. methyl- or phenyl-dimethylaminosulfoxonium methylide, or a dialkylsulfoxonium methylide, e.g. dimethyl- or diethyl-sulfoxonium methylide.
The relevant sulfur-ylide compound is expediently prepared in situ from the corresponding sulfonium or sulfoxonium salt and a base, e.g. sodium hydride, in a dipolar aprotic solvent, e.g. dimethyl sulfoxide, or an ether, e.g. tea~ahydrofuran or 1,2-dimethoxyethane, and then reacted with compounds of formula XiX or XIX A. The reaction is normally carried out at room temperature, with cooling e.g. to -20°C, or with gentle heating e.g. up to 40°C. The 2~~2'~~~

simultaneously formed sulfide, sulfinamide or sulfoxide is removed during the subsequent aqueous working-up. , The reaction with a sulfur-ylide i~ carried out especially preferably analogously to the conditions mentioned in J. Org. Chem. 50, 4515 (1985).
The campound of formula XX (preferably XX A) can also be obtained from a compound of formula XIX (preferably XIX A), as defined above, by reaction thereof with a tri-lower alkyl-silylmethyl-Grignard compound, e.g. prepared from the corresponding halo-methyl-silane, such as chloromethyl-trimethylsilane, in an inert solvent, e.g. an ether, such as dioxane or diethyl ether, at temperatures of from 0 to 50°C, e.g. from room temperature to approximately 40°C, subsequent removal of the silyl radical and formation of a double bond, e.g. by means of treatment with a Lewis acid, such as BF3, an amino-protecting group Rtp present preferably also being removed, in an inert solvent, e.g. an ether, such as diethyl ether, or a halogenated hydrocarbon, such as dichloromethane, or a mixture thereof, at temperatures of from -50°C to the reflex temperature, especially from 0 to 30°C, if necessary, acylation once more to introduce an amino-protecting group as Rlo, as defined above, and oxidation of the resulting double bond to the oxirane, preferably with a percarboxylic acid, e.g. m-chloroperbenzoic acid, in an inert solvent, e.g. a halogenated hydrocarbon, such as dichloromethane, at temperaturE;s of from -20°C to the reflex temp-erature of the mixture, e.g. at from 10 to 30°C.
The starting materials of Processes b), c) and d) are known or, if novel, can be prepared according to processes known ~ se, e.g. the compound of formula V can be prepared from suitable hydrazine derivatives of formula III wherein R9 is hydrogen and the remain-ing radicals are as defined for compounds of fornnula V, and suitable epoxides of formula IV wherein the radicals are as defined for compounds of formula V (Process b), the compound of formula VB can be prepared from suitable hydrazine derivatives of formula IIT wherein the radicals are as defined for compounds of formula VII, and suitable epoxides of formula IV wherein Rt is hydrogen and the remaining radicals are as defined for compounds of formula VII (Process c), and the compound of formula IX can be pre-pared from suitable hydrazine derivatives of formula III wherein R~ is hydrogen and the remaining radicals are as defined for compounds of formula IX (Process d) and suitable epoxides of formula IV wherein RI is hydrogen and the remaining radicals are as defined for compounds of formula IX (Process d), analogously to Process a), where appropriate with the use and removal of protecting groups.

The compounds of formula I' wherein the substituents are as defined,above can be pre-pared, for example, from compounds of formula III' H
I
HN eN / R9 (III') ~R$
wherein the radicals are as defined for compounds of formula I, in the manner described in Process b), by reaction with a compound of formula IV, wherein any functional groups present that are not to take part in the reaction are in protected form as described in that Process and can be freed after the reaction.
There are preferred for Process d) the starting materials of formula H
OH I ~
He/N~N~N/-H (II)~

H
wherein R3 is unsubstituted or substituted alkyl or cycloalkyl; aryl;
heterocyclyl; or unsubstituted or substituted alkenyl; and R~ is unsubstituted or substituted alkyl or cyclo-alkyl; aryl; heterocyclyl; or unsubstituted or substituted allcenyl, and the salts of the said compounds where salt-forming groups are present, which are intermediates according to the invention.
They may be protected especially at one or both amino groups and, in the case where two amino-protecting groups are present, these may be identical or different from one another.
There may be used as amino-protecting groups, for example, the amino-protecting groups mentioned above in Process a). The radicals R3 and R~ mentioned for compounds of formula II are as defined above for compounds of formula I in the definition of the radicals R3 and R~.
Especially preferred are compounds of formula II wherein R3 is cyclohexyl-lower alkyl, ~o~~~~~

phenyl-lower alkyl or p-fluorophenyl-lower alkyl and R~ is lower alkyl, cyclohexyl-lower alkyl, phenyl-lower alkyl, p-cyanophenyl-lower alkyl or p-fluorophenyl-lower alkyl, and the salts of the said compounds where salt-forming groups are present.
Especially preferred in particular are compounds of formula II wherein R3 is phenyl-lower akyl and R~ is lower alkyl, cyclohexyl-lower alkyl or phenyl-lower alkyl, and the salts of the said compounds where salt-forming groups are present.
More especially preferred are compounds of formula IT wherein R3 is cyclohexylmethyl, benzyl or p-fluorobenzyl and R~ is n-butyl, isobutyl, cyclohexylmethyl, benzyl, p-fluoro-benzyl or p-cyanobenzyl, and the salts of the said compounds where salt-forming groups are present.
More especially preferred in particular are compounds of formula II wherein R3 is benzyl and R~ is isobutyl, cyclohexylmethyl or benzyl, and the salts of the said compounds where salt-forming groups are present.
Preferred above all are the compounds of formula II mentioned in the.
Examples.
The compounds of formula II wherein the substituents are as defined, or their salts where salt-fornZing groups are present, are prepared, for example, by adding a hydrazine deriva-tive of formula R7-~-~'R11 (XVI), wherein Rlp is an amino-protecting group, to an epoxide of formula H
O
(~ A) wherein R11 is an amino-protecting group, and if desired, converting a compound of formula II having at least one salt-forming group obtainable according to the preceding Process a) into its salt or converting an obtainable 2072~~~

salt into the free compound or into a different salt and/or separating any isomeric mixtures that are obtainable and/or removing any protecting groups present in ,a compound of formula II and/or converting a compound of formula II according to the invention into a different compound of formula IT according to the invention.
The preparation and conversion of salts, the separation of isomeric mixtures, the removal of protecting groups and the conversion of compounds of formula II are carried out analo-gously to the processes described hereinbefore for compounds of formula I.
Especially preferred is the preparation of starting materials of formula II, wherein the sub-stituents are as defined, by the removal of protecting groups from compounds of formula II wherein one or both amino groups are protected by amino-protecting groups, especially under the conditions for the hydrolysis of compounds of formula I, as described in the additional process steps.
The methods for the addition of compounds of formula XVI to those of formula XX A are described above under Process a) in the preparation of compounds of formula I.
The preparation of the protected compounds of formula I is carried out, for example, according to any one of the processes mentioned so far, especially from compounds of formulae III and IV, wherein functional groups in those compounds are if desired protec-ted by protecting groups, as described in Process a).
The acids of formulae VI, VIII, XVII and XXI and the compounds having nucleofugal groups of formulae X, XI, XII, XIII, XIV and XV are known or, if novel, can be prepared according to processes known her se.
The fallowing Examples serve to illustrate the invention but do not limit the scope thereof m any way.
Temperatuxes are given in degrees Celsius (°C). If no temperature details are given, the reaction takes place at room temperature. The Itf values, which indicate the ratio of the seepage propagation of the substance in question to the seepage propagation of the eluant front, are ascertained on thin layer silica gel plates by thin layer chromatography (TLC) in the following solvent systems.

~?0'~2~~~

TLC eluant systems:
A chloroforrn/methanol/water/ 75:27:5:0.5 acetic acid ' B chloroform/methanol/water/ 90:10:1:0.5 acetic acid C chloroform/methanol/water/ 85:13:1.5:0.5 acetic acid D chlorofotm/methanol 8:1 E chloroform/methanol 95:5 F hexane%thyl acetate 2:1 G methylene chloride/diethyl 20:20:1 ether/

methanol I-I methylene chloride/diethyl 1:1 ether I toluene/ethyl acetate 2:1 K chlorofotm/rnethanol 5:1 J methylene chloride/diethyl 5:1 ether L hexane/ethyl acetate 4:1 Mf hexane/ethyl acetate 5:1 N hexane/ethyl acetate 1:1 O ethyl acetate P methylene chloride/ethanollNII3aq.90:10:1 Q methylene chlorideldiethyl 10:1 ether R hexane/ethyl acetate 3:1 S methylene chloride/diethyl 20:1 ether T: chloroform/methanol 30:1 U: chloroforn~/methanol 15:1 V: methylene chloride/diethyl 1:1:3 ether/

hexane W: methylene chloride/diethyl 20:1 ether X: methylene chloride/methanol 40:1 Y: toluene/ethyl acetate 4:1 The abbreviation "Rl(A)", for example, denotes that the Rf value was determined in solvent system A. The ratio of the amounts of solvent in relation to one another is always given in parts by volume.

20'~2'~~5 HPLC-gradients : , I: 20 % -> 100 % ~cetonitrile/0.05 % trifluoroacetic acid in water/0.05 % trifluoroacetic acid during 35 min.
II: 0 % -> 40 % acetonitrile/0.05 % trifluoroacetic acid in water/0.05 % trafluoroacetic acid during 30 min.
III: 20 % -> 60 % acetonitrile/0.05 % trifluoroacetic acid in water/O.OS % trifluoroacetic acid during 60 min.
IV: 10 % -> 50 % acetonitrile/0.05 % trifluoroacetic acid in water/O.OS % trifluoroacetic acid during 60 min.
Column (250 x 4.6 mm) filled with "reversed-phase" material Ct8-Nucleosil~ (S
~.m mean particle size, silica gel covalently derivatised with octadecylsilanes, Macherey & Nagel, Diixen, Federal Republic of Germany). Detection by UV-absorption at 215 nm.
The retention times (tRet) are given in minutes. Flow rate 1 ml/min.
The same abbreviations are used to indicate the eluant systems for the flash chromato-graphy and the medium pressure chromatography.
The other shortened names and abbreviations used have the following meanings:
' abs, absolute (indicates that the solvent is anhydrous) atm physical atmospheres (unit of pressure) - 1 atm corresponds to 1.013 bar Boc tent-butoxycarbonyl BOP benzotriazol-1-yl-oxy-tris(dimethylamino)-phosphonium hexafluorophosphate DIPE diisopropyl ether DMF dimethylformamide DMSO dimethyl sulfoxide ether diethyl ether ~o~~~~~

h hours HBTLJr O-benzotriazol-1-yl-N,N,N' ,N'-tetra-methyl-uronium hexafluorophosphate ~

H~Bt 1-hydroxybenzotriazole HV high vacuum min minutes) MS mass spectroscopy NMM N-methylmorpholine RT room temperature RE rotary evaporator brine saturated sodium chloride solution TFA trifluoroacetic acid 2 benzyloxycarbonyl Mass spectroscopic measurements are obtained either by conventional MS ar according to the "Fast-Atom-Bombardment" (FAB-MS) method. T'he mass details refer in the first instance to the unprotonated molecule ian (M)+ or to the protonated molecule ion (M+I-I)+.
The values for proton nuclear resonance spectroscopy (tH-NMR) are given in ppm (parts par million) based on tetramethylsilane as the internal standard, s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet, dd = double doublet, br = broad.
The values for IR spectra are given in cm-t, and the solvent in question is in round brackets. If quoted, s indicates a strong, m a medium and w a weak intensity of the band in question.
The residue referred to as -[PheNNPhe] denotes the divalent residue of 3(S)-amino-4-phenyl-1-(N-benzylhydrazino)-butan-2(S)-of and has the formula 2U°~~'~~35 ~ OH
-NH
N
~NH-The residue referred to as -[PheNNCha] denotes the divalent residue of 3(S)-amino-4-phenyl-1-(N-cyclohexylmethylhydrazino)-butan-2(S)-of and has the formula The residue referred to as -[PheNNLeu] denotes the divalent residue of 3(S)-amino-4-phenyl-1-(N-isobutylhydrazino)-butan-2(S)-of and has the formula N
eNH_ ~~°~2°~~5 The residue referred to as -[PheNNNle] denotes the residue of 3(S)-amino-4-phenyl-1-(N-n-butylhydrazino)-butan-2(S)-of and has the formula , OH
H ~N
~'NH-The residue referred to as -[PheNN(p-F)Phe] denotes the divalent residue of 3(S)-amino-4-phenyl-1-(N-(p-fluorophenylmethyl)-hydrazino)-butan-2(S)-of and has the formula /- ~ F
off w ~
-NH ~N _ ~NH-al The residue referred to as -[(p-F)PheNN(p-F)Phe] denotes the divalent residue of 3(S)-amino-4-(p-fluorophenyl)-1-(N-(p-fluorophenylmethyl)-hydxazino)-butan-2(S)-of and has the formula 2~'~2"~~5 F
F
The residue referred to as -[PheNN(p-CN)Phe] denotes the divalent residue of 3(S)-amino-4-phenyl-1-(N-(p-cyanophenylmethyl)-hydrazino)-butan-2(S)-of and has the formula c'%
OH
_NH \ . N
~~ ~NH-The residue refeixed to as -[ChaNNLeu] denotes the divalent residue of 3(S)-amino-4-cyclohexyl-1-(N-isobutyl-hydrazino)-butan-2(S)-of and has the formula OH
N
~NH-The abbreviations customarily used in peptide chemistry are used to name divalent 20~2'~~~

residues of natural a-amino acids. However, contrary to customary peptide nomenclature in which the amino terminus is on the left-hand side and the carboxy terminus is on the right-hand side, amino acids that are on the right-hand side of the zesidues -[PheNNPhe],' -[PheNNCha], -[PheNNLeu], -[PhaNNNle], -[PheNN(p-F)Phe], -[(p-F)PheNN(p-F)Phe], -[PheNN(p-CN)Phe] or -[ChaNNLeu] in the compound names, have the linking carboxy group on the left, which is indicated by an arrow (.-) symbolising the reversal of the direc-tion of linkage. The configuration at the a-cazbon atom, if it is known, is indicated by the prefix (L)- or (D)-. Tyrosine xesidues etherified at the phenolic hydroxy group by the radical R are designated by Tyr(OR). Nle denotes the residue of norleucine.
Example 1: Boc-fPheNNPheI-Boc:
A solution of 300 mg (1.14 mmol) of (2R)-[1'(S)-Boc-amino-2'-phenylethyl]oxirane (J.
Org. Chem. S0, 4615 (1985)) and 253 mg (1.14 mmol) of tent-butyl-3-benzyl-carbazate (J.
Chem. Sec., Perkin I, 1712 (1975)) in 4 ml of methanol is heated under reflux for 12 hours. After cooling the reaction mixture to 0° a large portion of the title compound precipitates. The mother liquor is concentrated by evaporation and the residue is dissolved in a small amount of methylene chloride. After the dropwise addition of hexane a further amount of the title compound is obtained in the form of a white precipitate.
FAB-MS:
(M+H)+=486, tRet(I)=26.8 min, R f(E)=0.70.
Example 2: Z-(L)-Val-fPheNNPheI.-((L)-Val-Z):
191 mg (0.76 mmol) of Z-(L)-valine, 336 mg (0.76 mmol) of BOP and 103 mg (0.76 mmol) of HOBt are dissolved in 5 ml of a 0.3M solution of NMM in DMF, and after minutes 100 mg (0.25 mmol) of H-[.PheNNPhe]-H~3HC1 are added and the mixture is stirred for 2 hours at RT under a nitrogen atmosphere. The reaction mixture is concentrated by evaporation, and the residue is dissolved in methylene chloride and washed twice with saturated sodium hydrogen carbonate solution. The organic phases are filtered through cotton wadding and concentrated by evaporation and the residue is purified by means of chromatography on silica gel with methylene chloride/ether (1:1).
Lyophilisation of the product-containing fractions from dioxane yields the title compound in the form of a white solid. FAB-MS: (M+H)+=752, tRet(I)=27.8 ruin, Rf(E)=0.45.
The starting material is prepared as follows:

~0~2"~~~

a) H-~PheNNPheI-H~3HCl:
A solution of 280 mg (0.58 mmol) of Boc-[PheNNPhe]-Boc from Example 1 in 10 ml of~
4N hydrogen chloride in dioxane is stirred for 2 hours at RT under a nitrogen atmosphere and then lyophilised. Lyophilisation once more from dioxane/tert-butanol yields the title compound in the form of a flocculent solid. FAB-MS: (M+H)+=286, tRet(m=23.1 min, R f(C)=0.17.
Example 3: Boc-(L~Val-fPheNNPhel~f(L)-Val-Boc):
The title compound is obtained in a manner analogous to that described in Example 2 from 50 mg (0.13 mmol) of H-[PheNNPhe]-H~3HC1, 83 mg (0.83 mmol) of Boc-(L)-valine, mg (0.38 mmol) of BOP, 51 mg (0.38 mmol) of HOBt and 2.5 ml of 0.3M NMM in DMF
after chromatographic purification on silica gel with chloroform/methanol (95:5) and lyophilisation from dioxane. FAB-MS: (M-t-H)+=684, tRet(I)=27.4 min, Rf(E)=0.38.
Example 4: Boc-f.PheNNChaI-Boc:
The title compound is obtained analogously to Example 1, from 231 mg (0.88 mmol) of (2R,3S)-1-[3-Boc-amino-2-phenylethyl]oxirane and 200 mg (0.88 rnmol) of tert-butyl-3-cyclohexylmethyl-carbazate, in the form of a white precipitate from hexane.
FAB-.MS:
(M+H)+=492, tRet(I)=30.4 min, Rf(E)=0.78.
The starting material is prepared as follows:
a) tert-But~3-cyclohex l~yl-carbazate:
10.2 g (45.1 mmol) of cyclohexylcarbaldehyde-tent-butoxycarbonylhydrazone, dissolved in 400 mI of methanol, are hydrogenated in the presence of 5.1 g of 5 %
platinum on carbon at RT and 4 atm hydrogen pressure. When the reaction is complete, the catalyst is removed by filtration and the filtrate is concentrated by evaporation. The residue is dissolved in methylene chloride and washed with water. Concentration by evaporation of the organic phase yields the title compound in the form of a colourless resin.

(200 MHz, CDC13): 6.1 (s, br, 1H), 3.9 (s, br, 1I-I), 2.65 (d, 2H), 1.8-0.75 (m, 11H), 1.45 (s, 9H), tRet(I)=32.0 min, Rf(E)=0.75.

20~~'~~5 b) Cyclohexylcarbaldehyde-tent-butoxycarbonylhydrazone:
A solution of 10.8 g (81.2 mmol) of tert-butylcarbazate and 10.1 g (90 mmol) of cyclo-hexylcarbaldehyde in 400 ml of ethanol is heated under reflux for 2 hours.
Half of the solvent is then removed by distillation and the title compound is precipitated by the addition of water. It is directly further used in a).
Example 5: H-(L)-Val-fPheNNPheI.-((L)-Val)-H~3HCl:
A solution of 40 mg (0.06 mmol) of Boc-(L)-Val-[PheNNPhe]~((L)-Val)-Boc from Example 3 in 4 ml of 4N hydrogen chloride in dioxane is stirred at RT for 1 h.
The mixture is then diluted with dioxane and, after lyophilisation, the title compound is obtained in the form of the hydrochloride. FAB-MS: (M+H)+=484, tRet(B)=25.8 min, R f(A)=0.45.
Example 6: N-Thiomorpholinocarbonyl-(L)-Val-fPheNNPheI.-(N-thiomorpholino-carbonyl-(L)-Val):
35 ltl (0.25 mmol) of triethylamine and 16 mg (0.1 mmol) of (4-thiomorpholinylcarbonyl)-chloride are added in succession at RT to a solution of 20 mg (0.03 mmol) of H-(L)-Val-[PheNNPhe]~((L)-Val)-H~3HC1 from Example 5 in 0.5 ml of DMF, and the mixture is stirred for 1 h at RT. The reaction mixture is diluted with chloroform and washed with saturated sodium hydrogen carbonate solution. The organic phase is filtered through cotton wadding and concentrated by evaporation, and the residue is chromatographed on silica gel with a gradient of chlorofotm/methanol (15:1 -> 8:1). The product fractions are concentrated by evaporation and precipitated with methylene chloride/DIPE.
Lyophilisa-tion from dioxane yields the title compound in the form of a flocculent solid.
FAB-MS:
(M+H)+=742, tRet(I)=21.6 min, R f(D)=0.54.
The starting material is prepared as follows:
a) (4-Thiomorpholinylcarbonyl)chloride:
A solution of 10 g (97 mmol) of thiomorpholine in 200 ml of toluene is added dropwise at Oo to a solution of 85 ml (165 mmol) of 20 % phosgene in toluene and the white suspen-sion is stirred for 1 h at RT. Excess phosgene is driven off by introducing nitrogen, the 2~°~2~~5 suspension is filtered, and the filtrate is concentrated by evaporation. The title compound is obtained in the form of a yellow oil. IR (CH2Cl2, cm-1): 1735, 1450, 1440, 1405, 1370, 1290, 1180.
Example 7: N-Morpholinocarbonyl-(L)-Val-lPheNNPheI.-(N-morpholino-carbonyl-(L)-Val):
210 p.1 (1.52 mmol) of triethylamine are added to a solution of 100 mg (0.25 mmol) of H-[PheNNPhe]-H~3HCl from Example 2a), 163 mg (0.76 mmol) of N-morpholino-carbonyl-(L)-valine and 288 mg (0.76 mmol) of HBTU in 2 ml of DMF and the mixture is stirred for 16 h at RT under a nitrogen atmosphere. The reaction mixture is fully concen-trated by evaporation, and the residue is dissolved in methylene chloride and washed with saturated sodium hydrogen carbonate solution. The organic phase is filtered through cotton wadding, concentrated by evaporation and chromatographed on silica gel with methylene chloride/methanol (15:1). The title compound is precipitated from methylene chlori.de/hexane and, after lyophilisation from dioxane/tert-butanol, is obtained in the form of a flocculent solid. FAB-MS: (M+H)+=710, tRet(I)'16.3 min, Rf(E)=0.16.
The starting material is prepared as follows:
a) N-Morpholinocarbonyl-(L)-valine:
2.7 g (8.4 mmol) of N-morpholinocarbonyl-(L)-valine-benzyl ester are dissolved in 75 ml of ethyl acetate and the solution is hydrogenated for 3 h in the presence of 500 mg of 10 %
palladium on carbon at 1 atm hydrogen pressure and RT. The catalyst is filtered off and, after concentrating the solvent by evaporation, the title compound is obtained in the form of a colourless oil. 1H-NMR (300 MHz, CD30D): 4.15 (m, 1H), 3.65 (m, 4H), 3.40 (m, 4H), 2.12 (m, 1H), 0.95 (2d, 6H).
b) N-Morpholinocarbonyl-(L)-valine-benzyl ester:
0.8 ml (8.1 mmol) of (morpholinacarbonyl)chloride (preparation: J. Mod. Chem.
31, 2277 (1988)) and 4.1 ml (24.1 mmol) of N-ethyldiisopropylamine are added to a solution of 4 g (10.5 mmol) of (L)-valine-benzyl ester 4-toluenesulfonate in 56 ml of methylene chloride and the mixture is stirred at RT for 24 h. The reaction mixture is diluted with ethyl acetate and washed in succession with 1N hydrochloric acid, water, saturated sodium hydrogen 20°~2~~5 carbonate solution and brine, The organic phase is dried over sodium sulfate and concen-trated by evaporation. Chromatography on silica gel with ethyl acetate yields N-morpholinocarbonyl-(L)-valine-benzyl ester in the form of a colourless oil.
The ester is directly further used in a).
Exam~h 8: Phenylace~l-(L)-Val-LheNNPheI.-(N-phenylacetyl-(L)-Val):
The title compound is obtained analogously to Example 7 from 100 mg (0.25 mmol) of H-[PheNNPhe]-H~3HCl from Example 2a), 143 mg (0.61 mmol) of phenylacetyl-(L)-valine (preparation: Mem. Tokyo Univ. Agric. 20, 51 (1978)), 230 mg (0.61 mmol) of HBTU and 200 ~.1 (1.42 mmol) of triethylamine after chromatographic purification with methylene chloride/ether/methanol (20:20:1) and lyophilisation from dioxane/tert-butmol.
FAB-MS: (M+H)+=720, tRet(I)=23~7 min, R f(G)=0.21.
Example 9: N-(3-P r~ld r~lacet~l)-(L)-Val-fPheNNPheI~-(N-(3-~yridylacetyl)-(L)-Val):
The title compound is obtained analogously to Example 7 in the form of a white solid from 100 mg (0.25 mmol) of H-[PheNNPhe]-I-I~3HC1 from Example 2a, 576 mg (1.52 mmol) of HBTU, 358 mg (1.52 mmol) of N-(3-pyridylacetyl)-(L)-valine and 316 y1 (2.3 rnmol) of triethylamine after chromatographic purification with chloroform/methanol (S:1) and lyophilisation from dioxane/tert-butanol. FAB-MS: (M+H)+=722, tRet(II)=27.9 min, Rf(A)=0.71.
The starting material is prepared as follows:
a) N-(3-Pyrid~lacetyl)-(L)-valine:
3.4 g of N-(3-pyridylacetyl)-(L)-valine-tent-butyl ester are dissolved in 20 ml of trifluoro-acetic acid/methylene chloride (1:l) and the solution is stirred at RT for 16 h. The reaction solution is fully concentrated by evaporation and the residue is digested with DIPE. The title compound is obtained in the form of a white amozphous solid. 1H-NMR (200 MHz, CD30D): 8.9-8.6 (m, broad, 1H), 8.5 (m, 1H), 7.95 (m, 1H), 4.33 (m, 1H), 3.93 (s, 2H), 2.2 (m, 1H), 0.98 (2d, 6H).
b) N-(3-Pyridylacet~~(L)-valine-ten-but leer:

~o~~7s~

4.2 ml of triethylamine are added dropwise at 0° to a solution of 3.36 g (16 mmol) of (L)-valine-tent-butyl ester~HCI, 2 g (14.5 mmol) of 3-pyridylacetic acid and 2.17 ml (14.3 mmol) of cyanophosphonic acid diethyl ester in 20 ml of DMF. The reaction mixture is stirred for 48 h at RT, and then diluted with methylene chloride and washed with 10 %
citric acid as well as saturated sodium hydrogen carbonate solution. The organic phase is filtered through cotton wadding and, after removal of the solvent by evaporation, yields N-(3-pyridylacetyl)-(L)-valine-tert-butyl ester, which is directly further used in a).
Example 10 : Boc-(L)-Val-fPheNNChaI~((L)-Val)-Boc:
The title compound is obtained analogously to Example 7 in the form of a flocculent solid starting from 500 mg (1,25 mmol) of H-[PheNNCha]-H~3HC1, 1.U8 g (4.98 mmol) of Boc-(L)-valine, 1.89 g (4.98 mmol) of HBTU and 1.39 ml (9.96 mmol) of triethylamine after chromatographic purification on silica gel with methylene chloride/ether (1:1) and lyophilisation from dioxane. FAB-MS: (M+H)+=690, tRet(I)=29.3 ruin, Rf(H)=0.48.
The starting material is prepared as follows:
a) H-(PheNNCha H~1 3HCl:
1.10 g (2.2 mrnol) of Boc-[PheNNCha]-Boc from Ex~unple 4 are dissolved in 20 ml of 4N
hydrogen chloride in dioxane and the solution is stirred at RT for 3 h.
Lyophilisation of the reaction solurion yields the title compound in the form of the hydrochloride. FAB-MS:
(M+H)+=292, tRet(B)=27.3 min.
Example 11: Z-(L)-Val-(PheNNChal~f(L)-Val)-Z:
The title compound is obtained analogously to Example 2 from 50 mg (0.12 mmol) of H-(PheNNCha]-H~3HC1 from Example 10a, 94 mg (0.37 mmol) of z-(L)-valine, 165 mg (0.37 mmol) of BOP, S 1 mg (0.37 mmol) of HOBt and 2.5 ml of 0.3M NMM in DMF
after chromatographic purification on silica gel with methylene chloride/ether (1:1) and lyophilisation from dioxane. FAB-MS: (M+H)+=758, tRet(n=29.1 min, R f(I-I)=O.SS.
Example 12: Boc-(PheNNLeuI-Boc:
The title compound is obtained analogously to Example 1, starting from 1.0 g (3.8 mmol) of (2R)-[1'(S)-Boc-amino-2'-phenylethyl]oxirane and 715 mg (3.8 mmol) of tertrbutyl-3-isobutyl-carbazate (preparation: J. Chem. Soc., Perlcin I, 1712 (1975)), in the form of a precipitate from hexane. FAB-MS: (M+H)+=452, tRet(I)=27.2 min, Rf(I)=0.55. ' Example 13: Z-(L)-Val-fPhe~Leul.-((L)-Val)-Z:
The title compound is obtained analogously to Example 2 starting from 60 mg (0.17 mmol) of H-[Phe~Leu]-H~3HC1, 125 mg (0.50 mmol) of Z-(L)-valine, 221 mg (0.50 mmol) of BOP, 67 mg (0.50 mmol) of HOBt and 3.3 ml of 0.3M NMM in DMF
after chromatographic purification on silica gel with methylene chloride/ether (3:l) and lyophilisation from dioxane. FAB-MS: (M+H)+= 718, tRet (~=26.8 min, Rf(H)=0.38.
The starting material is prepared as follows:
a) H-fPheNNLeuI-H~3HC1:
The title compound is obtained analogously to Example 10a), in the form of a lyophilisate, from 1.21 g (2.48 mmol) of Boc-[PheNNLeu]-Boc from Example 12. FAB-MS:
(M+H)+=252, tRet(n)=20.9 min, R f(K)=0.23.
Example 14: H-(L)-Val-fPheNNChaI~-((L)-Val)-H~3I°ICI:
The title compound is obtained analogously to Example 10a), from 632 mg (0.91 mmol) of Bac-(L)-Val-[PheNNCha]~((L)-Val)-Boc from Example 10, in the form of the hydro-chloride after lyophilisation. FAB-MS: (M+H)+=490, tRet(B)=29.4 min, Rf(K)=0.23.
Example 15: N-(3-PYridylacetyl)-(L)-Val-fPhe~Leul~-(N-(3-p °~idylacet~
L -_) Val):
The tide compound is obtained analogously to Example 9 from 90 mg (0.25 mmol) of H-[Phe~Leu]-H~3HC1 from Example 13 a), 358 mg (1.52 mmol) of N-(3-pyridylacetyl)-(L)-valine, 576 mg (1.52 mmol) of HBTU and 316 ~1 (2.5 mmol) of triethylamine after chromatographic purification with methylene chloride/methanol (15:1) and lyophilisation from dioxane/tert-butanol/water. FAB-MS: (M+H)+= 688, tRet(IV)= 15.5 min, Rf(D)=
0.37.
Example 16: N-Trifluoroacetyl-fPheNN(p-F)Phe]-Boc:

~o~~~~~

A solution of 4.0 g (15.4 mmol) of 2(R)-[1'(S)-(trifluoroacetylamino)-2'-phenylethyl]-oxirane and 3.89 g (16.2 mmol) of tert-butyl-3-(p-fluorophenyl-methyl)-carbazate in 35 ml of methanol are heated at 80°C for approximately 20 h in a bomb tube.
The reaction mixture is concentrated by evaporation, the residue is dissolved in a small amount of dichloromethane, and the title compound is precipitated therefrom using hexane (refrig-erator). Column chromatography (Si02, methylene chloride/ether 95:7) yields further product. TLC Rt(J)=0.57; tRet(I)=24.3 min; FAB-MS (M+H)~=500.
The starting materials are prepared as follows:
a) N-3(S)-Boc-amino)-2(R,S)-hydroxy-4-phenyl-1-trimethylsilyl-butane Under a nitrogen atmosphere, 24.7 g (1.02 mol) of magnesium are placed in 100 ml of abs.
ether and over a period of 35 minutes a small amount of iodine and, at the same time, 132.5 ml (0.95 mol) of chloromethyltrimethylsilane and 300 ml of ether am added, the temperature being maintained at 38°C by means of an ice bath. The reaction mixture obtained is then stirred for 1.5 h at RT. After the mixture has been cooled to -60°C, a suspension of 48.6 g (0.195 mol) of N-Boc-phenylalaninal (preparation: D.J.
Kempf, J.
Org. Chem. 51, 3921 (1986)) in 1.1 1 of ether is addedl over a period of 40 min. Over a period of 90 min the reaction mixture is warmed to R'T and stirred for a further 90 min at that temperature. The mixture is then poured onto 21 of ice-water and 1.51 of 10 %
aqueous citric acid. The separated aqueous phase is extracted twice with 500 m1 of ether.
All ether extracts are washed with 500 ml of 10 % citric acid and twice with brine. After drying over sodium sulfate the residue is concentrated in vacuo and the resulting title compound is further used without additional purificatian. TLC Rf(L)=0.6; FAB-MS
(M+H)+=338.
b) 1-Phenyl-3-buten-2(S)-amine:
35.6 ml (0.28 mol) of an approximately 48 % solution of boron trifluoride in ether are added at 5°C, over a period of 10 min, to a solution of 18.8 g (0.055 mol) of 3(S)-(Boc-amino)-2(R,S)-hydroxy-4-phenyl-1-trimethylsilyl-butane in 420 ml of methylene chloride.
The reaction mixture is then stirred at RT for 16 h, cooled to 10°C
and, over a period of 20 min, 276 ml of a 4N sodium hydroxide solution are added. The aqueous phase is removed and extracted twice with 400 ml of methylene chloride each time. The combined organic 20~2~~~

extracts are washed with brine and dried over sodium sulfate. The title product is. further used without additional purification. TLC Rf (C)= 0.15; IR (methylene chloride) (crri t):
3370, 3020, 2920, 1640, 1605. ~ ' c) N-Trifluoroacetyl-1-phenyl-3-buten-2(S)-amine:
17.0 ml (121 mmol) of trifluoroacetic acid anhydride are added dropwise, at 0°C, to 11.9 g (81 mmol) of 1-phenyl-3-buten-2(S)-amine dissolved in 210 ml of methylene chloride and 70 ml of pyridine. The mixture is stirred for O.S h at 0°C and then extracted twice with dilute HCI, water and brine. The aqueous phases are washed a further twice with methyl-ene chloride, dried with sodium sulfate and concentrated by evaporation: TLC
R~(M)=0.4.
d) 2(R)-f 1'(S)-(Trifluoroaceylamino)-2'=phenvlethyll-oxirane:
54.28 g (314 mmol) of m-chloroperbenzoic acid are added to a solution of 14.5 g (60 mmol) of N-trifluoroacetyl-1-phenyl-3-buten-2(S)-amine in 600 ml of chloroform and the mixture is stirred for 24 h at RT to complete the reaction. The reaction mixture is washed twice with 10 % sodium sulfite solution, twice with saturated sodium carbonate solution, water and brine. The aqueous phases are extracted a further twice with methylene chloride and the combined organic phases are dried with sodium sulfate and concentrated by evaporation to yield the title compound, which is used in the next step without being further purified: TLC Rt{N)=0.6.
e) p-Fluoro-phenylcarbaldehyde-tart-butoxycarbonylhydrazone:
32 g (242 mmol) of tart-butylcarbazate and 30 g (242 mmol) of p-fluorobenzaldehyde in 300 ml of ethanol are reacted analogously to Example 4 b) for 3 h at 80°C to form the title compound, which crystallises on cooling and diluting with water: TLC
RA(N)=0.48;
tttec(n=19.4 min.
f) test-Butyl-3-(p-fluorophenyl-methyl)-carbazate:
55 g (231 mmol) of p-fluorophenylcarbaldehyde-tart-butoxycarbonylhydrazone in 500 ml of THF are hydrogenated with 5.5 g of palladium (5 %) on carbon analogously to Example 4 a) to yield the title compound: tH-NMR (200 MHz, CD30D): 7.35 (dd, 8 and 6 Hz, 2 H), 7.05 (t, 8 Hz, 2 H), 3.9 (s, 2 I-I), 1.45 (s, 9 H).

20'~2~~5 Example 17: N-Morpholinocarbonyl-(L)-Val-fPhe~(p-F)Phel-Boc:
A mixture of 185 mg (0.80 mmol) of N-morpholinocarbonyl-(L)-valine (for preparation see Example 7 a)), 270 mg (0.67 mmol) of H-[Phe~(p-F)Phe]-Boc, 311 mg (0.70 moral) of BOP and 95 mg (0.70 mmol) of HOBT is dissolved at RT in 6.8 ml of 0.3M
NMM/DMF and stirred for 5 h at RT. The xeaction mixture is concentrated by evaporation under HV and the residue is partitioned between 4 portions of methylene chloride and 2 portions of 1M sodium carbonate solution, water and brine. The combined organic phases are dried over sodium sulfate, concentrated by evaporation and purified by column chromatography (Si02, ethyl acetate): TLC Rr(O)=0.38; tRec(n=21.8 min; FAB-MS
(M+H)+=616.
The starting material is prepared as follows:
a) H-fPhe~(p-F)Phel-Boc:
At 70°C, 15 mi of a 1M aqueous solution of potassium carbonate are added dropwise to a solution of 0.3 g (0.6 mmol) of N-trifluoroacetyl-[.Phe~(p-F)Phe]-Boc (for preparation see Example 16) in 50 ml of methanol under a nitrogen atmosphere and the mixture is stirred for 25 h at that temperature. The reaction mixture is concentrated by evaporation under HV, methylene chloride is added to the residue and the mixture is washed twice with water and brine. The aqueous phases are extracted twice with methylene chloride and the organic phases are dried with sodium sulfate and concentrated by evaporation. The crude product is used in the next step without being further purified:
tRe~(I)=16.2 min.
Example 18 _ N-- Mornholinocarbonyl-(L)-Val-fF'he~(p-F)Phel~((L)-Val)-Z:
129 mg (0.34 mmol) of HBTU are added to a solution of 86 mg (0.34 mmoi) of Z-(L)-Val and 160 mg (0.31 mmol) of N-morpholinocarbonyl-(L)-Val-[Phe~(p-F)Phe]-H in 2.7 ml of 0.25M NMM/CH3CN (0.25M NMM in CH3CN). After 4 h at RT the mixture is con-centrated by evaporation and the residue is partitioned between 3 portions of methylene chloride and 2 portions of saturated sodium hydrogen carbonate solution and brine. The organic phases are dried with sodium sulfate and concentrated by evaporation to yield the title compound which is obtained in pure form after digestion from methylene chloride/-ether 1:1: TLC Rt(P)=0.4; tRe~(I)=22.4 min; FAB-MS (M+H)+=749.

~0'~27~5 The starting material is prepared as follows:
a) N-Morpholinocarbonyl-(L,)-Val-iPhe~(p-F)Phe]-H:
210 mg (0.34 mmol) of N-morpholinocarbonyl-(I,)-Val-[Phe~(p-F)Phe]-Boc (Example 17) are dissolved in 105. ml of formic acid and the solution is stirred for 4 h at RT and then concentrated by evaporation. The residue is taken up in methylene chloride and the solution is washed with saturated sodium hydrogen carbonate solution and brine. Extrac-tion of the aqueous phases with 2 portions of methylene chloride, drying the organic phases with sodium sulfate and concentrating by evaporation yields the title compound, which is used in the next step without being further purified: tRe~(I)=12.9.
Example 19: N-Morpholinocarbonvl-(L)-Val-[Phe~(p F)Phe].-((L)-Val 160 mg (0.2.1 mmol) of N-morpholinocarbonyl-(L)-Val-[Phe~(p-F)Phe].-((L)-Val)-Z
(Example 18) in 6 ml of ethanol are hydrogenated with 40 mg of palladium (10 %) on carbon at normal pressure. Filtration through Celite~ (siliceous earth, filter aid from Fluka, Buchs, Switzerland), concentration by evaporation and lyophilisation from dioxane yield the title compound: tRec(hYdrochloride, I)=13.4 tnin; FAB-MS (M+H)+=615.
Example 2U: N-Morpholinocarbonyl-(L)-Val-fPhew(p-F)Phel~((L)-Val).-(N-morpholino-carbonvl-Glv):
54 mg (0.143 mmol) of HBTU are added to a solution of 26.9 mg (0.143 mmol) of N-morpholinocarbonyl-glycine and 80 mg (0.130 mmol) of N-morpholinocarbonyl-(L)-Val-[Phe~(p-F)Phe].-((L)-Val)-H in 1.1 ml of 0.25M NMM/CH3CN and the mixture is stirred for 16 h at RT. The mixture is concentrated by evaporation and the residue is partitioned between 3 portions of ethyl acetate and water and 2 portions of saturated sodium hydrogen carbonate solution, water and brine. The organic phases are dried with sodium sulfate and concentrated by evaporation to yield the title compound which, after dissolving in a small amount of DMF and precipitating with RIPE is obtained in pure form:
tRet(I)=15.1 min;
FAB-MS (M+H)*=785.
The starting material is prepared as follows:

20~~7~~

a) N-Motpholinocarbo~l-~lycine-benzyl ester:
Analogously to Example 7 b), 7.69 g (22.8 mmol) of glycine-benzyl ester 4-toluenesulfon-ate and 2.8 g (19 mmol) of (morpholinocarbonyl)chloride in 118 ml of methylene chloride and 9 ml (53 mmol) of N-ethyldiisopropylarnine are reacted for 18 h. The title compound is obtained in pme form after extraction with methylene chloride and digestion with hexane: tRe~(I)=11.6 min.
b) N-Morpholinocarbonyl-gl cy ine:
Analogously to Example 7 a), 4.8 g (18.3 mmol) of N-morpholinocarbonyl-glycine-benzyl ester in 100 ml of ethyl acetate are hydrogenated with 1 g of palladium (10 %) on carbon to yield the title compound: tH-NMR (300 MHz, CDCI3): 3.88 (s, 2 H), 3.64 (s, 4 I-I), 3.50 (s, 2 H), 3.35 (s, 4 I-I).
Example 21: Z-(L)-Val-(Phe~(p-F)Phel-Boc:
463 mg (1.22 mmol) of HBTLJ are added to a solution of 335 mg (1.33 mmol) of Z-(L)-Val and 448 mg (1.11 mmol) of H-[Phe~(p-F)Phe]-l3oc (for preparation see Example 17 a)) in 9.4 ml of 0.25M NMM/CH3CN (0.25M NMM in CI-I3CN). After stirring for 16 h at RT, the mixture is concentrated by evaporation and the residue is partitioned between 3 portions of methylene chloride and 2 portions of saturated sodium hydrogen carbonate solution and brine. The organic phases are dried with sodium sulfate and concentrated by evaporation to yield the title compound, which is purified by column chromatography (Si02, hexane/ethyl acetate 4:1 >1:l): tRec(I)=26.6 min; FAB-MS (M+H)+=637.
Example 22: Z-(L)-Val-(Phe~(p-F~hel.-((L)-Val)-Boc:
Analogously to Example 18, 165 mg (0.76 mmol) of Boc-(L)-Val and 371 mg (0.69 mmol) of Z-(L)-Val-[Phe~(p-F)Phe]-H in 6 ml of 0.25M NMh4/CH3CN are reacted with 289 mg (0.76 mmol) of HBTU to yield the title compound, which can be crystallised directly from the reaction solution and filtered off:
t~e~(I)=27.2 min; FAB-MS
(M+H)+=736.
The starting material is prepared as follows:

a) Z-(I,)-Val-[Phe~(p-F)Phel-H:
Analogously to Example 18 a), 440 mg (0.69 mmol) of Z-(L)-Val-[Phe~(p-F)Phe]-Boc are deprotected with 212 ml of formic acid to yield the title compound:
tRe~(I)=17.8 min.
Example 23: Z-(L)-Val-fPhe~(p-F)Phe].-((L)-Val)-H:
Analogously to Example 18 a), 250 mg (0.34 mmol) of Z-(L)-Val-[Phe~(p-F)Phe).-((L)-Val)-Boc (Example 22) are deprotected with 50 ml of formic acid to yield the title compound: tRe~(I)=18.0 min; FAB-MS (M+H)+=636.
Example 24: Z-(L)-Val-fPhe~(p-F)Phel~((L)-Val).-(N-mor~holinocarbo~l-Gly):
Analogously to Example 20, 32 mg (0.17 mmol) of N-morpholinocarbonyl-glycine (Example 20 b)) and 99 mg (0.16 mmol) of Z-(L)-Val-[Phe~(p-F)Phe].-((L)-Val)-lH in 1.3 ml of 0.25M NMM/CH3CN are reacted with 65 mg (0.17 mmol) of HBTU to yield the title compound, which crystallises directly from the reaction solution:
t~°~(I)=21.1 min;
FAB-MS (M+H)+=806.
Example 25: Z-(L)-Asn-fPhe~(p-F)Phel-Boc:
3.0 g (7.8 mmol) of Z-(L)-asparagine-p-nitrophenyl ester (Bachem, Bubendorf/Switzer-land) are added to a solution of 2.09 g (5.2 rnmol) of H-[Phe~(p-F)Phe]-Boc (for prepar-ation see Example 17 a)) in 68 ml of DMF and 2.7 ml (16 mmol) of N-ethyl-diisopropyl-amine. The mixture is stirred for 16 h at RT and concentrated by evaporation under IIV, and the residue is taken up in a large amount of methylene chloride (poorly soluble) and washed with 2 portions of 5 % potassium carbonate solution. The aqueous phases are extracted twice more with a large amount of methylene chloride, and the combined organic phases are dried with sodium sulfate and concentrated by evaporation.
The title compound is obtained by dissalving the crude product in a small amount of methanal and precipitating by the addition of toluene at -20°C: tgei(I)=21.2 min.
Example 26: H-(L)-Asn-[Phe~(p-F)Phe]-Boc:
Analogously to Example 19, 0.40 g (0.61 mmol) of Z-(L)-Asn-[Phe~(p-F)Phe]-Boc are hydrogenated in 20 ml of methanol to yield the title compound: tRe~(I)=14.9 min.

20'~~7~5 Examt~Ie 27: Ouinoline-2-carbonyl-(L)-Asn-fPhe~(p-F)Phe -Boc:
Analogously to Example 17, 134 mg (0.78 mmol) of quinoline-2-carboxylic acid (Fluke, Buchs/Switzerland) in 4 ml of 0.3M NMM/DMF are reacted with 344 mg (0.78 mmol) of BOP, 105 mg {0.78 mmol) of HOBT and 268 mg (0.52 mmol) of H-{L)-Asn-[Phe~{p-F)Phe]-Boc. Since, according to HPL.C, there is still some H-(L)-Asn-[Phe~(p-F)Phe]-Boc present after stirnng for 16 h at RT, a further 299 mg of BOP, 70 mg of HOST, $9 mg of quinaldic acid and 113 p.1 of NMM are added. After a further 16 h the mixture is concentrated by evaporation and the residue is partitioned between 3 portions of methyiene chloride and 2 portions of saturated sodium hydrogen carbonate solution and brine. The combined organic phases are dried with sodium sulfate and con-centrated by evaporation. The crude product is dissolved in a small amount of DMF, precipitated with DIPS and cooled to -20°C to yield the title compound:
tR~~(I)=22.8 min;
FAB-MS (M+I-I)+=673.
Example 28: Z-~L~ Asn-fPhe~(p-F)Phel.-((L)-Val)-'T.,_:
88 mg (0.35 mmol) of Z-(L)-Val in 3.8 ml of 0.3N NMM/DMF are activated with 153 mg (0.35 mmol) of BOP and 47 mg (0.35 mmol) of I-IOBT and, after 15 ruin, 144 mg (0.23 mmol) of Z-(L)-Asn-[Phe~(p-F)Phe]-hI>2HC1 are added. The reaction mixture is stirred for 14 h at RT and then concentrated by evaporation, the residue is dissolved in 2 ml of methanol and partitioned between 3 portions of methylene chloride and 2 portions of 1M sodium carbonate solution, and the organic phases are dried with sodium sulfate and concentrated by evaporation. Repeated dissolution of the crude product in a small amount of DMF and precipitation with DIPE yield the title compound:
tRecCI)=22.2 min;
FAB-MS (M+H)*=785.
The starting material is prepared as follows:
a) Z-(L)-Asn-fPhe~~p-F)Phel-H~2HC1:
Under a nitrogen atmosphere, 2 ml of 4N HCl/dioxane (Fluke, Buchs/Switzerland) are added to a solution of 150 mg (0.23 mmol) of Z-(L)-Asn-[Phe~(p-F)Phe]-Boc (Example 25) in 1 ml of dioxane. The reaction mixture is stirred for 1.5 h at RT and then lyophilised, and the lyophilisate is directly further reacted.

2072'~~~

Example 29: Trifluoroacet 1-fPhe~ p-F)Phel.-((L)-Val)-Z:
Analogously to Example 17, 239 mg (0.95 mmol) of Z-(L)-Val in 10.5 ml of 0.3M
NMM/DMF are reacted for 15 h with 421 mg (0.95 mmol) of BOP, 129 mg (0.95 mmol) of HOBT and 0.3 g (0.63 mmol) of N-trifluoroacetyl-[Phe~(p-F)Phe]-H. Column chrom-atography (Si02, methylene chloride/ether 10:1) and precipitation from DMF
solution with DIPE yield the title compound: TLC Rf(Q)=0.15; tRec(I)=25.9 min; FAB-MS
(M+H)+=633.
The starting material is prepared as follows:
a) N-Trifluoroacetyl-fPhe~(p-F)Phel-H:
At 0°C, 5 ml of trifluoroacetic acid are added to 0.20 g (0.40 mmol) of N-trifluoroacetyl-[Phe~(p-F)Phe]-Boc (for preparation see Example 16) in 5 ml of methylene chloride. The reaction mixture is stirred for 4 h at 0°C and for 2 h at RT and then concentrated by e~rap-oration. Lyophilisation of the residue from dioxane yields the title compound, which is further reacted without being purified: tRe~(I)=14.7 min.
Example 30: Z-(L)-Asn-[Phe~Phal-Boc:
Analogously to Example 25, 167 mg (0.34 mmol) of H-[Phe~Phe]-Boc in 3.6 ml of DMF
and 0.18 ml (1 mmol) of N-ethyl-diisopropylamine are reacted with 0.20 g (0.52 mmol) of Z-(L)-asparagine-p-nitrophenyl ester to yield the title compound, which is obtained in pure form by column chromatography (Si02, ethyl acetate): TLC Rt(O)=0.19;
tRe~(1)=20.9 min.
The starting material is prepared as follows:
a) N-Trifluoroacetyl-fPhe~Phe1-Boc:
Analogously to Example 16, 1.82 g (7.0 mmol) of 2(R)-[1'(S)-(trifluoroacetylamino)-2'-phenylethyl]-oxirane (Example 16 d)) and 1.58 g (7.1 mmol) of tert-butyl-3-benzyl-carbazate (J. Chem., Perlcin I, 1712 (1975)) in 15 ml of methanol are reacted in a bomb tube to yield the title compound, which is isolated by column chromatography (Si02, methylene chloride/ether 50:1): TLC Rp(J)=0.38; tRec(I)=24.5 min.

20'~2'~~~

b) H-fPhe~Phel-Boc:
Analogously to Example 17 a), 258 mg (0.53 mmol) of N-trifluoroacetyl-[Phe~Phe]-Boc in 60 ml of methanol are reacted with 10.7 ml of 1M potassium carbonate solution to yield the title compound.
Example 31: Z-(L)-Val-f (p-F)Phe~(~F)Phel-Boc:
Analogously to Example 21, 18 mg (0.070 mmol) of Z-(L)-Val and 27 mg (0.064 mmol) of H-[(p-F)Phe~(p-F)Phe]-Boc in 0.6 ml of 0.25M NMM/CH3CN are reacted with 26.6 mg (0.070 mmol) of HBTU to yield the title compound, which is purified by dissolv-ing in a small amount of methylene chloride and precipitating with DIPE: FAB-MS
(M+H)+=655.
The starting material is prepared as follows:
a) N-Boc-(p-fluoro~henylalanine In 0.41 of dioxane/water 1:120 g (109 mmol) of p-fluorophenylalanine (Fluka, Buchs, Switzerland) are reacted with 35.5 g (163 mmol) of Boc-anhydride and 150 g (1.09 mol) of potassium carbonate. After 4 h, the reaction mixture is acidified with citric acid solution and extracted with 3 portions of ethyl acetate. The organic phases are washed with 10 citric acid, water and brine, dried with sodium sulfate and concentrated by evaporation.
Dissolution of the residue in a small amount of methylene chloride and crystallisation by the addition of hexane yields the title compound: tR~~(I)=16.9 min.
b) N-Boc-(p-fluorophenylalaninol):
At from -5°C to -10°C 9.66 ml (69 mmol) of triethylamine are added to a solution of 17.9 g (63 mmol) of N-Boc-(p-fluorophenylalanine) in 73 ml of abs. THF, and a solution of 9.05 ml (69 mmol) of chloroformic acid isobutyl ester in 44 ml of abs. THF
is added dropwise thereto. After stirring for 0.5 h at RT, the resulting precipitate is filtered off with suction. The filtrate is added dropwise, with cooling, to 4.77 g (126 mmol) of sodium borohydride in 28 ml of water. The mixture is stirred for 4 h at RT and acidified with 10 %
citric acid, the THF is partially removed by evaporation using a RE and the residue is partitioned between 3 portions of ethyl acetate and 2 portions of 2N sodium hydroxide 20'~2°~~5 solution, water, saturated sadaum hydrogen carbonate solution and brine. The organic phases axe dried with sodium sulfate, concentrated by evaporation, dissolved in a small amount of methylene chloride and crystallised by the addition of hexane to yield the title' compound: TLC Rt{N)=0.36; tRet(n=16.8 min; 1H-NMR (200 MHz, CD30D): 7.24 (dd, and 5 Hz, 2 H), 6.98 (t, 8 Hz, 2 H), 3.73 (m, 1 H), 3.47 (d, 5 Hz, 2 H), 2.88 (dd, 13 and 6 Hz, 1 H), 2.62 (dd, 13 and 8 Hz, 1 H), 1.36 (s, 9 H).
c) N-Boc-(p-fluorophenylalaninal):
Under a nitrogen atmosphere, 4.44 ml (62.4 mmol) of DMSO dissolved in 76 ml of methylene chloride are added dropwise to a solution, cooled to -60°C, of 4.0 ml (46.8 mmol) of oxalyl chloride in 44 ml of methylene chloride. After stirring for 15 minutes, resulting in a clear reaction solution, 8.4 g (31.2 mmol) of N-Boc-(p-fluoro-phenylalaninol) in the form of a solution in 185 ml of rnethylene chloride~THF
1:1 are added (-~ precipitation) and the mixture is then stirred for 25 min. 17.3 ml (124.8 mmol) of triethylamine dissolved in 38 ml of methylene chloride are then added.
After the mixture has been stirred for 30 min, 278 ml of a 20 % potassium hydrogen sulfate solution are added dropwise, followed by 220 ml of hexane. The mixture is left to warm to .RT, and the aqueous phase is removed and extracted with 2 portions of ether. The organic phases are washed with saturated sodium hydrogen carbonate solution, water and brine, dried with sodium sulfate and concentrated by evaporation to yield the title compound, which is used in the next step without being further purified: tH-NMR (200 MHz, CDCl3):
9.63 (s, 1 H), 6.9-7.2 (2m, 4 H), 5.04 (m, 1 H), 4.42 (m, 1 I-I), 3.10 (m, 2 H), 1.43 (s, 9 H).
d) N-3(S)-(Boc-amino)-2(R,S)-hey-4-(p-fluorophenvl)-1-trimethvlsilvl-butane:
Analogously to Example 16 a), 1.63 g (67 mmol) of magnesium in 33 ml of abs.
ether are reacted with 8.3 ml (60 mmol) of chloromethyltrimethylsilane to formr the Grignard compound which, after reaction with 13 mmol of N-Boc-(p-fluorophenylalaninal), extrac-tion and column chromatography (Si02, hexane/ethyl acetate 5:1 ~ 4:1), yields the title compound in the form of a diastereoisomeric mixture: TLC Rr(L)=0.32;
tRec(I)=24.9 min (22 %)/25.5 min (78 %); FAB-MS (M+H)+=356.
e) 1-(L-Fluorophen~)-3-buten-2(S)-amine:
Analogously to Example 16 b), 1.1 g (3.1 mmol) of N-3(S)-(Boc-amino)-2(R,S)-hydroxy-.2~~~7~5 4-(p-fluorophenyl)-1-trimethylsilyl-butane in 22 ml of methylene chloride are reacted with 1.9 ml (15.5 mmol) of an approximately 48 % solution of boron trifluoride in ether to yield the title compound: tH-NMR (300 MHz, CDC13): 7.2-7.10 and 7.05-6.9 (2m, each 2 H), 5.9-5.8 (m, 1 H), 5.2-5.0 (m, 2 H), 3.57 (m, 1 H), 2.79 (dd, 12 and 6 Hz, 1 H), 2.62 (dd, 12 and 8 Hz, 1 H), 1.7 (sb, 2 H).
f) N-Trifluoroacet~(p-fluorophenyl)-3-buten-2(S)-amine:
Analogously to Example 16 c), 364 mg (2.2 mmol) of 1-(p-fluorophenyl)-3-buten-2(S)-amine in 1.8 ml of methylene chloride and 5.4 ml of pyridine are reacted with 460 ~tl (3.3 mmol) of trifluoroacetic acid anhydride to yield the title compound, which after digestion with hexane is obtained in pure form: TLC Rt{F)=0.58; MS (M)+=261.
g} 2(R)-f 1'(S)-(Trifluoroace~lamino)-2'- p-fluorophen 1~~11-oxirane:
Analogously to Example 16 d), 359 rng (1.37 mmol) of N-trifluoroacetyl-1-(p-fluoro-phenyl)-3-buten-2(S)-amine in 9 ml of chloroform are: oxidised with 1.18 g (6.87 mmol) of m-chloroperbenzoic acid to yield the title compound: TLC Rt(R)=0.45.
h) N-Trifluoroacetyl-[(p-F)Phe~(p-F)Phel-Boc:
Analogously to Example 16, 41S mg (1.49 mmol) of 2(R)-[1'(S)-(trifluoroacetylamino)-2'-(p-fluorophenyl)ethyl]-oxirane and 377 mg (1.57 mmol) of tert-butyl-3-(p-fluoro-phenyl-methyl)-carbazate in 9 ml of methanol are reacted to yield the title compound:
TLC Rt(S)=0.53; FAB-MS (M+H)~=518; tH-NMR (300 MHz, CD30D): 7.4-7.3 and 7.3-7.2 (2m, each 2 H), 7.05-6.9 (m, 4 H), 4.23 (m, 1 H), 3.90-3.65 (m, 3 H), 3.03-2.78 and 2.74-2.60 (2m, each 2 H}, 1.30 (s, 9 H}.
i) H-[(p-F)Phe~ p-F)Phel-Boc:
Analogously to Example 17 a), 285 mg (0.55 mmol) of N-trifluoroacetyl-[(p-F)Phe~(p-F)Phe]-Boc in 45 ml of methanol are reacted with 14 ml of 1M
potassium carbonate solution to yield the title compound: tR~~(I)=16.4 min.
Example 32: Z-(L)-Val-f(p-F)Phe~(p-F)Phel-H:

20'~2~~5 Analogously to Example 18 a), 215 mg (0.33 mmol) of Z-(L)-Val-[(p-F)Phe~(p-F)Phe]-Boc are deprotected with 100 ml of formic acid to yield the title compound:
FAB-MS
(M+H)~=555.
Example 33: Z-(L)-Val-((p-F)Phew(~F)Phel.-(N-(N-(2-pyridylmeth~)-N-methylamino-carbonyl)-(L)-Val):
Analogously to Example 18, 23.6 mg (0.089 mmol) of N-(N-(2-pyridylmethyl)-N-methyl-aminocarbonyl)-(L)-valine (for preparation see EP 402646 A1, 19th Dec. 1990) and 45 mg (0.081 mmol) of Z-(L)-Val-[(p-F)Phe~(p-F)Phe]-H are reacted with 33.8 mg (0.089 mmol) of HBTU in 0.76 ml of 0.25M NMM/CH3CN to yield the title compound which is recrystallised with DMF/DIPE: TLC Rt(O)=0.39; FAB-MS (M+H)+=802.
Example 34: Z-(L)-Val-f(p-F)Phew(p-F)Phel~(N-(2(R,S)-carbamoyl-3-phen~=pro-ip onyl)(L,)Val):
Analogously to Example 18, 26.0 mg (0.089 mmol) of N-(2(R,S)-carbamoyl-3-phenyl-propionyl)-(L)-valine (preparation: Synth., Struct., Funct., Proc. Am. Pept.
Symp., 7'}', 85, (1981)) and 45 mg (0.081 mmol) of Z-(L)-Val-j(p-F):Phe~(p-F)Phe]-H (Example 32) are reacted with 33.8 mg (0.089 mmol) of I-IBTU in 0.76 ml of 0.25M NMM/CH3CN to yield the tide compound which is recrystallised with DMF/DIPE: Rt{P)=0.64; FAB-MS
(M+H)+=829.
)xample 35: Acetyl-Val-(Phe~Phel.-(N-acetyl-Val):
Analogously to Example 7, the title compound is obtained from 100 mg (0.25 mmol) of H-[Phe~Phe]-He3HC1 from Example 2a), 121 mg (0.76 mmol) of N-acetyl-(L)-valine, 288 mg (0.76 mmol) of HBTU and 0.211 ml (1.52 mmol) of triethylamine in DMF
after lyophilisation from dioxane. FAB-MS: (iVI+H)+=568, tRec(I)=15.0 min., Rt(B)=0.46.
Example 36: Z-(D)-Val-fPhe~Phel~-((D)-Val)-Z:
Analogously to Example 2, the title compound is obtained from 50 mg (0.123 mmol) of H-[Phe~Phe]-Ha3HCl from Example 2a), 95 mg (0.38 mmol) of Z-(D)-valine, 168 mg (0.38 mmol) of BOP, 5I mg (0.38 mmol) of HOBt and 2.53 ml of 0.3M NMM in DMF
after lyophilisation from dioxane. FAB-MS: (M+H)+=752, tRec(I)=26.4 min, Rf(H)=0.21.

2~'~~'~~5 Example 37: Quinoline-2-carbonyl-Val- f Phe~Phel~-(N-nuinoline-2-carbon~al2 145 mg (0.53 mmol) of N-(quinoline-2-carbonyl)-(L)-valine, 235 mg (0.53 mmol) of BOP
and 72 mg (0.53 mmol) of HOBt are dissolved in 3.5 ml of a 0.3M solution of NMM in DMF, after 10 min 70 mg (0.18 mmol) of H-[Phe~Phe]-H=HCl (Example 2a)) are added, and the mixture is stirred for 5 h at RT under a nitrogen atmosphere. The reaction mixture is concentrated by evaporation and the residue is dissolved in methylene chloride and washed twice with saturated sodium hydrogen carbonate solution, once with 10 %
citric acid and once again with saturated sodium hydrogen carbonate solution. The organic phases are filtered through cotton wadding and concentrated by evaporation, and the residue is precipitated twice from methylene chloride/methanol by the addition of DIPE.
Lyophilisation from dioxane yields the title compound in the form of a white solid (mixture of two diastereoisomers differentiable by HPLC). FAB-MS: (M+I-I)+=794, tR~~(A)=29.1 and 29.3 min, Rt{B)=0.81.
a) N-( uinoline-2-carbonyl)-(L)_valine:
3.28 g (15.9 mmol) of N,N-dicyclohexylcarbodiimide; and 2.0 ml (14.5 mmol) of triethyl-amine are added to a solution of 2.5 g (14.5 mmol) of (L)-valyl-tert-butyl ester and 2.5 g (14.5 mmol) of quinoline-2-carboxylic acid in 100 ml of methylene chloride/1~IIF (10:1) and the mixture is stirred for 18 h at RT. The reaction mixture is cooled to -18° and filtered off from the urea. The filtrate is concentrated by evaporation, and the residue is dissolved in methylene chloride and washed once with saturated sodium hydrogen carbonate solution and once with water. The organic phases are filtered through cotton wadding, concentrated by evaporation and, after chromatographic purification on silica gel with hexane/ethyl acetate (2:1), yield N-(quinoline-2-carbonyl)-(L)-valyl-tert-butyl ester.
2.59 g (12.2 mmol) thereof are left at RT in methylene chloride/TFA (1:1) for 4.5 h. After concentration by evaporation the residue is purified by chromatography on silica gel with hexane/ethyl acetate (2:1). The product-containing fractions are concentrated by evapora-tion, dissolved in methylene chloride again, and converted into the hydrochloride of the title compound by washing with 1N sodium hydroxide solution and 1N
hydrochloric acid.
tH-NMR (200 MHz, CD30D): 1.05 and 1.07 (2d, J=6Hz, 6H), 2.40 (m, 1H), 4.65 (m, 1H), 7.70 (m, 1H), 7.85 (m, 1H), 8.00 (dxd, 1H), 8.20 (m, 2H), 8.48 (d, 1H).
Example 38: Acetyl-(L.)-Val-fPhe~Chal.-(N-acet~-(L)-Val):

~0~27~~

Analogously to Example 37, the title compound is obtained from 160, mg (0.40 mmol) of H-[Phe~Cha]-H~3HC1 from Example 10a), 190 mg (1.19 mmol) of N-acetyl-(L)-valine, 525 mg (1.19 mmol) of BOP, 160 mg (1.19 mmol) of HOBt and 7.9 ml of 0.3M NMM
in DMF after precipitation from chloroform/methanol with DIPE and lyophilisation from dioxane. FAB-MS: (M+H)+=574, tRec(I)=18.1 min, RI(B)=0.30.
Example 39: N-(3-P~rfidylacetyl)-(L)-Val-(Phe~Chal.-(N-(3-pyrid~et 1y )-~)_ Val)~3HCl:
Analogously to Example 7, the title compound is obtained from 100 mg (0.25 mmol) of H-[Phe~Cha]-H~3HC1 from Example 10a), 358 mg (1.52 mmol) of N-(3-pyridylacetyl)-(L)-valine from Example 9a), 576 mg (1.52 mmol) of HBTU and 0.316 ml (2.28 mmol) of triethylamine in DMF after chromatographic purification on silica gel with methylene chloride/methanol (15:1) and lyophilisation of the product-containing fractions from dioxane. FAB-MS: (M+H)+=728, tR~i(I)=11.3 min, Rp(IJ)=0.21.
Example 40: Acetyl-Ile-(Phe~Chal~-(N-acetyl-Ile):
Analogously to Example 37, the title compound is obtained from 160 mg (0.40 mmol) of H-[Phe~Cha]-H~3HC1 from Example 10a), 206 mg (1.19 mmol) of N-acetyl-(L)-iso-leucine, 525 mg (1.19 mmol) of BOP, 160 mg (1.19 mmol) of HOBt and 7.9 ml of 0.3M
NMM in DMF after precipitation from methylene chloride/methanol by the addition of DIPS and lyophilisation from dioxane/tezt-butanol (mixture of 2 diastereoisomers differentiable by HPLC). FAB-MS: (M+H)'''=602, iRec(~=20.4 and 20.7 min, Rf(D)=0.33.
Example 41: Thiomort~holinocarbonyl-(L)-Val-fPhe~Chal.-(N-thiomorpholina-carbonyl-(I,)-Val):
Analogously to Example 6, the title compound is obtained starting from 70 mg (0.12 mmol) of H-(L-Val)-[Phe~Cha].-(N-(L)-Val)-H~3HCl from Example 14, 58 mg (0.35 mmol) of (4-thiornorpholinylcarbonyl)chloride from Example 6a) and 0.127 ml of triethylamine in 2 ml of DMF after chromatographic purification on silica gel with methylene chloride/methanol (95:5) and lyophilisation of the product-containing fractions from dioxane. PAB-MS: (M+H)~=748, tRe~(I)=24.0 min, Rf(B)=0.70.

2~'~27~5 Example 42: Z-(L)-Glu-~Phe~''t(p-F)Phel.-(CL)-Glu)-Z:
A solution of 130 mg (0.14 mmol) of Z-(L)-Glu(O-tent-but5~1)-(Phe~(p-F)Phe].-((L)-Glu(O-tent-butyl))-Z [(Glu(O-terf-butyl) here denotes the radical of glutamic acid ester-ified at they-carboxy group by a tent-butyl radical] in 8 ml of methylene chloride/TFA
(i:1) is stirred for 3 h at RT. The solvent is evaporated off under reduced pressure and the residue is precipitated from methylene chloride by the addition of DIPE. The title compound is obtained after lyophilisation from dioxane/tert-butanol. FAB-MS:
(M+H)+=830, tRe,(I)=19.6 min, Rt(B)=0.32.
a) Z-(L)-Glu(O-tert-but r~ fPhew(p-F)Phel~-((L)-Glu(O-tert-butyl))-Z:
Analogously to Example 37, the title compound is obtained from 100 mg (0.24 mmol) of H-[Phe~(p-F)Phe]-H~3HC1, 245 mg (0.73 mmol) of Z-(L)-glutamic acid ten-butyl ester, 321 mg (0.73 mmol) of BOP, 98 mg (0.73 mmol) of HOBt and 4.8 ml of 0.3M NMM in DMF after chromatographic purification on silica gel with methylene chloride/ether (1:1).
tRec(I)=30.2 min, Rf(H)=0.17.
b) I3-fPhe~(p-F)Phe]-H~3HCl:
Analogously to Example 2a), the title compound is obtained from 1.77 g (3.51 mmol) of Boc-[Phe~(p-F)Phe]-Boc after lyophilisation. FAB-MS: (M+H)+=304, Rt{K)=0.19.
c) Boc-FPhe~(p-F)Phel-Bac:
Analogously to Example 1, the title compound is obtained starting from 2.0 g (7.60 mmol) of (2R)-[1'(S)-Boc-amino-2'-phenylethyl]oxirane and 2.17 g (9.04 mmol) of tent-butyl-3-(4-fluorophenyl-methyl)-carbazate from Example 16 f) after chromatographic purification on silica gel with hexane/ethyl acetate (2:1). FAB-MS: (M+H)+=504, tRec(I)=26.2 min, R f(F)=0.26.
Example 43: N-(2-Pyridylmethyl)-N-methylaminocarbonyl-(L)-Val-iPhe~(p-F)-Phel~(N-(N-(2-p"~ridylmethyl)-N-methylaminocarbonyl)-(L)-V al):
Analogously to Example 37, the title compound is obtained from 70 mg (0.17 mmol) of H-[Phe~(p-F)Phe]-H~3HCl from Example 42b), 135 mg (0.51 mmol) of N-(N-(2-pyridyl-2~"~27~~

methyl)-N-methylaminocarbonyl)-(L)-valine (preparation as described in EP 0 Al of 19th Dec. 1990), 225 mg (0.51 mmol) of BOP, 69 mg (0.51 m~nol) of HOBt and 3.4 ml of 0.3M NMM in DMF after chromatography on silica gel with methylene chloride/methanol (15:1) and lyophilisation of the product-containing fractions from dioxane. FAB-MS: (M+H)*=798, tRec(IV)=35 min, Rf(U)=0.21.
Example 44: N-(3-(Tetrazol-1-yl)-pr~ionyl)-Val-[Phew(p-F)Phel~~(N-(3-(tetrazol-1-yl)-propionyl)-Val):
Analogously to Example 37, the title compound is obtained from 100 mg (0.24 mmol) of H-[Phe~)p-F)Phe]-H~3HC1 (from Example 42b), 146 mg (0.61 mmol) of N-(3-{tetrazol-I-yl)-propionyl)-(L)-valine, 268 mg (0.61 mmol) of BOP, 82 mg (0.61 mmol) of HOBt and 4 ml of 0.3M NMM in DMF after precipitation from methylene chloride by the addition of DIPE and lyophilisation from dioxane (4 diastereoisomers differentiable by HPLC). FAB-MS: (M+H)*=750, tR~t(IlI)=30.8; 31.4; 32.4 and 32.8 min, Rt(K)=0.5.
Example 44a: N-(3-(Tetrazol-1-~Zpropionyl)-(L)-valine:
Analogously to Example 9b, starting from 4 g (16.4 mmol) of (L)-valine-benzyl ester~HCI, 2.1 g (14.9 mmol) of 3-(tetrazol-1-yl)-propionic acid (preparation: US 4 794 109 A of 27th Dec. 1988), 2.4 ml of cyanophosphonic acid diethyl ester and 4.4 ml of triethylamine in DMF, N-(3-(tetrazol-1-yl)-propionyl)-(L)-valine-benzyl ester is obtained after chromato-graphic purification on silica gel with methylene chloride/methanol (30:1).
2.66 g (8.03 mmol) thereof are hydrogenated in methanol/water (9:1) in the presence of 530 mg of 10 % palladium on carbon, at 1 atm hydrogen pressure, to yield the title compound after precipitation from methanol/DIPE. 1H-NMR (200 MHz, CD30D): 0.9 (d, J=7I-Iz, 6H), 2.1 (m, 1H), 2.95 (m, 2H), 4.29 (d, J=6Hz, 1H), 4.78 (m, 2H), 9.15 (s> 1H).
Example 45: Z-(L)-Val-(Phe~(p-F)Phel.-((L)-VaI~Z:
Analogously to Example 37, the title compound is obtained from 100 mg (0.24 mmol) of H-[Phe~{p-F)Phe]-H~3HCl (from Example 42b), 182 mg (0.38 mmol) of Z-(L)-valine, 321 mg (0.73 mmol) of BOP, 98 mg (0.73 mmol) of HOBt and 4.8 ml of 0.3M NMM in DMF after precipitation from methylene chloride by the addition of DIPE and lyophilisa-tion from dioxane. FAB-MS: (M+1-1)*=770, IRet(I)=26.3 min, Rf(H)=0.25.

2~72~~~

Example 46: Acetyl-Val-fPhe~(p-F)Phe].-(N-acet 1-Analogously to Example 37, the title compound is obtained from 80 mg (0.19 mmol) of H-[Phe~(p-F)Phe]-H~3HCi from Example 42b), 124 mg (0.78 mmol) of N-acetyl-(L)-valine, 344 mg (0.78 mmol) of BOP, 105 mg (0.76 mmol) of HOBt and 4.5 ml of 0.3M
NMM in DMF after reprecipitation twice from methylene chloride/methanol by the addition of DIPE and lyophilisation from dioxane/tert-butanol. FAB-MS:
(M+H)+=586, tR~c(I)=15.8 min, Rf (F)=0.32.
Example 47: Acetyl-Val-fPheNN(p-CN)Phe].-(N-acetyl-Val):
Analogously to Example 37, the title compound is obtained in the form of a mixture of 2 diastereoisomers differentiable by HPLC from 80 mg (0.19 mmol) of H-[Phe~(p-CN)Phe]-H~3HC1, 124 mg (0.78 mmol) of N-acetyl-(L)-valine, 344 mg (0.78 mmol) of BOP, 105 mg (0.78 mmol) of I-IOBt and 4.5 ml of 0.3M NMM in DMF after precipitation from methylene chloride/methanol by the addition of DIPE and lyophilisation from dioxane. FAB-MS: (M-t-H)+=593, tRet(I)=14.4 and 14.6 min, Rt(D)=0.39.
a) H-fPhe~(L-CN)Phe]-H~3HC1:
Analogously to Example 2a), the title compound is obtained from 2.69 g (5.27 mmol) of Boc-[Phe~(p-CN)Phe]-Boc after lyophilisation. FAB-MS: (M+H)+=311, Rt(K)=0.16.
b) Boc-[Phe~(p-CN)Phe]-Boc:
Analogously to Example 1, the title compound is obtained from 2.0 g (7.60 mmol) of (2R)-[1'(S)-Boc-amino-2'-phenylethyl]oxirane and 1.87 g (7.6 mmol) of tent-butyl-3-(4-cyanophenyl-methyl)-carbazate after crystallisation from methanol/D1PE. FAB-MS:
(M+H)+=511, tRe~(I)=25 min, RA(Y)=0.19.
c) tent-Butyl-3-(4-cyanophen 1-~yl)-carbazate:
Analagously to Example 4b), 10 g (76.3 mmol) of 4-cyartobenzaldehyde and 10 g (76.3 mmol) of tent-butylcarbazate in ethanol are reacted to yield 4-cyanophenylcarb-aldehyde-tort-butoxycarbonylhydrazone. 11.1 g thereof are hydrogenated in 150 ml of T'HF in the presence of 2 g of 10 % palladium on carbon at 2 atm hydrogen pressure to 20°~2~~~

yield the title compound. 1H-NMR (200 MHz, CDCl3): 7.65 (d, J=BHz, 2H), 7.45 (d, J=8 Hz, 2H), 6.08 (s> br, 1H), 4.3 (s, br, 1H), 4.02 (s, 2H), 1.45 (s, 9H). , Example 48: Z-CL)-Val-fPhe~(~-CN)Phel~((L)-VaD-Z:
Analogously to Example 37, the title compound is obtained from 70 mg (0.17 mmol) of H-[Phe~(p-CN)Phe]-H~3HCl (from Example 47a)), 125 mg (0.5 mmol) of Z-(L)-valine, 221 mg (0.5 mmol) of BOP, 68 mg (0.5 mmol) of HOBt and 3.33 ml of 0.3M NMM in DMF after precipitation from methylene chloride by the addition of hexane and lyophilisa-tion from dioxane. FAB-MS: {M+H)+=777, tR~t(I)=25.3 min, R~D)=0.69.
Example 49: Z-(L)-Ile-fPhe~Leul.-((L)-Ile)-Z:
Analogously to Example 37, the title compound is obtained from 70 mg (0.19 mmol) of H-[Phe~Leu]-H~3HC1 (from Example 13a)), 154 mg (0.58 mmol) of Z-(L)-isoleucine, 257 mg (0.58 mmol) of BOP, 79 mg (0.58 mmol) of HOBt and 3.88 ml of 0.3M NMM
in DMF after chromatography on silica gel with methylene chloride/ether (3:1) and precipita-tion of the product-containing fractions from methylene chloride/DIPE and lyophilisation from dioxane. FAB-MS: (M+H)+=746, tRe~(~=28.2 min, Rf(H)=0.39.
Example 50: Isobutox c~arbonyli~',l-Val-fPhe~Leul~-(N-isobutoxycarbonyl-(L)-Val):
Analogously to Example 37, the title compound is obtained from 70 mg (0.19 mmol) of H-[Phe~Leu]-H~3HCl (from Example 13a)), 130 mg (0.58 rnmol) of N-(isobutoxy-carbonyl)-(L)-valine, 256 rng (0.58 mmol) of BOP, 78 mg (0.S8 mmol) of HOBt and 3.9 ml of 0.3M NMM in DMF after chromatography on silica gel with rnethylene ' chloride/ether (1:1) and lyophilisation of the product-containing fractions from dioxane.
FAB-MS: (M+H)~'=650, tRei(>)=26.4 min, Rf(H)=0.38.
a) N-(Isobutox~carbonyl)-(L)-valine:
11.2 ml (85.3 mmol) of isobutyl chlorofonnate are added to a solution of 10 g (85.3 rnrnol) of (L)-valine in 100 ml of 2N sodium hydroxide solution and the solution is stirred at RT
for 18 h. The reaction solution is washed with methylene chloride, acidified with 4N
hydrochloric acid and extracted with methylene chloride. The organic extracts are washed with brine and filtered through cotton wadding to yield the title compound in the form of a 20'~~7~5 colourless resin after concentration by evaporation. tH-NMR (200 MHz, CD30D):
0.95 (m, 12H), 1.9 (rn, 1H), 2.15 (m, 1H), 3.85 (d, J=7Hz, 2H), 4.05 (d broad, 1H).
Example 5i: N-(3-(Tetrazol-1-Yl)-propionyl)-(L)-Val-fPhe~Leul.-(N-3-(tetrazol-propionYl-(L)-Val):
Analogously to Example 37, the title compound is obtained from 150 mg (0.42 mmol) of H-[Phe~Leu]-H~3HC1 (from Example 13a)), 251 mg (1.04 mmol) of N-(3-(tetrazol-1-yl-propionyl)-(L)-valise from Example 44a, 460 mg (1.04 mmol) of BOP, 140 mg (1.04 mmol) of HOBt and 6.9 ml of 0.3M N-methylmorpholine in DMF after precipitation from methylene chloride/DIPE and lyophilisation from dioxane/tert-butanol/water.
FAB-MS: (M+H)+=689, tRe~(I)=14.7 min, R~(K)~.36.
Example 52: Acetvl-Val-fPhe~Leul~(N-acetyl-VaD:
Analogously to Example 37, the title compound is obtained from 70 mg (0.19 mmol) of H-[Phe~Leu]-H~3HCl (from Example 13a)), 184 mg (1.16 mmol) of N-acetyl-(L)-valise, 512 mg (1.16 mmol) of BOP, 156 mg (1.16 mmol) of HOBt and 7.8 ml of 0.3M NMM
in DMF after precipitation from methylene chloride/methanol by the addition of DIPE and lyophilisation from dioxane/tert-butanol/water (2 diastereoisomers differentiable accord-iIlg to HPLC). FAB-MS: (M+H)+=534, tR~~(I)=14.7 and 15.1 min, Rf(D)=0.35.
Example 53: Boc-(L)-Val-fPhe~Leul~-((L)-Val)-Boc:
Analogously to Example 7, the title compound is obtained from 300 mg (0.83 mmol) of H-[Phe~Leu]-H~3HC1 (from Example 13a)), 722 mg (3.33 mmol) of Boc-(L)-valise, 1.262 g (3.33 mmol) of HBTU and 0.927 ml (6.66 mmol) of triethylamine in DMF
after chromatographic purification on silica gel with methylene chloride/ether (1:l), precipita-tion of the product-containing fractions and lyophilisation from dioxane. FAB-MS:
(M+H)+=650, tRe~(I)=26.3 min. Rt(II)~.64.
Example 54: H-(L)-Val-fPhe~Leul.-((L)-Val)-H~3HC1:
Analogously to Example 5, the title compound is obtained from 396 mg (0.61 mmol) of Boc-(L)-Val-[Phe~Leu].-((L)-Val)-Boc from Example 53 and 10 ml 4N hydrogen chloride in dioxane after lyophilisation of the reaction solution. FAB-MS:
(M+H)+=450, ~O'~~"~~

tRec(B)=24.1 min, Rf{K)=0.25.
Example 55: N-Thiomorpholinocarbonyl-(L)-Val-lPhe~Leu.-(N-thiomorpholino-carbon~(L)-Val): . ' Analogously to Example 6, the title compound is obtained in the form of an amorphous solid starting from 100 mg (0.16 mmol) of H-(L)-Val-[Phe~Leu)~(L)-Val-H~3HC1, 78.5 mg (0.47 mmol) of (4-thiomorpholinylcarbonyl)chloride from Example 6a and 0.172 ml of triethylamine in DMF after chromatographic purification on silica gel with methylene chloride/methanol (95:5), precipitation of the product-containing fractions from methylene chloride/hexane and lyophilisation from dioxane. FAB-MS: (M+H)+=708, tRet(n=21.4 min, Rf(E)=0.45.
Example 56: 2(R,S)-Tetrahydrofurlrl-methox c~ 1-(L)-Val-f Cha~Leul.-(N-2(R,S)-tetrahvdrofurlrl-methoxycarbonyl- L( )~Val) Analogously to Example 37, the tide compound is obtained from 80 mg (0.22 mmol) of H-[Cha~Leu]-H~3HC1, 160 mg (0.65 mmol) of N-(2(R,S)-tetxahydrofuryl-methoxycar-bonyl)-(L)-valine, 289 mg (0.65 mmol) of BOP, 88 m,g (0.65 mmol) of HOBt and 4.35 ml of 0.3M NMM in DMF after chromatographic purification on silica gel with ethyl acetate and lyophilisation of the product-containing fractions from dioxane. FAB-MS:
(M+H)+=712, tRe~(I)=22.4 min, Rt(E)=0.21.
a) H-lCha~Leui-H~3HC1:
Analogously to Example 5, 100 mg (83 %) of the title compound are obtained from 150 mg (0.33 mmol) of Boc-[Cha~Leu]-Boc and 10 ml of 4N hydrogen chloride in dioxane after lyophilisation of the reaction solution. R~(K)=0.26.
b) Boc-lCha~Leui-Boc A solution of 200 mg (0.24 mmol) of Boc-[Phe~Leu]-Boc (Example 12) in 15 ml of methanol is hydrogenated for 4 h at 1 atm hydrogen pressure in the presence of 10 mg of Nishimura-catalyst (Rh(III)- and Pt(1V)-oxide tnonohydrate, Degussa). The catalyst is removed by filtration, the solvent is fully concentrated by evaporation and the title compound is obtained after crystallisation from methylene chloride/hexane.
tRec(I)=26.7 ~072"~~5 069 _ min, Rx(V )=0.21.
c) N-(2(R,S)-Tetrahydrofuryl-methoxycarbonyl)-(L)-valine:
Analogously to Example 50a, the title compound is obtained in the form of a mixture of 2 diastereoisomers from 7 g (60 mmol) of (L)-valine and 9.8 g (60 mmol) of 2(R,S)-tetra-hydrofurylmethyl-chloroformate (Hetexocycles 27, 1155 (1988)) in 100 ml of 2N
sodium hydroxide solution and 30 ml of dioxane. tR~~(II)=23.5 and 23.8 min.
Example 57: Z-Val-iPhe~Leul.-(N-(3-(tetrazol-1-yl)-propionyl)-Val):
Analogously to Example 37, the title compound is obtained (in the form of 2 diastereo-isomers differentiable by HPLC) from 100 mg (0.21 mmol) of Z-(L)-Val-[Phe~Leu]-H, 75 mg (0.31 mmol) of N-(3-(tetrazol-1-yl)-propionyl)-(L)-valine from Example 44a, 137 mg (0.31 mmol) of BOP, 42 mg (0.31 mmol) of HOBt and 2 ml of 0.3M NMM in DMF after precipitation from methylene chloride/hexane and lyophilisation from dioxane/tert-butanol. FAB-MS: (M+H)'"=708, tRec(I)-.21.1 and 21.1 min, Rf(D)=0.45.
a) Z-(L.)-Val-fPhe~LeuLH:
A solution of 250 mg (0.43 mmol) of Z-(L)-Val-[Phe~Leu]-Boc in 5 ml of .formic acid is stirred for 7.5 h at RT. After that time no more starting material can be detected by HPLC
analysis (tRec(1)=27.5 min), and the reaction solution is concentrated by evaporation. The residue is dissolved in chloroform and washed with saturated sodium hydrogen carbonate solution. The chloroform phase is filtered through cotton wadding and yields the crude .
title compound after removal of the solvent by evaporation. tRei(I)=16.7 min, R f(K)=0.21. , zo~27~~

b) Z-(L,)-Val-fPhe~Leul-Boc:
Analogously to Example 37, the title compound is obtained from 230 mg (0.653 mmol) of H-[Phe~Leu]-Boc, 247 mg (0.98 mmol) of Z-(L)-valine, 434 mg (0.98 mmol) of BOP, , 133 mg (0.98 mmol) of HOBt and 6.5 ml of 0.3M NMM in DMF after precipitation from methylene chloride/methanol by the addition of DIPE. FAB-MS: (M+H)+=585, tRec(I)=27.5 min, Rf(C)=0.71.
c) H-fPhe~Leul-Boc:
Analogously to Example 17a), the title compound is obtained starting from 1.27 g (2.84 mmol) of N-trifluoroacetyl-[Phe~Leu]-Boc and 24 ml of 1N aqueous sodium carbonate solution in 90 ml of methanol by precipitation from methylene chloride by the addition of DIPE. tR~~(I)=14.9 min, Rf(K)=0.38.
d) N-Trifluoroacetyl-fPhe~Leul-Boc:
Analogously to Example 16, the title compound is obtained starting from 3 g (11.57 mrnol) of 2(R)-[1'(S)-(trifluoroacetylamino)-2'-phenylethyl]-oxirane from Example 16d) and 2.3 g (12.15 mmol) of tart-butyl-3-isobutyl-carbazate (preparation: J.
Chem. Soc. Perltin I, 1712 (1975)) after chromatographic purification on silica gel with methylene chloride/ether (20:1). tRec(I)=24.7 min, Rt(W)=0,36.
Example 58: Acetyl-Val-fPhe~Leul~(N-(2(R S)-carbamoyl-3-phenyl-prapion~V
Analogously to Example 37, the title compound is obtained (in the form of 2 diastereo-isomers differentiable by HPLC) from 140 mg (0.3 mmol) of acetyl-(L)-Val-[Phe~Leu]-H~2HC1, 132 mg (0.45 mmol) of N-(2(R,S)-carbamoyl-3-phenyl-propionyl)-(L)-valine (preparation: Synth., Struct., Funct., Proc. Am. Pept. Symp., 7~, 85, (1981)), 199 mg (0.45 mmol) of BOP, 61 mg (0.45 mmol) of HOBt and 3.5 ml of 0.3M NMM in DMF after precipitatian from methylene chloride/DIPE and lyophilisation from dioxane.
FAB-MS: (M+H)+=667, tRe~(I)=17.9 and 18.4 min, Rf(D)=0.33.
a) Acetyl-Val-fPhe~Leul-I-I~2HCl:
Analogously to Example 2a), the title compound is obtained starting from 230 mg ~o~~~~~

(0.46 mmol) of acetyl-(L)-Val-[Phe~Leu]-Boc after lyophilisation, tket(I)=10.5 min, Rt{D)=0.38. , b) Acetyl-Val-fPhe~Leul-Boc: ' Analogously to Example 37, the title compound is obtained from 2S0 mg (0.71 mmol) of H-[Phe~Leu]-Boc from Example 57c), 170 mg (1.07 mmol) of N-acetyl-(L)-valine, 471 mg (1.07 mmol) of BOP, 144 mg (1.07 mmol) of I-IOBt and 7.1 ml of 0.3M NMM
in DMF after precipitation from methylene chloride by the addition of DLPE and lyophilisa-tion from dioxane. FAB-MS: (M+H)+=493, tRet(I)=20.5 min, Rf(D)=0.59.
Example 59: N-Morpholinocarbonyl-(L)-Val-fPhe~Leui~(N-(3-(tetrazol-1-yl)-prop-ionyl)-Val):
Analogously to Example 37, the title compound is obtained (in the form of 2 diastereo-isomers differentiable by HPLC) from 100 mg (0.19 mmol) of N-rnorpholinocarbonyl-(L)-Val-[Phe~Leu]-H~2HCl, 67 mg (0.38 mmol) of N-(3-(tetrazol-1-yl)-propionyl)-(L)-valine from Example 44a, 124 mg (0.28 mmol) of BOP, 38 mg (0.28 mmol) of HOBt and 2.1 ml of 0.3M NMM in DMF after precipitation from methylene chloride by the addition of DIPE and lyophilisation from dioxane. FAB-MS: (M+H)~=687, tR~c(I)=15.2 and 15.4 min, Rp(D)=0.25.
a) N-Morpholinocarbonyl-(L)-VaI-[Phe~Leul-H~2HC1:
Analogously to Example 2a), the title compound is obtained starting from 279 mg (0.49 mmol) of N-morpholinocarbonyl-(L)-Val-[Phe~Leu]-Boc after lyaphilisation.
FAB-MS: (M+H)~"=464, tRec(B)=30.3 min, Rf(D)=0.46.
b) N-Morpholinocarbonyl-(L)-Val-fPhe~Leul-Boc:
Analogously to Example 37, the title compound is obtained from 250 mg (0.71 mmol) of H-[Phe~Leu]-Boc (from Example 57c)), 265 mg (1.07 mmol) of N-morpholino-carbonyl-(L)-valine from Example 7a), 471 mg (1.07 mmol) of BOP, 144 mg (1.07 mmol) of HOBt and 7.1 ml of 0.3M NMM in DMF after precipitation from methylene chloride/-hexane and lyophilisation from dioxane. FAB-MS: (M+H)+=564, tRe~(I)=21.5 min, Rt(K)=0.69.

Example 60: N-Trifluoroacetyl-(Phe~Leul.-(N-(2(R S)-carbam~l-3-phenyl-propionyl)-L -Val Analogously to Example 37, the title compound is obtained (in the form of 2 diastereo-isomers differentiable by HPLC) from 136 mg (0.32 mmol) of N-trifluoroacetyl-[Phe~Leu]-H~2HC1,142 mg (0.49 mmol) of N-(2(R,S)-carbamoyl-3-phenyl-propionyl)-(L)-valine (preparation: Synth., Struct., Funct., Proc. Am. Pept. Symp., 7a', 85, (1981)), 215 mg (0.49 mmol) of BOP, 66 mg (0.49 mmol) of HOBt and 3.5 ml of 0.3M NMM in DMF after chromatographic purification on silica gel with chloroform/methanol (15:1), precipitation of the product-containing fractions from methylene chloride/DIPE
and lyophilisation from dioxane/tert-butanol. FAB-MS: (M+H)~=622, tRec{T)=21.6 and 22.0 min, Rf(K)=0.26.
a) N-Trifluoroacetyl-(Phe~Leul-H~2HC1:
Analogously to Example 2a), the title compound is obtained starting from 300 mg (0.67 mmol) of N-trifluoroacetyl-[Phe~Leu]-Boc from Example 57d) after lyophilisation.
Rt{W)<0.1.
Example 61: Z-~L)-Val-(Phe~Nlel.-(N-(2(R S)-(N-(:Z-morpholinoethyl)-carbamoyl)-methyl)-butyr~:
Analogously to Example 37, the title compound is obtained (in the form of 2 diastereo-isomers differentiable by HPLC) from 100 mg (0.17 mmol) of Z-(L)-Val-[Phe~Nle]-H~2HC1, 69 mg {0.27 mmol) of 2(R,S)-(N-(2-morpholinoethyl)-carbamoyl)-3-methylbutyric acid (isopropylmalonic acid N-(2-morpholinoethyl)monoamide), 119 mg (0.27 mmol) of BOP, 36 mg (0.27 mmol) of HOBt and 2.1 ml of 0.3M NMM in DMF
after precipitation from methylene chloride/DIPE and lyophilisation from dioxane.
FAB-MS: (M+H)+=725, tRec{I)=17.2 and 17.6 rnin, R,f(D)=0.56.
a) Z-(L)-Val-(Phe~Nle1-H~2HC1:
Analogously to Example 2a), the title compound is obtained starting from 310 mg (0.53 mmol) of Z-(L)-Val-[Phe~Nle]-Boc after lyophilisation. tRec(1)=16.4 min, Rt(U)=0.25.

b) Z-(L)-~lal-fPhe~Nlel-Boc:
Analogously to Example 37, the title compound is obtained from 250 mg (0.71 mmol) of H-(Phe~Nle]-Boc, 268 mg (1.07 mmol) of Z-(L)-valine, 472 mg (1.07 mmol) of BOP, 144 mg (1.07 mmol) of HOBt and 7.1 ml of 0.3M NMM in DMF after chromatographic purification on silica gel with methylene chloride/methanol (40:1) and precipitation of the product-containing fractions from methylene chloride/DIPE. tRec(I)=25.6 min, Rf(X)=0.17.
c) H-fPhe~Nlel-Boc:
Analogously to Example 17a), the title compound is obtained starting from 830 mg (1.85 mmol) of N-trifluoroacetyl-(Phe~NIe]-Boc after precipitation fzorn methylene chloride/DIPE. tR~c(I)=15.4 min, Rf(K)=0.54.
d) N-Trifluoroacetyl-fPhe~NIel-Boc:
Analogously to Example 16, the title compound is obtained stwting from 1 g (3.86 mmol) of 2(R)-(1'-(S)-(triouoroacetylamino)-2'-phenylethyl]-oxirane from Example 16d) and 720 mg (3.86 mmol) of tert-butyl-3-butyl-carbazate after chromatographic purification on silica gel with methylene chloride/ether (20:1). tR~~(I)=:25.3 min, Rt(Q)=0.43.
e) tent-Butyl-3-butyl-carbazate:
Analogously to Example 4b), the corresponding tert-butoxycarbonyl-hydrazone (25 g, 99 %) is obtained from 18.0 g (136.2 mmol) of tent-butyl-carbazate and 12.3 ml (136.2 mmol) of n-butanal in the form of a crude product, which is hydrogenated as described in Example 4a) in the presence of 10 g of 5% platinum on carbon at 4 atm hydrogen pressure. Chromatographic pzu-ification of the crude product on silica gel with hexane%thyl acetate (1:1) yields the title compound. Rf(N)=0.44,1H-NMR (200 MHz, CD30D). 0.92 (t, J=7Hz, 3H), 1.43 (s, 9H), 1.30 to 1.50 (m, 4H), 2.75 (t, J=7I-Iz, 2H).
f) 2(R,S)-(N-(2-Morpholinoeth~l)-carbarnoyl)-3-methylbutyric acid Analogously to Example 9b) there is obtained from 7 g (43.7 mmol) of racemic isopropyl-malonic acid monomethyl ester CChem. Ber. 119, 1196 (1986)), 6.3 m1 (48.1 mmol) of 20'~2'~~~

aminoethyl-morpholine, 6.6 ml (43.7 mmol) of cyanophosphonic acid diethyl ester and 12.8 ml (91.8 mmol) of triethylamine in DMF, 2(R,S)-(N-(2-morpholinoethyl)-carbamoyl)-3-methyl-butyric acid methyl ester (isopropylmalonic acid N-morpholino-ethylamide methyl ester). This is 'stirred for 5 h in a mixture of 28 ml of 2N
sodium hydroxide solution and 28 ml of dioxane at RT, acidified with 2N hydrochloric acid and fully concentrated by evaporation. The residue is digested with ethanol, filtered off, and concentration by evaporation of the filtrate yields the title compound. lI-I-NMR (200 MHz, CD30D): 0.95 and 1.00 (2d, J=7H, 6H), 2.25 (m, 4H), 2.70 (m, 6H), 2.75 (d, J=8Hz, 1H), 3.45 (m, 2H), 3.75 (m, 4H).
Exam 1p a 62: Z-(L)-Val-fPhe~Nlel~(N-(3-(tetrazol-1-~_propionyl)-Val):
Analogously to Example 37, the title compound is obtained (in the form of 2 diastereo-isomers differentiable by HPLC) from 1(?0 mg (0.18 mmol) of Z-(L)-Val-[Phe~Nle]-H~2HCl (from Example 61a)), 65 mg (0.27 mmol) of N-(3-(tetrazol-1-yl)-propionyl)-(L)-valine from Example 44a, 119 mg (0.27 mmol) of BOP, 36 mg (0.27 mmol) of HOBt and 2.1 ml of 0.3M N-methylmorpholine in DMF after precipitation from methylene chloride/-DIPE and lyophilisation from dioxane/tert-butanol. F,AB-MS: (M+H)+=708, tR~~(I)=20.3 and 20.6 min, Rf(D)=0.43.
ExamQe 63: Z-CL)-Val-fPhe~Nlel~(N-(2(R,S)-(N-(2-pvridylmethyl)-carbamoyl)-3-methyl)-butyryp (dibenzenesulfonate):
Analogously to Example 37, the title compound is obtained in the form of the free amine from 95 mg (0.17 mmol) of Z-(L)-Val-[Phe~Nle]-H~2HC1 from Example 61a), 60 mg (0.26 mmol) of (R,S)-isopropylmalonic acid N-(2-picolyl)-monoamide, 113 mg (0.26 mmol) of BOP, 35 mg (0.26 mmol) of HOBt and 2.0 ml of 0.3M NMM in DMF
after chromatographic purification on silica gel with methylene chloride/methanol (15:1).
The free amine is dissolved in methylene chloride, 2 eduivalents of benzenesulfonic acid are added, and precipitation is effected by the addition of DIPE.
Lyophilisation from tert-butanol yields the dibenzenesulfonate salt (in the form of 2 diastereoisomers differentiable by HPLC). FAB-MS: (M+H)+=703, tRec(I)=17.7 and 18.0 min, Rf(D)=0.54.
a) Isopropylmalonic acid N-(2-picolyl)monoamide:
10.6 ml (103 mmol) of N-methylmorpholine are added to a solution of 15 g (93.6 mmol) 20°~2'~~~

of isopropylmalonic acid monomethyl ester (preparation: Chem. Ber. 119, 1196 (1986)) in 150 ml of THF and subsequently 13.5 ml (103 mmol) of isobutyl chlproformate are added dropwise thereto. After 30 min 15.3 ml (150 mmol) of 2-picolylamine are added and the resulting suspension is.stirred for 2 h. The reaction mixture is diluted with 1N sodium hydroxide solution and water and washed with methylene chloride, and the organic phase is filtered through cotton wadding and concentrated by evaporation.
Crystallisation of the residue yields isopropylmalonic acid N-(2-picolylamide) methyl ester, which is hydro-lysed in 2N sodium hydroxide solution and dioxane as described in Example 61f) to yield the title compound. tRec(B)=16.0 min.
Example 64: Z-(L)-Val-(Phew(p-F)Phel.-(N-(3-(tetrazol-1- 1~)-propionyl)-(L)-Val) (benzenesulfonate):
Analogously to Example 37, the title compound is obtained in the form of the free amine from 100 mg (0.16 mmol) of 2-(L)-Val-[Phe~(p-F)Phe]-H from Example 22a), 59 mg (0.25 mmol) of N-(3-(tetrazol-1-yl)-propionyl)-(L)-valine from Example 44a, 109 mg (0.25 mmol) of BOP, 33 mg (0.25 mmol) of HOBt and 1.19 ml of 0.3M N-methyl-morpholine in DMF after precipitation from methylene chloride/DIPE. The free amine is dissolved in methylene chloride/methanol, 1 equivalent of benzenesulfonic acid is added, and precipitation is effected by adding hexane. Lyophilisation from tert-butmol yields the title compound in the form of the benzenesulfonate salt. FAB-MS: (M+H)'"'=760, tRe~(1)=21.6 min, R~B)=0.49.
Examyle 65: Methylsulfonyl-fPhe~Phel.-(N,=phenylacetyl-(L)-ValO
132 mg (0.28 mmol) of methylsulfonyl-[Phe~Phe]-H-2HC1 is reacted analogously to Example 7 with 197 mg (0.84 mmol) of N-phenylacetyl-(L)-valine (preparation:
Mem.
Tokyo Univ. Agric. 20, Sl (1978)), 317 mg (0.S4 mmol) of HBTU and 0.23 ml (1.67 mmol) of triethylamine in DMF to yield the title compound after precipitaton from methanol by the addition of ether. FAB-MS: (M+H)+=581, tRec(I)=20.2 min, Rr(B)=0.64.
a) Methvlsulfonvl-fPhe~Phei-H~2HCl:
Analogously to Example 2a), the title compound is obtained starting from 130 mg (0.28 mmol) of methylsulfonyl-[Phe~Phe]-Boc after lyophilisation. FAB-MS:
(M+H)~=364, tRe~(II)=28.5 min, Rf (K)=0.56.

2072~~~

b) MethvlsulfonYl-fPhe~Phel-Boc:
Analogously to Example 16a), tht; title compound is obtained as a diastereoisomeric mixture in a ratio of 4:1 starting from 1.1 g (4.56 mmol) of 2(R)-[1'(S)-(methylsulfonyl-amino)-2'-phenylethyl]oxirane and 1,11 g (5.02 mmol) of tert-butyl-3-benzyl-carbazate (preparation: J. Chem. Soc. Perlcin I, 1712 (1975)). By crystallisation from methylene chloride/hexane the ratio in favour of the 2S-diastereoisomer is improved to 10:1.
FAB-MS: (M+H)+=464, tRet(~=21.3 min, RA(N)=0.26.
c) 2(R)-(1'(S)-(Methylsulfonylamino)-2'-phen 1y ethylloxirane~
2.36 g (13.6 mmol) of methansulfonic acid anhydride and 1.88 ml (13.6 mmol) of triethyl-amine are added at O~C to a solution of 1 g (6.8 mmol) of 1-phenyl-3-buten-2(S)-amine from Example 16b) in 10 ml methylene chloride and the mixture is stirred for 1 h. The xeaction mixture is washed with water and saturated sodium hydrogen carbonate solution and the organic phase is filtered through cotton wadding and concentrated by evaporation to yield 2(S)-methylsulfonylamino-1-phenyl-3-butene. 1 g (4.4 mmol) of that crude product is dissolved in 30 ml of methylene chloride, 3.05 g (17.7 mmol) of 4-chloroper-benzoic acid are added at RT and stirring is earned oust for 18 h. The reaction solution is washed 5 times with 10 % aqueous sodium sulfite solution, filtered through cotton wadding and fully concentrated by evaporation. According to iH-NMR the crude product contains both the (2R)- and the (2S)-epimer in a ratio of 4:1. tH-NMR (200 MHz, CD30D); 2.30 and 2.52 (2 s, together 3H), 2.6 to 3.2 (m, 5H), 3.55 (m, 1H), 7.32 (m, 5H).
Example 66: Methox c~yi-(L)-Val-[Phe~Leul~(N-methox cy arbonyl-(L,)-VaIO
Analogously to Example 37, the title compound is obtained from 200 mg (0.55 mmol) of H-[Phe~Leu]-H~3HC1 (from Example 13a)), 291 mg (1.66 mmol) of N-methoxycar-bonyl-(L)-valine (preparation: Chem. Lett. 705, (1980)), 735 mg (1.66 mmol) of BOP, 225 mg (1.66 mmol) of HOBt and 11 ml of 0.3M NMM in DMF after precipitatian from rnethylene chloridelDlPE and lyophilisation from dioxane. FAB-MS: (M+H)~=566, tttet(I)=18.6 min, Rt(U)=0.33.

20'?'27~~

Example 67: Methox~carbon~-(L)-Val-fPhe~(p-F)Phel--(N-methoxycarbonyl-(L)-Val):
Analogously to Example 37, the title compound is obtained from 200 mg (0.48 mmol) of H-jPhe~(p-F)Phe]-H~3HCl (from Example 42b)), 255 mg (1.45 mmol) of N-methoxy-carbonyl-(L)-valine (preparation: Chem. Lett. 705, (1980)), 643 mg (1.45 mmol) of BOP, 196 mg (1.45 mmol) of HOBt and 9.7 ml of 0.3M NMM in DMF after precipitation from methylene chloride/DIPE and lyophilisation from dioxane. FAB-MS: (M+H)+=618, tR~,(1)=19.5 min, R~U)=0.22.
Example 68: Methoxycarbonyl-(L)-Val-fPhe~(p-CN)Phel~(N-methoxycarbonyl-(L)-V
Analogously to Example 37, the title compound is obtained from 200 mg (0.48 mmol) of H-[Phe~(p-CN)Phe]-H~3HC1 (from Example 47a)), 250 mg (1.43 mmol) of N-methoxy-carbonyl-(L)-valine (preparation: Chem. Lett. 705, (1980)), 631 mg (1.43 mmol) of BOP, 193 mg (1.43 mmol) of HOBt and 9.5 ml of 0.3M NMM in DMF after chromatographic purification on silica gel with methylene chloride/methanol (15:1) and lyophilisation of the product-containing fractions from dioxane. FAB-MS: (M+H)+=625, tRe~(I)=18 min, Rt(U)=0.31.
Exam 1-p a 69: Z-(L)-Val-f (p-F)Phew(p-F)Phel.-(N-(2(R,S)-(N-(2-morpholinoeth 1 -carb-amoyl)-3-methyl)-butyr~):
Analogously to Example 18, 23.0 mg (0.089 mmol) of 2(R,S)-(N-(2-morpholinoethyl)-carbamoyl)-3-methylbutyric acid (Example 61 f)) and 45 mg (0.081 mmol) of Z-(L)-Val-j(p-F)Phe~(p-F)Phe]-H (Example 32) are reacted with 33.8 mg (0.089 mmol) of HBTU
in 0.76 ml of 0.25M NMM/CH3CN to yield the title compound which is reprecipitated with DMF/DIPE: TLC Rt{P)=0.42; FAB-MS (M+H)~'=795.
Example 70: Z-(L)-Va1-f (p-F)Phe~(~ F)Phel~(N-(2(R,S)-(N-(2-pyridylmethyD-carb-amo~l)-3-methyl)-butyr Analogously to Example 18, 21.0 mg (0.089 mmol) of rac. isopropylmalonic acid N-(2-picolyl)amide (Example 63 a)) and 45 mg (0.081 mmol) of Z-(L)-Val-[(p-F)Phe~(p-F)Phe]-H (Example 32) are reacted with 33.8 mg (0.089 mmol) of HBTU in 0.76 ml of 0.25M NMM/CI-33CN to yield the title compound which is reprecipitated with 20"~~'~~5 DMF/DIPE: TLC R;f(P)=0.52; FAB-MS (M+H)+=773.
Example 71:
The following compounds can be prepared analogously to one of the afore-mentioned processes:
a) Z-(L)-Val-[(p-F)Phew(p-F)Phe].-((L)-Val).-(N-morpholinocarbonyl-Gly);
b) N-Morpholinocarbonyl-(L)-Val-[(p-F)Phew(p-F)Phe].-((L)-Val).-(N-morpholino-carbonyl-Gly);
c) N-(Quinoline-2-carbonyl)-(L)-Asn-[Phe~(p-F)Phe]~((L)-Val)-Z
d) N-(Mozpholinosulphonyl)-(L)-Val-[Phe~Leu].-(N(morpholinosulphonyl)-(L)-Val) Example 72: Gelatine solution:
A sterile-Filtered aqueous solution, with 20 % cyclodextrins as solubilisers, of one of the compounds of formula I mentioned in the preceding Examples as active ingredient, is so mixed under aseptic conditions, with hearing, with a sterile gelatine solution containing phenol as preservative, that 1.0 ml of solution has the following composition:
active ingredient 3 mg gelatine 150.0 mg phenol 4.7 mg dirt. water with 20 % cyclodextrins as solubilisers 1.0 ml Example 73: Sterile dry substance for infection:
mg of one of the compounds of formula I mentioned in the preceding Examples as active ingredient are dissolved in 1 ml of an aqueous solution with 20 mg of mannitol and 20 %
cyclodextrins as solubilisers. The solution is sterile-filtered and introduced under aseptic conditions into a 2 ml ampoule, deep-frozen and lyophilised. Before use, the lyophilisate is dissolved in 1 ml of distilled water or 1 ml of a physiological saline solution. The 20'~2"~~~5 solution is administered intramuscularly or intravenously. This formulation can also be introduced into a twin-chambered injection ampoule.
Examgle 74: Nasal spray;
S00 mg of finely ground (<S.0 N.m) powder of one of the compounds of formula I
men-tioned in the preceding Examples is suspended as active ingredient in a mixture of 3.S ml of Myglyol 812 and 0.08 g of benzyl alcohol. The suspension is introduced into a container with a metering valve. S.0 g of Freon 12~ are introduced under pressure through ' the valve into a container. The "Freon" is dissolved in the Myglyol/benzyl alcohol mixture "
by shaking. The spray container contains approximately 100 single doses which can be administered individually.
Example 7S: Film-coated tablets The following ingredients are used for the preparation of 10 000 tablets each containing 100 mg of active ingredient:
active ingredient 1000 g corn starch 680 g colloidal silica 200 g magnesium stearate 20 g stearic acid 50 g sodium carboxymethyl starch 2S0 g water quantum satis A mixture of one of the compounds of formula I mentioned in the preceding Examples as active ingredient, SO g of corn starch and the colloidal silica is processed with a starch paste, made from 2S0 g of corn starch and 2.2 kg of demineralised water, to form a moist mass. This is forced through a sieve having a mesh size of 3 rnm and dried at 4S° for 30 min in a fluidised bed drier. The dry granules are pressed through a sieve having a mesh size of 1 mm, mixed with a pre-sieved mixture (1 mm sieve) of 330 g of corn starch, the magnesium stearate, the stearic acid and the sodium carboxymethyl starch, and compressed to form slightly biconvex tablets.

Claims (14)

1. A compound of formula wherein R1 and R9 are each independently of the other - hydrogen, - lower alkoxycarbonyl, - 2-halo-lower alkoxycarbonyl, - aryloxycarbonyl wherein aryl has from 6 to 14 carbon atoms, - aryl-lower alkoxycarbonyl wherein aryl has from 6 to 14 carbon atoms, - heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- and cyclohepta-fused derivative of those radicals, optionally fully or partially saturated, - 2-tri-lower alkylsilyl-lower alkoxycarbonyl, - 2-triarylsilyl-lower alkoxycarbonyl wherein aryl is phenyl or 1- or 2-naphthyl, - a radical, bonded via a carboxy group, of an amino acid selected from glycine, alanine, valine, norvaline, leucine, isoleucine, norleucine, serine, homoserine, threonine, methionine, cysteine, proline, trans-3- and trans-4-hydroxyproline, phenylalanine, tyrosine, 4-aminophenylalanine, 4-chlorophenylalanine, 4-carboxyphenylalanine, .beta.-phenylserine, phenylglycine, .alpha.-naphthylalanine, cyclohexylalanine, cyclohexylglycine, tryptophan, indoline-2-carboxylic acid, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, aspartic acid, asparagine, aminomalonic acid, aminomalonic acid monoamide, glutamic acid, glutamine, histidine, arginine, lysine, .delta.-hydroxylysine, ornithine, .alpha., .gamma.-diaminobutyric acid and .alpha., .beta.-diaminopropionic acid, wherein each amino acid is in the D-, L- or (D, L)-form, and wherein the .alpha.-amino group is unsubstituted or mono- or di-N-alkylated by lower alkyl, by amino-lower alkyl by phenyl- or naphthyl-amino-lower alkyl, or by piperazinylcarbonyl-lower alkyl substituted at the nitrogen atom by lower alkyl, or is optionally N-acylated by lower alkanoyl; by aryl-lower alkanoyl wherein aryl is selected from phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl and fluorenyl and is unsubstituted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylaminosulfonyl, nitro and/or by cyano, wherein phenyl is optionally present up to three times, and wherein lower alkanoyl is unsubstituted or substituted by lower alkyl, heterocyclyl selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, .beta.-carbolinyl and .alpha. benzo-, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof which is optionally fully or partially saturated, hydroxy, lower alkoxy, lower alkanoyloxy, acetoacetoxy, amino- or benzyloxy-carbonylamino-lower alkanoyloxy, aryl-lower alkanoyloxy wherein aryl has from 6 to 10 carbon atoms, lower alkoxycarbonyloxy, mono- or di-lower alkylaminocarbonyloxy, aryloxycarbonyloxy wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyloxy wherein aryl has from 6 to 14 carbon atoms, sulfonyloxy, lower alkylsulfonyloxy, phenylsulfonyloxy, 2- or 4-toluenesulfonyloxy or 1- or 2-naphthylsulfonyloxy, carboxy, esterified carboxy selected from lower alkoxycarbonyl, aryloxycarbonyl wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyl wherein aryl has from 6 to 12 carbon atoms, lower alkanoyl, lower alkylsulfonyl, hydroxy-lower alkoxyphosphoryl and di-lower alkoxyphosphoryl, carbamoyl, carbamoyl substituted by one or two radicals selected from lower alkyl, carboxy-lower alkyl, lower alkoxycarbonyl-lower alkyl, di-lower alkylamino-lower alkyl, aminocarboxy-lower alkyl, hydroxy-lower alkyl and di-lower alkoxy-lower alkyl or carbamoyl substituted by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene, in which a carbon atom is optionally replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and is optionally unsaturated, and also sulfamoyl, phosphono, benzofuranyl, oxo and/or by cyano and is branched or unbranched; by heterocyclyl-lower alkanoyl selected from thienyl-, furyl-, pyranyl-, pyrrolyl-, imidazolyl-, pyrazolyl-, oxazolyl-, isoxazolyl-, thiazolyl-, furazanyl, pyridyl-, pyrazinyl-, pyrimidinyl-, pyridazinyl-, azepinyl-, indolyl-, benzimidazolyl-, 1H-indazolyl-, quinolyl-, isoquinolyl-, quinoxalinyl-, quinazolinyl-cinnolyl-, purinyl-, pteridinyl-, naphthyridinyl-, 4H-quinolizinyl-, 3,1-benzofuranyl-, Benz-[e]indolyl-, 4,1-benzoxazinyl-, 4,1-benzothiazinyl-, carbazolyl-, .beta.-carbolinyl-, phenazinyl-, phenanthridyl-, acridyl-, phenoxazinyl-, phenothiazinyl-, 1-azaacenaphthenyl-, cyclohexa[b]pyrrolyl-, cyclohepta[b]pyrrolyl-, cyclohexa[d]pyrazolyl-, cyclohexa[b]-pyridyl-, cyclohexa[b]pyrazinyl-, cyclohexa [b] pyrimidinyl-, cyclohexa [b] -1, 4-oxazinyl-, cyclohexa[b]-1,4-thiazinyl-, pyrrolidinyl-, pyrrolinyl-, imidazolidinyl-, 2-imidazolinyl-, 2,3-dihydropyridyl-, piperidyl-, piperazinyl-, 2,3,5,6-tetrahydropyrazinyl-, morpholinyl-, thiomorpholinyl-, S,S-dioxothiomorpholinyl-, indolinyl-, isoindolinyl-, 4,5,6,7-tetrahydroindolyl-, 1,2,3,4-tetrahydroquinolyl-, 1,2,3,4-tetrahydroisoquinolyl-, chroman-, thiochroman-, 1,2,3,4-tetrahydro-3,1-benzodiazinyl-, 3,4-dihydro-3H-4,1-benzoxazinyl-, 3,4-dihydro-3H-4,1-benzothiazinyl-, 2,3,4,5-tetrahydro-1H-5,1-benzazepinyl- and 5,6-dihydrophenanthridinyl-lower alkanoyl, the heterocyclyl radicals being unsubstituted or substituted by lower alkyl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, hydroxy-lower alkyl, lower alkoxy-lower alkyl, phenoxy- or naphthyloxy-lower alkyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, lower alkanoyloxy-lower alkyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, lower alkoxycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyloxy-lower alkyl, amino-lower alkyl, carboxy-lower alkyl, hydroxy, lower alkoxy, phenyl- or naphthyl-lower alkoxy, amino, lower alkylamino, di-lower alkylamino, carboxy, lower alkoxycarbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, halogen, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, dialkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, hydroxy- or carboxy-lower alkylcarbamoyl, sulfamoyl, nitro, oxo and/or by cyano; by heterocyclyl-lower alkenoyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof, which is optionally fully or partially saturated;
by lower alkoxycarbonyl; by aryl-lower alkoxycarbonyl wherein aryl has from 6 to 14 carbon atoms; by heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, b-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof, which is optionally fully or partially saturated and unsubstituted or substituted by lower alkyl;
by carboxy-lower alkanoyl; by lower alkoxycarbonyl-lower alkanoyl; by hydroxy-lower alkoxy-lower alkanoyl; by amino-lower alkanoyl; or by benzyloxy-carbonylamino-lower alkanoyl wherein the amino group is not bonded in the .alpha.- or .beta.-position; by carbamoyl; by phenyl-lower alkylaminocarbonyl; by N-di-lower alkylamino-lower alkyl-N-lower alkylaminocarbonyl; by N-dihydroxy-lower alkyl-N-lower alkylaminocarbonyl; by 2- or 3-pyridyl-lower alkylaminocarbonyl; by N-2-pyridyl-lower alkyl-N-lower alkylaminocarbonyl; by sulfonyl; by lower alkylsulfonyl; by arylsulfonyl wherein aryl has from 6 to 10 carbon atoms and is unsubstituted or substituted by lower alkyl or by lower alkoxy; by heterocyclylsulfonyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, a-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof, which is optionally fully or partially saturated; by sulfamoyl; or by sulfamoyl substituted by heterocyclyl-lower alkyl wherein heterocyclyl is as last defined, and/or by lower alkyl;
a carboxy group of the side chain is present in free form or in esterified form as a lower alkyl ester group, as an aryl ester group or as an aryl-lower alkyl ester group, wherein aryl is phenyl, 4-nitrophenyl, naphthyl or biphenylyl, or in amidated form as a carbamoyl, lower alkylcarbamoyl, di-lower alkylaminocarbamoyl, mono- or di-(hydroxy-lower alkyl)-carbamoyl or mono- or di-(carboxy-lower alkyl)-carbamoyl group, an amino group of the side chain is present in free form or in alkylated form as mono- or di-lower alkylamino or in acylated form as lower alkanoylamino, as amino-lower alkanoylamino, as aryl-lower alkanoylamino wherein aryl has from 6 to 14 carbon atoms and is unsubstituted or substituted by lower alkyl, hydroxy, lower alkoxy, carboxy, carbamoyl or by sulfamoyl, as a lower alkoxycarbonylamino group, an arylmethoxycarbonylamino group wherein aryl has from 6 to 14 carbon atoms, as piperidyl-1-carbonyl, morpholinocarbonyl, thiomorpholinocarbonyl or as S,S-dioxothiomorpholinocarbonyl and/or a hydroxy group of the side chain is present in free form or in esterified or esterified form as a lower alkoxy, aryl-lower alkoxy, lower alkanoyloxy or lower alkoxycarbonyloxy group, - lower alkylsulfonyl, -2- or 3-pyrrolyl-, 2-thienyl-, 2-furyl-, 1-pyrazolyl-, 2-, 3- or 4-pyridyl-, 2-, 3- or 5-indolyl-, (1-methyl-,
2-methyl-, 5-methoxy-, 5-benzyloxy-, 5-chloro- or 4,5-dimethyl-indol-2-yl)-, (1-benzylindol-2-yl or -3-yl)-, 4,5,6,7-tetrahydroindol-2-yl-, (2-, 3- or 4-quinolyl or 4-hydroxyquinol-2-yl)-, (1-, 3- or 4-isoquinolyl or 1-oxo-1,2-dihydroisoquinol-3-yl)-, 3-pyrrolidinyl-, (3- or 4-hydroxypyrrolidin-2-yl)-, 5-oxopyrrolidin-2-yl-, (2- or
3-morpholinyl)-, (2- or 3-thiomorpholinyl)-, (S,S-dioxothiomorpholin-2- or -3-yl)-, (2- or 3-indolinyl)-, 1,2,3,4-tetrahydroquinol-2-, -3- or -4-yl)- or (1,2,3,4-tetrahydroisoquinol-1-, -2- or -3-yl)-methylsulfonyl, -phenyl- or 1- or 2-naphthyl-sulfonyl that is unsubstituted or mono- or di-substituted by lower alkyl, - lower alkoxysulfonyl, or - benzyloxysulfonyl or 1- or 2-naphthyloxysulfonyl, and wherein not more than one of the radicals R1 and R9 is hydrogen, and R2 and R8 are each independently of the other hydrogen or the same radical as R1 and R9, or pairs of substituents R1 and R9, and R2 and R8, each independently of the other, together with the bonding nitrogen atom and a radical selected from ethylene, trimethylene, tetramethylene and pentamethylene in which a carbon atom is optionally replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which is optionally unsaturated, form a heterocyclic ring, R3 is - cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms and is unsubstituted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxy-phosphoryl, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro, and/or by cyano and is bonded to lower alkyl, or - aryl-lower alkyl wherein aryl is selected from phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl and fluorenyl, which is unsubstituted or mono-to tri-substituted by lower alkyl, halo-lower alkyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano, wherein phenyl is optionally present up to three times, and wherein lower alkyl is unsubstituted or substituted by lower alkyl, heterocyclyl selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof, which is optionally fully or partially saturated, hydroxy, lower alkoxy, lower alkanoyloxy, acetoacetoxy, amino- or benzyloxycarbonylamino-lower alkanoyloxy, aryl-lower alkanoyloxy wherein aryl has from 6 to 10 carbon atoms, lower alkoxycarbonyloxy, mono- or di-lower alkylaminocarbonyloxy, aryloxycarbonyloxy wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyloxy wherein aryl has from 6 to 12 carbon atoms, sulfonyloxy, lower alkylsulfonyloxy, phenylsulfonyloxy, 2- or
4-toluenesulfonyloxy or 1- or 2-naphthylsulfonyloxy, amino, mono- or di-lower alkylamino, N-lower alkoxy-N-lower alkylamino, mono- or di-(phenyl- or naphthyl-lower alkyl)-amino, lower alkanoylamino, carboxy, esterified carboxy selected from lower alkoxycarbonyl, aryloxycarbonyl wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyl wherein aryl has from 6 to 12 carbon atoms, lower alkanoyl, lower alkylsulfonyl, hydroxy-lower alkoxyphosphoryl and di-lower alkoxyphosphoryl, carbamoyl, carbamoyl substituted by one or two radicals selected from lower alkyl, from carboxy-lower alkyl or lower alkoxycarbonyl-lower alkyl, from di-lower alkylamino-lower alkyl, from aminocarboxy-lower alkyl, from hydroxy-lower alkyl and from di-lower alkoxy-lower alkyl, or carbamoyl substituted by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene in which a carbon atom is optionally replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and which is optionally unsaturated, and also sulfamoyl, phosphono, benzofuranyl, oxo and/or by cyano and is unbranched or branched, R4 is hydrogen, R5 i s hydroxy and R6 is hydrogen, or R5 and R6 together are oxo and R7 is - lower alkyl, - cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms and is unsubstituted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro, and/or by cyano and is bonded to lower alkyl, - bicycloalkyl-lower alkyl wherein bicycloalkyl contains from 5 to 10 carbon atoms, - tricycloalkyl-lower alkyl wherein tricycloalkyl contains from 8 to 10 carbon atoms, - aryl-lower alkyl wherein aryl is selected from phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl and fluorenyl, which is unsubstituted or mono-to tri-substituted by lower alkyl, halo-lower alkyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy, N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, halogen, carboxy, lower alkoxycarbonyl, benzyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano, wherein phenyl is optionally present up to three times, and wherein lower alkyl is unsubstituted or substituted by lower alkyl, heterocyclyl selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof, which is optionally fully or partially saturated, hydroxy, lower alkoxy, lower alkanoyloxy, acetoacetoxy, amino- or benzyloxycarbonylamino-lower alkanoyloxy, aryl-lower alkanoyloxy wherein aryl has from 6 to 10 carbon atoms, lower alkoxycarbonyloxy, mono- or di-lower alkylaminocarbonyloxy, aryloxycarbonyloxy wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyloxy wherein aryl has from 6 to 12 carbon atoms, sulfonyloxy, lower alkylsulfonyloxy, phenylsulfonyloxy, 2- or 4-toluenesulfonyloxy, 1- or 2-naphthylsulfonyloxy, amino, mono- or di-lower alkylamino, N-lower alkoxy-N-lower alkylamino, mono- or di-(phenyl- or naphthyl-lower alkyl)amino, lower alkanoylamino, carboxy, esterified carboxy selected from lower alkoxycarbonyl, aryloxycarbonyl wherein aryl has from 6 to 10 carbon atoms, aryl-lower alkoxycarbonyl wherein aryl has from 6 to 12 carbon atoms, lower alkanoyl, lower alkylsulfonyl, hydroxy-lower alkoxyphosphoryl and di-lower alkoxyphosphoryl, carbamoyl, carbamoyl substituted by one or two radicals selected from lower alkyl, from carboxy-lower alkyl, from lower alkoxycarbonyl-lower alkyl, from di-lower alkylamino-lower alkyl, from aminocarboxy-lower alkyl, from hydroxy-lower alkyl and from di-lower alkoxy-lower alkyl, or carbamoyl substituted by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene in which a carbon atom is optionally replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen and is optionally unsaturated, and also sulfamoyl, phosphono, benzofuranyl, oxo (which is not bonded to the carbon atom that is linked to the nitrogen atom bonding the radical R7) and/or by cyano and is unbranched or branched, - heterocyclyl-lower alkyl, - hydroxy-lower alkyl, - lower alkoxy-lower alkyl, - phenoxy-lower alkyl or nitrophenoxy-lower alkyl, - naphthyloxy-lower alkyl, - lower alkanoyloxy-lower alkyl, - acetoacetoxy-lower alkyl, - arylmercapto-lower alkyl wherein aryl has from 6 to 10 carbon atoms, - amino-lower alkyl, - mono- or di-lower alkylamino-lower alkyl, - phenyl- or naphthyl-amino-lower alkyl, - lower alkanoylamino-lower alkyl, - piperazinylcarbonyl-lower alkyl substituted at the nitrogen atom by lower alkyl, - lower alkoxycarbonylamino-lower alkyl, - phenyl-lower alkoxycarbonylamino-lower alkyl, - aminocarbonylamino-lower alkyl, - N-phenyl-lower alkyl-N-lower alkylaminocarbonylamino-lower alkyl, - halo-lower alkyl, - carboxy-lower alkyl, - lower alkoxycarbonyl-lower alkyl, - 2-halo-lower alkoxycarbonyl-lower alkyl, - phenyl- or naphthyl-lower alkoxycarbonyl-lower alkyl, - heterocyclyl-lower alkoxycarbonyl-lower alkyl wherein heterocyclyl is selected from fully or partially saturated pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof, - lower alkylsulfonyl-lower alkyl, - arylsulfonyl-lower alkyl wherein aryl has from 6 to 10 carbon atoms, - carbamoyl-lower alkyl, - lower alkylcarbamoyl-lower alkyl, - di-lower alkylcarbamoyl-lower alkyl, - hydroxy-lower alkylcarbamoyl- or di(hydroxy-lower alkyl)carbamoyl-lower alkyl, - N-lower alkoxy-lower alkoxy-lower alkylcarbamoyl-lower alkyl, - carboxy-lower alkylcarbamoyl- or di(carboxy-lower alkyl)carbamoyl-lower alkyl, - carbamoyl-lower alkyl substituted at the nitrogen atom by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom is optionally replaced by nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen, wherein the radical so formed is optionally fully or partially unsaturated, - N-lower alkyl-N-heterocyclyl-lower alkylcarbamoyl-lower alkyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof, which is optionally fully or partially saturated, - sulfamoyl-lower alkyl, - N-(phenyl- or naphthyl-lower alkyl)sulfamoyl-lower alkyl, - sulfamoyl-lower alkyl substituted at the nitrogen atom by one radical selected from ethylene, trimethylene, tetramethylene and pentamethylene wherein a carbon atom is optionally replaced by nitrogen, lower alkyl-substituted nitrogen, oxygen, sulfur or by sulfur mono- or di-substituted by oxygen wherein the radical so formed is optionally fully or partially unsaturated, - oxo-lower alkyl (wherein oxo is not bonded to the carbon atom that is linked to the nitrogen atom that carries R7), - cyano-lower alkyl, - hydroxy-carboxy-lower alkyl, - .alpha.-naphthyloxy-carboxy-lower alkyl, - hydroxy-lower alkoxycarbonyl-lower alkyl, - .alpha.-naphthyloxy-lower alkoxycarbonyl-lower alkyl, - lower alkylcarbonyl-halo-lower alkyl, - .alpha.-naphthyloxyethoxycarbonyl-lower alkyl, - .alpha.-naphthyloxy-benzyloxycarbonyl-lower alkyl, - esterified hydroxy-lower alkoxycarbonyl-lower alkyl wherein the hydroxy group is esterified by lower alkanoyl, cycloalkyl-lower alkanoyl wherein cycloalkyl has from 3 to 7 carbon atoms, bicycloalkyl-lower alkanoyl wherein bicycloalkyl has from 5 to 10 carbon atoms, tricycloalkyl-lower alkanoyl wherein tricycloalkyl has from 8 to 10 carbon atoms, aryl-lower alkanoyl wherein aryl has from 6 to 14 carbon atoms and may be unsubstituted or mono- to tri-substituted by lower alkyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy or N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, di-lower alkoxyphosphoryl, carbamoyl, sulfamoyl, nitro and/or by cyano, lower alkoxycarbonyl, 2-halo-lower alkoxycarbonyl or by phenyl- or fluorenyl-lower alkoxycarbonyl, - dihydroxy-carboxy-lower alkyl, - dihydroxy-lower alkoxycarbonyl-lower alkyl, - dihydroxy-lower alkoxycarbonyl-lower alkyl esterified by lower alkanoyl, lower alkoxycarbonyl, phenyl- or fluorenyl-lower alkoxycarbonyl, lower alkylsulfonyl or by toluenesulfonyl, - .alpha.-naphthyloxy-di-lower alkylamino-lower alkyl, - .alpha.-naphthyloxy-carbamoyl-lower alkyl, - .alpha.-naphthyloxy-oxo-lower alkyl (wherein oxo is not bonded to the carbon atom that is linked to the nitrogen atom that carries R7) , or - .alpha.-naphthyloxy-cyano-lower alkyl, or a salt thereof, where a salt-forming group is present.

2. A compound of formula I according to claim 1, wherein R1 or R9, the amino acid is in the L-form.

3. A compound of formula I, or salt thereof, according to claim 1, wherein R7, in the heterocyclyl-lower alkyl, the heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinolyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative thereof, which is optionally fully or partially saturated.

4. A compound of formula I, or salt thereof, according to claim 1, wherein R7, the heterocyclyl-lower alkyl is 4-pyrrolidinylmethyl, 1-imidazolylmethyl, 2-pyridylmethyl, 3-pyridylmethyl, quinolin-2-ylmethyl or indol-2-ylmethyl.
5. A compound of formula I

wherein 195a R1 and R9 are each independently of the other hydrogen; lower alkanoyl; aryl-lower alkanoyl wherein aryl is phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl and may be unsubstituted or mono-to tri-substituted by lower alkyl, halo-lower alkyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy, N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylaminosulfonyl, nitro and/or by cyano, wherein phenyl may be present up to three times, and wherein lower alkanoyl is unsubstituted or substituted by carbamoyl or by carbamoyl substituted at the nitrogen atom by one or two radicals selected from lower alkyl, carboxy-lower alkyl, lower alkoxycarbonyl-lower alkyl, di-lower alkylamino-lower alkyl, amino-carboxy-lower alkyl, hydroxy-lower alkyl and di-lower alkoxy-lower alkyl; heterocyclyl-lower alkanoyl wherein lower alkanoyl is unsubstituted and wherein heterocyclyl is selected from thienyl, furyl, pyranyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, tetrazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, azepinyl, indolyl, benzimidazolyl, 1H-indazolyl, quinolyl, isoquinolyl, quinoxalinyl, quinazolinyl, cinnolyl, purinyl, pteridinyl, naphthyridinyl, 4H-quinolizinyl, 3,1-benzofuranyl, 4,1-benzoxazinyl, 4,1-benzothiazinyl, cyclohexa[b]pyrrolyl, cyclohepta[b]pyrrolyl, cyclohexa [d] pyrazolyl, cyclohexa [b] pyridyl, cyclohexa[b]pyrazinyl, cyclohexa[b]pyrimidinyl, cyclohexa[b]-1,4-oxazinyl, cyclohexa[b]-1,4-thiazinyl, pyrrolidinyl, pyrrolinyl, imidazolidyl, 2-imidazolinyl, 2,3-dihydropyridyl, piperidyl, piperazinyl, 2,3,5,6-tetrahydropyrazinyl, morpholinyl, thiomorpholinyl, S,S-dioxo-thiomorpholinyl, indolinyl, isoindolinyl, 4,5,6,7-tetrahydroindolyl, 1,2,3,4-tetrahydroquinolyl, 1,2,3,4-tetrahydroisoquinolyl, chromanyl, thiochromanyl, 1,2,3,4-tetrahydro-3,1-benzodiazinyl, 3,4-dihydro-3H-4,1-benzoxazinyl and 3,4-dihydro-3H-4,1-benzothiazinyl, the mentioned heterocyclyl radicals being unsubstituted or substituted by lower alkyl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, hydroxy-lower alkyl, lower alkoxy-lower alkyl, phenoxy- or naphthoxy-lower alkyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, lower alkanoyloxy-lower alkyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, lower alkoxycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyloxy-lower alkyl, amino-lower alkyl, carboxy-lower alkyl, hydroxy, lower alkoxy, phenyl- or naphthyl-lower alkoxy, amino, lower alkylamino, di-lower alkylamino, carboxy, lower alkoxycarbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, halogen, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or dialkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, hydroxy- or carboxy-lower alkyl-carbamoyl, sulfamoyl, nitro, oxo and/or by cyano; amino-lower alkanoyl substituted at the amino nitrogen atom by heterocyclyl-lower alkanoyl wherein heterocyclyl-lower alkanoyl is as defined for heterocyclyl-lower alkanoyl R1 and R9; halo-lower alkanoyl containing up to three halogen atoms;
(N-heterocyclyl-lower alkylcarbamoyl)-lower alkanoyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinoyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, from morpholine and from thiomorpholine; lower alkoxycarbonyl;
aryl-lower alkoxycarbonyl wherein aryl is phenyl, biphenylyl, 1- or 2-naphthyl, fluorenyl, or phenyl mono- or poly-substituted by lower alkyl, hydroxy, lower alkoxy, halogen and/or by nitro; heterocyclyl-lower alkoxycarbonyl wherein heterocyclyl is selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, oxazolyl, thiazolyl, pyridyl, pyrazinyl, pyrimidinyl, indolyl, quinolyl, isoquinoyl, quinoxalinyl, .beta.-carbolinyl and a benzo-fused, cyclopenta-, cyclohexa- or cyclohepta-fused derivative of those radicals, which may also be fully or partially saturated, or from morpholine or thiomorpholine and is unsubstituted or substituted by lower alkyl; lower alkylsulfonyl; morpholinosulfonyl, thiomorpholinosulfonyl, piperidinosulfonyl, 4-methylpiperazinylsulfonyl or piperazinosulfonyl; N-heterocyclyl-lower alkyl-N-lower alkylcarbamoyl wherein heterocyclyl is selected from thienyl, furyl, pyranyl, pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, azepinyl, indolyl, benzimidazolyl, 1H-indazolyl, quinolyl, isoquinoyl, quinoxalinyl, quinazolinyl, cinnolyl, purinyl, pteridinyl, naphthyridinyl, 4H-quinolizinyl, 3,1-benzofuranyl, benz [e] indolyl, 4,1-benzoxazinyl, 4,1-benzothiazinyl, carbazolyl, .beta.-carbolinyl, phenazinyl, phenanthridyl, acridyl, phenoxazinyl, phenothiazinyl, 1-azaacenaphthenyl, cyclohexa [b] pyrrolyl, cyclohepta [b) pyrrolyl, cyclohexa [d] pyrazolyl, cyclohexa [b] pyridyl, cyclohexa [b] pyrazinyl, cyclohexa [b] pyrimidinyl, cyclohexa[b]-1,4-oxazinyl, cyclohexa[b]-1,4-thiazinyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, 2-imidazolinyl, 2,3-dihydropyridyl, piperidyl, piperazinyl, 2,3,5,6-tetrahydropyrazinyl, morpholinyl, thiomorpholinyl, S,S-dioxothiomorpholinyl, indolinyl, isoindolinyl, 4,5,6,7-tetrahydroindolyl, 1,2,3,4-tetrahydroquinolyl, 1,2,3,4-tetrahydroisoquinolyl, chromanyl, thiochromanyl, 1,2,3,4-tetrahydro-3,1-benzodiazinyl, 3,4-dihydro-3H-4,1-benzoxazinyl, 3,4-dihydro-3H-4,1-benzothiazinyl, 2,3,4,5-tetrahydro-1H-5,1-benzazepinyl and 5,6-dihydrophenanthridinyl, the mentioned radicals being unsubstituted or substituted by lower alkyl, phenyl, 1- or 2-naphthyl, phenyl-lower alkyl, hydroxy-lower alkyl, lower alkoxy-lower alkyl, phenoxy- or naphthoxy-lower alkyl, phenyl-lower alkoxy- or naphthyl-lower alkoxy-lower alkyl, lower alkanoyloxy-lower alkyl, phenyl- or naphthyl-lower alkanoyloxy-lower alkyl, lower alkoxycarbonyloxy-lower alkyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyloxy-lower alkyl, amino-lower alkyl, carboxy-lower alkyl, hydroxy, lower alkoxy, phenyl- or naphthyl-lower alkoxy, amino, lower alkylamino, di-lower alkylamino, carboxy, lower alkoxycarbonyl, phenyl- or naphthyl-lower alkoxycarbonyl, halogen, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or dialkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, hydroxy- or carboxy-lower alkylcarbamoyl, sulfamoyl, nitro, oxo and/or by cyano; or an acyl radical of an amino acid the amino function of which is free or has been acylated by one of the other radicals mentioned hitherto for R1 and R9, the amino acids being selected from glycine, alanine, valine, norvaline, leucine, isoleucine, norleucine, serine, homoserine, threonine, methionine, cysteine, proline, trans-3- and trans-4-hydroxyproline, phenylalanine, tyrosine, 4-aminophenylalanine, 4-chlorophenylalanine, 4-carboxyphenylalanine, .beta.-phenylserine, phenylglycine, .alpha.-naphthylalanine, cyclohexylalanine, cyclohexylglycine, tryptophan, indoline-2-carboxylic acid, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, aspartic acid, asparagine, aminomalonic acid, aminomalonic acid monoamide, glutamic acid, glutamine, histidine, arginine, lysine, .delta.-hydroxylysine, ornithine, 3-aminopropanoic acid, .alpha.,.gamma.-diaminobutyric acid and .alpha.,.beta.-diaminopropionic acid, wherein each of the mentioned amino acid residues (with the exception of glycine) is in the D-, L- or (D, L)-form; with the proviso that not more than one of the radicals R1 and R9 is hydrogen, R2, R4, R6 and R8 are hydrogen, R3 is lower alkyl; cycloalkyl-lower alkyl wherein cycloalkyl has from 3 to 7 carbon atoms and may be unsubstituted or mono- to tri-substituted by lower alkyl, halo-lower alkyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy, N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl or di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylaminocarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano; or is aryl-lower alkyl wherein aryl is phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl and is unsubstituted or mono- to tri-substituted by lower alkyl, isopropyl, halo-lower alkyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy, N,N-di-lower alkylcarbamoyl-lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, halogen, carboxy, lower alkoxycarbonyl, phenyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano, wherein phenyl may be present up to three times, R5 is hydroxy, and R7 is unsubstituted lower alkyl; or cycloalkyl-lower alkyl as last described for cycloalkyl-lower alkyl R3;
or aryl-lower alkyl wherein aryl is phenyl, indenyl, indanyl, naphthyl, anthryl, phenanthryl, acenaphthyl or fluorenyl and is unsubstituted or mono- to tri-substituted by lower alkyl, isopropyl, halo-lower alkyl, phenyl, 1- or 2-naphthyl, hydroxy, lower alkoxy, carbamoyl-lower alkoxy, N-lower alkylcarbamoyl-lower alkoxy, N,N-di-lower alkylcarbamoyl- lower alkoxy, amino, mono- or di-lower alkylamino, lower alkanoylamino, halogen, carboxy, lower alkoxycarbonyl, benzyl-, naphthyl- or fluorenyl-lower alkoxycarbonyl, lower alkanoyl, sulfo, lower alkylsulfonyl, phosphono, hydroxy-lower alkoxyphosphoryl, di-lower alkoxyphosphoryl, carbamoyl, mono- or di-lower alkylcarbamoyl, sulfamoyl, mono- or di-lower alkylsulfamoyl, nitro and/or by cyano, wherein phenyl may be present up to three times, or a salt thereof where at least one salt-forming group is present.
6. A compound of formula I
wherein R1 and R9 are each independently of the other hydrogen, lower alkanoyl, phenyl-lower alkanoyl, phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carbamoyl; morpholino-lower alkanoyl, thiomorpholino-lower alkanoyl, pyridyl-lower alkanoyl, quinolyl-lower alkanoyl, tetrazolyl-lower alkanoyl, amino-lower alkanoyl substituted at the amino nitrogen atom by N-morpholino- or N-thiomorpholino-carbonyl; halo-lower alkanoyl containing up to three halogen atoms, 2-(N-morpholino-lower alkylcarbamoyl)-lower alkanoyl, 2-(N-pyridyl-lower alkylcarbamoyl)-lower alkanoyl, 2(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-3-methyl-butyryl, lower alkoxycarbonyl, phenyl-lower alkoxycarbonyl, benzyloxycarbonyl, tetrahydrofuranyl-lower alkoxycarbonyl, lower alkylsulfonyl, morpholinosulfonyl, thiomorpholinosulfonyl, N-pyridyl-lower alkyl-N-lower alkylcarbamoyl, or an acyl radical of an amino acid selected from glycine, alanine, valine, leucine, isoleucine, glutamic acid and asparagine in the (D)-, (L)- or (D, L)-form, wherein the a-amino group is unsubstituted or acylated by a radical selected from lower alkanoyl, phenyl-lower alkanoyl, phenyl-lower alkanoyl wherein the lower alkanoyl radical is substituted by carbamoyl; morpholino-lower alkanoyl, thiomorpholino-lower alkanoyl, pyridyl-lower alkanoyl, quinolyl-lower alkanoyl, tetrazolyl-lower alkanoyl, amino-lower alkanoyl substituted at the amino nitrogen atom by N-morpholino- or N-thiomorpholino-carbonyl; halo-lower alkanoyl containing up to three halogen atoms, 2-(N-morpholino-lower alkylcarbamoyl)-lower alkanoyl, 2-(N-pyridyl-lower alkylcarbamoyl)-lower alkanoyl, 2(R,S)-(N-(2-pyridylmethyl)-carbamoyl)-3-methyl-butyryl, lower alkoxycarbonyl, phenyl-lower alkoxycarbonyl, benzyloxycarbonyl, tetrahydrofuranyl-lower alkoxycarbonyl, lower alkylsulfonyl, morpholinosulfonyl, thiomorpholinosulfonyl, and N-pyridyl-lower alkyl-N-lower alkylcarbamoyl, with the proviso that not more than one of the radicals R1 and R9 is hydrogen, R2, R4, R6 and R8 are hydrogen, R3 is lower alkyl; cyclohexyl-lower alkyl; or phenyl-lower alkyl that is unsubstituted or substituted by halogen, lower alkoxy or by cyano;

202a R5 is hydroxy, and R7 is lower alkyl; cyclohexyl-lower alkyl; or phenyl-lower alkyl that is unsubstituted or substituted by halogen, lower alkoxy or by cyano;
or a salt thereof where salt-forming groups are present.
7. The compound of formula I according to claim 1 wherein R1 and R9 are each the monovalent residue of the amino acid (L)-valine bonded via the carboxy group and acylated by benzyloxycarbonyl at the amino nitrogen atom, R2 and R8 are hydrogen, R3 is benzyl, R4 is hydrogen, R5 is hydroxy, R6 is hydrogen and R7 is benzyl, and the asymmetric carbon atoms carrying the radicals R3 and R5 are in the S-configuration, or a pharmacologically acceptable salt thereof.
8. The compound of formula I according to claim 1 wherein R1 and R9 are each the monovalent residue of the amino acid (L)-valine bonded via the carboxy group and acylated by 4-thiomorpholinocarbonyl at the amino nitrogen atom, R2 and R8 are hydrogen, R3 is benzyl, R4 is hydrogen, R5 is hydroxy, R6 is hydrogen and R7 is isobutyl, and the asymmetric carbon atoms carrying the radicals R3 and R5 are in the S-configuration, or a pharmacologically acceptable salt thereof.
9. A pharmaceutical composition comprising a compound of formula I according to any one of claims 1 to 8 or a pharmaceutically acceptable salt of such a compound having at least one salt-forming group together with a pharmaceutically acceptable carrier.
10. A use of a compound of formula I as defined in any one of claims 1 to 8 or a pharmaceutically acceptable salt of such a compound having at least one salt-forming group for the preparation of a pharmaceutical composition.
11. A use of a compound of formula I as defined in any one of claims 1 to 8 or a pharmaceutically acceptable salt of such a compound having at least one salt-forming group for preparation of a pharmaceutical composition for inhibiting the action of the enzyme HIV-gag-protease.
12. A compound according to any one of claims 1 to 8 or a pharmaceutically acceptable salt thereof wherein the compound has at least one salt-forming group for use in treatment of AIDS.
13. A process for the preparation of a compound of formula I according to claim 1, wherein the substituents are as defined in claim 1, or a salt thereof, which comprises a? adding a hydrazine derivative of the formula wherein the radicals R7 to R9 are as defined in claim 1, to an epoxide of the formula wherein the radicals R1 to R4 and R6 are as defined in claim 1, and free functional groups, with the exception of those participating in the reaction, are optionally in protected form, and removing any protecting groups present, or b) for the preparation of a compound of formula I
wherein R1 and R9 are acyl; sulfo; sulfonyl substituted by unsubstituted or substituted alkyl, aryl, heterocyclyl, alkoxy, which is unsubstituted or substituted, or by aryloxy; sulfamoyl that is unsubstituted or substituted at the nitrogen atom; or phosphoryl substituted by one or two identical or different radicals selected from substituted or unsubstituted alkyl, unsubstituted or substituted cycloalkyl, aryl, hydroxy, unsubstituted or substituted alkoxy, cycloalkoxy and aryloxy; R2 and R8 are hydrogen, unsubstituted or substituted alkyl, alkenyl or alkynyl, or heterocyclyl, and the remaining radicals R3 to R7 are as defined in claim 1, condensing an amino compound of the formula wherein the radicals R3 to R7 are as defined in claim 1, and R1, R2 and R8 are as defined immediately above, with an acid of the formula or with a reactive acid derivative thereof, wherein R9 is as defined immediately above, and free functional groups, with the exception of those participating in the reaction, are optionally in protected form, and removing any protecting groups present, or c) for the preparation of a compound of formula I
wherein R1 and R9 are acyl; sulfo; sulfonyl substituted by unsubstituted or substituted alkyl, aryl, heterocyclyl, alkoxy, which is unsubstituted or substituted, or by aryloxy; sulfamoyl that is unsubstituted or substituted at the nitrogen atom; or phosphoryl substituted by one or two identical or different radicals selected from substituted or unsubstituted alkyl, unsubstituted or substituted cycloalkyl, aryl, hydroxy, unsubstituted or substituted alkoxy, cycloalkoxy and aryloxy; R2 and R8 are hydrogen, unsubstituted or substituted alkyl, alkenyl or alkynyl, or heterocyclyl, and the remaining radicals R3 to R7, are as defined in claim 1, condensing an amino compound of the formula wherein the radicals R3 to R7 are as defined in claim 1, and R2, R8 and R9 are as defined immediately above, with an acid of the formula R1 -OH (VIII), or with a reactive acid derivative thereof, wherein R1 is as defined immediately above and free functional groups, with the exception of those participating in the reaction, are optionally in protected form, and removing any protecting groups present, or d) for the preparation of a compound of formula I
wherein R1 and R9 are two identical radicals selected from acyl; sulfo; sulfonyl substituted by unsubstituted or substituted alkyl, aryl, heterocyclyl, alkoxy, which is unsubstituted or substituted, or by aryloxy; sulfamoyl that is unsubstituted or substituted at the nitrogen atom; and phosphoryl that is substituted by one or two identical or different radicals selected from substituted or unsubstituted alkyl, unsubstituted or substituted cycloalkyl, aryl, hydroxy, unsubstituted or substituted alkoxy, cycloalkoxy and aryloxy; R2 and R8 are hydrogen, unsubstituted or substituted alkyl, alkenyl or alkynyl, or heterocyclyl, and the remaining radicals R3 to R7 are as defined in claim 1, condensing a diamino compound of formula wherein the radicals R3 to R7 are as defined in claim 1, and R2 and R8 are as defined immediately above, with an acid suitable for introducing the identical radicals R1 and R9 as defined immediately above, or with a reactive acid derivative thereof, wherein R1 and R9 are as defined in claim 1, and free functional groups, with the exception of those participating in the reaction, are optionally in protected form, and removing any protecting groups present, or e) for the preparation of a compound of formula I
wherein in place of the radical R7 there is a radical R7"
which is unsubstituted or substituted alkyl or cycloalkyl, in a compound of formula I' wherein R7' is hydrogen and the remaining radicals R1 to R6, R8 and R9 are as in claim 1, introducing the radical R7" by substitution with a compound of formula XII, R7"-X (XII) wherein X is a leaving group and R7" is unsubstituted or substituted alkyl or cycloalkyl, and free functional groups, with the exception of those participating in the reaction, are optionally in protected form, and removing any protecting groups present, or f) in a compound of formula I wherein the substituents are as defined in claim 1, with the proviso that, in the compound of formula I in question, at least one functional group is protected by protecting groups, and removing the protecting groups, and optionally, one or more further steps selected from: (i) converting a compound of formula I obtainable in accordance with any one of processes a) to f) above having at least one salt-forming group, into a salt;
(ii) converting an obtainable salt into a free compound or into a different salt; (iii) separating any isomeric mixtures that are obtainable; and (iv) converting a compound of formula I as defined in claim 1 into a different compound of formula I as defined in claim 1.
14. A compound of formula wherein R3 and R7 are as defined in claim 1, or a salt of such a compound where salt-forming groups are present.
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US5753652A (en) * 1991-07-03 1998-05-19 Novartis Corporation Antiretroviral hydrazine derivatives
US6071895A (en) 1992-03-11 2000-06-06 Narhex Limited Polar-substituted hydrocarbons
US5888992A (en) 1992-03-11 1999-03-30 Narhex Limited Polar substituted hydrocarbons
US5679688A (en) * 1992-03-11 1997-10-21 Narhex Limited Quinaldoyl-amine derivatives of oxo-and hydroxy-substituted hydrocarbons
AU681342B2 (en) * 1992-03-11 1997-08-28 Narhex Limited Amine derivatives of oxo- and hydroxy-substitued hydrocarbons
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US5559256A (en) * 1992-07-20 1996-09-24 E. R. Squibb & Sons, Inc. Aminediol protease inhibitors
DE59303870D1 (en) 1992-12-23 1996-10-24 Ciba Geigy Ag Antiretroviral hydrazine derivatives
US5461067A (en) * 1993-02-25 1995-10-24 Abbott Laboratories Retroviral protease inhibiting compounds
EP0626178A1 (en) * 1993-05-17 1994-11-30 Ciba-Geigy Ag Use of inhibitors of HIV-protease for the treatment of tumorous diseases
IL110898A0 (en) * 1993-09-10 1994-11-28 Narhex Australia Pty Ltd Polar-substituted hydrocarbons
AU3150395A (en) * 1994-08-09 1996-03-07 Abbott Laboratories Retroviral protease inhibiting 1,2,4-triazacycloheptanes
ES2177816T3 (en) 1995-11-21 2002-12-16 Novartis Ag DERIVATIVES OF AZAHEXANO AS ISOSTEROS DE SUBSTRATE OF ASPARTATO PROTEASAS RETROVIRICAS.
US5849911A (en) * 1996-04-22 1998-12-15 Novartis Finance Corporation Antivirally active heterocyclic azahexane derivatives
TW409125B (en) * 1996-04-22 2000-10-21 Novartis Ag Antivirally active heterocyclic azahexane derivatives
ES2251022T3 (en) * 1996-05-10 2006-04-16 Bayer Cropscience Ag NEW REPLACED PIRIDYLCETOENOLS.
AU2959397A (en) * 1996-05-31 1998-01-05 Novartis Ag Process for the preparation of hydrazine derivatives useful as intermediates for the preparation of peptide analogues
US6642261B2 (en) * 1997-11-21 2003-11-04 Athena Neurosciences, Inc. N-(aryl/heteroarylacety) amino acid esters, pharmaceutical compositions comprising same, and methods for inhibiting β-amyloid peptide release and/or its synthesis by use of such compounds
EP1299352B1 (en) * 2000-06-30 2005-12-28 Elan Pharmaceuticals, Inc. Compounds to treat alzheimer's disease
WO2008011116A2 (en) * 2006-07-21 2008-01-24 Gilead Sciences, Inc. Aza-peptide protease inhibitors
ES2574831T3 (en) 2006-07-21 2016-06-22 Gilead Sciences, Inc. Antiviral Protease Inhibitors
JOP20180009A1 (en) 2017-02-06 2019-01-30 Gilead Sciences Inc Hiv inhibitor compounds
TWI829205B (en) 2018-07-30 2024-01-11 美商基利科學股份有限公司 Anti-hiv compounds
CN115197118B (en) * 2022-06-21 2024-01-23 贵州医科大学 Synthesis method of 3, 3-disubstituted vulcanized oxindole derivative

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US5142056A (en) 1989-05-23 1992-08-25 Abbott Laboratories Retroviral protease inhibiting compounds
US4794109A (en) 1982-11-16 1988-12-27 Ciba-Geigy Corporation 6-hydroxy-lower alkylpenem compounds, pharmaceutical preparations that contain these compounds, and the use of the latter
FI870474A (en) 1986-02-07 1987-08-08 Ciba Geigy Ag MED SVAVELHALTIGA GRUPPER SUBSTITUERADE 5-AMINO-4-HYDROXIVALERYLDERIVAT.
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