TREA

SULFONYLTRYPTOPHANOLS

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  • Patent Application
  • 20080255117
  • Publication Number
    20080255117
  • Date Filed
    February 29, 2008
    16 years ago
  • Date Published
    October 16, 2008
    15 years ago
Information
Abstract
The present invention relates to sulfonyltryptophanols of the general formula I,
Description

The present invention relates to the use of sulfonyltryptophanols as FSH-receptor antagonists. The present invention also relates to novel sulfonyltryptophanols, process for their preparation, pharmaceutical compositions comprising the compounds according to the invention, their use for fertility control in men or women, and their use for the treatment and/or prevention of osteoporosis.


Follicle-stimulating hormone (FSH) and luteinizing hormone (LH) are together responsible for the control of male and female fertility and of the production of sex steroids.


In the female mammal, FSH controls the early ripening of ovarian primary follicles and the biosynthesis of sex steroids. In the advanced stage of differentiation (preantral follicles), the influence of LH becomes increasingly important for further development of the follicles until ovulation occurs.


In male mammals, FSH is primarily responsible for the differentiation and stimulation of Sertoli cells. Their function consists of assisting spermatogenesis on many levels. LH is primarily responsible for stimulating the Leydig cells and thus androgen production.


FSH, LH and TSH (thyrotropic hormone) together form the group of glycoprotein hormones which are formed in the pituitary and are secreted from there. Whereas the alpha subunit is common to the three hormones, their specificity of action is determined by the beta chain which is unique in each case. The molecular weight of FSH including the sugar portion is about 30 kD.


FSH and the other glycoprotein hormones act specifically via their selectively expressed G protein-coupled receptor (GPCR). FSH stimulates, through binding to its receptor, the association thereof with a stimulating G protein (Gs) which is thereby stimulated to hydrolyse guanosine triphosphate (GTP) and to activate the membrane-associated adenylate cyclase. Cyclic adenosine monophosphate (cAMP) is accordingly an important and readily quantifiable secondary messenger substance of FSH (G. Vassart, L. Pardo, S. Costagliola, Trends Biochem. Sci. 2004, 29, 119-126).


The importance of FSH for male fertility is the subject of intensive research. It has been possible to show that FSH influences several processes of spermatogenesis such as the proliferation of spermatogonia, the antiapoptotic effect on spermatogonia and spermatocytes and the stimulation of sperm maturation including motility thereof.


The following arguments are also in favour of the FSH receptor as target for male fertility control:

  • 1. The FSH receptor is exclusively expressed on Sertoli cells (high specificity).
  • 2. Contraceptive vaccination against FSH beta chain or the FSH receptor induces infertility in male primates (N. R. Mougdal, M. Jeyakumar, H. N. Krishnamurthy, S. Sridhar, H. Krishnamurthy, F. Martin, Human Reproduction Update 1997, 3, 335-346).
  • 3. Naturally occurring mutations in the FSH receptor or the FSH beta chain may lead to sub- or infertility in men (I. Huhtaniemi, Journal of Reproduction and Fertility 2000, 119, 173-186; L. C. Layman, P. G. McDonough, Molecular and Cellular Endocrinology 2000, 161, 9-17).
  • 4. Neutralizing FSH antiserum has no effect on testis weight and testosterone production (V. Sriraman, A. J. Rao, Molecular and Cellular Endocrionology 2004, 224, 73-82). Adverse effects of FSH blockade on androgen production therefore appear unlikely.


In line with these arguments, FSH antagonists are expected to be suitable for spermatogenesis inhibition (prevention) in men. Moreover, a suitable FSH antagonist may just as well lead to infertility in women, because it suppresses follicle ripening and thus also ovulation. On the other hand, the skilled person expects advantages from non-peptidergic FSH agonists when used to promote fertility in women (stimulation of follicle ripening). There are no reports of experience on the use of FSH or FSH agonists in male infertility, but specific indications are also conceivable in this connection.


New findings demonstrate that there is also a direct effect of FSH on cells of bone metabolism. There are two fundamentally different cell types in bones: osteoclasts and osteoblasts. While osteoclasts play a central role in bone resorption (breakdown of bone), osteoblasts simulate bone density (anabolic effect).


FSH receptors have been detected in osteoclasts but not in osteoblasts. In vitro, FSH stimulates bone resorption by mouse osteoclasts (Li Sun et al. Cell 2006; 125: 247-60). A clinical correlation between the height of the serum FSH levels and low bone density has been observed in postmenopausal women (Devleta et al, J. Bone Miner. Metab. 2004, 22: 360-4).


These findings among others suggest that FSH stimulates loss of bone mass, and accordingly FSH antagonists will display an antiresorptive effect on bone and are therefore suitable for the therapy and/or prevention of peri- and postmenopausal loss of bone mass and osteoporosis.


FSH receptor modulators are compounds that have a mixed profile of both FSH receptor antagonistic and/or FSH receptor agonistic properties. FSH receptor modulators of various compound classes of low molecular weight, have been reported on recently.


FSH receptor modulators are disclosed in WO 2004/056779, WO 2004/056780; J. Med. Chem. 2005, 48, 1697 [tetrahydroquinolines]; WO 02/70493, Bioorg. Med. Chem. Lett. 2004, 14, 1713 and 1717 [diketopiperazines]; and WO 01/47875 [sulphonamides]. FSH receptor agonists are disclosed in WO 02/09706; J. Comb. Chem. 2004, 6, 196 [Thiazolidinones]; WO 2003/020726 and WO 03/20727, Chem. Biochem. 2002, 10, 1023 {thieno[2,3-d]pyrimidines)}; WO 01/87287 [pyrazoles]; WO 00/08015 [carbazoles]; WO 06/117023, WO 06/117368, WO 06/117370, WO 06/117371, [hexahydroquinolines].


FSH receptor antagonists are disclosed in WO 03/004028 [tetrahydroquinolines], WO 02/09705 [thiazolidinones], WO 00/58277, Bioorg. Med. Chem. 2002, 10, 639 [sulphonic acids]; WO 00/58276, Endocr. 2002, 143, 3822; Synth. Comm. 2002, 32, 2695 [azo compounds]; US 2006/0199806, US 2006/0258644, US 2006/0258645, US 2006/0287522 [pyrrolobenzodiazepines], WO 2007/017289 [acyltryptophanols].


JP11-3432795 describes a broad scope of compounds of sulfonamide-type as a tumor necrosis factor alpha inhibitors. JP11-3432795 discloses sulfonyltryptophanols in claim 10 genericly and discloses one specific compound namely p-tolylethynyl-thiophene-2-sulfonic acid [1-hydroxymethyl-2-(1H-indol-3-yl)-ethyl]-amide [example 37].


In view of the prior art, the objective technical problem to be solved according to the present invention may therefore be seen in providing alternative means of controlling the fertility in men (male fertility control) or women (female contraception), or providing alternative treatment and/or prevention of osteoporosis.


The technical problem has been solved according to the present invention by the use of compounds of the formula I







in which

  • R1 may be hydrogen, C1-C6-alkyl, C3-C6-alkenyl, C3-C6-alkynyl, C3-C7-cycloalkyl, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6-alkyl)amino-C1-C6-alkylene, phenyloxy-C1-C6-alkylene;
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano, hydroxy, amino or the groups:







  • R2 may be hydrogen, halogen, cyano, —SO2Me, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkyloxy or benzyloxy,
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine;

  • R3 may be hydrogen, hydroxy, halogen, nitro, amino, cyano, C1-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C3-C7-cycloalkyl, hydroxy-C1-C6-alkylene, hydroxy-C3-C6-alkenylene, hydroxy-C3-C6-alkynylene, C1-C6-alkyloxy, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy, C3-C7-cycloalkyl-C1-C6-alkylenoxy, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkyloxy-C3-C6-alkenylene, C1-C6-alkyloxy-C3-C6-alkynylene, C1-C6-alkyloxyphenyl-C1-C6-alkylene, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6-alkyl)amino-C1-C6-alkylene, phenyloxy-C1-C6-alkylene;
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano, hydroxy, amino or the groups








  • R4, R5, R6 may be independently of one another hydrogen, hydroxy, halogen, nitro, amino, cyano, phenyl, C1-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C6-alkylene, C3-C7-heterocycloalkyl, where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano or the radicals:










    • or

    • independently of one another hydroxy-C1-C6-alkylene, hydroxy-C3-C6-alkenylene, hydroxy-C3-C6-alkynylene, C1-C6-alkyloxy, C3-C7-cycloalkyloxy, C3-C7-cycloalkyl-C1-C6-alkylenoxy, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkyloxy-C3-C6-alkenylene, C1-C6-alkyloxy-C3-C6-alkynylene, C1-C6-alkyloxyphenyl-C1-C6-alkylene, phenyloxy-C1-C6-alkylene,

    • C1-C6-alkylamino, di(C1-C6-alkyl)amino, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6)-alkylamino-C1-C6-alkylene, C3-C7-cycloalkyl-(C0-C6-alkyl)amino,

    • C1-C6-acyl-(C0-C6-alkyl)amido, C1-C6-alkylaminocarbonyl, di(C1-C6-alkyl)aminocarbonyl, (C3-C7-cycloalkyl)aminocarbonyl, di(C3-C7-cycloalkyl)aminocarbonyl, C3-C7-cycloalkyl-C1-C6-alkyleneaminocarbonyl,

    • C1-C6-alkylcarbonyl, C3-C7-cycloalkylcarbonyl,

    • carboxy, carboxamido [—C(O)NH2], C1-C6-alkyloxycarbonyl, C1-C3-alkylsulphanyl, C1-C6-alkysulphonyl, C3-C7-cycloalkylsulphonyl, C3-C7-cycloalkyl-C1-C6-alkylenesulphonyl,

    • C1-C6-alkylaminosulphonyl, di(C1-C6-alkyl)aminosulphonyl, (C3-C7-cycloalkyl)aminosulphonyl, di(C3-C7-cycloalkyl)aminosulphonyl, C3-C7-cycloalkyl-C1-C6-alkyleneaminosulphonyl, C1-C6-alkylsulphonylamido, —N(C0-C6-alkyl)-C(O)—C1-C6-alkyl, —N(C0-C6-alkyl)-C(O)—C3-C7-cycloalkyl, —N(C0-C6-alkyl)-C(O)—N-di(C0-C6-alkyl), —N(C0-C6-alkyl)-C(O)—O—(C0-C6)alkyl, —N(C0-C6-alkyl)-C(O)—NH—C3-C7-cycloalkyl, —N(C0-C6-alkyl)-SO2—C1-C6-alkyl, —N(C0-C6-alkyl)-SO2—C3-C7-cycloalkyl, —N(C0-C6-alkyl)-SO2—N-di(C0-C6-alkyl), —N(C0-C6-alkyl)-SO2—NH—(C3-C7)-cycloalkyl,

    • —C(O)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine, —C(O)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine, —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine, —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkyl)amine,

    • —S(O2)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine, —S(O2)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine, —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine, —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkylene)amine,

    • —O—C2-C6-alkylene-(C1-C6-alkyl)amine, —O—C2-C6-alkylene-[di(C1-C6-alkylene)]amine,

    • or the radicals:













  • R5 and R6 may together form heterocycloalkyl, cycloalkyl;

  • R7, R8 may be independently of one another hydrogen, methyl, ethyl, where the methyl and ethyl radicals may be fluorinated one or more times;

  • Q may be an aryl or heteroaryl group
    • or the group










    • in which

    • A is a monocyclic aryl or a monocyclic heteroaryl group;

    • V is a cycloalkylen, cycloalkenylen, heterocycloalkylen or heterocycloalkenylen group;



  • X may be a bond, C1-C4-alkylene, C2-C4-alkenylene, C2-C4-alkynylene;

  • W may be an aryl or heteroaryl group;


    where

  • R2 may substitute one or more positions of the aryl or heteroaryl ring in the indole residue;

  • R3 may substitute one or more positions of the aryl or heteroaryl ring in the radical Q and or the radical V.



The present invention relates to both possible enantiomeric forms at the stereocentre of the tryptophanol residue.


The unbranched C1-C6-alkyl groups for the radicals R1 to R6 may be for example a methyl, ethyl, propyl, butyl, pentyl or a hexyl group; and the branched C3-C6-alkyl groups for the radicals R1 to R6 may be an isopropyl, isobutyl, sec-butyl, tert-butyl, isopentyl, 2-methylbutyl, 1-methylbutyl, 1-ethylpropyl, neopentyl, 1,1-dimethylpropyl, 4-methylpentyl, 3-methylpentyl, 2-methylpentyl, 1-methylpentyl, 2-ethylbutyl, 1-ethylbutyl, 3,3-dimethylbutyl, 2,2-dimethylbutyl, 1,1-dimethylbutyl, 2,3-dimethylbutyl, 1,3-dimethylbutyl or a 1,2-dimethylbutyl group.


The branched or unbranched C3-C6-alkenyl groups for the radical R1 may be for example an allyl, (E)-2-methylvinyl, (Z)-2-methylvinyl, homoallyl, (E)-but-2-enyl, (Z)-but-2-enyl, (E)-but-1-enyl, (Z)-but-1-enyl, pent-4-enyl, (E)-pent-3-enyl, (Z)-pent-3-enyl, (E)-pent-2-enyl, (Z)-pent-2-enyl, (E)-pent-1-enyl, (Z)-pent-1-enyl, hex-5-enyl, (E)-hex-4-enyl, (Z)-hex-4-enyl, (E)-hex-3-enyl, (Z)-hex-3-enyl, (E)-hex-2-enyl, (Z)-hex-2-enyl, (E)-hex-1-enyl, (Z)-hex-1-enyl, isopropenyl, 2-methylprop-2-enyl, 1-methylprop-2-enyl, 2-methylprop-1-enyl, (E)-1-methylprop-1-enyl, (Z)-1-methylprop-1-enyl, 3-methylbut-3-enyl, 2-methylbut-3-enyl, 1-methylbut-3-enyl, 3-methylbut-2-enyl, (E)-2-methylbut-2-enyl, (Z)-2-methylbut-2-enyl, (E)-1-methylbut-2-enyl, (Z)-1-methylbut-2-enyl, (E)-3-methylbut-1-enyl, (Z)-3-methylbut-1-enyl, (E)-2-methylbut-1-enyl, (Z)-2-methylbut-1-enyl, (E)-1-methylbut-1-enyl, (Z)-1-methylbut-1-enyl, 1,1-dimethylprop-2-enyl, 1-ethylprop-1-enyl, 1-propylvinyl, 1-isopropylvinyl, 4-methylpent-4-enyl, 3-methylpent-4-enyl, 2-methylpent-4-enyl, 1-methylpent-4-enyl, 4-methylpent-3-enyl, (E)-3-methylpent-3-enyl, (Z)-3-methylpent-3-enyl, (E)-2-methylpent-3-enyl, (Z)-2-methylpent-3-enyl, (E)-1-methylpent-3-enyl, (Z)-1-methylpent-3-enyl, (E)-4-methylpent-2-enyl, (Z)-4-methylpent-2-enyl, (E)-3-methylpent-2-enyl, (Z)-3-methylpent-2-enyl, (E)-2-methylpent-2-enyl, (Z)-2-methylpent-2-enyl, (E)-1-methylpent-2-enyl, (Z)-1-methylpent-2-enyl, (E)-4-methylpent-1-enyl, (Z)-4-methylpent-1-enyl, (E)-3-methylpent-1-enyl, (Z)-3-methylpent-1-enyl, (E)-2-methylpent-1-enyl, (Z)-2-methylpent-1-enyl, (E)-1-methylpent-1-enyl, (Z)-1-methylpent-1-enyl, 3-ethylbut-3-enyl, 2-ethylbut-3-enyl, 1-ethylbut-3-enyl, (E)-3-ethylbut-2-enyl, (Z)-3-ethylbut-2-enyl, (E)-2-ethylbut-2-enyl, (Z)-2-ethylbut-2-enyl, (E)-1-ethylbut-2-enyl, (Z)-1-ethylbut-2-enyl, (E)-3-ethylbut-1-enyl, (Z)-3-ethylbut-1-enyl, 2-ethylbut-1-enyl, (E)-1-ethylbut-1-enyl, (Z)-1-ethylbut-1-enyl, 2-propylprop-2-enyl, 1-propylprop-2-enyl, 2-isopropylprop-2-enyl, 1-isopropylprop-2-enyl, (E)-2-propylprop-1-enyl, (Z)-2-propylprop-1-enyl, (E)-1-propylprop-1-enyl, (Z)-1-propylprop-1-enyl, (E)-2-isopropylprop-1-enyl, (Z)-2-isopropylprop-1-enyl, (E)-1-isopropylprop-1-enyl, (Z)-1-isopropylprop-1-enyl, (E)-3,3-dimethylprop-1-enyl, (Z)-3,3-dimethylprop-1-enyl- or a 1-(1,1-dimethylethyl)ethenyl group.


The C3-C6-alkynyl groups for the radical R1 may be for example a prop-1-ynyl, prop-2-ynyl, but-1-ynyl, but-2-ynyl, but-3-ynyl, pent-1-ynyl, pent-2-ynyl, pent-3-ynyl, pent-4-ynyl, hex-1-ynyl, hex-2-ynyl, hex-3-ynyl, hex-4-ynyl, hex-5-ynyl, 1-methylprop-2-ynyl, 2-methylbut-3-ynyl, 1-methylbut-3-ynyl, 1-methylbut-2-ynyl, 3-methylbut-1-ynyl, 1-ethylprop-2-ynyl, 3-methylpent-4-ynyl, 2-methylpent-4-ynyl, 1-methylpent-4-ynyl, 2-methylpent-3-ynyl, 1-methylpent-3-ynyl, 4-methylpent-2-ynyl, 1-methylpent-2-ynyl, 4-methylpent-1-ynyl, 3-methylpent-1-ynyl, 2-ethylbut-3-ynyl, 1-ethylbut-3-ynyl, 1-ethylbut-2-ynyl, 1-propylprop-2-ynyl, 1-isopropylprop-2-ynyl, 2,2-dimethylbut-3-ynyl, 1,1-dimethylbut-3-ynyl, 1,1-dimethylbut-2-ynyl or a 3,3-dimethylbut-1-ynyl group.


The C2-C6-alkenyl groups for the radicals R2 to R6 may, in addition to the C3-C6-alkenyl groups mentioned for the radical R1, be for example a vinyl group.


The C2-C6-alkynyl groups for the radicals R2 to R6 may, in addition to the C3-C6-alkynyl groups mentioned for the radical R1, be for example an ethynyl group. The C1-C6-alkyloxy groups for the radicals R2 to R6 may be for example a methyloxy, ethyloxy, propyloxy, isopropyloxy, butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, pentyloxy, isopentyloxy, (2-methylbutyl)oxy, (1-methylbutyl)oxy, (1-ethylpropyl)oxy, neopentyloxy, (1,1-dimethylpropyl)oxy, hexyloxy, (4-methylpentyl)oxy, (3-methylpentyl)oxy, (2-methylpentyl)oxy, (1-methylpentyl)oxy, (1-ethylbutyl)oxy, (2-ethylbutyl)oxy, (3,3-dimethylbutyl)oxy, (2,2-dimethylbutyl)oxy, (1,1-dimethylbutyl)oxy, (2,3-dimethylbutyl)oxy, (1,3-dimethylbutyl)oxy or a (1,2-dimethylbutyl)oxy group.


The halogens for the radicals R2 to R6 are fluorine, chlorine, bromine or iodine.


The C1-C3-alkylsulphanyl groups for the radicals R4 to R6 may be for example a methylsulphanyl (CH3S—), ethylsulphanyl (CH3CH2S—), propylsulphanyl, isopropylsulphanyl group.


The C1-C6-alkylaminocarbonyl groups for the radicals R4 to R6 may be for example a methylaminocarbonyl-, ethylaminocarbonyl-, propylaminocarbonyl-, isopropylaminocarbonyl-, butylaminocarbonyl-, isobutylaminocarbonyl-, sec-butylaminocarbonyl-, tert-butylaminocarbonyl-, pentylaminocarbonyl-, isopentylaminocarbonyl-, (2-methylbutyl)aminocarbonyl-, (1-methylbutyl)aminocarbonyl-, (1-ethylpropyl)aminocarbonyl-, neo-pentylaminocarbonyl-, (1,1-dimethylpropyl)aminocarbonyl-, hexylaminocarbonyl-, (4-methylpentyl)aminocarbonyl-, (3-methylpentyl)aminocarbonyl-, (2-methylpentyl)aminocarbonyl-, (1-methylpentyl)aminocarbonyl-, (1-ethylbutyl)aminocarbonyl-, (2-ethylbutyl)aminocarbonyl-, (3,3-dimethylbutyl)aminocarbonyl-, (2,2-dimethylbutyl)aminocarbonyl-, (1,1-dimethylbutyl)aminocarbonyl-, (2,3-dimethylbutyl)aminocarbonyl-, (1,3-dimethylbutyl)aminocarbonyl- or a (1,2-dimethylbutyl)aminocarbonyl group.


The hydroxy-C1-C6-alkylene groups for the radicals R3 to R6 may be a hydroxymethyl (HOCH2—), 2-hydroxyethyl (HOCH2CH2—), 1-hydroxyethyl [CH3CH(OH)—], 3-hydroxypropyl (HOCH2CH2CH2—), 2-hydroxypropyl [CH3CH(OH)CH2—], 1-hydroxypropyl [CH3CH2CH(OH)—], 2-hydroxy-1-methylethyl [HOCH2CH(CH3)—], 1-hydroxy-1-methylethyl [(CH3)2C(OH)—], 4-hydroxybutyl (HOCH2CH2CH2CH2—), 3-hydroxybutyl [CH3CH(OH)CH2CH2—], 2-hydroxybutyl [CH3CH2CH(OH)CH2—], 1-hydroxybutyl [CH3CH2CH2CH(OH)—], 3-hydroxy-1-methylpropyl [HOCH2CH2CH(CH3)—], 2-hydroxy-1-methylpropyl [CH3CH(OH)CH(CH3)—], 1-hydroxy-1-methylpropyl [CH3CH2C(CH3)(OH)—], 1-(hydroxymethyl)propyl [CH3CH(CH2OH)—], 3-hydroxy-2-methylpropyl [HOCH2CH(CH3)CH2—], 2-hydroxy-2-methylpropyl [(CH3)2C(OH)CH2—], 1-hydroxy-2-methylpropyl [CH3CH(CH3)CH(OH)—] or a 2-hydroxy-1,1-dimethylethyl group [HOCH2C(CH3)2—].


The heterocycloalkyl groups which may form the radicals R4 and R5 together may be for example the following groups:







The cycloalkyl groups which may form the radicals R4 and R5 together may be for example the following groups:







The C3-C7-cycloalkyl groups for the radicals R1 to R6 may be for example a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl group.


The C3-C7-heterocycloalkyl groups for the radicals R1 to R6 may be for example a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl group in which one or two carbon atoms of the ring are replaced independently of one another by an oxygen, nitrogen or sulphur atom.


The monocyclic aryl group for A may be for example a phenyl group which is linked via substitutable positions


The aryl group for W or Q may be for example a phenyl, naphthyl group which is linked via substitutable positions.


The monocylic heteroaryl group for A may be for example a pyridinyl, pyrimidinyl, furanyl, thienyl, oxazolyl, isoxazolyl, thiazolyl, pyrrolyl, pyrazolyl or an imidazolyl group which is linked via substitutable positions.


The heteroaryl group for W or Q may be for example a pyridinyl, pyrimidinyl, quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, phthalazinyl, 1.5-naphthyridinyl, 1,6-naphthyridinyl, 1,7-naphthyridinyl, 1,8-naphthyridinyl, benzofuranyl, benzothienyl, 1,3-benzodioxolyl, 2,1,3-benzothiadiazolyl, indolyl, indazolyl, furanyl, thienyl, oxazolyl, isoxazolyl, thiazolyl, pyrrolyl, pyrazolyl or an imidazolyl group which is linked via substitutable positions.


The heterocycloalkylen groups for V may be for example the following groups:










The heterocycloalkenylen groups for V may be for example the following groups:







The cycloalkylen groups for V may be for example the following groups:







The cycloalkenylen groups for V may be for example the following groups:







The C1-C4-alkylene groups for the radicals X may be for example a methylene (—CH2—), ethylidene [—CH(CH3)—], ethylene (—CH2CH2—), prop-1,3-ylene (—CH2CH2CH2—), prop-1,2-ylene [—CH2CH(CH3)—], but-1,4-ylene (—CH2CH2CH2CH2—), but-1,3-ylene [—CH2CH2CH(CH3)—], but-1,2-ylene [—CH2CH(CH2CH3)—], but-2,3-ylene [—CHCH(CH3)—], 2-methylprop-1,2-ylene [—CH2C(CH3)2—] or a 2-methylprop-1,3-ylene group [—CH2CH(CH3)CH2—].


The C2-C4-alkenylene groups for the radical X may be for example an ethen-1,2-ylidene (—CH═CH—), prop-2-en-1,3-ylidene (—CH2—CH═CH—), prop-1-en-1,3-ylidene (—CH═CH—CH2—), but-1-en-1,4-ylidene (—CH═CH—CH2—CH2—), but-2-en-1,4-ylidene (—CH2—CH═CH—CH2—) or a but-3-en-1,4-ylidene group (—CH2—CH2—CH═CH—).


The C2-C4-alkynylene groups for the radical X may be for example an ethyn-1,2-ylidene (—C≡C—), prop-2-yn-1,3-ylidene (—CH2—C≡C—), prop-1-yn-1,3-ylidene (—C≡C—CH2—), but-1-yn-1,4-ylidene (—C≡C—CH2—CH2—), but-2-yn-1,4-ylidene (—CH2—C≡C—CH2—) or a but-3-yn-1,4-ylidene group (—CH2—CH2—C≡C—).


The C1-C3-alkyleneoxy groups for the radical X may be for example an oxymethylene (—O—CH2—), methyleneoxy (—CH2—O—), ethane-1,2-diyloxy (—CH2—CH2—O—), oxyethane-1,2-diyl (—O—CH2—CH2—), propane-1,3-diyloxy (—CH2—CH2—CH2—O—) or an oxypropane-1,3-diyl (—O—CH2—CH2—CH2—) group.


The C1-C3-alkyleneoxy-C1-C3-alkyl groups for the radical X may be for example an oxybis(methylene) (—CH2—O—CH2—), methyleneoxyethane-2,1-diyl [—CH2—O—(CH2)2—], ethane-1,2-diyloxymethylene [—(CH2)2—O—CH2—], methyleneoxypropane-3,1-diyl [—CH2—O—(CH2)3—], propane-1,3-diyloxymethylene [—(CH2)3—O—CH2—], oxybis(ethane-2,1-diyl) [—(CH2)2—O—(CH2)2—], propane-1,3-diyloxyethane-2,1-diyl [—(CH2)3—O—(CH2)2—], ethane-1,2-diyloxypropane-3,1-diyl [—(CH2)2—O—(CH2)3—] or an oxybis(propane-3,1-diyl) group [—(CH2)3—O—(CH2)3—].


The C3-C7-cycloalkyloxy groups for the radicals R1 to R6 may be for example a cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy group.


The C1-C6-alkylamino groups for the radicals R1 to R6 may be for example methylamino, ethylamino, propylamino, isopropylamino, butylamino, isobutylamino, sec-butylamino, tert-butylamino, pentylamino, isopentylamino, (2-methylbutyl)amino, (1-methylbutyl)amino, (1-ethylpropyl)amino, neopentylamino, (1,1-dimethylpropyl)amino, hexylamino, (4-methylpentyl)amino, (3-methylpentyl)amino, (2-methylpentyl)amino, (1-methylpentyl)amino, (1-ethylbutyl)amino, (2-ethylbutyl)amino, (3,3-dimethylbutyl)amino, (2,2-dimethylbutyl)amino, (1,1-dimethylbutyl)amino, (2,3-dimethylbutyl)amino, (1,3-dimethylbutyl)amino or a (1,2-dimethylbutyl)amino group.


In the di(C1-C6-alkyl)amino groups for the radicals R1 to R6, each of the two radicals on the nitrogen atom of the dialkylamino group may be chosen independently of one another from the following radicals: possible examples are a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the C3-C7-cycloalkyl-C1-C6-alkyleneoxy groups for the radicals R1 to R6 it is possible to combine each of the C3-C7-cycloalkyl groups of the C3-C7-cycloalkyl-C1-C6-alkyleneoxy group, for example of a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group, independently of one another with each C0-C6-alkyleneoxy group, for example with a methyleneoxy, ethyleneoxy, propyleneoxy, butyleneoxy, pentyleneoxy, hexyleneoxy group.


In the hydroxy-C3-C6-alkenylene groups for the radicals R1 to R6 it is possible for the hydroxy group to be located on any desired position of the C3-C6-alkenyl group, for example of an allyl, (E)-2-methylvinyl, (Z)-2-methylvinyl, homoallyl, (E)-but-2-enyl, (Z)-but-2-enyl, (E)-but-1-enyl, (Z)-but-1-enyl, pent-4-enyl, (E)-pent-3-enyl, (Z)-pent-3-enyl, (E)-Pent-2-enyl-, (Z)-Pent-2-enyl-, (E)-Pent-1-enyl-, (Z)-Pent-1-enyl-, hex-5-enyl-, (E)-hex-4-enyl, (Z)-hex-4-enyl, (E)-hex-3-enyl, (Z)-hex-3-enyl, (E)-hex-2-enyl, (Z)-hex-2-enyl, (E)-hex-1-enyl, (Z)-hex-1-enyl, isopropenyl, 2-methylprop-2-enyl, 1-methylprop-2-enyl, 2-methylprop-1-enyl, (E)-1-methylprop-1-enyl, (Z)-1-methylprop-1-enyl, 3-methylbut-3-enyl, 2-methylbut-3-enyl, 1-methylbut-3-enyl, 3-methylbut-2-enyl, (E)-2-methylbut-2-enyl, (Z)-2-methylbut-2-enyl, (E)-1-methylbut-2-enyl, (Z)-1-methylbut-2-enyl, (E)-3-methylbut-1-enyl, (Z)-3-methylbut-1-enyl, (E)-2-methylbut-1-enyl, (Z)-2-methylbut-1-enyl, (E)-1-methylbut-1-enyl, (Z)-1-methylbut-1-enyl, 1,1-dimethylprop-2-enyl, 1-ethylprop-1-enyl, 1-propylvinyl, 1-isopropylvinyl, 4-methylpent-4-enyl, 3-methylpent-4-enyl, 2-methylpent-4-enyl, 1-methylpent-4-enyl, 4-methylpent-3-enyl, (E)-3-methylpent-3-enyl, (Z)-3-methylpent-3-enyl, (E)-2-methylpent-3-enyl, (Z)-2-methylpent-3-enyl, (E)-1-methylpent-3-enyl, (Z)-1-methylpent-3-enyl, (E)-4-methylpent-2-enyl, (Z)-4-methylpent-2-enyl, (E)-3-methylpent-2-enyl, (Z)-3-methylpent-2-enyl, (E)-2-methylpent-2-enyl, (Z)-2-methylpent-2-enyl, (E)-1-methylpent-2-enyl, (Z)-1-methylpent-2-enyl, (E)-4-methylpent-1-enyl, (Z)-4-methylpent-1-enyl, (E)-3-methylpent-1-enyl, (Z)-3-methylpent-1-enyl, (E)-2-methylpent-1-enyl, (Z)-2-methylpent-1-enyl, (E)-1-methylpent-1-enyl, (Z)-1-methylpent-1-enyl, 3-ethylbut-3-enyl, 2-ethylbut-3-enyl, 1-ethylbut-3-enyl, (E)-3-ethylbut-2-enyl, (Z)-3-ethylbut-2-enyl, (E)-2-ethylbut-2-enyl, (Z)-2-ethylbut-2-enyl, (E)-1-ethylbut-2-enyl, (Z)-1-ethylbut-2-enyl, (E)-3-ethylbut-1-enyl, (Z)-3-ethylbut-1-enyl, 2-ethylbut-1-enyl, (E)-1-ethylbut-1-enyl, (Z)-1-ethylbut-1-enyl, 2-propylprop-2-enyl, 1-propylprop-2-enyl, 2-isopropylprop-2-enyl, 1-isopropylprop-2-enyl, (E)-2-propylprop-1-enyl, (Z)-2-propylprop-1-enyl, (E)-1-propylprop-1-enyl, (Z)-1-propylprop-1-enyl, (E)-2-isopropylprop-1-enyl, (Z)-2-isopropylprop-1-enyl, (E)-1-isopropylprop-1-enyl, (Z)-1-isopropylprop-1-enyl, (E)-3,3-dimethylprop-1-enyl, (Z)-3,3-dimethylprop-1-enyl or a 1-(1,1-dimethylethyl)ethenyl group, and to be combined independently of one another.


In the hydroxy-C3-C6-alkynyl groups for the radicals R1 to R6 it is possible for the hydroxy group to be located at any desired position of the C3-C6-alkynyl group, for example of a prop-1-ynyl, prop-2-ynyl, but-1-ynyl, but-2-ynyl, but-3-ynyl, pent-1-ynyl, pent-2-ynyl, pent-3-ynyl, pent-4-ynyl, hex-1-ynyl, hex-2-ynyl, hex-3-ynyl, hex-4-ynyl, hex-5-ynyl, 1-methylprop-2-ynyl, 2-methylbut-3-ynyl, 1-methylbut-3-ynyl, 1-methylbut-2-ynyl, 3-methylbut-1-ynyl, 1-ethylprop-2-ynyl, 3-methylpent-4-ynyl, 2-methylpent-4-ynyl, 1-methylpent-4-ynyl, 2-methylpent-3-ynyl, 1-methylpent-3-ynyl, 4-methylpent-2-ynyl, 1-methylpent-2-ynyl, 4-methylpent-1-ynyl, 3-methylpent-1-ynyl, 2-ethylbut-3-ynyl, 1-ethylbut-3-ynyl, 1-ethylbut-2-ynyl, 1-propylprop-2-ynyl, 1-isopropylprop-2-ynyl, 2,2-dimethylbut-3-ynyl, 1,1-dimethylbut-3-ynyl, 1,1-dimethylbut-2-ynyl or a 3,3-dimethylbut-1-ynyl group.


In the C1-C6-alkyloxy-C3-C6-alkenylene groups for the radicals R1 to R6 it is possible for the C1-C6-alkyloxy group, for example a methyloxy, ethyloxy, propyloxy, isopropyloxy, butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, pentyloxy, isopentyloxy, (2-methylbutyl)oxy, (1-methylbutyl)oxy, (1-ethylpropyl)oxy, neopentyloxy, (1,1-dimethylpropyl)oxy, hexyloxy, (4-methylpentyl)oxy, (3-methylpentyl)oxy, (2-methylpentyl)oxy, (1-methylpentyl)oxy, (1-ethylbutyl)oxy, (2-ethylbutyl)oxy, (3,3-dimethylbutyl)oxy, (2,2-dimethylbutyl)oxy, (1,1-dimethylbutyl)oxy, (2,3-dimethylbutyl)oxy, (1,3-dimethylbutyl)oxy or a (1,2-dimethylbutyl)oxy group, to be located on any desired position of the C3-C6-alkenyl group, for example of an allyl, (E)-2-methylvinyl, (Z)-2-methylvinyl, homoallyl, (E)-but-2-enyl, (Z)-but-2-enyl, (E)-but-1-enyl, (Z)-but-1-enyl, pent-4-enyl, (E)-pent-3-enyl, (Z)-pent-3-enyl, (E)-pent-2-enyl, (Z)-pent-2-enyl, (E)-pent-1-enyl, (Z)-pent-1-enyl, hex-5-enyl, (E)-hex-4-enyl, (Z)-hex-4-enyl, (E)-hex-3-enyl, (Z)-hex-3-enyl, (E)-hex-2-enyl, (Z)-hex-2-enyl, (E)-hex-1-enyl, (Z)-hex-1-enyl, isopropenyl, 2-methylprop-2-enyl, 1-methylprop-2-enyl, 2-methylprop-1-enyl, (E)-1-methylprop-1-enyl, (Z)-1-methylprop-1-enyl, 3-methylbut-3-enyl, 2-methylbut-3-enyl, 1-methylbut-3-enyl, 3-methylbut-2-enyl, (E)-2-methylbut-2-enyl, (Z)-2-methylbut-2-enyl, (E)-1-methylbut-2-enyl, (Z)-1-methylbut-2-enyl, (E)-3-methylbut-1-enyl, (Z)-3-methylbut-1-enyl, (E)-2-methylbut-1-enyl, (Z)-2-methylbut-1-enyl, (E)-1-methylbut-1-enyl, (Z)-1-methylbut-1-enyl, 1,1-dimethylprop-2-enyl, 1-ethylprop-1-enyl, 1-propylvinyl, 1-isopropylvinyl, 4-methylpent-4-enyl, 3-methylpent-4-enyl, 2-methylpent-4-enyl, 1-methylpent-4-enyl, 4-methylpent-3-enyl, (E)-3-methylpent-3-enyl, (Z)-3-methylpent-3-enyl, (E)-2-methylpent-3-enyl, (Z)-2-methylpent-3-enyl, (E)-1-methylpent-3-enyl, (Z)-1-methylpent-3-enyl, (E)-4-methylpent-2-enyl, (Z)-4-methylpent-2-enyl, (E)-3-methylpent-2-enyl, (Z)-3-methylpent-2-enyl, (E)-2-methylpent-2-enyl, (Z)-2-methylpent-2-enyl, (E)-1-methylpent-2-enyl, (Z)-1-methylpent-2-enyl, (E)-4-methylpent-1-enyl, (Z)-4-methylpent-1-enyl, (E)-3-methylpent-1-enyl, (Z)-3-methylpent-1-enyl, (E)-2-methylpent-1-enyl, (Z)-2-methylpent-1-enyl, (E)-1-methylpent-1-enyl, (Z)-1-methylpent-1-enyl, 3-ethylbut-3-enyl, 2-ethylbut-3-enyl, 1-ethylbut-3-enyl, (E)-3-ethylbut-2-enyl, (Z)-3-ethylbut-2-enyl, (E)-2-ethylbut-2-enyl, (Z)-2-ethylbut-2-enyl, (E)-1-ethylbut-2-enyl, (Z)-1-ethylbut-2-enyl, (E)-3-ethylbut-1-enyl, (Z)-3-ethylbut-1-enyl, 2-ethylbut-1-enyl, (E)-1-ethylbut-1-enyl, (Z)-1-ethylbut-1-enyl, 2-propylprop-2-enyl, 1-propylprop-2-enyl, 2-isopropylprop-2-enyl, 1-isopropylprop-2-enyl, (E)-2-propylprop-1-enyl, (Z)-2-propylprop-1-enyl, (E)-1-propylprop-1-enyl, (Z)-1-propylprop-1-enyl, (E)-2-isopropylprop-1-enyl, (Z)-2-isopropylprop-1-enyl, (E)-1-isopropylprop-1-enyl, (Z)-1-isopropylprop-1-enyl, (E)-3,3-dimethylprop-1-enyl, (Z)-3,3-dimethylprop-1-enyl or a 1-(1,1-dimethylethyl)ethenyl group and to be combined independently of one another.


In the C1-C6-alkyloxy-C3-C6-alkynylene groups for the radicals R1 to R6 it is possible for the C1-C6-alkyloxy group, for example a methyloxy, ethyloxy, propyloxy, isopropyloxy, butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, pentyloxy, isopentyloxy, (2-methylbutyl)oxy, (1-methylbutyl)oxy, (1-ethylpropyl)oxy, neopentyloxy, (1,1-dimethylpropyl)oxy, hexyloxy, (4-methylpentyl)oxy, (3-methylpentyl)oxy, (2-methylpentyl)oxy, (1-methylpentyl)oxy, (1-ethylbutyl)oxy, (2-ethylbutyl)oxy, (3,3-dimethylbutyl)oxy, (2,2-dimethylbutyl)oxy, (1,1-dimethylbutyl)oxy, (2,3-dimethylbutyl)oxy, (1,3-dimethylbutyl)oxy or a (1,2-dimethylbutyl)oxy group, to be located at any desired position of the C3-C6-alkynyl group, for example of a prop-1-ynyl, prop-2-ynyl, but-1-ynyl, but-2-ynyl, but-3-ynyl, pent-1-ynyl, pent-2-ynyl, pent-3-ynyl, pent-4-ynyl, hex-1-ynyl, hex-2-ynyl, hex-3-ynyl, hex-4-ynyl, hex-5-ynyl, 1-methylprop-2-ynyl, 2-methylbut-3-ynyl, 1-methylbut-3-ynyl, 1-methylbut-2-ynyl, 3-methylbut-1-ynyl, 1-ethylprop-2-ynyl, 3-methylpent-4-ynyl, 2-methylpent-4-ynyl, 1-methylpent-4-ynyl, 2-methylpent-3-ynyl, 1-methylpent-3-ynyl, 4-methylpent-2-ynyl, 1-methylpent-2-ynyl, 4-methylpent-1-ynyl, 3-methylpent-1-ynyl, 2-ethylbut-3-ynyl, 1-ethylbut-3-ynyl, 1-ethylbut-2-ynyl, 1-propylprop-2-ynyl, 1-isopropylprop-2-ynyl, 2,2-dimethylbut-3-ynyl, 1,1-dimethylbut-3-ynyl, 1,1-dimethylbut-2-ynyl or a 3,3-dimethylbut-1-ynyl group, and to be combined independently of one another.


In the C1-C6-alkyloxyphenyl-C1-C6-alkylene groups for the radical R1 to R6 it is possible for the C1-C6-alkyloxy group to be selected independently of one another from methyloxy, ethyloxy, propyloxy, isopropyloxy, butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, pentyloxy, isopentyloxy, (2-methylbutyl)oxy, (1-methylbutyl)oxy, (1-ethylpropyl)oxy, neopentyloxy, (1,1-dimethylpropyl)oxy, hexyloxy, (4-methylpentyl)oxy, (3-methylpentyl)oxy, (2-methylpentyl)oxy, (1-methylpentyl)oxy, (1-ethylbutyl)oxy, (2-ethylbutyl)oxy, (3,3-dimethylbutyl)oxy, (2,2-dimethylbutyl)oxy, (1,1-dimethylbutyl)oxy, (2,3-dimethylbutyl)oxy, (1,3-dimethylbutyl)oxy or a (1,2-dimethylbutyl)oxy, and to be combined independently of one another with C1-C6-alkylene groups such as, for example, methylene, ethylene, propylene, butylene, pentylene, hexylene.


In the C3-C7-cycloalkyl-(C0-C6)-alkyleneamino groups of the radicals R3 to R6 it is possible for each of the C3-C7-cycloalkyl groups of the C3-C7-cycloalkyl-(C0-C6)-alkyleneamino group, for example of a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group, to be combined independently of one another with each C0-C6-alkylene group, for example with a bond, a methylene, ethylene, propylene, butylene, pentylene, hexylene group.


In the C1-C6-alkyloxy-C1-C6-alkylene groups for the radical R1 to R6, it is possible for the C1-C6-alkyloxy group to be selected independently for example from methyloxy, ethyloxy, propyloxy, isopropyloxy, butyloxy, isobutyloxy, sec-butyloxy, tert-butyloxy, pentyloxy, isopentyloxy, (2-methylbutyl)oxy, (1-methylbutyl)oxy, (1-ethylpropyl)oxy, neopentyloxy, (1,1-dimethylpropyl)oxy, hexyloxy, (4-methylpentyl)oxy, (3-methylpentyl)oxy, (2-methylpentyl)oxy, (1-methylpentyl)oxy, (1-ethylbutyl)oxy, (2-ethylbutyl)oxy, (3,3-dimethylbutyl)oxy, (2,2-dimethylbutyl)oxy, (1,1-dimethylbutyl)oxy, (2,3-dimethylbutyl)oxy, (1,3-dimethylbutyl)oxy or a (1,2-dimethylbutyl)oxy and to be combined independently of one another with C1-C6-alkylene groups such as, for example, methylene, ethylene, propylene, butylene, pentylene, hexylene.


In the di(C1-C6-alkyl)amino-C1-C6-alkylene group for the radical R1 it is possible for each of the two radicals on the nitrogen atom of the amino group to be selected independently for example from methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group, and to be combined with C1-C6-alkylene groups such as, for example, methylene, ethylene, propylene, butylene, pentylene, hexylene.


The C3-C7-cycloalkyl-C1-C6-alkylene groups for the radicals R1 to R6 may be for example a cyclopropyloxymethylene, cyclopropyloxyethylene, cyclopropyloxypropylene, cyclopropyloxybutylene, cyclopropyloxypentylene, cyclopropyloxyhexylene, cyclobutyloxymethylene, cyclobutyloxyethylene, cyclobutyloxypropylene, cyclobutyloxybutylene, cyclobutyloxypentylene, cyclobutyloxyhexylene, cyclopentyloxymethylene, cyclopentyloxyethylene, cyclopentyloxypropylene, cyclopentyloxybutylene, cyclopentyloxypentylene, cyclopentyloxyhexylene, cyclohexyloxymethylene, cyclohexyloxyethylene, cyclohexyloxypropylene, cyclohexyloxybutylene, cyclohexyloxypentylene, cyclohexyloxyhexylene, cycloheptyloxymethylene, cycloheptyloxyethylene, cycloheptyloxypropylene, cycloheptyloxybutylene, cycloheptyloxypentylene, cycloheptyloxyhexylen group.


In the C1-C6-alkylamino-C1-C6-alkylene groups for the radicals R1 to R6 it is possible for the C1-C6-alkylamino group to be selected independently for example from methylamino, ethylamino, propylamino, isopropylamino, butylamino, isobutylamino, sec-butylamino, tert-butylamino, pentylamino, isopentylamino, (2-methylbutyl)amino, (1-methylbutyl)amino, (1-ethylpropyl)amino, neopentylamino, (1,1-dimethylpropyl)amino, hexylamino, (4-methylpentyl)amino, (3-methylpentyl)amino, (2-methylpentyl)amino, (1-methylpentyl)amino, (1-ethylbutyl)amino, (2-ethylbutyl)amino, (3,3-dimethylbutyl)amino, (2,2-dimethylbutyl)amino, (1,1-dimethylbutyl)amino, (2,3-dimethylbutyl)amino, (1,3-dimethylbutyl)amino or a (1,2-dimethylbutyl)amino and to be combined with C1-C6-alkylene groups such as, for example, methylene, ethylene, propylene, butylene, pentylene, hexylene.


The phenyloxy-C1-C6-alkylene groups for the radicals R1 to R6 may be for example a phenyloxymethyl, phenyloxyethyl, phenyloxypropyl, phenyloxybutyl, phenyloxypentyl, phenyloxyhexyl group.


In the C1-C6-acyl-(C0-C6-alkyl)amido groups for the radicals R4 to R6, it is possible for each of the C1-C6-acyl groups, for example a formyl, acetyl, propionyl, 2-methylpropionyl, 2,2-dimethylpropionyl, butyryl, 2-methylbutyryl, 3-methylbutyryl, 2,2-dimethylbutyryl, 2-ethylbutyryl, pentanoyl, 2-methylpentanoyl, 3-methylpentanoyl, 4-methylpentanoyl or a hexanoyl group, to be combined independently of one another with each (C0-C6-alkyl)amido group, for example a hydrogen atom, a methylamido, ethylamido, propylamido, isopropylamido, butylamido, isobutylamido, sec-butylamido, tert-butylamido, pentylamido, isopentylamido, (2-methylbutyl)amido, (1-methylbutyl)amido, (1-ethylpropyl)amido, neopentylamido, (1,1-dimethylpropyl)amido, hexylamido, (4-methylpentyl)amido, (3-methylpentyl)amido, (2-methylpentyl)amido, (1-methylpentyl)amido, (1-ethylbutyl)amido, (2-ethylbutyl)amido, (3,3-dimethylbutyl)amido, (2,2-dimethylbutyl)amido, (1,1-dimethylbutyl)amido, (2,3-dimethylbutyl)amido, (1,3-dimethylbutyl)amido or a (1,2-dimethylbutyl)amido group.


The C1-C6-alkylaminocarbonyl groups for the radicals R4 to R6 may be for example a methylaminocarbonyl, ethylaminocarbonyl, propylaminocarbonyl, isopropylaminocarbonyl, butylaminocarbonyl, isobutylaminocarbonyl, sec-butylaminocarbonyl, tertbutylaminocarbonyl, pentylaminocarbonyl, isopentylaminocarbonyl, (2-methylbutyl)aminocarbonyl, (1-methylbutyl)aminocarbonyl, (1-ethylpropyl)aminocarbonyl, neopentylaminocarbonyl, (1,1-dimethylpropyl)aminocarbonyl, hexylaminocarbonyl, (4-methylpentyl)aminocarbonyl, (3-methylpentyl)aminocarbonyl, (2-methylpentyl)aminocarbonyl, (1-methylpentyl)aminocarbonyl, (1-ethylbutyl)aminocarbonyl, (2-ethylbutyl)aminocarbonyl, (3,3-dimethylbutyl)aminocarbonyl, (2,2-dimethylbutyl)aminocarbonyl, (1,1-dim ethylbutyl)aminocarbonyl, (2,3-dimethylbutyl)aminocarbonyl, (1,3-dimethylbutyl)aminocarbonyl or a (1,2-dimethylbutyl)aminocarbonyl group.


In the di(C1-C6-alkyl)aminocarbonyl groups for the radicals R4 to R6, each of the two C1-C6-alkyl radicals on the nitrogen atom of the di(C1-C6-alkyl)aminocarbonyl group may be independently of one another for example a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


The (C3-C7-cycloalkyl)aminocarbonyl groups for the radicals R4 to R6 may be for example a cyclopropylaminocarbonyl, cyclobutylaminocarbonyl, cyclopentylaminocarbonyl, cyclohexylaminocarbonyl or cycloheptylaminocarbonyl group.


In the di(C3-C7-cycloalkyl)aminocarbonyl groups for the radicals R4 to R6, each of the two C3-C7-cycloalkyl radicals on the nitrogen atom of the di(C3-C7-cycloalkyl)aminocarbonyl group may be independently of one another for example a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group.


In the C3-C7-cycloalkyl-C1-C6-alkyleneaminocarbonyl groups of the radicals R4 to R6 it is possible for each of the C3-C7-cycloalkyl groups of the C3-C7-cycloalkyl-C1-C6-alkyleneaminocarbonyl groups, for example of a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group, to be combined independently of one another with each C1-C6-alkyleneaminocarbonyl group, for example with a methyleneaminocarbonyl, ethyleneaminocarbonyl, propyleneaminocarbonyl, butyleneaminocarbonyl, pentyleneaminocarbonyl, hexyleneaminocarbonyl group.


The C1-C6-alkylcarbonyl groups for the radicals R4 to R6 may be for example a methylcarbonyl, ethylcarbonyl, propylcarbonyl, isopropylcarbonyl, butylcarbonyl, isobutylcarbonyl, sec-butylcarbonyl, tert-butylcarbonyl, pentylcarbonyl, isopentylcarbonyl, (2-methylbutyl)carbonyl, (1-methylbutyl)carbonyl, (1-ethylpropyl)carbonyl, neopentylcarbonyl, (1,1-dimethylpropyl)carbonyl, hexylcarbonyl, (4-methylpentyl)carbonyl, (3-methylpentyl)carbonyl, (2-methylpentyl)carbonyl, (1-methylpentyl)carbonyl, (1-ethylbutyl)carbonyl, (2-ethylbutyl)carbonyl, (3,3-dimethylbutyl)carbonyl, (2,2-dimethylbutyl)carbonyl, (1,1-dimethylbutyl)carbonyl, (2,3-dimethylbutyl)carbonyl, (1,3-dimethylbutyl)carbonyl or a (1,2-dimethylbutyl)carbonyl group.


The C3-C7-cycloalkylcarbonyl groups for the radicals R4 to R6 may be for example a cyclopropylcarbonyl, cyclobutylcarbonyl, cyclopentylcarbonyl, cyclohexylcarbonyl or cycloheptylcarbonyl group.


The C1-C6-alkyloxycarbonyl groups for the radicals R4 to R6 may be for example a methyloxycarbonyl, ethyloxycarbonyl, propyloxycarbonyl, isopropyloxycarbonyl, butyloxycarbonyl, isobutyloxycarbonyl, sec-butyloxycarbonyl, tert-butyloxycarbonyl, pentyloxycarbonyl, isopentyloxycarbonyl, (2-methylbutyl)oxycarbonyl, (1-methylbutyl)oxycarbonyl, (1-ethylpropyl)oxycarbonyl, neopentyloxycarbonyl, (1,1-dimethylpropyl)oxycarbonyl, hexyloxycarbonyl, (4-methylpentyl)oxycarbonyl, (3-methylpentyl)oxycarbonyl, (2-methylpentyl)oxycarbonyl, (1-methylpentyl)oxycarbonyl, (1-ethylbutyl)oxycarbonyl, (2-ethylbutyl)oxycarbonyl, (3,3-dimethylbutyl)oxycarbonyl, (2,2-dimethylbutyl)oxycarbonyl, (1,1-dimethylbutyl)oxycarbonyl, (2,3-dimethylbutyl)oxycarbonyl, (1,3-dimethylbutyl)oxycarbonyl or a (1,2-dimethylbutyl)oxycarbonyl group.


The C1-C6-alkylsulphonyl groups for the radicals R4 to R6 may be for example a methylsulphonyl, ethylsulphonyl, propylsulphonyl, isopropylsulphonyl, butylsulphonyl, iso-butylsulphonyl, sec-butylsulphonyl, tert-butylsulphonyl, pentylsulphonyl, isopentylsulphonyl, (2-methylbutyl)sulphonyl, (1-methylbutyl)sulphonyl, (1-ethylpropyl)sulphonyl, neopentylsulphonyl, (1,1-dimethylpropyl)sulphonyl, hexylsulphonyl, (4-methylpentyl)sulphonyl, (3-methylpentyl)sulphonyl, (2-methylpentyl)sulphonyl, (1-methylpentyl)sulphonyl, (1-ethylbutyl)sulphonyl, (2-ethylbutyl)sulphonyl, (3,3-dimethylbutyl)sulphonyl, (2,2-dimethylbutyl)sulphonyl, (1,1-dimethylbutyl)sulphonyl, (2,3-dimethylbutyl)sulphonyl, (1,3-dimethylbutyl)sulphonyl or a (1,2-dimethylbutyl)sulphonyl group.


The C3-C7-cycloalkylsulphonyl groups for the radicals R4 to R6 may be for example a cyclopropylsulphonyl, cyclobutylsulphonyl, cyclopentylsulphonyl, cyclohexylsulphonyl or cycloheptylsulphonyl group.


In the C3-C7-cycloalkyl-C1-C6-alkylenesulphonyl groups of the radicals R4 to R6 it is possible for each of the C3-C7-cycloalkyl groups of the C3-C7-cycloalkyl-C1-C6-alkylenesulphonyl groups, for example of a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group, to be combined independently of one another with each C1-C6-alkylenesulphonyl group, for example with a methylenesulphonyl, ethylenesulphonyl, propylenesulphonyl, butylenesulphonyl, pentylenesulphonyl, hexylenesulphonyl group. The C1-C6-alkylaminosulphonyl groups for the radicals R4 to R6 may be for example a methylaminosulphonyl, ethylaminosulphonyl, propylaminosulphonyl, isopropylaminosulphonyl, butylaminosulphonyl, isobutylaminosulphonyl, sec-butylaminosulphonyl, tert-butylaminosulphonyl, pentylaminosulphonyl, isopentylaminosulphonyl, (2-methylbutyl)aminosulphonyl, (1-methylbutyl)aminosulphonyl, (1-ethylpropyl)aminosulphonyl, neopentylaminosulphonyl, (1,1-dimethylpropyl)aminosulphonyl, hexylaminosulphonyl, (4-methylpentyl)aminosulphonyl, (3-methylpentyl)aminosulphonyl, (2-methylpentyl)aminosulphonyl, (1-methylpentyl)aminosulphonyl, (1-ethylbutyl)aminosulphonyl, (2-ethylbutyl)aminosulphonyl, (3,3-dimethylbutyl)aminosulphonyl, (2,2-dimethylbutyl)aminosulphonyl, (1,1-dimethylbutyl)aminosulphonyl, (2,3-dimethylbutyl)aminosulphonyl, (1,3-dimethylbutyl)aminosulphonyl or a (1,2-dimethylbutyl)aminosulphonyl group.


In the di(C1-C6-alkyl)aminosulphonyl groups for the radicals R4 to R6, each of the two C1-C6-alkyl radicals on the nitrogen atom of the di(C1-C6-alkyl)aminosulphonyl group may be independently of one another for example a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


The (C3-C7-cycloalkyl)aminosulphonyl groups for the radicals R4 to R6 may be for example a cyclopropylaminosulphonyl, cyclobutylaminosulphonyl, cyclopentylaminosulphonyl, cyclohexylaminosulphonyl or cycloheptylaminosulphonyl group.


In the di(C3-C7-cycloalkyl)aminosulphonyl groups for the radicals R4 to R6, each of the two C3-C7-cycloalkyl radicals on the nitrogen atom of the di(C3-C7-cycloalkyl)aminosulphonyl group may be independently of one another for example a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group.


In the C3-C7-cycloalkyl-C1-C6-alkyleneaminosulphonyl groups of the radicals R4 to R6, each of the C3-C7-cycloalkyl groups of the C3-C7-cycloalkyl-C1-C6-alkyleneaminosulphonyl groups, for example of a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group, can be combined independently of one another with each C1-C6-alkyleneaminosulphonyl group, for example with a methyleneaminosulphonyl, ethyleneaminosulphonyl, propyleneaminosulphonyl, butyleneaminosulphonyl, pentyleneaminosulphonyl, hexyleneaminosulphonyl group.


The C1-C6-alkylsulphonylamido groups for the radicals R4 to R6 may be for example a methylsulphonylamido, ethylsulphonylamido, propylsulphonylamido, isopropylsulphonylamido, butylsulphonylamido, isobutylsulphonylamido, sec-butylsulphonylamido, tert-butylsulphonylamido, pentylsulphonylamido, isopentylsulphonylamido, (2-methylbutyl)sulphonylamido, (1-methylbutyl)sulphonylamido, (1-ethylpropyl)sulphonylamido, neopentylsulphonylamido, (1,1-dimethylpropyl)sulphonylamido, hexylsulphonylamido, (4-methylpentyl)sulphonylamido, (3-methylpentyl)sulphonylamido, (2-methylpentyl)sulphonylamido, (1-methylpentyl)sulphonylamido, (1-ethylbutyl)sulphonylamido, (2-ethylbutyl)sulphonylamido, (3,3-dimethylbutyl)sulphonylamido, (2,2-dimethylbutyl)sulphonylamido, (1,1-dimethylbutyl)sulphonylamido, (2,3-dimethylbutyl)sulphonylamido, (1,3-dimethylbutyl)sulphonylamido or a (1,2-dimethylbutyl)sulphonylamido group.


In the —N(C0-C6-alkyl)-C(O)—C1-C6-alkyl groups of the radicals R4 to R6, each of the (C0-C6-alkyl) groups on the nitrogen atom of the —N(C0-C6-alkyl)-C(O)—C1-C6-alkyl groups, for example a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group, may be combined independently of one another with each C1-C6-alkyl group on the carbonyl group of the amide, for example with a methyl, ethyl, propyl, iso-propyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —N—(C0-C6-alkyl)-C(O)—C3-C7-cycloalkyl groups of the radicals R4 to R6, each of the (C0-C6-alkyl) groups on the nitrogen atom of the —N(C0-C6-alkyl)-C(O)—C1-C6-alkyl groups, for example a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group, may be combined independently of one another with each C3-C7-cycloalkyl group on the carbonyl group of the amide, for example with a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group.


In the —N(C0-C6-alkyl)-C(O)—N-di(C0-C6-alkyl) groups of the radicals R4 to R6, all three (C0-C6-alkyl) groups may be independently of one another a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —N(C0-C6-alkyl)-C(O)—O—(C0-C6-alkyl) groups of the radicals R4 to R6, both (C0-C6-alkyl) groups may be independently of one another a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —N(C0-C6-alkyl)-C(O)—NH—(C3-C7-cycloalkyl) groups of the radicals R4 to R6, each of the (C0-C6-alkyl) groups on the nitrogen atom of the —N(C0-C6-alkyl)-C(O)—NH—(C3-C7-cycloalkyl) groups, for example a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, iso-butyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group, may independently of one another be combined with each C3-C7-cycloalkyl group on the terminal nitrogen atom of the urea, for example with a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group.


In the —N(C0-C6-alkyl)-SO2—(C1-C6-alkyl) groups of the radicals R4 to R6, each of the (C0-C6-alkyl) groups on the nitrogen atom of the —N(C0-C6-alkyl)-SO2—(C1-C6-alkyl) group, for example a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group, may independently of one another be combined with each C1-C6-alkyl group on the sulphonyl group of the sulphonamide, for example with a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —N(C0-C6-alkyl)-SO2—C3-C7-cycloalkyl groups of the radicals R4 to R6, each of the (C0-C6-alkyl) groups on the nitrogen atom of the —N(C0-C6-alkyl)-SO2—C3-C7-cycloalkyl group, for example a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group, may be combined independently of one another with each C3-C7-cycloalkyl group on the sulphonyl group, for example with a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group.


In the —N(C0-C6-alkyl)-SO2—N-di(C0-C6-alkyl) groups of the radicals R4 to R6, all three (C0-C6-alkyl) groups may be independently of one another a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —N(C0-C6-alkyl)-SO2—NH—(C3-C7)-cycloalkyl groups of the radicals R4 to R6, the C0-C6-alkyl group of the —N(C0-C6-alkyl)-SO2—NH—(C3-C7)-cycloalkyl group, for example a hydrogen, a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group, may be combined independently of one another with each C3-C7-cycloalkyl group, for example with a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group.


In the —C(O)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine groups of the radicals R4 to R6, each of the C2-C6-alkylene groups on the nitrogen atom of the —C(O)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each C1-C6-alkyl group on the amino group, for example with a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —C(O)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine groups of the radicals R4 to R6, each of the C2-C6-alkylene groups on the nitrogen atom of the —C(O)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each of the two identically or different C1-C6-alkyl groups on the amino group, for example with a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl-, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine groups of the radicals R4 to R6, each of the (C2-C6-alkylene) groups of the —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each C3-C7-cycloalkyl group on the amine, for example with a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group.


In the —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkylene)amine groups of the radicals R4 to R6, each of the (C2-C6-alkylene) groups of the —C(O)—N(H)—C2-C6-alkylene-(C3-C6-cycloalkyl-C1-C6-alkylene)amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each C3-C7-cycloalkyl-C1-C6-alkylene group on the amine, for example with a cyclopropylmethylene, cyclopropylethylene, cyclopropylpropylene, cyclopropylbutylene, cyclopropylpentylene, cyclopropylhexylene, cyclobutylmethylene, cyclobutylethylene, cyclobutylpropylene, cyclobutylbutylene, cyclobutylpentylene, cyclobutylhexylene, cyclopentylmethylene, cyclopentylethylene, cyclopentylpropylene, cyclopentylhexylene, cyclohexylmethylene, cyclohexylethylene, cyclohexylpropylene, cyclohexylbutylene, cyclohexylpentylene, cyclohexylhexylene, cycloheptylmethylene, cycloheptylethylene, cycloheptylpropylene, cycloheptylbutylene, cycloheptylpentylene or cycloheptylhexylene group.


In the —S(O2)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine groups of the radicals R4 to R6, the (C2-C6-alkylene) groups of the —S(O2)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each C1-C6-alkyl group on the amino group, for example with a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —S(O2)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine groups of the radicals R4 to R6, the C2-C6-alkylene group of the —S(O2)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each of the two C1-C6-alkyl groups on the amino group, for example with a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neo-pentyl, (1,1-dimethylpropyl), hexyl-, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine groups of the radicals R4 to R6, the C2-C6-alkylene group of the —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each C3-C7-cycloalkyl group on the amino group, for example with a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl group.


In the —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkylene)amine groups of the radicals R4 to R6, each C2-C6-alkylene group of the —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkylene)amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each C3-C7-cycloalkyl-C1-C6-alkylene group on the amine, for example with a cyclopropylmethylene, cyclopropylethylene, cyclopropylpropylene, cyclopropylbutylene, cyclopropylpentylene, cyclopropylhexylene, cyclobutylmethylene, cyclobutylethylene, cyclobutylpropylene, cyclobutylbutylene, cyclobutylpentylene, cyclobutylhexylene, cyclopentylmethylene, cyclopentylethylene, cyclopentylpropylene, cyclopentylhexylene, cyclohexylmethylene, cyclohexylethylene, cyclohexylpropylene, cyclohexylbutylene, cyclohexylpentylene, cyclohexylhexylene, cycloheptylmethylene, cycloheptylethylene, cycloheptylpropylene, cycloheptylbutylene, cycloheptylpentylen or cycloheptylhexylene group.


In the —O—C2-C6-alkylene-(C1-C6-alkyl)amine groups of the radicals R4 to R6, the C2-C6-alkylene group of the —O—C2-C6-alkylene-(C1-C6-alkyl)amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with each C1-C6-alkyl group on the amino group, for example a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


In the —O—C2-C6-alkylene-[di(C1-C6-alkyl)]amine groups of the radicals R4 to R6, the C2-C6-alkylene group of the —O—C2-C6-alkylene-[di(C1-C6-alkyl)]amine group, for example an ethylene, propylene, butylene, pentylene or hexylene group, may be combined independently of one another with two freely selectable C1-C6-alkyl groups on the amino group, for example with a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, (2-methylbutyl), (1-methylbutyl), (1-ethylpropyl), neopentyl, (1,1-dimethylpropyl), hexyl-, (4-methylpentyl), (3-methylpentyl), (2-methylpentyl), (1-methylpentyl), (1-ethylbutyl), (2-ethylbutyl), (3,3-dimethylbutyl), (2,2-dimethylbutyl), (1,1-dimethylbutyl), (2,3-dimethylbutyl), (1,3-dimethylbutyl) or a (1,2-dimethylbutyl) group.


Preferred according to the present invention is the use of compounds of formula I in which

  • R3 may be hydroxy, halogen, nitro, amino, cyano, C1-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C3-C7-cycloalkyl, hydroxy-C1-C6-alkylene, hydroxy-C3-C6-alkenylene, hydroxy-C3-C6-alkynylene, C1-C6-alkyloxy, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy, C3-C7-cycloalkyl-C1-C6-alkylenoxy, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkyloxy-C3-C6-alkenylene, C1-C6-alkyloxy-C3-C6-alkynylene, C1-C6-alkyloxyphenyl-C1-C6-alkylene, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6-alkyl)amino-C1-C6-alkylene, phenyloxy-C1-C6-alkylene;
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano, hydroxy, amino or the groups







  • R4 may be hydrogen, hydroxy, halogen, nitro, amino, cyano, phenyl, C1-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C3-C7-cycloalkyl,
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano or the radicals:










    • or

    • independently of one another hydroxy-C1-C6-alkylene, C1-C6-alkyloxy, C1-C6-alkyloxyphenyl-C1-C6-alkylene, phenyloxy-C1-C6-alkylene, C1-C6-alkylamino, di(C1-C6-alkyl)amino

    • C1-C6-acyl-(C0-C6-alkyl)amido,

    • C1-C6-alkylcarbonyl,

    • carboxy, C1-C6-alkyloxycarbonyl,

    • C1-C3-alkylsulphanyl, C1-C6-alkysulphonyl, —N(C0-C6-alkyl)-C(O)—N-di(C0-C6-alkyl),



  • and

  • R1, R2, R5, R6, R7, R8, Q, X and W have the same meaning as defined in formula I.



The present invention also relates to compounds as such of formula I which are novel over JP11-3432795.


Preferred according to the present invention are the compounds of formula I and use thereof, namely

  • 1 4,3′,4′,5′-Tetramethoxy-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amide
  • 10 4-Isopropoxy-3′,4′,5′-trimethoxy-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 11 5-Pyridin-2-yl-thiophene-2-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide
  • 12 4′-Trifluoromethyl-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide
  • 13 4′-Methyl-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide
  • 14 5-(2-Methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-thiophene-2-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide.


These compounds are not disclosed in JP11-3432795 and are thus novel.


Likewise, preferred are compounds of formula I and use thereof, in which

  • R3 may be hydroxy-C3-C6-alkenylene, hydroxy-C3-C6-alkynylene, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy, C3-C7-cycloalkyl-C1-C6-alkylenoxy, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkyloxy-C3-C6-alkenylene, C1-C6-alkyloxy-C3-C6-alkynylene, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6-alkyl)amino-C1-C6-alkylene,
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano, hydroxy, amino or the groups







  • R4 may be hydrogen, hydroxy, halogen, nitro, amino, cyano, phenyl, C1-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C3-C7-cycloalkyl,
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano or the radicals:










    • or

    • independently of one another hydroxy-C1-C6-alkylene, C1-C6-alkyloxyC1-C6-alkyloxyphenyl-C1-C6-alkylene, phenyloxy-C1-C6-alkylene,

    • C1-C6-alkylamino, di(C1-C6-alkyl)amino C1-C6-acyl-(C0-C6-alkyl)amido,

    • C1-C6-alkylcarbonyl,

    • carboxy, C1-C6-alkyloxycarbonyl,

    • C1-C3-alkylsulphanyl, C1-C6-alkysulphonyl, —N(C0-C6-alkyl)-C(O)—N-di(C0-C6-alkyl),



  • and

  • R1, R2, R5, R6, R7, R8, Q, X and W have the same meaning as defined in formula I.



This subrange of formula I defined above does not overlap with the range of formulas disclosed in JP11-3432795 and is thus novel.


Likewise preferred according to the present invention are those compounds of formula I and use thereof


in which

  • R4 may be C3-C7-cycloalkyl-C1-C6-alkylene, C3-C7-heterocycloalkyl,
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano or the radicals:









    • or

    • independently of one another hydroxy-C3-C6-alkenylene, hydroxy-C3-C6-alkynylene, C3-C7-cycloalkyloxy, C3-C7-cycloalkyl-C1-C6-alkylenoxy, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkyloxy-C3-C6-alkenylene, C1-C6-alkyloxy-C3-C6-alkynylene, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6)-alkylamino-C1-C6-alkylene, C3-C7-cycloalkyl-(C0-C6-alkyl)amino,





C1-C6-alkylaminocarbonyl, di(C1-C6-alkyl)aminocarbonyl, (C3-C7-cycloalkyl)aminocarbonyl, di(C3-C7-cycloalkyl)aminocarbonyl, C3-C7-cycloalkyl-C1-C6-alkyleneaminocarbonyl,

    • C3-C7-cycloalkylcarbonyl,
    • carboxamido [—C(O)NH2],
    • C3-C7-cycloalkylsulphonyl, C3-C7-cycloalkyl-C1-C6-alkylenesulphonyl, C1-C6-alkylaminosulphonyl, di(C1-C6-alkyl)aminosulphonyl, (C3-C7-cycloalkyl)aminosulphonyl, di(C3-C7-cycloalkyl)aminosulphonyl, C3-C7-cycloalkyl-C1-C6-alkyleneaminosulphonyl, C1-C6-alkylsulphonylamido, —N(C0-C6-alkyl)-C(O)—C1-C6-alkyl, —N(C0-C6-alkyl)-C(O)—C3-C7-cycloalkyl, —N(C0-C6-alkyl)-C(O)—O—(C0-C6)alkyl, —N(C0-C6-alkyl)-C(O)—NH—C3-C7-cycloalkyl,
    • —N(C0-C6-alkyl)-SO2—C1-C6-alkyl, —N(C0-C6-alkyl)-SO2—C3-C7-cycloalkyl, —N(C0-C6-alkyl)-SO2—N-di(C0-C6-alkyl), —N(C0-C6-alkyl)-SO2—NH—(C3-C7)-cycloalkyl,
    • —C(O)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine, —C(O)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine, —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine, —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkyl)amine,
    • —S(O2)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine, —S(O2)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine, —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine, —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkylene)amine,
    • —O—C2-C6-alkylene-(C1-C6-alkyl)amine, —O—C2-C6-alkylene-[di(C1-C6-alkylene)]amine,
    • or the radicals:










  • R4 and R5 may together form heterocycloalkyl, cycloalkyl;


    and the groups R1, R2, R3, R5, R6, R7, R8, Q, X and W have the same meaning as defined in formula I.



This subrange of formula I defined above does not overlap with the range of formulas disclosed in JP11-3432795 and is thus novel.


Particularly preferred are compounds of formula II and use thereof







in which

  • R4 may be C3-C7-cycloalkyl-C1-C6-alkylene, C3-C7-heterocycloalkyl,
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano or the radicals:









    • or

    • independently of one another hydroxy-C3-C6-alkenylene, hydroxy-C3-C6-alkynylene, C3-C7-cycloalkyloxy, C3-C7-cycloalkyl-C1-C6-alkylenoxy, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkyloxy-C3-C6-alkenylene, C1-C6-alkyloxy-C3-C6-alkynylene, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6)-alkylamino-C1-C6-alkylene, C3-C7-cycloalkyl-(C0-C6-alkyl)amino,

    • C1-C6-alkylaminocarbonyl, di(C1-C6-alkyl)aminocarbonyl, (C3-C7-cycloalkyl)aminocarbonyl, di(C3-C7-cycloalkyl)aminocarbonyl, C3-C7-cycloalkyl-C1-C6-alkyleneaminocarbonyl,

    • C3-C7-cycloalkylcarbonyl, carboxamido [—C(O)NH2],

    • C3-C7-cycloalkylsulphonyl, C3-C7-cycloalkyl-C1-C6-alkylenesulphonyl, C1-C6-alkylaminosulphonyl, di(C1-C6-alkyl)aminosulphonyl, (C3-C7-cycloalkyl)aminosulphonyl, di(C3-C7-cycloalkyl)aminosulphonyl, C3-C7-cycloalkyl-C1-C6-alkyleneaminosulphonyl, C1-C6-alkylsulphonylamido, —N(C0-C6-alkyl)-C(O)—C1-C6-alkyl, —N(C0-C6-alkyl)-C(O)—C3-C7-cycloalkyl, —N(C0-C6-alkyl)-C(O)—O—(C0-C6)alkyl, —N(C0-C6-alkyl)-C(O)—NH—C3-C7-cycloalkyl,

    • —N(C0-C6-alkyl)-SO2—C1-C6-alkyl, —N(C0-C6-alkyl)-SO2—C3-C7-cycloalkyl, —N(C0-C6-alkyl)-SO2—N-di(C0-C6-alkyl), —N(C0-C6-alkyl)-SO2—NH—(C3-C7)-cycloalkyl,

    • —C(O)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine, —C(O)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine, —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine, —C(O)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkyl)amine,

    • —S(O2)—N(H)—C2-C6-alkylene-(C1-C6-alkyl)amine, —S(O2)—N(H)—C2-C6-alkylene-[di(C1-C6-alkyl)]amine, —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl)amine, —S(O2)—N(H)—C2-C6-alkylene-(C3-C7-cycloalkyl-C1-C6-alkylene)amine,

    • —O—C2-C6-alkylene-(C1-C6-alkyl)amine, —O—C2-C6-alkylene-[di(C1-C6-alkylene)]amine,

    • or the radicals:













  • R4 and R5 may together form heterocycloalkyl, cycloalkyl;


    and


    R1, R2, R3, R5, R6, R7, R8, X and W have the same meaning as defined in formula I.



Formula II does not overlap with the range of the formula disclosed in JP11-3432795 and is thus novel.


More particularly preferred according to the present invention are compounds of formula II and use thereof, namely

  • 2 3-Chloro-2′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-biphenyl-4-carboxylic acid methylamide;
  • 3 3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4′-methoxybiphenyl-4-carboxylic acid methylamide;
  • 4 3-Chloro-4′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-biphenyl-4-carboxylic acid methylamide;
  • 5 3′-Chloro-4′-(morpholine-4-carbonyl)-5-trifluoromethyl-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 6 3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-5′-trifluoromethyl-biphenyl-4-carboxylic acid methylamide;
  • 7 3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-5′-trifluoromethyl-biphenyl-4-carboxylic acid amide;
  • 8 4′-Bromo-3-chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-biphenyl-4-carboxylic acid amide;
  • 9 3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4′-iso-propoxy-biphenyl-4-carboxylic acid methylamide;
  • 15 3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4′-methoxy-biphenyl-4-carboxylic acid amide;
  • 16 3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4′-methoxy-biphenyl-4-carboxylic acid methylamide;
  • 17 3′-Chloro-4-methoxy-4′-(morpholine-4-carbonyl)-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-amide;
  • 18 4-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide
  • 19 3-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide;
  • 20 3-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-propoxy-phenylethynyl}-N-methyl-benzamide;
  • 21 4-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-propoxy-phenylethynyl}-N-methyl-benzamide;
  • 22 4-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide
  • 23 3-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide;
  • 24 2-Chloro-4-{7-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-N-methyl-benzamide
  • 35 2-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-benzamide;
  • 38 4-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-N-methyl-benzamide;
  • 42 3-Fluoro-5-{7-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-N-methyl-benzamide;
  • 47 3-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-benzamide;
  • 50 N-(3-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-benzyl)-acetamide;
  • 52 5-(4-Cyanomethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 54 5-Benzo[1,3]dioxol-5-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 58 5-(3-Methanesulfonylamino-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide.


Likewise preferred according to the present invention are compounds of formula III and use thereof







in which

  • R4 may be hydrogen, hydroxy, halogen, nitro, amino, cyano, phenyl, C1-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C3-C7-cycloalkyl,
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano or the radicals:









    • or

    • independently of one another hydroxy-C1-C6-alkylene, C1-C6-alkyloxy, C1-C6-alkyloxyphenyl-C1-C6-alkylene, phenyloxy-C1-C6-alkylene, C1-C6-alkylamino, di(C1-C6-alkyl)amino

    • C1-C6-acyl-(C0-C6-alkyl)amido,

    • C1-C6-alkylcarbonyl,

    • carboxy, C1-C6-alkyloxycarbonyl,

    • C1-C3-alkylsulphanyl, C1-C6-alkysulphonyl, —N(C0-C6-alkyl)-C(O)—N-di(C0-C6-alkyl);


      and


      R1, R2, R3, R5, R6, R7, R8, X, V and W have the same meaning as defined in formula I.





Formula III does not overlap with the range of the formula disclosed in JP11-3432795 and is thus novel.


Particularly preferred are compounds of formula IV and use thereof







in which

  • R4 may be hydrogen, hydroxy, halogen, nitro, amino, cyano, phenyl, C1-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C3-C7-cycloalkyl,
    • where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano or the radicals:









    • or

    • independently of one another hydroxy-C1-C6-alkylene, C1-C6-alkyloxy, C1-C6-alkyloxyphenyl-C1-C6-alkylene, phenyloxy-C1-C6-alkylene, C1-C6-alkylamino, di(C1-C6-alkyl)amino

    • C1-C6-acyl-(C0-C6-alkyl)amido,

    • C1-C6-alkylcarbonyl,

    • carboxy, C1-C6-alkyloxycarbonyl,

    • C1-C3-alkylsulphanyl, C1-C6-alkysulphonyl, —N(C0-C6-alkyl)-C(O)—N-di(C0-C6-alkyl);


      and


      R1, R2, R3, R5, R6, R7, R8, A, V, X and W have the same meaning as defined in formula I.





More particularly preferred are compounds of formula IV and use thereof, namely

  • 25 5-(3,4,5-Trimethoxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 26 5-(4-Acetyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide
  • 27 5-(4-Methylsulfanyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 28 5-(3-Amino-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 29 5-(3-Trifluoromethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 30 5-(4-Hydroxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 31 5-(4-Fluoro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 32 5-(4-Cyano-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 33 5-Naphthalen-1-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 34 5-(4-Chloro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 36 5-(6-Methoxy-pyridin-3-yl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 37 5-(2-Fluoro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 39 5-Quinolin-6-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 40 5-((E)-Styryl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 41 5-(3-Hydroxymethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 43 5-(3-Fluoro-5-methoxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 44 N-(4-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-phenyl)-acetamide;
  • 45 5-(3,5-Dimethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 46 5-Quinolin-3-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 48 5-(2-Fluoro-pyridin-3-yl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 49 5-(5-Cyano-thiophen-2-yl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 51 5-(2-Methoxy-pyrimidin-5-yl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 53 5-(3-Cyano-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 55 N-(3-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-phenyl)-acetamide;
  • 56 5-Biphenyl-2-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 57 5-o-Tolyl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 59 5-(4-Trifluoromethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 60 5-Benzo[b]thiophen-3-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 61 5-Biphenyl-3-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 62 5-(3-Acetyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 63 5-(3-Fluoro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 64 2′,3′-Dihydro-[2,5′]bibenzofuranyl-7′-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 65 5-Benzo[b]thiophen-2-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 66 5-(3-Chloro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 67 5-p-Tolyl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 68 5-Naphthalen-2-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 69 5-(3-Methoxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 70 5-(4-Methoxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;
  • 71 5-Thiophen-3-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide.


The present invention also relates to a process for preparing the compounds according to the invention. Compounds of the general formula I can be prepared as shown in Scheme 1 by an sulfonamide-formation reaction between the tryptophanol derivative V and the sulfonyl chloride VI. The sulfonyl chloride VI reacts with the tryptophanol derivative V in a suitable solvent and where appropriate in the presence of a base (an organic or inorganic base) which are known to the skilled person. It is possible to generate the sulfonyl chloride VI in situ from the corresponding sulfonic acid by treatment with reagents known to the skilled person, for example thionyl chloride, POCl3, sulfonyl chloride, PCl3 or PCl5.







Compounds of the general formula II can be prepared as shown in Scheme 2 by an sulfonamide-formation reaction between the tryptophanol derivative V and the sulfonyl chloride VII. The sulfonyl chloride reacts with the tryptophanol derivative in a suitable solvent and where appropriate in the presence of a base which are known to the skilled person. It is possible to generate the sulfonyl chloride in situ from the corresponding sulfonic acid by treatment with reagents known to the skilled person, for example thionyl chloride, POCl3, sulfonyl chloride, PCl3 or PCl5.







Compounds of the general formula III can be prepared as shown in Scheme 3 by an sulfonamide-formation reaction between the tryptophanol derivative V and the sulfonyl chloride VIII. The sulfonyl chloride VIII reacts with the tryptophanol derivative V in a suitable solvent and where appropriate with a base which are known to the skilled person. It is possible to generate the sulfonyl chloride in situ from the corresponding sulfonic acid by treatment with reagents known to the skilled person, for example thionyl chloride, POCl3, sulfonyl chloride, PCl3 or PCl5.







Compounds of the general formula IV can be prepared as shown in Scheme 4 by an sulfonamide-formation reaction between the tryptophanol derivative V and the sulfonyl chloride IX. The sulfonyl chloride IX reacts with the tryptophanol derivative V in a suitable solvent and where appropriate with a base which are known to the skilled person. It is possible to generate the sulfonyl chloride in situ from the corresponding sulfonic acid by treatment with reagents known to the skilled person, for example thionyl chloride, POCl3, sulfonyl chloride, PCl3 or PCl5.







Alternatively, compounds of the general formula I can also be prepared as shown in Scheme 5 by a metal catalyzed cross coupling reaction between the aryl halide XI (wherein Hal stands for chlorine, bromine or iodine) and the correspondingly functionalized building block X known to the skilled person, for example: a Suzuki reaction (R═—B(OH)2), a Sonogashira coupling (R═H, X═—C≡C—), a Negishi coupling (R═Zn-Hal) or a Stille coupling (R═Sn(alkyl)3). Preferred metal catalysts used are typically those containing palladium or nickel, depending on the nature of the cross-coupling reaction. For a more detailed description of the metal catalyzed cross-coupling reactions applied and applicable for the synthesis of compounds of the formula I, see e.g. S. Takahashi, Y. Kuroyama, K. Sonogashira and N. Hagihara, Synthesis, 1980, 627; Metal catalyzed Cross-coupling Reactions, ed. F. Diederich and P. J. Stang, Wiley-VCH, Weinheim, 1998; K. Sonogashira, J. Organomet. Chem., 2002, 653 (1-2), 46.







Likewise, compounds of the general formula II can be prepared as shown in Scheme 6 by a metal catalyzed cross coupling reaction between the aryl halide XII and the correspondingly functionalized building block X known to the skilled person.







Likewise, compounds of the general formula III can be prepared as shown in Scheme 7 by a metal catalyzed cross coupling reaction between the aryl halide XIII and the correspondingly functionalized building block X known to the skilled person.







Likewise, compounds of the general formula IV can be prepared as shown in Scheme 8 by a metal catalyzed cross coupling reaction between the aryl halide XIV and the correspondingly functionalized building block X known to the skilled person.







The present invention further relates to the aryl halides of the formulae XI, XII, XIII and XIV as intermediates of the process according to the invention for preparing the compounds according to the invention, namely:

  • 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-methoxy-benzenesulfonamide
  • 2-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-benzenesulfonamide
  • 4-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-benzenesulfonamide
  • 3-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-5-trifluoromethyl-benzenesulfonamide
  • 2,5-Dibromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-benzenesulfonamide
  • 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-isopropoxy benzenesulfonamide
  • 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-2-methoxy-benzenesulfonamide
  • 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-propoxy-benzenesulfonamide
  • 5-Bromo-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide


Pharmacological Experiments

HTRF Assay for Measuring cAMP in Cells


The method is based on a competitive immunoassay between native cAMP, which has been produced by the cells, and cAMP which is labelled with cAMPD2 conjugate. The tracer binding was visualized by a monoclonal antibody, anti-cAMP labelled with cryptate [HTRF=homogeneous time-resolved fluorescence].


The specific signal is inversely proportional to the cAMP concentration of the samples employed.


The 665 nm/620 nm fluorescence ratio was evaluated.


The following material was used: 96-well plates for the tissue culture, 96-well plates with black edge and black base (e.g. Fluotrac 600 from Greiner), 96-well plates for the substance dilutions of polypropylene and cAMP Femtomolar (4000 wells Kit, CIS Bio International # 62AM5PEJ).


The following reagents were used: BSA (bovine serum albumin) Fraction V protease-free, IBMX (3-isobutyl-1-methylxanthine), hFSH (human follicle stimulating hormone), Triton X-100 analytical grade, potassium fluoride analytical grade, G 418 (Geneticin) and Accutase.


Buffer 1 (washing and testing buffer) contained PBS, 1 mM CaCl2, 1 mM MgCl2, 0.2% glucose; 0.1% BSA, 1 mM IBMX.


Buffer 2 (2× lysis buffer) contained 1% Triton X-100 in PBS (without CaCl2 and MgCl2).


Buffer 3 (assay buffer) contained 50 mM potassium phosphate buffer (pH 7.0); 800 mM potassium fluoride; 0.2% BSA (always added fresh).


Procedure:

On day 1, the cells were seeded in 96-well plates (3×104 cells per well hFSHR clone 16 cells (CHO cells stably transfected with the human FSH receptor in 150 μl of medium). The next day, test substance dilutions were made up. For this purpose, all the substances were diluted in ice-cold buffer 1 (with or without hFSH), and the substance dilutions were placed on ice until applied to the cells.


The cell supernatant was then aspirated off, and the cells were washed 2× with 200 μl of buffer 1. The cells were treated with 60 μl of the appropriate substance concentrations at 37° C. for 2 h. The cells were then lysed with 60 μl of buffer 2 (put onto the supernatant) (on a plate shaker at RT for 30 min).


The test conjugates (cAMP-D2 and anti-cAMP cryptate, CIS Bio) were diluted in buffer 3 in accordance with the manufacturers' information. The actual mixture for measurement was pipetted into a black 96-well plate (in each case 15 μl of the cell lysate diluted with 35 μl of buffer 1; firstly 25 μl of cAMP-D2 conjugate were pipetted and, after 10 min, 25 μl of the anti-cAMP cryptate were added). This is followed by incubation at RT for 90 minutes. The measurement was carried out in a PheraStar (BMG).












Tissue culture conditions


















1) hFSHr clone 16
Ham's F12




PSG




10% FCS




700 μg/ml G 418 (Geneticin) from PAA.










Dose-effect curve (hFSH) for the human receptor: 1e-8, 3e-9, 1e-9, 3e-10, 1e-10, 3e-11, 1e-11, 3e-12 mol/l.


The test substances were employed in suitable dilutions in the absence (test for agonism) and in the presence of 1e-9 mol/l hFSH.


Evaluation

The values of the well ratio were averaged and then entered directly in SigmaPlot versus the concentrations. The maximum and minimum values were determined for each plate, and half the difference is to be regarded as IC50.


The test results (Table 1) show that the compounds according to the invention have an FSH-antagonistic effect.









TABLE 1







FSH antagonistic effect of selected


compounds in the HTRF assay










Compound [Ex. #]
IC50















1
3.5
μM



3
4
μM



9
180
nM



18
2.5
μM



22
3.5
μM



39
5
μM



52
10
μM










Being antagonists of the FSH receptor, compounds of the general formula I and their pharmaceutically acceptable salts can thus be used for the fertility control in male and/or in a female animals, in particular in men and/or women; as well as for the treatment and/or prevention of osteoporosis.


Pharmaceutical Compositions

The invention further relates to compounds of the general formula I or pharmaceutically acceptable salts thereof as therapeutic active ingredients, and to pharmaceutical compositions comprising at least one compound of the general formula I or pharmaceutically acceptable salts thereof, where appropriate together with pharmaceutically suitable excipients and/or carriers.


Pharmaceutically acceptable salts of the compounds of the general formula I can be prepared by methods known to the skilled person, depending on the nature of the compound of formula I, either by using as inorganic acids inter alia hydrochloric acid, hydrobromic acid, sulphuric acid and phosphoric acid, nitric acid, as carboxylic acids inter alia acetic acid, propionic acid, hexanoic acid, octanoic acid, decanoic acid, oleic acid, stearic acid, maleic acid, fumaric acid, succinic acid, benzoic acid, ascorbic acid, oxalic acid, salicylic acid, tartaric acid, citric acid, lactic acid, glycolic acid, malic acid, mandelic acid, cinnamic acid, glutamic acid, aspartic acid, and as sulphonic acids inter alia methanesulphonic acid, ethanesulphonic acid, toluenesulphonic acid, benzenesulphonic acid and naphthalenesulphonic acid; or by using an appropriate base as inorganic base inter alia alkalimetal hydroxide, carbonate, or hydrogencarbonate, as organic base inter alia tertiary amines and N-heterocycles.


These pharmaceutical compositions and medicaments may be intended for oral, rectal, subcutaneous, transdermal, percutaneous, intravenous or intramuscular administration. They comprise besides conventional carriers and/or diluents at least one compound of the general formula I.


The medicaments of the invention are formulated using the customary solid or liquid carriers or diluents and the excipients customarily used in pharmaceutical technology, in accordance with the desired mode of administration with a suitable dosage in a known manner: i.e. by processing the active ingredient with the carrier substances, fillers, substances which influence disintegration, binders, humectants, lubricants, absorbents, diluents, test modifiers, colorants etc. which are used in pharmaceutical technology, and converting into the desired administration form. Reference should be made in this connection to Remington's Pharmaceutical Science, 15th ed. Mack Publishing Company, East Pennsylvania (1980) and to Gennaro, A. R. et al., Remington: The Science and Practice of Pharmacy (20th Edition., Lippincott Williams & Wilkins 2000, see especially Part 5: Pharmaceutical Manufacturing).


Pharmaceutical compositions according to the present invention are preferably administered orally. Suitable for oral administration are in particular tablets, (film)-coated tablets, sugar-coated tablets capsules, pills, powders, granules, pastilles, suspensions, emulsions, solutions or depot forms.


Appropriate tablets can be obtained for example by mixing the active ingredient with known excipients, for example inert diluents such as dextrose, sugar, sorbitol, mannitol, polyvinylpyrrolidone, disintegrants such as maize starch or alginic acid, binders such as starch or gelatine, lubricants such as magnesium stearate or talc and/or agents to achieve a depot effect such as carboxylpolymethylene, carboxylmethylcellulose, cellulose acetate phthalate or polyvinyl acetate. The tablets may also consist of a plurality of layers.


Correspondingly, coated tablets can be produced by coating cores which have been produced in analogy to the tablets with agents normally used in tablet coatings, for example polyvinylpyrrolidone or shellac, gum Arabic, talc, titanium oxide or sugar. The tablet coating may also consist of a plurality of layers, it being possible to use the excipients mentioned above for tablets.


Solutions or suspensions with the compounds according to the invention of the general formula I may additionally comprise taste-improving agents such as saccharin, cyclamate or sugar and, for example, flavourings such as vanillin or orange extract.


They may additionally comprise suspending aids such as sodium carboxymethylcellulose or preservatives such as p-hydroxybenzoates.


Capsules comprising the compounds of the general formula I can be produced for example by the compound(s) of the general formula I being mixed with an inert carrier such as lactose or sorbitol and encapsulated in gelatine capsules.


Parenteral preparations such as solutions for injection are also suitable. Preparations for injection and infusion are possible for parenteral administration. Appropriately prepared crystal suspensions can be used for intraarticular injection. Aqueous and oily solutions for injection or suspensions and corresponding depot preparations can be used for intramuscular injection. The novel compounds can be used for rectal administration in the form of suppositories, capsules, solutions (e.g. in the form of enemas) and ointments both for systemic and for local therapy.


Suitable suppositories can be produced for example by mixing with carriers intended for this purpose, such as neutral fats or polyethylene glycol or derivatives thereof.


Formulations suitable for topical application include gels, ointments, greasy ointments, creams, pastes, dusting powders, milk and tinctures. Topical use can also take place by means of a transdermal system, for example a patch. The concentration of the compounds of the general formula I in these preparations should typically be in the range of 0.01%-20% in order to achieve an adequate pharmacological effect.


The invention further relates to pharmaceutical compositions in combination with packaging material suitable for said composition, wherein said packaging material including instructions for the use of the composition.


Dose

Suitable doses for the compounds according to the present invention may vary from 0.005 mg to 50 mg per day per kg of body weight, depending on the age and constitution of the patient. It is possible to administer the necessary daily dose by single or multiple delivery. The preferred daily dose for larger mammals, for example humans, may vary in the range from 10 μg to 30 mg per kg of body weight.


The exact dose and regimen of administration of the drug substance (active ingredient, or a pharmaceutical composition thereof, may however vary with the particular compound, the route of administration, and the age, sex and condition of the individual to whom the medicament is administered. The dose, the dosage as well as the regimen of the administration may thus differ between a male and a female considerably.


The compounds according to the invention of the general formula I can be prepared as described below.


ABBREVIATIONS USED



  • ACN Acetonitrile

  • DIBAC Diisobutylaluminium hydride

  • DMF N,N-Dimethylformamide

  • EDC N-Ethyl-N′-(3-dimethylaminopropyl)carbodiimide

  • EtOH Ethanol

  • HATU O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate

  • FMOC (9H-Fluoren-9-ylmethoxy)carbonyl

  • HOBt 1-Hydroxy-1H-benzotriazole

  • MeCN Acetonitrile

  • MeOH Methanol

  • MTBE Methyl tert-butyl ether

  • NMM 4-methylmorpholine

  • NMP N-Methylpyrrolidinone

  • Rf Reflux

  • RT Room temperature

  • TBAF Tetrabutylammonium fluoride

  • TFA Trifluoroacetic acid

  • THF Tetrahydrofuran



Compounds of the general formula I can in principle be prepared as shown in Scheme 9 by an sulfonamide forming reaction between a tryptophanol derivative V and a sulfonyl chloride VI. Typically the reaction is performed in the presence of a base.







The tryptophanol derivatives of the formula V with R7=R8=H can be prepared as shown in Scheme 10 from the corresponding amino acids which can be purchased or are known from the literature.







Compounds of the general formula I can in principle also be prepared as shown in Scheme 11 via an Grignard reaction from the corresponding esters XV.







Compounds of the general formula XV can in principle be prepared as shown in Scheme 12 by an sulfonamide forming reaction between a tryptophan derivative XVI and a sulfonyl chloride VI. Typically the reaction is performed in the presence of a base.







Compounds of the general formula I can in principle also be prepared as shown in Scheme 13 via Suzuki reaction of aryl halide XI and boronic acid XVII.







The acetylene derivatives of formula XVIII can in principle also be prepared according to Scheme 14 via a Sonogashira type coupling of terminal acetylene XIX or XXI with the corresponding aryl halides XX or XI.







The acetylene derivatives of formula XIX can in principle also be prepared according to Scheme 15 via a Sonogashira type coupling from aryl halide XI. The aryl halide XI itself can be prepared via an sulfonamide forming reaction from the tryptophanol derivative V and sulfonyl chloride XXII.












Synthesis of the Compounds According to the Invention
EXAMPLE 1
4,3′,4′,5′-Tetramethoxy-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide






1a) 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-methoxy-benzenesulfonamide

To a solution of (R)-Tryptophanol (67 mg) and triethylamine (0.12 ml) in THF (2.8 ml) was added slowly a solution of 5-Bromo-2-methoxy-benzenesulfonyl chloride (100 mg) in THF (2 ml) and the mixture was stirred for 1 h at room temperature. Water (2 ml) and brine (8 ml) were added, the aqueous phase extracted with ethyl acetate (2×20 ml) and the combines organic phases reduced in vacuo. Flash chromatography of the residue on silica gel afforded 50 mg of the title compound. 1H-NMR (DMSO-d6): 10.69 s (1H); 7.69 d (J=2.5 Hz, 1H); 7.58 dd (J=2.5 Hz/8.8 Hz, 1H); 7.24 d (J=8.1 Hz, 1H); 7.20 d (J=7.8 Hz, 1H); 7.17 m (1H); 7.02-6.98 m (2H); 6.96 d (J=8.8 Hz, 1H); 6.89 m (1H); 4.68 d (J=5.3 Hz, 1H); 3.77 s (3H); 3.35 m (1H); 3.27 m (2H); 2.89 dd (J=6.6 Hz/14.4 Hz, 1H); 2.64 dd (J=6.3 Hz/14.4 Hz, 1H).


1b) 4,3′,4′,5′-Tetramethoxy-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide

A solution of 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-methoxy-benzenesulfonamide (200 mg), 3,4,5-Trimethoxy-benzene boronic acid (97 mg) and Pd(PPh3)4 (26 mg) in ethanol (2 mL), toluene (10 mL) and an aqueous sodium carbonate solution (2M, 2 mL) was stirred at reflux for 4 h. The solvent was evaporated and the solid purified by flash chromatography to yield 61 mg of the title compound.



1H-NMR (DMSO-d6): 10.69 s (1H); 7.89 s (1H); 7.76 dd (J=2.3 Hz/8.6 Hz, 1H); 7.21 d (J=8.1 Hz); 7.12 m (2H); 7.00 s (1H); 6.99 m (1H); 6.92 m (1H); 6.77 s (2H); 6.72 m (1H); 4.64 m (1H); 3.82 s (6H); 3.66 s (3H); 3.28 m (2H); 2.85 m (1H); 2.65 m (1H).


The following compounds were obtained in analogy to the preparation methods described in detail:


















Method

1H-NMR




Product;
analagous
(400 MHz) δ


Ex.
reagents
to
[ppm]
Structure







2
3-Chloro-2′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfa-moyl]-biphenyl-4-carboxylic acidmethylamide;2-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-benzenesulfonamideand3-Chloro-4-methylcarbamoyl-phenyl boronic acid
1

1H-NMR (DMSO-d6):10.79 s (1H); 8.40 q (J =4.7 Hz, 1H); 7.84 d (J =7.0 Hz, 1H); 7.55 m (1H);7.45 d (J = 6.4 Hz, 1H);7.42-7.26 m (6H); 7.22dd (J = 0.9 Hz/6.9 Hz,1H); 7.07, d (J = 2.3 Hz,1H); 7.04 m (1H); 6.93 m(1H); 4.76 t (J = 5.1 Hz,1H); 3.44-3.23 m (3H);2.93 dd (J = 6.6 Hz/14.5Hz, 1H); 2.77 d (J = 4.5Hz, 3H); 2.75 m (1H).










3
3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4′-methoxy-biphenyl-4-carboxylic acidmethylamide;5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-methoxy-benzenesulfonamideand3-Chloro-4-methylcarbamoyl-phenyl boronic acid
1

1H-NMR (DMSO-d6):10.86 s (1H); 8.38 q (J =4.9 Hz, 1H); 7.91 d (J =2.5 Hz, 1H); 7.81 dd (J =2.3 Hz/8.5 Hz, 1H); 7.67d (J = 1.5 Hz, 1H); 7.59dd (J = 1.7 Hz/8.1 Hz,1H); 7.50 d (J = 7.9 Hz,1H); 7.20 m (2H); 7.12 d(J = 8.9 Hz, 1H); 7.03broad s (1H); 7.01 d (J =1.9 Hz, 1H); 6.93 m (1H);6.74 m (1H); 4.68 broad s(1H); 3.85 s (3H); 3.39 m(2H); 3.26 m (1H); 2.89dd (J = 6.2 Hz/14.3 Hz,1H); 2.78 d (J = 4.5 Hz,1H); 2.68 dd (J = 6.2 Hz/14.3 Hz, 1H).










4
3-Chloro-4′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-biphenyl-4-carboxylic acid methylamide;4-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-benzenesulfonamideand3-Chloro-4-methylcarbamoyl-phenyl boronic acid
1

1H-NMR (DMSO-d6):10.67 s (1H); 8.42 q (J =4.7 Hz, 1H); 7.79 d (J =1.7 Hz, 1H); 7.68 m (2H);7.63 s (4H); 7.54 d (J =7.9 Hz, 1H); 7.26 d (J =7.5 Hz, 1H); 7.15 d (J =7.9 Hz, 1H); 7.05 d (J =2.1 Hz, 1H); 6.93 m (1H);6.85 m (1H); 4.77 t (J =5.5 Hz, 1H); 3.4 m (1H);3.28 m (1H); 2.95 dd (J =5.8 Hz/13.9 Hz, 1H);2.78 d (J = 4.5 Hz, 3H);2.61 dd (J = 6.6 Hz/14.1Hz, 1H).










5
3′-Chloro-4′-(morpholine-4-carbonyl)-5-trifluoromethyl-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amide;3-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-5-trifluoromethyl-benzene-sulfonamideand3-Chloro-4-(morpholine-4-carbonyl)-phenyl boronic acid
1

1H-NMR (DMSO-d6):10.59 s (1H); 8.16 d (J =8.5 Hz, 1H); 7.96 d (J =7.0 Hz, 1H); 7.92 s (1H);7.90 d (J = 1.5 Hz, 1H);7.75 dd (J = 1.3 Hz/7.7Hz, 1H); 7.53 d (J = 8.1Hz, 1H); 7.27 d (J = 7.5Hz, 1H); 7.15 d (J = 8.1Hz, 1H); 6.97 d (J = 1.9Hz, 1H); 6.91 m (1H);6.78 m (1H); 4.80 t (J =5.3 Hz, 1H); 3.7 m (4H);3.57 m (2H); 3.40 m (2H);3.31 m (1H); 3.19 m (2H);2.90 dd (J = 8.7 Hz/14.5Hz, 1H); 2.62 dd (J = 6.4Hz/14.5 Hz, 1H).










6
3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl-sulfamoyl]-5′-trifluoromethyl-biphenyl-4-carboxylic acidmethylamide;3-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-5-trifluoromethyl-benzene-sulfonamideand3-Chloro-4-methylcarbamoyl-phenyl boronic acid
1

1H-NMR (DMSO-d6):10.58 s (1H); 8.43 q (J =4.7 Hz, 1H); 8.18 s (1H);8.13 s (1H); 7.97 d (J =6.6 Hz, 1H); 7.92 s (1H);7.87 d (J = 1.5 Hz, 1H);7.72 dd (J = 1.5 Hz/8.1Hz, 1H); 7.56 d (J = 8.1Hz, 1H); 7.26 d (J = 7.7Hz, 1H); 7.16 d (J = 7.9Hz, 1H); 6.99 d (J = 1.9Hz, 1H); 6.92 m (1H);6.79 m (1H); 4.79 t (J =5.5 Hz,1H); 3.48-3.26 m(3H); 2.91 dd (J = 7.5 Hz/14.3 Hz, 1H); 2.79 d (J =4.7 Hz, 3H); 2.63 dd (J =6.2 Hz/14.3 Hz, 1H).










7
3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-5′-trifluoro-methyl-biphenyl-4-carboxylicacid amide;3-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-5-trifluoromethyl-benzene-sulfonamideand3-Chloro-4-carbamoyl-phenylboronic acid
1

1H-NMR (DMSO-d6):10.59 s (1H);8.18 s (1H);8.13 s (1H); 7.96 broad s(2H); 7.92 s (1H); 7.92 s(1H); 7.86 d (J = 1.7 Hz,1H); 7.72 dd (J = 1.7 Hz/8.1 Hz, 1H); 7.68 s (1H);7.58 d (J = 8.1 Hz, 1H);7.26 d (J = 7.7 Hz, 1H);7.16 d (J = 8.1 Hz, 1H);6.99 d (J = 2.1 Hz, 1H);6.93 m (1H); 6.79 m (1H);4.79 m (1H); 3.46-3.26m (3H); 2.91 dd (J= 6.6Hz/14.5 Hz, 1H); 2.63dd (J = 6.8 Hz/14.5 Hz,1H).










8
4′-Bromo-3-chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethylsulfamoyl]-bi-phenyl-4-carboxylic acid amide;2,5-Dibromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-benzenesulfonamideand3-Chloro-4-carbamoyl-phenylboronic acid
1

1H-NMR (DMSO-d6):10.65 s (1H); 8.10 d (J =2.3 Hz, 1H); 8.13 s (1H);7.93 s (1H); 7.87-7.61 m(5H); 7.59 dd (J = 1.7 Hz/8.1 Hz, 1H); 7.54 d (J =7.9 Hz, 1H); 7.23 d (J =7.9 Hz, 1H); 7.18 d (J =8.1 Hz, 1H); 7.04 d (J =2.1 Hz, 1H); 6.90 m (1H);6.75 m (1H); 4.81 t (J =5.3 Hz, 1H); 3.53-3.34 m(3H); 2.94 dd (J = 6.4 Hz/14.7 Hz, 1H); 2.71 dd (J =6.2 Hz/14.3 Hz, 1H).














EXAMPLE 9
3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4′-isopropoxy-biphenyl-4-carboxylic acid methylamide






9a) 5-Bromo-2-hydroxy-benzenesulfonyl chloride

Chloro sulphonic acid (13.5 ml) was cooled to 0° C. and 4-Bromo-phenol (5 g) slowly added in small portions. The clear colourless solution was allowed to warm to room temperature and stirred for 16 h. The mixture was poured over ice and a fine precipitate formed. Filtration afforded 2.02 g the title compound as a white pasty solid that was not further purified. Extraction of the aqueous filtrate with ethyl acetate, drying of the combined organic phases with sodium sulfate and removal of solvent afforded another 2.32 g of the title compound. 1H-NMR (DMSO-d6): 7.46 d (J=2.5 Hz, 1H); 7.32 dd (J=2.5 Hz/8.8 Hz, 1H); 6.73 (J=8.6 Hz, 1H); no sharp signal corresponding to the phenolic hydroxy-proton detected.


9b) (R)-2-(5-Bromo-2-hydroxy-benzenesulfonylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

To a solution of (R)-Tryptophane methyl ester hydrochloride (493 mg) and triethylamine (0.77 ml) in DMF (5 ml) was added crude 5-Bromo-2-hydroxy-benzenesulfonyl chloride (500 mg) and the solution stirred for 16 h. Upon addition of water and hydrochloric acid (2 M) a white precipitate formed. The mixture was extracted with ethyl acetate, the combined organic phases washed with saturated aqueous sodium bicarbonate solution, dried over sodium sulfate and reduced in vacuo. Flash chromatography on silica gel afforded 138 mg of the title compound.



1H-NMR (CDCl3): 8.65 d (J=4.1 Hz, 1H); 8.21 s (1H); 7.64 d (J=2.5 Hz, 1H); 7.48 d (J=7.7 Hz, 1H); 7.38 dd (J=2.5 Hz/8.9 Hz, 1H); 7.33 m (1H); 7.22 m (1H); 7.13 m (1H); 7.07 d (J=2.5 Hz, 1H); 6.81 d (J=8.7 Hz, 1H); 4.34 m (1H); 3.61 s (3H); 3.32 dd (J=4.9 Hz/14.7 Hz, 1H); 3.26 dd (J=6.1 Hz/14.7 Hz, 1H).


9c) (R)-2-(5-Bromo-2-isopropoxy-benzenesulfonylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

To a solution of (R)-2-(5-Bromo-2-hydroxy-benzenesulfonylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester (138 mg) in DMF (6 ml) were added potassium carbonate (105 mg) and 2-Iodo-propane (0.061 ml) and the mixture was heated to 60° C. for 2 h. Water and sulphuric acid (1 M) were added and the mixture extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate, the solvent removed in vacuo and the residue chromatographed on silica gel to afford 75 mg of the title compound. 1H-NMR (CDCl3): 8.11 s (1H); 7.97 d (J=2.5 Hz, 1H); 7.57-7.52 m (2H); 7.37 d (J=8.1 Hz, 1H); 7.21 m (1H); 7.13 m (1H); 7.12 d (J=2.5 Hz, 1H); 6.79 d (J=8.9 Hz, 1H); 5.67 d (J=8.1 Hz, 1H); 4.57 sept. (J=6.0 Hz, 1H); 4.41 m (1H); 3.47 (3H); 3.36 m (2H); 1.34 d (J=6.0 Hz, 3H); 1.26 d (J=6.0 Hz, 3H).


9d) 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-isopropoxy benzenesulfonamide

A solution of (R)-2-(5-Bromo-2-isopropoxy-benzenesulfonylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester (171 mg) was dissolved in THF (4 mL) and a solution of lithium borohydride (2 M in THF, 518 μL) was added at 0° C. followed by methanol (77 μL). The reaction was allowed to warm to room temperature and stirred overnight, then quenched with methanol and water. The solvent was distilled off under reduced pressure and the title compound was obtained after flash chromatography in 82% yield (161 mg). 1H-NMR (DMSO-d6): 10,72 s (1H); 7.76 d (J=2.5 Hz, 1H); 7.60 dd (J=2.8 Hz/9.1 Hz, 1H); 7.24 d (J=8.1 Hz, 1H); 7.19 d (J=7.8 Hz, 1H); 7.06 d (J=9.1 Hz, 1H); 7.01 d (J=2.0 Hz, 1H); 6.98 m (1H); 6.88 m (1H); 6.59 d (J=7.1 Hz, 1H); 4.72-4.64 m (2H); 3.32 m (1H); 3.25 m (2H); 2.85 dd (J=8.1 Hz/14.2 Hz, 1H); 2.67 dd (J=5.3 Hz/14.2 Hz, 1H); 1.26 d (J=5.8 Hz, 3H); 1.23 (J=5.8 Hz, 3H).


9e) 3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4′-isopropoxy-biphenyl-4-carboxylic acid methylamide

To a solution of 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-isopropoxy benzenesulfonamide (64 mg) and 3-Chloro-4-methylcarbamoyl-benzeneboronic acid (32 mg) in toluene (1.8 ml) and EtOH (1.8 ml) were added aqueous Na2CO3 (1 M, 340 μL) and Pd(PPh3)4 (16 mg) and the mixture was stirred at 100° C. for 4 h. After addition of water and brine the mixture was extracted with ethyl acetate, the combined organic phases washed with brine, dried over Na2SO4 and reduced in vacuo. Flash chromatography on silica gel afforded 56 mg of the title compound (74%). 1H-NMR (DMSO-d6): 10,71 s (1H); 8.36 q (J=4.6 Hz, 1H); 7.98 d (J=2.3 Hz, 1H); 7.83 dd (J=2.5 Hz/8.6 Hz, 1H); 7.68 d (J=1.5 Hz, 1H); 7.59 dd (J=1.8 Hz/8.1 Hz, 1H); 7.47 d (J=7.8 Hz, 1H); 7.21 m (2H); 7.18 d (J=7.8 Hz, 1H); 7.00 d (J=2.0 Hz, 1H); 6.93 m (1H); 6.75 m (1H); 4.78 m (1H); 4.72 t (J=5.5 Hz, 1H); 3.33 m (1H); 3.25 m (2H); 2.85 dd (J=8.3 Hz/14.4 Hz, 1H); 2.75 d (J=4.6 Hz, 3H) 2.70 dd (J=5.8 Hz/14.4 Hz, 1H); 1.31 d (J=6.1 Hz, 3H); 1.28 (J=5.8 Hz, 3H).


The following compounds were obtained in analogy to the preparation methods described in detail:


















Method

1H-NMR




Product;
analagous
(400 MHz) δ


Ex.
reagents
to
[ppm]
Structure







10
4-Isopropoxy-3′,4′,5′-trimethoxy-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-isopropoxy-benzenesulfon-amide and3,4,5-Trimethoxyphenylboronicacid
9

1H-NMR (DMSO-d6):10.77 s (1H); 8.01 d (J =2.5 Hz, 1H);7.83 dd (J =2.5 Hz/8.8 Hz, 1H); 7.26d (J = 7.1 Hz, 1H); 7.23 d(J = 6.1 Hz, 1H);7.06 d (J =2.3 Hz, 1H); 7.03 d (J =8.6 Hz, 1H); 6.98 m (1H);6.83 s (2H); 6.79 m (1H);6.46 d (J = 7.1 Hz, 1H);4.82 m (1H); 4.75 t (J =5.5 Hz, 1H); 3.85 s (6H);3.69 s (3H); 3.38 m (1H);3.31-3.21 m (2H); 2.88dd (J = 8.8 Hz/14.4 Hz,1H); 2.76 dd (J = 5.3 Hz/14.4 Hz, 1H); 1.34 d (J =6.1 Hz, 3H); 1.31 (J = 5.8Hz, 3H).














EXAMPLE 11
5-Pyridin-2-yl-thiophene-2-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)ethyl]-amide






To a solution of (R)-Tryptophanol (75 mg) and triethylamine (0.14 ml) in THF (3.1 ml) was added slowly a solution of 5-Pyridin-2-yl-thiophene-2-sulfonyl chloride (100 mg) in THF (2 ml) and the mixture stirred for 1 h at room temperature. Water (2 ml) and brine (8 ml) were added, the aqueous phase extracted with ethyl acetate (2×20 ml) and the combines organic phases reduced in vacuo. Flash chromatography of the residue on silica gel afforded 87 mg of the title compound. 1H-NMR (DMSO-d6): 10.72 s (1H); 8.56 d (J=4.6 Hz, 1H); 7.95 d (J=7.8 Hz, 1H); 7.92-7.87 m (2H); 7.59 d (J=4.0 Hz, 1H); 7.39-7.35 m (3H); 7.17 d (J=8.1 Hz, 1H); 7.07 d (J=2.0 Hz, 1H); 6.93 m (1H); 6.84 m (1H); 4.75 t (J=5.6 Hz, 1H); 3.47-3.24 m (3H); 2.95 dd (J=7.1 Hz/14.2 Hz, 1H); 2.68 dd (J=6.3 Hz/14.4 Hz, 1H).


The following compounds were obtained in analogy to the preparation methods described in detail:


















Method

1H-NMR




Product;
analagous
(400 MHz) δ


Ex.
reagents
to
[ppm]
Structure







12
4′-Trifluoromethyl-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;4′-Trifluoromethyl-biphenyl-3-sulfonyl chlorideand(D)-Tryptophanol
11

1H-NMR (DMSO-d6):10.67 s (1H); 8.04 t (J =1.5 Hz, 1H); 7.92-7.83m (5H); 7.72 m (2H); 7.54t (J = 7.7 Hz, 1H); 7.24 m(1H); 7.01 d (J = 2.1 Hz,1H); 6.96 m (1H); 6.81 m(1H); 4.74 t (J = 5.1 Hz,1H); 3.39-3.21 m (3H);2.91 dd (J = 9.2 Hz/14.3Hz, 1H); 2.62 dd (J = 5.8Hz/14.3 Hz, 1H).










13
4′-Methyl-biphenyl-3-sulfonicacid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;4′-Methyl-biphenyl-3-sulfonylchlorideand(D)-Tryptophanol
11

1H-NMR (DMSO-d6):10.71 s (1H); 8.04 t (J =1.3 Hz, 1H); 7.8 d (J = 7.9Hz, 1H); 7.67 m (2H);7.60-7.47 m (3H); 7.31 dJ = 8.1 Hz, 1H) 7.25 d (J =8.1 Hz, 1H); 7.02 d (J =2.1 Hz, 1H); 6.98 m (1H);6.83 m (1H); 4.70 t (J =5.3 Hz, 1H); 3.37-3.20m (3H); 2.89 dd (J = 7.2Hz/14.0 Hz, 1H); 2.64dd (J = 5.3 Hz/14.0 Hz,1H); 2.36 s (3H).










14
5-(2-Methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-thiophene-2-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-(2-Methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-thiophene-2-sulfonyl chlorideand(D)-Tryptophanol
11

1H-NMR (DMSO-d6):10.69 s (1H); 8.04 broads (1H); 7.39 m (1H); 7.30d (J = 4.0 Hz, 1H); 7.23 d(J = 4.0 Hz, 1H); 7.13 m(1H); 7.06 d (J = 1.7 Hz,1H); 7.03 s (1H); 6.96-6.85 m (2H); 4.85 t (J =5.5 Hz, 1H); 3.96 s (3H);3.44 m (2H); 3.37-3.28m (1H, overlapping withwater signal); 3.00 dd (J =5.5 Hz/14.3 Hz, 1H);2.66 dd (J = 7.5 Hz/14.3Hz, 1H).














EXAMPLE 15
3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4′-methoxy-biphenyl-4-carboxylic acid amide






15a) (R)-2-(5-Bromo-2-methoxy-benzenesulfonylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester

A solution of 5-Bromo-2-methoxy-benzenesulfonyl chloride (1.0 g) in dichloromethane (10 mL) was added to a solution of (R)-2-Amino-3-(1H-indol-3-yl)-propionic acid methyl ester hydrochloride (1.07 g) in dichloromethane (10 mL) and triethyl amine (1.46 mL) at ambient temperature. The reaction was stirred at ambient temperature over night and quenched by the addition of hydrochloric acid (1 N). The phases were separated and the organic phase was washed with saturated aqueous sodium carbonate solution, and dried over sodium sulphate. The solvent was distilled off under reduced pressure. The title compound was obtained in 95% yield (1.55 g) as a colourless foam.



1H-NMR (DMSO-d6): 10.82 s (1H); 8.19 d (J=8.3 Hz, 1H); 7.65 m (2H); 7.28 d (J=8.1 Hz, 1H); 7.25 d (J=8.3 Hz, 1H); 7.08 d (J=2.0 Hz, 1H); 7.03 m (2H); 6.94 m (1H); 4.08 m (1H); 3.76 s (3H); 3.39 s (3H); 3.09 dd (J=14.6, 6.8 Hz, 1H); 2.94 dd (J=14.4, 7.8 Hz, 1H).


15b) 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-2-methoxy-benzenesulfonamide

A solution of methyl lithium (6.4 mL, 1.6 M in diethyl ether) was added dropwise to a solution of (R)-2-(5-Bromo-2-methoxy-benzenesulfonylamino)-3-(1H-indol-3-yl)propionic acid methyl ester (1.89 g) in tetrahydrofurane (20 mL) at 0° C. The mixture was brought to room temperature an stirred for six hours. Additional methyl lithium (2.5 mL, 1.6 M in diethyl ether) was added to the mixture. The reaction was quenched after 30 minutes by the addition of water. The mixture was extracted with ethyl acetate. The organic phase was dried over magnesium sulphate, filtered and concentrated in vacuo. Purification by flash chromatography afforded the title compound in 29% yield (557 mg).



1H-NMR (DMSO-d6): 10.33 s (1H); 7.32 m (2H); 7.13 d (J=2.6 Hz, 1H); 7.10 d (J=8.1 Hz, 1H); 6.95 m (2H); 6.87 m (1H); 6.81 d (J=1.7 Hz, 1H); 6.70 d (J=9.0 Hz, 1H); 4.41 (1H); 3.75 s (3H); 3.51 m (1H); 3.06 dd (J=14.1, 2.5 Hz, 1H); 2.60 dd (J=14.7, 10.2 Hz, 1H); 1.17 s (3H); 1.16 s (3H).


15c) 3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4′-methoxy-biphenyl-4-carboxylic acid amide

A solution of 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-2-methoxy-benzenesulfonamide (101 mg), 3-Chloro-4-carboxamide-phenyl boronic acid (42 mg), Pd(PPh3)4 (7.1 mg) and aqueous sodium carbonate solution (2M, 0.22 mL) in ethanol (1.3 mL) and toluene (2.0 mL) was stirred in a sealed microwave reactor at 100° C. for 30 minutes. The solvent was evaporated and the solid purified by flash chromatography to yield 55% of the title compound (64 mg).



1H-NMR (DMSO-d6): 10.25 d (J=1.9 Hz, 1H); 7.88 s (1H); 7.61 s (1H); 7.56 dd (J=8.5, 2.5 Hz, 1H), 7.48 d (J=7.9 Hz, 1H), 7.35 m (4H); 6.97 m (1H); 6.90 d (J=8.7 Hz, 2H); 6.76 m (3H); 4.42 s (1H); 3.83 s (3H); 3.56 m (1H); 3.08 dd (J=14.9, 2.6 Hz, 1H); 2.61 dd (J=14.9, 10.6 Hz, 1H); 1.20 s (3H); 1.18 s (3H).


The following compounds were obtained in analogy to the preparation methods described in detail:


















Method

1H-NMR




Product;
analagous
(400 MHz) δ


Ex.
reagents
to
[ppm]
Structure







16
3-Chloro-3′-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4′-methoxy-biphenyl-4-carboxylic acidmethylamide;5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-2-methoxy-benzenesulfonamideand3-Chloro-4-(N-methylcarbamoyl)benzeneboronic acid
15

1H-NMR (DMSO-d6): 10.24s (1H); 8.36 q (J = 4.6 Hz,1H); 7.56 dd (J = 8.6, 2.5Hz, 1H), 7.44 d (J = 7.8Hz, 1H); 7.38 m (1H); 7.35dd (J = 8.1, 1.8 Hz, 1H);7.31 m (2H); 6.96 m (1H);6.89 d (J = 8.6 Hz, 2H);6.75 m (3H); 4.43 s (1H);3.83 s (3H); 3.55 m (1H);3.08 m (1H); 2.78 d (J =4.6 Hz, 3H); 2.61 dd (J =14.7, 12.9 Hz,1H); 1.20 s(3H); 1.18 s (3H).










17
3′-Chloro-4-methoxy-4′-(morpholine-4-carbonyl)-biphenyl-3-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-amide5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-2-methoxy-benzenesulfonamideand3-Chloro-4-(Morpholine-4-carbonyl)benzene boronic acid
15

1H-NMR(DMSO-d6):10.23 s (1H); 7.58 dd (J =8.6, 2.0 Hz, 1H), 7.44 d (J =7.3 Hz, 1H); 7.40 s(2H); 7.31 m (2H); 6.96 m(1H); 6.90 m (2H); 6.74 m(3H); 4.43 s (1H); 3.83 s(3H); 3.67 m (4H); 3.55 m(3H); 3.19 t (J = 4.3 Hz,2H); 3.07 m (1H); 2.60 dd(J = 14.7, 10.4 Hz, 1H);1.20 s (3H); 1.17 s (3H).














EXAMPLE 18
4-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide






18a) (R)-2-(5-Bromo-2-methoxy-benzenesulfonylamino)-3-(1H-indol-3-yl)-propionic acid methyl ester was prepared as described above
18b) 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-methoxy-benzenesulfonamide

A solution of (R)-2-(5-Bromo-2-methoxy-benzenesulfonylamino)-3-(1H-indol-3-yl)propionic acid methyl ester (1.48 g) was dissolved in THF (30 mL) and a solution of lithium borohydride (2M in THF, 4.75 mL) was added at ambient temperature. The reaction was stirred 72 hours, then quenched with hydrochloric acid (4 M). The mixture was extracted with ethyl acetate The organic phase was dried over magnesium sulphate and the solvent was distilled off under reduced pressure. The title compound was obtained after flash chromatography in 30% yield (420 mg). 1H-NMR (DMSO-d6): 10.70 s (1H); 7.69 d (J=2.6 Hz, 1H); 7.59 dd (J=8.9, 2.6 Hz, 1H); 7.24 d (J=7.9 Hz, 1H); 7.19 m (2H); 6.98 m (3H); 6.89 m (1H); 4.68 m (1H); 3.77 s (3H); 3.29 m (3H); 2.89 dd (J=14.3, 6.4 Hz, 1H); 2.64 dd (J=14.5, 6.0 Hz, 1H).


18c) 4-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide

A solution of 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-methoxy-benzenesulfonamide (100 mg), Pd(PPh3)2Cl2 (9 mg), 4-Ethynyl-N-methyl-benzamide (38 mg), TBAF×3 water (180 mg) in THF (3 mL) and ethanol (0.3 mL) was stirred at 110° C. in a sealed microwave reactor for 30 min. The solvents were distilled off under reduced pressure. The crude mixture was taken up in ethyl acetate and extracted with water. The organic phase was reduced in vacuo and the title compound was obtained in 35% yield (41 mg) after flash chromatography. 1H-NMR (DMSO-d6): 10.70 s (1H); 8.54 q (J=4.6 Hz, 1H); 7.88 d (J=8.1 Hz, 2H); 7.82 d (J=2.3 Hz, 1H); 7.65 m (3H); 7.25 d (J=8.6 Hz, 2H); 7.13 d (J=6.3 Hz, 1H); 7.08 d (J=8.8 Hz, 1H); 6.99 m (2H); 6.89 t (J=7.1 Hz, 1H); 4.68 t (J=5.3 Hz, 1H); 3.82 s (3H); 3.31 m (3H); 2.90 dd (J=14.7, 6.8 Hz, 1H); 2.80 d (J=4.3 Hz, 3H); 2.68 dd (J=14.4, 6.1 Hz, 1H).


The following compound was obtained in analogy to the preparation methods described in detail:


















Method

1H-NMR




Product;
analagous
(400 MHz) δ


Ex.
reagents
to
[ppm]
Structure







19
3-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide;5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-methoxy-benzenesulfonamideand3-Ethynyl-N-methyl-benzamide
18

1H-NMR (DMSO-d6):10.71 s (1H); 8.56 m(1H); 8.02 m (1H); 7.86 m(1H); 7.82 d (J = 2.3 Hz,1H); 7.70 m (1H); 7.66 dd(J = 8.7, 2.1 Hz, 1H); 7.53t (J = 7.7 Hz, 1H); 7.25 d(J = 8.3 Hz, 2H); 7.13 d (J =5.8 Hz, 1H); 7.09 d (J =8.7 Hz, 1H); 6.99 m (2H);6.89 m (1H); 4.67 t (J =4.9 Hz, 1H); 3.82 s (3H);3.31 m (3H); 2.91 dd (J =14.1, 5.7 Hz, 1H); 2.80 d(J = 4.5 Hz,3H); 2.67 dd(J = 14.0, 5.1 Hz, 1H).














EXAMPLE 20
3-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-propoxy-phenylethynyl}-N-methyl-benzamide






20a) 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-propoxy-benzenesulfonamide

A solution of 5-Bromo-2-propoxy-benzenesulfonyl chloride (5.0 g) in tetrahydrofurane (50 mL) was added to a solution of (R)-2-Amino-3-(1H-indol-3-yl)-propan-1-ol (3.64 g) in tetrahydrofurane (50 mL) and diisopropyl ethyl amine (8.19 mL) at 0° C. The reaction mixture was warmed to room temperature, stirred over night and then concentrated under reduced pressure. The title compound was obtained in 82% yield (6.1 g). 1H-NMR (DMSO-d6): 10.70 s (1H); 7.73 d (J=2.5 Hz, 1H); 7.56 dd (J=8.6, 2.5 Hz, 1H); 7.23 m (2H); 7.00 m (2H); 6.90 m (2H); 6.68 d (J=6.3 Hz, 1H); 4.76 t (J=5.3 Hz, 1H); 3.89 m (2H); 3.32 m (3H); 2.90 dd (J=14.4, 7.1 Hz, 1H); 2.69 dd (J=14.4, 6.3 Hz, 1H); 1.72 m (2H); 0.95 t (J=7.3 Hz, 3H).


20b) 3-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-propoxy-phenylethynyl}-N-methyl-benzamide

A solution of 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-propoxy-benzenesulfonamide (100 mg), Pd(PPh3)2Cl2 (7 mg), 3-Ethynyl-N-methyl-benzamide (34 mg), TBAF×3 water (280 mg) in THF (3 mL) and ethanol (0.3 mL) was stirred at 110° C. in a sealed microwave reactor for 30 min. The solvents were distilled off under reduced pressure. The crude mixture was taken up in ethyl acetate and extracted with water. The organic phase was reduced in vacuo and the title compound was obtained in 38% yield (44 mg) after flash chromatography.



1H-NMR (DMSO-d6): 10.71 s (1H); 8.55 q (J=4.3 Hz, 1H); 8.02 m (1H); 7.86 m (2H); 7.70 m (1H); 7.63 dd (J=8.7, 2.3 Hz, 1H); 7.53 t (J=7.7 Hz, 1H); 7.27 d (J=7.5 Hz, 1H); 7.26 d (J=7.9 Hz, 1H); 7.01 m (3H); 6.89 t (J=7.4 Hz, 1H); 6.62 d (J=5.7 Hz, 1H); 4.75 m (1H); 3.94 m (2H); 3.32 m (3H); 2.92 dd (J=14.7, 7.2 Hz, 1H); 2.80 d (J=4.5 Hz, 3H); 2.72 dd (J=14.3, 5.7 Hz, 1H); 1.73 m (2H); 0.96 t (J=7.5 Hz, 3H).


The following compound was obtained in analogy to the preparation methods described in detail:


















Method

1H-NMR




Product;
analagous
(400 MHz) δ


Ex.
reagents
to
[ppm]
Structure







21
4-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-4-propoxy-phenylethynyl}-N-methyl-benzamide;5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-2-propoxy-benzenesulfonamideand4-Ethynyl-N-methyl-benzamide
20

1H-NMR (DMSO-d6):10.76 s (1H); 8.59 m(1H); 7.89 m (2H); 7.85 d(J = 2.3 Hz, 1H); 7.65 m(3H); 7.27 m (2H); 7.01 m(3H); 6.88 t (J = 7.5 Hz,1H); 6.64 d (J = 6.6 Hz,1H); 4.79 m (1H); 3.93 m(2H); 3.37 m (2H); 3.27 m(1H); 2.91 dd (J = 14.7,7.3 Hz, 1H); 2.80 d (J =4.6 Hz, 3H); 2.72 dd (J =14.5, 6.1 Hz, 1H); 1.73 m(2H); 0.96 t (J = 7.6 Hz,3H).














EXAMPLE 22
4-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide






22a) 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-2-methoxy-benzenesulfonamide was prepared as described above
22b) 4-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide

A solution of 5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-2-methoxy-benzenesulfonamide (85 mg), Pd(PPh3)2Cl2 (6 mg), 4-Ethynyl-N-methylbenzamide (30 mg), TBAF×3 water (140 mg) in THF (3 mL) and ethanol (0.3 mL) was stirred at 110° C. in a sealed microwave reactor for 30 min. The solvents were distilled off under reduced pressure. The crude mixture was taken up in ethyl acetate and extracted with water. The organic phase was reduced in vacuo and the title compound was obtained in 27% yield (27 mg) after flash chromatography. 1H-NMR (DMSO-d6): 10.35 s (1H); 8.54 q (J=4.6 Hz, 1H); 7.88 d (J=8.5 Hz, 2H); 7.62 d (J=8.3 Hz, 2H); 7.42 dd (J=8.5, 2.1 Hz, 1H); 7.35 d (J=7.7 Hz, 1H); 7.28 d (J=2.3 Hz, 1H); 7.12 d (J=7.7 Hz, 1H); 6.90 m (5H); 4.41 s (1H); 3.77 s (3H); 3.52 m (1H); 3.08 m (1H); 2.80 d (J=4.3 Hz, 3H); 2.62 dd (J=14.5, 10.1 Hz, 1H); 1.15 s (6H).


The following compound was obtained in analogy to the preparation methods described in detail:


















Method

1H-NMR




Product;
analogous
(400 MHz) δ


Ex.
reagents
to
[ppm]
Structure







23
3-{3-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propylsulfamoyl]-4-methoxy-phenylethynyl}-N-methyl-benzamide;5-Bromo-N-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-2-methyl-propyl]-2-methoxy-benzenesulfonamideand3-Ethynyl-N-methyl-benzamide
22

1H-NMR (DMSO-d6):10.35 m (1H); 8.55 m(1H); 7.99 m (1H); 7.86 m(1H); 7.67 m (1H); 7.52 t(J = 7.7 Hz, 1H); 7.42 dd(J = 8.5, 2.1 Hz, 1H); 7.35d (J = 7.4 Hz, 1H); 7.29 d(J = 2.1 Hz, 1H); 7.13 d (J =7.5 Hz, 1H); 6.90 m(5H); 4.40 s (1H); 3.78 s(3H); 3.52 m (1H); 3.08 m(1H); 2.81 d (J = 4.5 Hz,3H); 2.62 dd (J = 14.7,10.5 Hz, 1H); 1.15 s (6H).














EXAMPLE 24
2-Chloro-4-{7-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-N-methyl-benzamide






24a) 5-Bromo-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide

5-Bromo-2,3-dihydro-benzofuran-7-sulfonyl chloride (300 mg) was added to a solution of (D)-Trypophanol (240 mg) in dichloromethane (6 mL) and pyridine (1 mL) at ambient temperature. The reaction was stirred at ambient temperature for one our and quenched by the addition of sulphuric acid (2N). The reaction mixture was diluted with brine and dichloromethane and the phases were separated. The organic phases were dried over sodium sulphate and the solvent was distilled off under reduced pressure. The title compound was obtained in 29% yield (130 mg) after flash chromatography.



1H-NMR (DMSO-d6): 10.60 s (1H); 7.35 d (J=7.3 Hz, 1H); 7.28 s (2H); 7.23 m (2H); 6.96 m (2H); 6.87 m (1H); 4.72 m (1H); 4.43 m (2H); 3.41 m (1H); 3.34 m (1H); 3.23 m (1H); 3.04 m (2H); 2.88 m (1H); 2.57 m (1H).


24b) 2-Chloro-4-{7-[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-N-methyl-benzamide

A solution of 5-Bromo-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide (35 mg), 3-Chloro-4-methylcarbamoyl-phenyl boronic acid (18 mg), Pd(PPh3)4 (9 mg) in ethanol (1.04 mL), toluene (1.04 mL) and sodium carbonate (21 mg) in water (190 μL) was stirred at 100° C. overnight. The solvent was evaporated and the solid purified by flash chromatography to yield 69% of the title compound (29 mg). 1H-NMR (DMSO-d6): 10.56 s (1H); 8.34 d (J=4.6 Hz, 1H); 7.55 s (1H); 7.48 m (4H); 7.26 d (J=6.8 Hz, 1H); 7.19 m (2H); 6.95 s (1H); 6.88 m (1H); 6.71 m (1H); 4.71 m (1H); 4.52 m (2H); 3.42 m (1H); 3.33 m (1H); 3.24 m (1H); 3.12 m (2H); 2.87 m (1H); 2.62 m (1H).


The following compound was obtained in analogy to the preparation methods described in detail:


















Method

1H-NMR




Product;
analogous
(400 MHz) δ


Ex.
reagents
to
[ppm]
Structure







25
5-(3,4,5-Trimethoxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzofuran-7-sulfonic acid[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amideand3,4,5-Trimethoxy-phenylboronic acid
24

1H-NMR (DMSO-d6):10,83 s (1H); 7.56m (2H);7.22 m (3H); 6.98 d (J =2.0 Hz, 1H); 6.93 m (1H);6.75 m (1H); 6.72 s (2H);4.67 m (1H); 4.53 m (2H);3.81 s (6H); 3.65 s (3H);3.35 m (2H); 3.23 m (1H);3.15 m (1H); 2.87 m (1H);2.63 m (1H).














EXAMPLE 26
5-(4-Acetyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide






5-Bromo-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)ethyl]-amide (0.15 mmol, 0.2M in THF), 4-Acetyl-phenylboronic acid (1.5 equivalents, 0.4 M in THF), palladium-(II)-acetate (0.1 equivalents, 0.0375M in THF), trisorthotolyl-phosphine (0.2 equivalents, 0.05 M in THF), triethylamine (1.2 equivalents, 0.6 M in THF) and water (200 μL) were stirred under microwave irradiation at 130° C. for 45 minutes. The reaction mixture was cooled to ambient temperature, the solvent was removed under reduced pressure, DMSO (2 mL) were added and the crude product was purified via HPLC to yield the title compound.


HPLC purification: Column X-Bridge RP C18 4.6×50 3.5 μM; detection wavelength 214 nm; flow rate 2 ml/min; eluents A: 0.1% TFA in H2O, B 0.1% TFA in ACN; gradient in each case based on B: 1% to 99% (5′) to 99% (1′) to 1% (0.25°) to 1% (1.75°).


Molecular peak (ESI, M+1): 492; Retention time: 3.49 min.


The following compound was obtained in analogy to the preparation methods described in detail:


















Method





Product;
analogous


Ex.
reagents
to
HPLC-MS
Structure







27
5-(4-Methylsulfanyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Methylsulfanyl-phenylboronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):496Retention time: 4.03 min.










28
5-(3-Amino-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Amino-phenyl boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):465Retention time: 2.65 min.










29
5-(3-Trifluoromethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Trifluoromethyl-phenylboronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):518Retention time: 4.11 min.










30
5-(4-Hydroxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Hydroxy-phenyl boronicacid
26
HPLC purification: ColumnX-Bridge RP 018 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):466Retention time: 3.22 min.










31
5-(4-Fluoro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzofuran-7-sulfonic acid[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amideand4-Fluoro-phenyl boronic acid
26
HPLC purification: ColumnX-Bridge RP 018 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):468Retention time: 3.86 min.










32
5-(4-Cyano-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Cyano-phenyl boronicacid
26
HPLC purification: ColumnX-Bridge RP 018 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):475Retention time: 3.59 min.










33
5-Naphthalen-1-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandNaphthalene-1- boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):500Retention time: 4.22 min.










34
5-(4-Chloro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Chloro-phenyl boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):484Retention time: 4.16 min.










35
2-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethyl-sulfamoyl]-2,3-dihydro-benzofuran-5-yl}-benz-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand2-Carbamoyl-phenyl boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):493Retention time: 3.07 min.










36
5-(6-Methoxy-pyridin-3-yl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand6-Methoxy-pyridine-3-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):481Retention time: 3.21 min.










37
5-(2-Fluoro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand2-Fluoro-phenyl boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each case Hbased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):468Retention time: 3.87 min.










38
4-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethyl-sulfamoyl]-2,3-dihydro-benzofuran-5-yl}-N-methyl-benzamide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Methylcarbamoyl-phenylboronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):507Retention time: 2.99 min.










39
5-Quinolin-6-yl-2,3-dihydro-benzofuran-7-sulfonic acid[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandQuinoline-6-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):501Retention time: 2.65 min.










40
5-((E)-Styryl)-2,3-dihydro-benzofuran-7-sulfonic acid[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand(E)-2-Phenyl-etheneboronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):476Retention time: 4.07 min.










41
5-(3-Hydroxymethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Hydroxymethyl-phenylboronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):480Retention time: 3.22 min.










42
3-Fluoro-5-{7-[(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethylsulfamoyl]-2,3-dihydro-benzofuran-5-yl}-N-methyl-benzamide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Fluoro-5-methylcarba-moyl-phenyl boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 50


3.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):525Retention time: 3.23 min.










43
5-(3-Fluoro-5-methoxy-phenyl)-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Fluoro-5-methoxy-phenylboronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 50


3.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):498Retention time: 3.87 min.










44
N-(4-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethyl-sulfamoyl]-2,3-dihydro-benzofuran-5-yl}-phenyl)-acetamide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Acetamido-phenyl boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):507Retention time: 3.1 min.










45
5-(3,5-Dimethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3,5-Dimethyl-phenyl boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):478Retention time: 4.28 min.










46
5-quinolin-3-yl-2,3-dihydro-benzofuran-7-sulfonic acid[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandQuinoline-3-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):501Retention time: 2.72 min.










47
3-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethyl-sulfamoyl]-2,3-dihydro-benzofuran-5-yl}-benz-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Carbamoyl-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):493Retention time: 2.97 min.










48
5-(2-Fluoro-pyridin-3-yl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand2-Fluoro-pyridine-3-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):469Retention time: 3.34 min.










49
5-(5-Cyano-thiophen-2-yl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand2-Cyano-thiophene-5-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):481Retention time: 3.59 min.










50
N-(3-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethyl-sulfamoyl]-2,3-dihydro-benzofuran-5-yl}-benzyl)-acetamide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-(Acetylamino-methyl)-phenyl boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):521Retention time: 3.09 min.










51
5-(2-Methoxy-pyrimidin-5-yl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand2-Methoxy-pyrimidine-5-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):482Retention time: 3.01 min.










52
5-(4-Cyanomethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Cyanomethyl-phenyl-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):489Retention time: 3.62 min.










53
5-(3-Cyano-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Cyano-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):475Retention time: 3.6 min.










54
5-Benzo[1,3]dioxol-5-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandBenzo[1,3]dioxole-5-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):494Retention time: 3.71 min.










55
N-(3-{7-[(R)-2-Hydroxy-1-(1H-indol-3-ylmethyl)-ethyl-sulfamoyl]-2,3-dihydro-benzofuran-5-yl}-phenyl)-acetamide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Acetamido-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):507Retention time: 3.19 min.










56
5-Biphenyl-2-yl-2,3-dihydro-benzofuran-7-sulfonic acid[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandBiphenyl-2-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):526Retention time: 4.37 min.










57
5-o-Tolyl-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand2-Methyl-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM;detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):464Retention time: 4.02 min.










58
5-(3-Methanesulfonylamino-phenyl)-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amideand3-Methanesulfonylamino-phenyl-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):543Retention time: 3.34 min.










59
5-(4-Trifluoromethyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Trifluoromethyl-phenyl-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):518Retention time: 4.18 min.










60
5-Benzo[b]thiophen-3-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandBenzo[b]thiophene-3-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):506Retention time: 4.29 min.










61
5-Biphenyl-3-yl-2,3-dihydro-benzofuran-7-sulfonic acid[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandBiphenyl-3-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):526Retention time: 4.36 min.










62
5-(3-Acetyl-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Acetyl-phenylboronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):492Retention time: 3.52 min.










63
5-(3-Fluoro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Fluoro-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):468Retention time: 3.88 min.










64
2′,3′-Dihydro-[2,5′]bibenzo-furanyl-7′-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandBenzofuran-2-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):490Retention time: 4.07 min.










65
5-Benzo[b]thiophen-2-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandBenzothiophen-2-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):506Retention time: 4.18 min.










66
5-(3-Chloro-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Chloro-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):484Retention time: 4.12 min.










67
5-p-Tolyl-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Methyl-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detectionwave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):464Retention time: 4.04 min.










68
5-Naphthalen-2-yl-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandNaphthalene-2-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):500Retention time: 4.2 min.










69
5-(3-Methoxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand3-Methoxy-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):480Retention time: 3.88 min.










70
5-(4-Methoxy-phenyl)-2,3-dihydro-benzofuran-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideand4-Methoxy-phenyl-boronicacid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):480Retention time: 3.77 min.










71
5-Thiophen-3-yl-2,3-dihydro-benzofuran-7-sulfonic acid[(R)-2-hydroxy-1-(1H-indol-3-ylmethyl)-ethyl]-amide;5-Bromo-2,3-dihydro-benzo-furan-7-sulfonic acid [(R)-2-hydroxy-1-(1H-indol-3-yl-methyl)-ethyl]-amideandThiophene-3-boronic acid
26
HPLC purification: ColumnX-Bridge RP C18 4.6 × 503.5 μM; detection wave-length 214 nm; flow rate 2ml/min; eluents A: 0.1%TFA in H2O, B 0.1% TFA inACN; gradient in each casebased on B: 1% to 99% (5′)to 99% (1′) to 1% (0.25′) to1% (1.75′).Molecular peak (ESI, M + 1):456Retention time: 3.77 min.













Claims
  • 1. A method of using a compound of the formula I
  • 2. Method of claim 1 for fertility control in men or women.
  • 3. Method according to claim 1, characterised in that in formula I R3 may be hydroxy, halogen, nitro, amino, cyano, C1-C6-alkyl, C2-C6-alkenyl or C2-C6-alkynyl, C3-C7-cycloalkyl, hydroxy-C1-C6-alkylene, hydroxy-C3-C6-alkenylene, hydroxy-C3-C6-alkynylene, C1-C6-alkyloxy, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy, C3-C7-cycloalkyl-C1-C6-alkylenoxy, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkyloxy-C3-C6-alkenylene, C1-C6-alkyloxy-C3-C6-alkynylene, C1-C6-alkyloxyphenyl-C1-C6-alkylene, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6-alkyl)amino-C1-C6-alkylene, phenyloxy-C1-C6-alkylene; where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano, hydroxy, amino or the groups
  • 4. A compound which is
  • 5. Compounds of formula I of claim 1 characterised in that R3 may be hydroxy-C3-C6-alkenylene, hydroxy-C3-C6-alkynylene, C1-C6-alkyloxy-C1-C6-alkylene, C3-C7-cycloalkyloxy, C3-C7-cycloalkyl-C1-C6-alkylenoxy, C3-C7-cycloalkyloxy-C1-C6-alkylene, C1-C6-alkyloxy-C3-C6-alkenylene, C1-C6-alkyloxyC3-C6-alkynylene, C1-C6-alkylamino-C1-C6-alkylene, di(C1-C6-alkyl)amino-C1-C6-alkylene, where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano, hydroxy, amino or the groups
  • 6. Compounds of formula I of claim 1 characterised in that R4 may be C3-C7-cycloalkyl-C1-C6-alkylene, C3-C7-heterocycloalkyl, where the hydrocarbon chains therein may optionally be substituted one or more times by fluorine, cyano or the radicals:
  • 7. Compounds according to claim 6 having the formula II
  • 8. Compounds according to claim 6, namely
  • 9. Compounds of formula III
  • 10. Compounds according to claim 9 having the formula IV
  • 11. Compounds according to claim 9, namely
  • 12. Process for preparing compounds of the formula I of claim 1, wherein a tryptophanol derivative of the formula V
  • 13. Process for preparing compounds of the formula II of claim 7, wherein a tryptophanol derivative of the formula V is coupled with a sulfonyl chloride of the formula VII
  • 14. Process for preparing compounds of the formula III of claim 9, wherein a tryptophanol derivative of the formula V is coupled with a sulfonyl chloride of the formula VIII
  • 15. Process for preparing compounds of the formula IV of claim 10, wherein a tryptophanol derivative of the formula V is coupled a sulfonyl chloride of the formula IX
  • 16. Process for preparing compounds of the formula I of claim 1, wherein the building block of the formula X
  • 17. Process for preparing compounds of the formula II of claim 7, wherein the building block of the formula X is coupled with an aryl halide of the formula XII
  • 18. Process for preparing compounds of the formula III of claim 9, wherein the building block of the formula X is coupled with an
  • 19. Process according to claim 10 for preparing compounds of the formula IV of claim 10, wherein the building block of the formula X is coupled with an aryl halide of the formula XIV.
  • 20. Aryl halides as intermediates in a process according to claim 16, namely
  • 21. Pharmaceutical compositions comprising at least one of the compounds according to claim 4 and pharmaceutically suitable excipients and/or carriers.
Parent Case Info

This application claims the benefit of the filing date of U.S. Provisional Application Ser. No. 60/892,371 filed Mar. 1, 2007.

Provisional Applications (1)
Number Date Country
60892371 Mar 2007 US