SI9300375A - Imidazole,triazole and tetrazoles derivates - Google Patents

Abstract

A group of substituted imidazole derivatives, triazoles and tetrazole are selective 5-HT1-like angonists receptors and are therefore useful in treatment clinical conditions, especially migraines and related conditions, for which selective angonists of these receptors are indicated.

Description

DERIVATIVES OF IMIDAZOLE, TRIAZOLE AND TETRAZOLE

The present invention relates to a group of substituted imidazole, triazole and tetrazole derivatives that act on 5-hydroxytryptamine (5HT) receptors as selective agonists, e.g. 5-HT1-like receptors. Therefore, they are useful in the treatment of clinical conditions for which selective agonists of these receptors are indicated.

5-HT1-receptor receptor agonists that are active as selective vasoconstrictors have recently been described as useful in the treatment of migraine (see, for example, A. Doenicke et al., The Lancet, 1988, Vol. 1, 1309-11). Thus, the compounds of the present invention, as selective 5-HT1-receptor receptor agonists, are particularly useful in the treatment of migraine and related conditions, for example, certain types of cluster headache, chronic paroxysmal hemicrania, headache coupled with vascular disorders, headaches that it is caused by pressure and pediatric migraines.

EP-A-0313397 describes a group of tryptamine derivatives substituted with a five-membered heteroaliphatic ring, which are said to be specific for a particular type of 5-HT 1-receptor and therefore effective therapeutic agents for the treatment of clinical conditions, especially migraines, which require this activity. However, EP-A-0323397 neither discloses nor lists the imidazole, triazole and tetrazole derivatives provided by the present invention.

The present invention provides a compound of formula I, or a salt or prodrug thereof:

(I) in which a broken circle means two non-adjacent double bonds at any position of a five-membered ring;

two, three or ¹ four of V, W, X, Y and Z represent nitrogen and the rest carbon if, when two of V, W, X, Y and Z represent nitrogen and other carbon, said nitrogen atoms at non-adjacent positions in a five-member ring;

E represents hydrogen, hydrocarbon, heterocyclic group, halogen, cyano, trifluoromethyl, -O R ^x , -SR ^X , -NR ^X R 4, -NR ^x CO ₂ Ry, or -NR ^Z CTNR ^X R 4;

Ό

A represents an unbound electron pair when four of V, W, X, Y and Z represent nitrogen and the other represents carbon; or, when two or three of V, o

W, X, Y and Z are nitrogen and the rest are carbon, A is hydrogen, hydrocarbon, heterocyclic group, halogen, cyano, trifluoromethyl, -OR \ -SR ^X , -NR ^X R ^, -NR ^x COR ^y , -NR ^X CO2R ^, -NR ^X SO2R ^ or NR ^Z CTNR ^X R ^;

E represents a bond or a straight or branched alkylene chain having 1 to 4 carbon atoms;

F represents a group of formula

U represents nitrogen or C-R4;

Oh

B represents oxygen, sulfur or N-R;

R ¹ represents -CH ₂ .CHR ₁ .NR (R) or a group of formula

in which the broken line represents any chemical bond;

R ^, R ³ , R ^, RS, R® and R? independently represent hydrogen or C1-8 or kil;

R ^x and R ^y independently represent a hydrogen, hydrocarbon or heterocyclic group, or R ^x and R 4 together represent a C ₂ .g group;

R ^z represents hydrogen, hydrocarbon or heterocyclic group;

T represents oxygen, sulfur or a group of formula = N.G; and · '

G represents a hydrocarbon, a heterocyclic group or an electron attracting group.

The present invention also provides compounds of formula (I) above, wherein three or four of V, W, X, Y and Z are nitrogen and the rest are carbon;

A ² represents an unbound electron pair when four of V, W, X, Y and Z represent nitrogen and the other represents carbon; or, when three of V, W, X, Y and Z represent nitrogen and the other carbon, A ² represents hydrogen, hydrocarbon, heterocyclic group, halogen, cyano, trifluoromethyl, -OR ^x , -SR ^X , -NR ^x R ^y , -NR ^x COR ^y , -NR ^x CO2R ^y , -NR ^x SO2R ^y or -NR ^with CTNR ^x R ^y ; and

A ^, E, F, R ^x , R ^y , R ^z and T are as defined above. _L For use in medicine, salts of compounds of Formula I will be non-toxic pharmaceutically acceptable salts. However, other salts may be useful in the preparation of the compounds of the invention or their non-toxic pharmaceutically acceptable salts. Suitable pharmaceutically acceptable salts of the compounds of this invention include acid addition salts, which can be obtained, for example, by mixing a solution of a compound of the invention with a solution of a pharmaceutically acceptable non-toxic acid such as hydrochloric acid, formic acid, maleic acid, succinic acid, acetic acid, benzoic acid , oxalic acid, citric acid, tartaric acid, carbonic acid or phosphoric (V) acid. Further, where the compounds of the invention have an acidic group, their pharmaceutically acceptable salts may include alkali metal salts, for example, sodium or potassium salts; alkaline earth metal salts, for example calcium or magnesium salts; and salts formed with suitable organic ligands, for example quaternary ammonium salts.

The term hydrocarbon as used herein includes straight chain, branched chain and cyclic groups containing up to 18 carbon atoms, up to 15 carbon atoms and up to 12 carbon atoms. Suitable hydrocarbon groups include, Cj.g alkyl, C ₂ _g alkenyl, C ₂ _g alkynyl, C3-7 cycloalkyl. C3-7 cycloalkyl (C1-8) alkyl, aryl and aryl (C1-8) alkyl.

The term heterocyclic group as used herein includes cyclic groups containing up to 18 carbon atoms and at least one heteroatom, preferably selected from oxygen, nitrogen and sulfur. The heterocyclic group suitably contains up to 15 carbon atoms and conveniently up to 12 carbon atoms, and is preferably bonded * via carbon. Examples of suitable heterocyclic compounds include heterocycloalkyl, C3-7 heterocycloalkyl (C1-8) alkyl, heteroaryl and heteroaryl (C1-8) alkyl groups.

Suitable alkyl groups include straight- and branched-chain alkyl groups containing from 1 to 6 carbon atoms. Typical examples include the methyl and ethyl groups and the straight or branched chain propyl and butyl groups. Special alkyl groups are methyl, ethyl and t-butyl.

Suitable alkenyl groups include straight or branched chain alkenyl groups containing from 2 to 6 carbon atoms. Typical examples include vinyl and allyl groups.

Suitable alkynyl groups include straight- or branched-chain alkynyl groups containing from 2 to 6 carbon atoms. Typical examples include the ethynyl and propargyl groups.

Suitable cycloalkyl groups include groups containing 3 to 7 carbon atoms. The cycloalkyl groups are cyclopropyl and cyclohexyl.

A special aryl group is phenyl.

Particular aryl (C1-8) alkyl groups include benzyl, phenethyl and phenylpropyl.

Suitable heterocycloalkyl groups include azetidinyl, pyrrolidyl, piperidyl, piperanisyl and morpholinyl groups.

Suitable heteroaryl groups include the pyridyl, quinolyl, isoquinolyl, pyridazinyl, pyrimidinyl, pyrazinyl, pyranyl, furyl, benzofuryl, dibenzofuryl, thienyl, benzthienyl, imidazolyl, oxadiazolyl and thiadiazolyl groups.

Particular heteroaryl (C1-8) alkyl groups include pyridylmethyl and pyrazinylmethyl.

The hydrocarbon and heterocyclic groups may be optionally further substituted by one or more groups selected from: C 1-6 alkyl, adamantyl, phenyl, halogen, C 1-8 haloalkyl, C 1-8 aminoalkyl, trifluoromethyl, hydroxy, C 1-6 alkoxy, aryloxy, keto, alkylenedioxy, nitroxyano , carboxy, alkoxycarbonyl Cg.g, Cg.g alkoxycarbonyl (Cj.g) alkyl, C2-5 alkylcarbonyloxy, arylcarbonyloxy, Cg_g arylcarbonyl, Cj_g alkylthio, Cj.g alkylsulphinyl, Cj.g alkylsulphonyl, arylsulphonyl, -NR ^V COR ^W , -NR ^V CO2R ^W , -NR ^v SO2R ^w , -CH2NR ^v SO2R ^w , -NHCONR ^v R ^w , SO2NR ^v R ^w and -CH2SO2NR ^V R ^W in which R ^v and R ^w independently represent hydrogen, Cj. g alkyl, aryl or aryl (Cj.g) alkyl, or R ^v and R ^w together represent a C2_g alkylene group.

When R ^x and R ^y, or R ^v and R ^w together represent a C ₂ _g alkylene group, this group is an ethylene, propylene, butylene, pentametilenska or hexamethylene group, preferably using butylene or penfametilenski.

When group G is an electron-attracting group, it is appropriate that this group be cyano, nitro, -COR ^X , -COgR * or -SO ^ R *, in which x is as defined above.

The term halogen as used herein includes fluorine, chlorine, bromine and iodine, especially fluorine.

The present invention also encompasses prodrugs of the compounds of formula (I) above. In general, such prodrugs will be functional derivatives of compounds of formula (I) that can be readily converted into the desired compound of formula (i) in vivo. of Prodrugs, ed. H, Bundgaard, Elsevier, 1985.

In case the compounds of the invention have at least one asymmetric center, they can therefore exist as enantiomers. Additionally, the compounds of the invention may have diastereoisomers if they have two or more asymmetric centers. It should be appreciated that the present invention encompasses all such isomers and mixtures thereof.

It will be appreciated that imidazole, triazole and tetrazole rings of formula I can exist in various canonical forms. This can be properly exemplified by IA to IT formulas as follows:

(ID) (IE) (IF) /

in which A ¹ , A ² , E and F are as defined above. The imidazole, triisole and tetrazole rings of the formula I that are recommended include the rings represented by the formulas IA, IC, IG, IH, IL, IM, IM, IP, and IQ above, especially IH.

The alkylene chain E may be, for example, methylene, ethylene, 1-methylethylene, propylene or 2-methylpropylene. Alternatively, group E may be a single bond such that group F in formula I is linked directly to a five-membered heteroaromatic ring.

Group F is indole, benzofuran or benzthiophene. a group of formula FA, or an indazole group of formula FB:

(FA) (FB) in which B, R ^, R ² and R ^{3 are} as defined above. Group F preferably means an indole group of FC structure:

(FC) wherein R ¹ , R ² and R ^{3 are} as defined above, in particular where R ² and R ³ are both hydrogen.

They will appreciate that group A ^{2 will be an} unbound electron pair when four of V, W, X, Y and Z represent nitrogen and the other is carbon. in case the Formula I ring is a tetrazole ring. Otherwise, A ^ and A ^{2 will} independently represent hydrogen, hydrocarbon, heterocyclic group, halogen, cyano, trifluoromethyl, -0R ^x , -SR ^X , -NR ^x R ^y , -NR ^x C0R7, -NR ^x CO2Ry, -NR ^X SO2R ^ or -NR ^with CTNR ^x R ^y .

Suitable values for the aM and / or A ² groups include C 1-8 alkyl, C 3-7 cycloalkyl, aryl, aryl (C 1-8) alkyl, ¢ 3.7 heterocycloalkyl 1, heteroaryl or heteroaryl (C 1-8) alkyl, each of these groups however, it may be optionally substituted; and hydrogen, halogen, cyano, trifluoromethyl, alkoxy Cj_g, Cj_g alkylthio or NR ^X R, where R ^x and R are as defined above. Examples of optional substituents on the groups A and / or A suitable include trifluoromethyl, Cj.g alkoxy, C ₂ .G alkyl carbonyl 1 1 Cj_g alkylsulfonyl, arylsulfonyl, amino, mono- or di (Cj_g) alkylamino, C ₂ _g alkylcarbonylamino, arylcarbonylamino , C ₂ -g alkylcarbonylamino, arylcarbonylamino, C ₂ -g alkoxycarbonylamino, C 1-8 alky 1sulfones 1amino, arylsulfonylamino, C 1-8 alkylsulfonylaminomethyl, aminocarbonylamino, mono- or di (C 1-8) alkyJaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminoalkylamino, mono- or di (C1-6) alkylaminocarbonyl, C1-6 alkylaminosulfonyl, aminosulfonylmethyl, mono- or di (C1-8) alkylaminosulfonylmethyl.

Specialty A ^ and / or A ^ specific hydrogen, , metilsulfonilaminoetil, aminokarboni1aminoeti 1 metilaminokarbonilaminoetil, t-butilaminokarbonilaminoetil, phenyl laminokarbonilaminoetil, pirolidilkarbonilaminoetil, cyclopropyl, phenyl, metilsulfonilaminofenil, aminokarboni1 phenyl-1, methyl laminokarboni1 phenyl-1, methylsulfonyl ami nometilfenil, aminosulfonilmetilfenil, methyl veins nose! sulfonyl Imetilfeni 1 dimetilaminosulfonilmetilfenil, benzyl, trifluoromethylbenzyl, methoxybenzyl, acetylaminobenzyl, methylsulfonylaminobenzyl, aminocarbonylaminobenzyl, aminocarbonylbenzyl, methylaminocarbonylbenzyl, methylsulfonylbenzyl, methylaminosulfonylbenzyl, pyridylmethylmethyl, methoxymethyl, methoxymethylmethyl, methoxypropylmethyl yl, amino, methylamino / benzylamino, dimethylamine, t-butoxycarbonylaminoethylamino and methylsulfonylaminoethylamino.

Preferred A 4 and / or A 4 values include hydrogen, methyl, ethyl, benzyl and amino.

Typical R 1 values include aminoethyl, N-methylaminoethyl, N, N-dimethylaminoethyl, 4-piperidyl, 1-methyl-4-piperidyl, 3-pyrrolidines 1, and 1methyl-3-pyrrolidinyl.

The preferred values of the groups up to R ⁷ are hydrogen and methyl.

A particular subtype of the compounds of the invention are compounds of formula IIA, salts or prodrugs thereof:

(IIA) in which χΐ represents nitrogen or A ^ -C n is zero, 1, 2 or 3;

means oxygen, sulfur or NR ^ ³ ;

A ¹¹ and A ¹² independently represent C 1-6 alkyl, C 3-6 alkenyl, C 1-8 alkynyl, C 1-5; cycloalkyl, aryl, aryl (C1-8) alkyl, C8,? heterocycloalkyl, heteroaryl or heteroaryl (C1-8) alkyl, each of these groups being optionally substituted; or hydrogen, halogen, cyano, trifluoromethyl, C _1-6 alkoxy, C 1-6 alkylthio or -NR ^x R ^y ;

R * ² , R * ³ , R ¹⁴ , R ¹⁶ and R ¹ ? independently represent hydrogen or C _1-6 alkyl; and

R ^x and R ^y independently represent a hydrogen, hydrocarbon or heterocyclic group, or R ^x and R 4 together represent a C 1-8 alkylene group.

Examples of any substituents on the groups A ^ and A ^ ² suitably include trifluoromethyl, C1-6 alkoxy, C1-8 alkoxycarbonyl, C1-8 alkylsulfonyl, arylsulfonyl, amino, mono- or di (C1-6) alkyamino, C 1-8 alkylcarbonylamino, arylcarbonylamino, arylcarbonyl alkoxycarbonylamino, C1-6 alkyl style background amino, arylsulfonylamino, C1-8 alkylsulfonylaminomethyl, aminocarbonylamino, mono- or di (C1-8) alkylaminocarbonylamino, mono- or diarylaminocarbonylamino, pyrrolidylcarbonylarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylamino C 1-6 alkylaminosulfonyl, aminosulfones Have 1, and mono- or di (C 1-8) alkylaminosulfonylmethyl.

Particular values of A ¹¹ and A ¹² , with respect to formula IIA, include hydrogen, methyl, ethyl, benzyl and amino. When A ^ ^{2 is} -C, then it is preferable that the group A ¹ * is hydrogen or methyl.

Preferably R ^ ² , R ^ ³ and R ^ each represent hydrogen. Preferred values for R ¹ ® and R 4, according to formula IIA, include hydrogen and methyl.

Another subtype of the compounds of the invention are compounds of formula IIB, and salts or prodrugs thereof:

(I I B) in which γϊ represents nitrogen or A ^ -C;

n is zero, 1, 2 or 3;

β2 represents oxygen, sulfur or NR ^ 3 _;

A ^ and A ^ZZ independently represent C1-6 alkyl, C8-8 alkenyl, C1-8 alkynyl, C3-7 cycloalkyl, aryl, aryl (C1-8) alkyl, C3-7 heterocycloalkyl, heteroaryl or heteroaryl (C1-8) alkyl, each of these groups may however be optionally substituted; or hydrogen, halogen, cyano, trifluoromethyl, C1-6 alkoxy, C1-8 alkylthio or -NR ^x R ^y .

R ^2, R 2 ^3, R 24, R 26 j _n R27 _neo epending hydrogen or Cj_g alkyl; and

R ^x and R ^y independently represent a hydrogen, hydrocarbon or heterocyclic group, or R ^x and R 4 together represent a C 1-8 alkylene group.

The examples of any substituents on the groups A ^ ¹ and A ^ 2 correspond to those indicated for groups A ¹¹ and A with respect to Formula IIA. Specific values of A ^ and A ^^ according to formula IIB include hydrogen, methyl, ethyl and benzyl.

Preferably R ^^, r23 j _n r24 _all ^ means hydrogen. Preferred values of R1 and R2 with respect to Formula IIB include hydrogen and methyl.

A further subset of the compounds of the invention are compounds of formula IIC, and salts or prodrugs thereof:

(IIC) in which

Y ^Z represents nitrogen or A ^ -C represents nitrogen or CH;

n is zero, 1, 2 or 3;

B ³ represents oxygen, sulfur or NR ³³ ;

ϋΐ 0 0

A and A independently represent a Cj.g alkyl, C ₂ _g alkenyl, C ₂ _g alkynyl, _C3 _7 cycloalkyl, aryl, aryl (Cj.g) alkyl, C ₃ .y heterocycloalkyl, heteroaryl or heteroaryl (Cj.g) alkyl , each of these groups may be optionally substituted; or hydrogen, halogen, cyano, trifluoromethyl · alkoxy, C1-8 alkylthio or -NR ^x R ^y .

R ³¹ stands for -CH ₂ .CHR ³⁴ .NR ³⁶ R

Ί-6 or

NR r ³ 2, r33, r34 * r35, r36 p37 _neoc | _in j _sno mean hydrogen or

C1-6 alkyl; and

R ^x and R neodvsino represent hydrogen, hydrocarbon or a heterocyclic group, or R ^x and R ^ together represent a C ₂ _g alkylene group.

About ί 00

The examples of any substituents on groups A and A correspond to those indicated for groups A ¹¹ and A ¹³ with respect to formula IIA. Specific values of A ³¹ and A 3 ^Z , according to formula IIC, include hydrogen, methyl, and amino.

Preferably R ³³ , R ³³ and R ³⁴ each represent hydrogen. Priority values R ³ ^, R ³ ® and R ³ ? include hydrogen and methyl.

A further subset of the compounds of the invention are compounds of formula IID, and salts or prodrugs thereof:

(IID) in which

H ¹ represents nitrogen or A ⁴² -C n is zero, 1, 2 or 3;

B ⁴ represents oxygen, sulfur or NR 4;

A ⁴ ^ and A ⁴² independently represent a Cj.g alkyl, C £ _g alkenyl, C ₂ .G alkynyl ¢ C3-7 cycloalkyl, aryl, aryl (Cj.g) alkyl, C3-7 heterocycloalkyl, heteroaryl or heteroaryl (Cj_g) alkyl , each of these groups may be optionally substituted; or hydrogen, halogen, cyano, trifluoromethyl, C1-6 alkoxy, C1-8 alkylthio or -NR ^x R ^y .

R ⁴ is -CH ₂ .CHR ⁴⁴ .NR ⁴ ®R ⁴⁷ or a group of formula

R ⁴² , R ⁴ ^, R ⁴⁴ , R ⁴⁵ , R ⁴ ® and R ⁴ ? independently represent hydrogen or C 1-6 alkyl; and

R ^x and R ^y neodvsino represent hydrogen, hydrocarbon or a heterocyclic group, or R ^x and R ^y together represent a C ₂ _g alkylene group.

The examples of any substituents on groups A ⁴¹ and A ⁴² are identical to those indicated for groups A ^ ¹ and a ¹² with respect to Formula IIA. The particular values of A ⁴ * and A ⁴² , according to formula IID, include hydrogen and methyl.

Preferably R ⁴² , R ⁴ ^ and R ⁴⁴ each represent hydrogen. Preferred values of R ⁴ , R ⁴⁶ and R ⁴⁷ include hydrogen and methyl.

Specific compounds within the scope of the invention include:

2- [5- (2-Benzyltetrazol-5-ylmethyl) -1H-indol-3-yl 2- {5- (1-benzyltetrazol-5-ylmethyl) -1H-indol-3-yl

N, N-dimethyl-2N, N-dimethyl-2N, N-dimethyl-2ethylamine; ethylamine;

5- (1-methyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethylamine; 5- (2-methyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethylamine; 5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-yl] ethylamine;

N, N-dimethyl-2- [5- (tetrazol-2-ylmethyl) -1H-indol-3-ylamine lamin;

N, N-dimethyl-2 ·

N, N-dimethyl-2

N, N-dimethyl-25- (tetrazol-1-ylmethyl 1) -IH-indol-3-yl] ethylamine;

5- (1-methyl-1,2,2-triazol-5-ylmethyl) -1H-indol-3-yl] ethylamine;

5- (1-methyl-1,2,4-triazol-3-ylmethyl) -1H-indol-3-ylmethylamine;

N, N-dimethyl-2- [5- (1,2,3-triazol-1-ylmethyl) -1H-indol-3-ethyl ethyl amine;

3- (2-aminoethyl) -5- (1-methyltetrazol-5-yl) -benzo [b] thiophene;

3- (2-aminoethyl) -5- (2-methyltetrazol-5-yl) -benzo (biothiophene;

3- [2- (N, N-dimethylamino) ethyl-5- (2-methyltetrazol-5-yl) benzo (biothiophene;

N, N-dimethyl 1 -2- [5- (2-methylimidazol-1-ylmethyl T) -1H-indol-3-yl] ethylamine;

N, N-dimethyl-2- [5- (imidazol-1-ylmethyl) -1H-indol-3-ylamine lamin;

N, N-dimethyl-2- (5- (2-methylimidazol-1-yl) -1H-indol-3-ylmethylamine;

N, N-dimethyl-2- [5- (2-ethyltetrazol-5-ylmethyl) -1H-indol-3-yl] lamine;

N, N-dimethyl-2- [5- (1-ethyltetrazol-5-ylmethyl) -1H-indol-3-ylamine lamine; _L N, N-dimethyl-2- {5- (1,2,4-triazol-1-yl) -1H-indol-3-yl] ethylamine;

1-methyl 1-4- (5- (2-methylimidazol-1-yl) -1H-indol-3-ylpiperidine;

1-methyl-4- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-ylpiperidine;

4- [5- (2-Methylimidazol-1-yl) -1H-indol-3-yl] piperidine;

4- [5- (1,2,4-Triazol-1-ylmethyl) -1H-indol-3-ylpiperidine;

3- [5- (2-Methylimidazol-1-yl) -1H-indol-3-yl] pyrrolidine;

1-Methyl 1-3- [5- (2-methylimidazol-1-yl) -1H-indol-3-ylpyrrolidine;

4- [5- (imidazol-1-yl) -1H-indol-3-yl] piperidine;

4-Γ.5- (1,2,3-tri azol-1-yl) -IH-indole-3-ylpiperidine;

1-Methyl-4-C5- (imidazol-1-yl) -1H-indol-3-ylpiperidine;

1-methyl-4- [5- {1,2,3-triazol-1-yl) -1H-indol-3-yl] piperidine;

1-methyl 1-3-C5- (1,2,3-triazol-1-yl) -1H-indol-3-ylpyrrolidine;

1-methyl-3- [5- (2-methylimidazol-1-ylmethyl) -1H-indol-3-yl] pyrrolidine;

1-Methyl 1-3-f 5- (imidazol-1-yl) -1H-indol-3-ylpyrrolidine;

1-methyl-3- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-ylpyrrolidine;

1-methyl-3-C5- (imidazol-1-ylmethyl) -1H-indol-3-ylpyrrolidine;

N, N-dimethyl-2- [5- (2-aminoimidazol-1-yl) -1H-indol-3-yl ethylamine;

N, N-dimethyl 1-2- [5- (2-aminoimidazol-1-ylmethyl) -1H-indol-3-ylmethylamine; N-methyl-2- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-ylmethyl amine;

and their salts and prodrugs.

The invention also provides pharmaceutical compositions containing one or more compounds of this invention together with a pharmaceutically acceptable carrier. Preferably, these compounds are in the form of dosage units such as tablets, pills,

9i capsules, powders, granules, sterile parenteral solutions or suspensions, metered aerosol or liquid dispensers, droplets, ampoules, auto-injector devices or suppositories; for oral, parenteral, intranasal, sublingual or rectal use, or for administration by inhalation or insufflation. For the preparation of solid compositions such as tablets, the main active ingredient is mixed with a pharmaceutical carrier, e.g. conventional tabletting ingredients such as cornstarch, lactose, sucrose, sorbitol, talc, stearic acid, magnesium stearate, dicalcium phosphate or resins, and other pharmaceutical diluents, e.g. water to form a solid preformulation composition comprising a homogeneous mixture of a compound of the invention or a non-toxic pharmaceutically acceptable salt thereof. When these preformulation compositions are referred to as homogeneous, we mean that the active ingredient is uniformly dispersed throughout the composition, so that the composition can easily be given to the smallest equally effective dosage unit forms, such as tablets, pills and capsules. The solid preformulation composition is then dispensed into dosage unit forms of the type described above containing from 0.1 to about 500 mg of the active ingredient of the present invention. The tablets or pills of the new composition may be coated or otherwise assembled to achieve a dosage form that benefits from long-lasting action. For example, a tablet or pill may contain an inner and outer dose component, the second in the form of an envelope above the first. These two components can be separated by an enteric layer that prevents disintegration in the stomach and allows the internal component to pass into the duodenum intact or to be relaxed. Various substances or coatings may be used for such enteric layers, such substances include multiple polymeric acids and mixtures of polymeric acids with substances such as shellac, cetyl alcohol and cellulose acetate.

Liquid forms for oral administration or injectable use into which new compositions of the present invention may be incorporated include aqueous solutions, suitably flavored syrups, aqueous or oily suspensions, and perfumed emulsions with edible oils such as cottonseed oil, sesame oil, coconut oil or peanut oil, as well as elixirs and similar pharmaceutical carriers. Suitable agents for dispersing or suspending in aqueous suspensions include synthetic or natural resins such as tragacanth, acacia, alginate, dextran, sodium carboxymethylcellulose, methylcellulose, polyvinylpyrrolidone or gelatin.

A suitable dose for migraine treatments is about 0.01 to 250 mg / kg per day, preferably about 0.05 to 100 mg / kg per day, and in particular about 0.05 to 5 mg / kg per day. The administration regimen of the compounds may be from 1 to 4 times daily.

The 1,2,4-triazole compounds of this invention can be prepared by a process comprising the reaction of a reactive carboxylic acid derivative of the formula

R ^a -CO ² H, with a compound of either formula III or formula IV, or a salt thereof:

NHR ^b

N

NHR ^b (IV) in which one of R ^a , R ' and R ^{c is a} group of formula A *, the second is a group of formula a ² , and the third is a group of formula -EF, as defined by reference to Formula I above .

Suitable reactive acid derivatives of R ^ COgH include esters, for example (4.4 alkyl esters, thioesters, for example pyridylthioesters, acid anhydrides, for example (R ^a -CO) 2O, acid halides, for example acid chlorides, orthoesters, and primary, secondary and tertiary amides.

Preference is given to the reactive acid derivative R ^a -CO2H, which is an iminoether derivative of formula V:

RO

where R is C _1-4 alkyl.

The reagent of formula III may be formed in situ, in a reaction mixture. For example, the reaction can be effected by treating a compound of formula V above with alkyl hydrazine, e.g. methyl chirazine followed by a suitable carboxylic acid such as formic acid.

Typically, the reaction is carried out by heating the reagents together, optionally in a solvent, for example tetrahydrofuran, dimethylformamide or lower alkanol, such as ethanol, propanol or isopropanol _t at about 20 ° C to 100 ° C for about 1 to 6 hours.

If R ^a is ^a group of formula -EF and group F is an indole moiety of the FC structure as defined above, a reactive carboxylic acid derivative of formula HO2C-EF can be prepared by converting a compound of formula VI:

(VI) in which Q represents a reactive carboxylate group and E is as defined above with a compound of formula VII or a carbonyl protected form thereof:

(n) wherein R ^ are as defined above and R ¹ * corresponds to the group R ^1, as defined above, or a group of the formula -CHg.CHR ^ D ^1, in which R \ are as defined above, means a group that is easily moved; this is followed, where necessary, by N-alkylation using standard methods to insert the R group.

Suitable carbonyl protected forms of the compounds of formula VII include dimethyl acetal or ketal derivatives.

The group in the compounds of Formula VII which is readily substituted is suitably a halogen atom, preferably chlorine. When the group R in compounds of formula VII, is a group of formula -CHg.CHR ^ D ^1, the substituent D * replaced in situ under the prevailing reaction conditions to sustain the end product of formula I in which R represents a group of the formula - CHg.CHR ^ .NHg. The terminal amino group may subsequently, if desired, be further refined using techniques known in the art to obtain a compound of formula I in which R1 represents the required group of formula -CHg.CHR2 .NR2R2.

The reactions of compounds VI and VII can be carried out in one step (Fischer indole synthesis) or with a starting state without cyclization, at a lower temperature to give the compound of formula VIII:

Q-E

(VIIIa): wherein Q, E, R ^ and R ^ ¹ are as defined above, followed, sledAciklizacija by using a suitable reagent, such as poly phosphate ester, to give a compound of the formula QEF.

Hydrazines of formula VI can be prepared from the corresponding anilines of formula IX:

Q-E

(IX) in which Q and E are as defined above, with diazotization followed by reduction. Diazotization is typically carried out using sodium nitrite / conc. HC1 and the resulting diazo product are reduced in situ using, for example, tin (II) chloride / conc. HCl or sodium sulfite / conc. HCl.

Anilines of formula IX can be prepared by reduction of the corresponding nitro compounds of formula X:

Q-E

(x) wherein Q and E are as defined above, typically by catalytic hydrogenation or by using tin (II) chloride.

When not commercially available, nitro compounds of formula X can be synthesized by standard methods well known in the art.

Where R ^a is ^a group of formula -EF and group F is an indazole group of FB structure, as defined above, a reactive carboxylic acid derivative of formula HO ₂ CEF can be prepared by cyclization of a compound of formula XI:

(XI) in which Q, E and R ^{1 are} as defined above and D ² represents a group which can be exchanged without difficulty; this is followed, where necessary, by N-alkylation by standard methods to introduce the R ³ group.

The cyclization of compound XI is usually carried out in a suitable organic solvent at elevated temperature, for example in a mixture of m-xylene and 2,6-lutidine, at a temperature in the range of 140 ° C.

The group D ² in the compounds of formula XI, which is easily removed, appropriately represents a C 1-4 alkanoyloxy group, preferably acetoxy. In the case of p

that in the desired compound of formula XI D is acetoxy, this compound can be conveniently prepared by treating the compound of formula XII:

(XII) wherein R ¹ , E and Q as defined above, or a protected derivative thereof, are hydroxylamine hydrochloride, preferably in pyridine at a solvent reflux temperature; followed by acetylation with acetic anhydride, appropriate in the presence of catalytic amounts of 4-dimethylaminopyridine, in dichloromethane, at room temperature.

The N-formyl protected derivatives of an intermediate of formula XII can be prepared in a conventional manner by ozonolysis of an indole derivative of formula XIII:

(XIII) wherein R ¹ , E and Q are as defined above followed by reduction, it is appropriate to use dimethylsulfide.

The indole derivative of formula XIII can be prepared by methods analogous to those described in the accompanying examples or by methods well known in the art.

In an alternative process, the triazole compounds of the invention can be prepared by a method comprising the reaction of a compound of formula XIV:

in which a \ E and F are as defined in claim 1, Hal represents halogen and two of V ^a , W ^a , X ^a , Y ^a and Z ^a , to one of which a group Hal is attached, are carbon and the others are nitrogen, with the reagent giving the anion 'AS where A ^{c is} as previously determined.

Reagents that can supply the anion 'A ² include Grignard's reagent A ² MgHal (where Hal is halogen), organobacrylic (I) reagents such as LiA ² 2Cu, organolithium reagents A ² Li, or compounds that stabilize the anion with an adjacent, an activating group, such as ester or ketone, which can be converted into a monolayer. In this case, the adjacent ester or ketone functional group may be retained or removed after the process is complete. For example, the ester group may be hydrolyzed and decarboxylated.

The 1,2,3-triazole compounds of the present invention can be prepared by a process comprising the cycloaddition of an alkyne of formula R ^a -CsC-Rk with an azide of formula RC-Νβ, wherein R ^a , R 4 and R ^{c are} as defined above .

The cycloaddition reaction can conveniently be carried out in a suitable solvent such as tetrahydrofuran, ideally by heating in an autoclave for 8 hours.

The tetrazole compounds of the invention can be prepared by a process comprising the cycloaddition of a nitrile of formula N = CR 2 with an azide of formula R 2, wherein one of R 4 and R ^e represents a group of formula A 4 and the other is a group of formula -EF. as previously determined.

The cycloaddition reaction is conveniently carried out by co-heating the reactants at elevated temperature, e.g. at a temperature in the range of 150 ° C, in a suitable solvent such as N-methylpyrrolid-2-one, it is useful in the presence of triethylamine hydrochloride. The product obtained in the cycloaddition reaction will typically be a mixture of isomers substituted with the A * group at positions 1 and 2 of the tetrazole ring corresponding to the IL and IM structures, as defined above. These isomers can be separated by conventional techniques such as chromatography.

In an alternative process, the tetrazole compounds of the invention can be prepared by a method that involves the reaction of a compound of formula R ^e -L with a tetrazole derivative of formula XV:

(xv) wherein one of R 4 and R ^e represents a group of formula A * and another group of formula -EF as defined in claim 1, and L represents a suitable leaving group in the presence of a base such as triethylamine.

The prominent group is suitably halogen, e.g. bromine or iodine, or a sulfonate derivative such as tosylate or mesylate.

The reaction is conveniently carried out in a suitable organic solvent, e.g. acetonitrile, at room temperature.

The tetrazole derivatives of formula XV can be prepared by cycloaddition of nitrile of formula N ^with C-Rd with sodium azide, useful under the conditions described above for the reaction between nitrile N ^ CR ^ and azide R ^e -N ₃ followed by acidification with inorganic acid such as hydrochloric acid.

In a further process, the compounds of the invention in which group F is an indole group with structure FC as defined above can be prepared by a method involving the reaction of a compound of formula XVI:

a '

(XVI) wherein V, W, X, Y, Z, A ¹ , and E are as defined above, with a compound of formula VII as defined above, or a carbonyl-protected form thereof, e.g. dimethyl acetal or ketal followed by, where necessary, N-alkylation by standard procedures to insert the R ^ group.

As in the case of Compounds VI and VII, the reaction between Compounds XVI and VII can be carried out in a single step (Fischer indole synthesis) or with an initial phase without cyclization, at a lower temperature, to obtain a compound of formula XVII:

A

H (χνιι) in which V, W, X, Y, Z, A *, A ?, E, R? and R ^ as defined above followed by cyclization using a suitable reagent e.g. of the polyphosphate ester.

Hydrazines of formula XVI can be prepared from the corresponding anilines of formula XVIII:

A ¹

(XVIII) wherein V, W, X, Y, Z, A ¹ , A ^ and E are as defined above, by methods analogous to those described above with reference to compounds of formula IX.

Anilines of formula XVIII can be prepared from the corresponding nitro compounds of formula XIX:

(XIX) in which V, W, X, Y, Z, A ¹ , A ^ and E are as defined above, by methods analogous to those described above with reference to compounds of formula X.

Nitro compounds of formula XIX can be prepared by various methods, which will be readily apparent to those skilled in the art. For example, if V is a nitrogen atom, the corresponding compounds of formula XIX will be prepared by converting an anion of formula XX with a compound of formula XXI:

A '

(xx) (XXI) in which W, X, Y, Z, A ^, and E as defined above, however, means a group which is easily displaced.

In case compound XX is a derivative of triazole or tetrazole, its anion may be formed by carrying out the reaction in a base such as triethylamine. In case the compound is a derivative of imidazole, its anion can be suitably produced if the reaction is carried out in sodium hydride using N, N-dimethylformamide as a solvent. In case the salts of the compounds of formula XX are commercially available, e.g. The 1,2,4-triazole sodium salt is advantageously used in solution in Ν, dim-dimethylformamide instead of the compounds of formula XX themselves, without the need to add bases to the reaction mixture.

The group in the compounds of Formula XXI that is easily displaced is

O preferably a halogen atom, bromine is preferred, except when group D is directly attached to the aromatic ring, i. when E is a bond - in this case fluorine is preferred.

if the nitro compounds of formula XXI above are not commercially available, they can be prepared by methods analogous to those described in the accompanying examples, or by methods well known in the art.

In an alternative approach to 1,23-triazole derivatives, nitro compounds of formula XIX can be prepared from those of formula X above, with appropriate modification of group Q, using, for example, methods analogous to those described above, with reference to compounds of formulas III and IV. Thus, for example, since Q in compounds of formula X represents a reactive carboxylate group, compounds of formula XIX can be prepared from them by metabolism with a compound of formula A ^ -C (= NNHA ^) NH2 or A ^ -C (^ NNHgJNHA ^ .

In a still further process, compounds of the invention in which group F is an indazole group with the structure FB as defined above can be prepared by a method comprising the cyclization of a compound of formula XXII:

(XXI I) in which V, W, X, Y, Z, A ¹ , A ² , E and R ¹ and D ^{2 are} as above, followed, where appropriate, by N-alkylation by standard methods ,

O to insert a group R.

As in the case of the cyclization of compound XI, this is conveniently achieved in the appropriate organic solvent at elevated temperature, for example in a mixture of m-xylene and 2,6-lutidine, at a temperature in the range of 140 ° C.

For example, compounds of formula XXII may be prepared from the corresponding compound of formula XXIII:

wherein V, W, X, Y, Z, A ^, A ² , E and R ^ are as defined above, or a protected derivative thereof, which may be prepared from the corresponding compound of formula XXIV, if necessary:

(XXIV)

H, wherein V, W, X, Y, Z, A ^, 2, E and R ^ are as defined above, using the methods described above by reference to the compounds of formula XII and XIII. For example, since Q in compounds of formula XIII represents a reactive carboxylate group, 1,2,4-triazole derivatives of formula XXIV can be prepared from them by reaction with a compound of formula A ² Ct-NNHAbNH ² or A ² -C ( = NNH ₂ ) NHA ¹ .

According to another further method, the compounds of the invention in which group F is a benzofuran or benzthiophene group can be prepared by a method comprising the cyclization of a compound of formula XXV: _L

(XXV) wherein V, W, X, Y, Z, A ¹ , A ² , E and R ^{2 are} as defined above, B ^a represents oxygen or sulfur and R ² ^ corresponds to the group R ^ as defined above, or it also means a precursor group, as explained below; this is followed, where necessary, by the conversion of the R ^C1 group to the desired R group by conventional means.

Cyclization is usually carried out using polyphosphoric acid or poly phosphate ester and is useful at elevated temperatures.

Compounds of formula XXV can be prepared by converting a compound of formula XXVI with a compound of formula XXVII:

(XXVI) (XXVII) in which V, W, X, Y, Z, A ¹ , A ² , E, B ^a , R ² and R ^{2 are} as defined above and Hal is halogen.

The reaction is usually carried out in the presence of a base such as sodium hydroxide.

Hydroxy and mercapto derivatives of formula XXVI can be prepared by a variety of methods that will be readily apparent to those skilled in the art. By one such method, convert the anion of a compound of formula XX, as defined above, with a compound of formula XXVIII:

(XXV III) in which D ^3, E and B ^a are as defined above, to give the intermediate of formula XXVI wherein V is nitrogen.

If the compounds of formula XXVII and XXVIII are not commercially available, they can be prepared by standard procedures well known in the art.

It is understood that any compound of formula I, initially obtained by any of the above processes, where appropriate, may subsequently be converted into a further compound of formula I by techniques known in the art. Of course, as will be appreciated, the compound of the above formula XV, wherein R ^ is a group of the formula -ef, in itself a compound of formula I in which is hydrogen, A ² represents non-bonded electron pair. In particular, the initially obtained compound of Formula I in which R ^{3 is} hydrogen can be converted to a compound of Formula I in which R ³ is θμθ alkyl, C 6 -g alkenyl or C 1 -C alkynyl by standard techniques such as alkali 1ring, at for example by treatment with alkyl iodide, e.g. methyl iodide, typically under basic conditions, e.g. sodium hydride in dimethylformamide or triethylamine in acetonitrile. Similarly, the initially obtained compound of formula I in which R ¹ represents a group of formula -CH 2 CHCH 2 NH 4 can be converted to a compound of formula I in which R ¹ represents a group of formula -CH 2 CH 2 N 4 N, wherein are R & R? as defined above, with the exception of hydrogen, for example by conventional Nalkylation or fi-arylation techniques, e.g. by treatment with a suitable aldehyde, in the presence of a reducing agent such as sodium cyanoborohydride.

When the preparation processes of the compounds of the invention described above result in the formation of a mixture of stereoisomers, these isomers may be separated by conventional techniques such as preparative chromatography.

The novel compounds can be prepared in racemic form, or as individual enantiomers, either by enantiospecific synthesis or by separation. For example, novel compounds can be separated into their constituent enantiomers by standard techniques such as the formation of diastereoisomeric pairs by the formation of salts with optically active acid, such as (-) - di-p-toluoyl-d-tartaric acid and / or (+ ) -di-p-toluoyl-1-tartaric acid followed by fractional crystallization and free base regeneration. The new compounds can be separated, also by forming diastereoisomeric esters or amides, followed by chromatographic separation and removal of the chiral auxiliary reagents.

During any of the above synthesis sequences, it may be necessary and / or desirable to protect the sensitive or reactive groups of any of the molecules involved. This can be achieved by conventional protecting groups such as those described in Protective Groups and Organsic Chemistry, ed. J.F.M. McOmie, Plenum Press, 1973; and T.W.Greene, Protective Groups in Organic Synthesis, John Wiley & Sons, 1981. Protective groups can be removed at a convenient later stage using methods known in the art.

Alternatively, certain of the functional groups on the desired product can be derived through the reaction sequence as precursor groups, and subsequently regenerated from these precursor groups at a later stage of the total synthesis. For example, where in the desired compound of formula I represents a group of formula - (CHglgNMg »this group may be formed from a cyano precursor -CH ₂ CN by reduction using, for example, borane / tetrahydrofuran. The cyano precursor may pass through the reaction sequence as a methyl group -CH ₃ , which can be properly converted to -CH ₂ CN by treatment with N-bromosuccinimide and benzoyl peroxide, in the presence of a strong light source followed by the conversion of the resulting bromo intermediate with sodium cyanide to dimethylsulfoxide.

The following examples illustrate the preparation of the compounds of the invention.

The ability of the test compounds to bind to 5-HT1-like receptors was measured with membranes prepared from porcine caudate, using the procedure described in J. Neurosci., 1987, 4, 894. The binding was determined by 2 nM 5-hydroxytryptamine creatinine sulfate, 5- [1,2- ³ H (N) J as the radioactive ligand. Cyanopindolol (100 nm) and mesulergin (100 nm) were included in the assay to block 5-HTj _A and 5-HTjq binding sites, respectively. The concentration of the compounds of the accompanying examples required to replace 50% specific binding (IC5) is in each case below 1 µM.

The activity of the test compounds, as agonists of 5-HT1-like receptors28, was measured as their ability to mediate the contraction of the New Zealand White Rabbit saphenous vein using the procedure described in Arch. Pharm., 1990, 342, 111. Agonistic efficacy was calculated as -logjgECgg (pEC ₅₀ ) values, from the curves of the percent 5-HT (ljjM) response against a given concentration of agonist. In this experiment, we found that the compounds of the accompanying examples of pECgg had values in no case less than 5.0.

EXAMPLE 1

2- [5 (2-Benzyltetrazol-5-ylraethyl) -1H-indol-3-yl] ethylaryl oxalate

1. 4-Hydrazinbenzylcyanide. hydrochloride

A solution of NaNO ₂ (80 g, 1.16 mol) was added dropwise while stirring dropwise (-10 ° C) to a suspension of 4-aminobenzyl cyanide (153.5 g, 1.16 ml) in concentrated HCl (1500 ml), with at such a rate that the temperature did not rise above -10 ° C. The mixture was stirred at -10 ° C for 0.25 hours before being rapidly filtered under vacuum to a funnel for addition. The solution was added portionwise over 0.25 hours to a mixture of SnCl ₂ .2H ₂ 0 (1.05 kg, 4.64 mol) in concentrated HCl (800 ml), which was stirred rapidly, maintaining the temperature below -5 ° C. The mixture was allowed to warm to room temperature and stirred for 0.25 hours before the precipitate of sand was filtered under vacuum and washed with ether (5 x 500 ml). The resulting solid was dried over P ₂ Og in a vacuum oven for 16 hours to give the title compound (213 g, 100%), m.p. 181-183 ° C; 1 H NMR (360MHz, D ₂ O) δ 3.90 (2H, s, CH ₂ ); 7.06 (2H, d, J = 8.7 Hz, Ar-H); 7.40 (2H, d, J = 8.7 Hz, Ar-H).

2. 2- (5-cyano & ethyl-1H-indol-3-yl) ethylanes n. hydrochloride

4-Chlorobutanal dimethylacetal (37.07 g, 0.24 mol) was added while stirring ratopine 4-hydrazinobenzyl cyanide hydrochloride (47.0 g, 0.26 mol) in EtOH / H ₂ O (5: 1; 21) and refluxed for 4.5 hours. The reaction mixture was evaporated to dryness under vacuum, MeOH (250 ml) was added and the mixture was allowed to stand at 0 ° C for 10 hours. The resulting pale yellow precipitate was filtered under vacuum, washed with Et ₂ O / MeOH (5: 1; 2 x 100 ml) and dried. The product was used without further purification (24.1 g, 40%), m.p. 239-241 ° C; R _f 0.4 in CH ₂ Cl ₂ / EtOH / NH ₃ (40: 8: 1); ¹ H NMR (360mHz, D ₂ O) 3.18 (2H, t, J = 7.1 Hz CH ₂ ); 3.36 (2H, t, J = 7.1 Hz, CH ₂ ); 4.02 (2H, s, CH ₂ ); 7.22 (1H, dd, J = 1.5 and 8.4Hz, Ar-H);

7.36 (1H, s, Ar-H); 7.56 (1H, d, J = 8.4 Hz, Ar-H); 7.66 (1H, s, Ar-H).

• r

3. 2- (5-Tetrazol-5-yl-ethyl-1H-indol-3-yl) ethylanine

A solution of 2- (5-cyanomethyl-1H-indol-3-yl) ethylamine hydrochloride (2.5 g, 10.6 mmol), triethylamine hydrochloride (2.2 g, 16.0 mmol) and sodium azide (2.1 g, 32.2 mmol) in 1-methylpyrrolidin-2-one (30 ^l ml) was heated at 140 ° C for 8 hours. 5 M hydrochloric acid (3 ml) was added and the solvents were removed by distillation under vacuum. The residue was chromatographed on silica gel with EtOH / Et ₂ O / H ₂ O / NH 3 (20: 30: 8: 1) as the eluent to afford the title tetrazole (1.76 g, 69%); δ (360ΜΗζ, CD3OD) 3.06 (2H, t, J = 7.2Hz, CH ₂ ); 3.19 (2H, t, J = 7.2 Hz, CH ₂ ); 4.29 (2H, s, CH ₂ ); 7.07 (1H, d, J = 8.4Hz, Ar-H); 7.13 (1H, s, Ar-H); 7.29 (1H, d, J = 8.4Hz, Ar-H); 7.44 (1H, s, Ar-H).

4. N-tert-butyl 1-oxy carbonyl -2- (5-tetrazol-5-ylaethyl-1H-indole-3-ylethylamine

To a suspension of 2- (5-tetrazol-5-ylmethyl-1H-indol-3-yl) ethylamine (1.76 g, 7.27 mmol) in dry CH ₂ Cl ₂ (40 ml) was added triethylamine (1, while stirring). 5 g, 14.9 mmol) and (BOC) ₂ O (1.9 g, 7.3 mmol) and the mixture was stirred for 16 hours. The solvent was removed in vacuo and the residue was chromatographed on silica gel eluting with EtOH / Et ₂ O / H ₂ O / NH 3 (20: 60: 8: 1) to give the title product (1.6 g, 64%); δ (360MHz, CD3OD) 1.41 (9H, s, 3 of CH3); 2.87 (2H, t, J = 7.4 Hz, CH ₂ ); 3.30 (2H, t, J = 7.4 Hz, CH _2), 4.32 (2H, s, CH _2), 6.99 (IH, d, J = 8.3 Hz, Ar-H); 7.04 (1H, s, Ar-H); 7.26 (1H, d, J = 8.3, Ar-H); 7.49 (1H, s, Ar-H).

5. N-tert-butyl 1-oxy carbonyl -2- [5- (2-benzyltetrazol-5-ylethyl) -1H-indol-3-yl] ethyl and 1 aai n and N-tert-butyloxycarbonyl 1 -2-15- (1-Benzyl 1 tetrazo 1 -5HaetH) -1H-indol-3-yl] ethylamine

Benzyl bromide (0.31 g, 1.8 mmol) was added to a solution of tetrazole grade 4 (0.62 g, 1.8 mmol) and triethylamine (0.37 g, 3.6 mmol) in dry acetonitrile (20 ml ). The mixture was stirred at room temperature for 2 hours, heated at 70 ° C for 1 hour and then stirred at room temperature for 16 hours. The solvent was removed in vacuo and the residue was chromatographed on silica gel eluting with CH ₂ Cl ₂ / MeOH (97: 3) to give 2 separate benzyltetrazoles. The less polar isomer was identified as 2-benzyltetrazole (0.17g, 22.4%); Δ (360MHz, CD ₃ Cl ₃ ) 1.43 (9H, s, 3 of CH ₃ ); 2.90 (2H, t, J = 6.8 Hz, CH ₂ ); 3.41 (2H, br t, CH ₂ ); 4.32 (2H, s, CH ₂ ); 5.70 (2H, with CH ₂ Ph); 7.00 (1H, s, Ar-H); 7.15 (1H, d, J = 8.4Hz, Ar-H); 7.28 (1H, d, J = 8.4HZ, Ar-H); 7.34 (5H, s, Ar-H); 7.50 (1H, s, Ar-H); 7.96 (1H, br s, NH).

The more polar component was determined to be 1-benzyltetrazole (0.2 g,

26.4%) δ (360 MHz, CDC1 ₃₎ 1.43 (9Η, s, 3 of CH3); 2.88 (2H, t, J = 7.0Hz,

CH ₂ ); 3.40 (1H; br t, CH ₂ ); 4.26 (2H, s, CH ₂ ); 5.29 (2H, s, CH ₂ -Ph); 6.92 (1H, d, J = 8.4 Hz, Ar-H); 7.01-7.05 (3H, m, Ar-H); 7.27-7.30 (5H, m, ArH); 8.08 (1H, br s, NH).

6. 2- [5- (2-Benzyltetrazol-5-ylBiethyl) -1H-indol-3-H] ethylasine oxalate

To a solution of the less polar component isolated in step 5 (0.17 g, 0.4 mmol) in CH ₂ C1 ₂ (5 ml) was added trifluoroacetic acid (1.5 ml) and stirred at room temperature for 1 hour . The solvents were removed in vacuo and the residue was chromatographed through silica gel eluting with CHglg / EtOH / N2 (40: 8: 1) to give the title tetrazole. Oxalic acid salt (65 mg) was prepared; m.p. 169-171 ° C; (found: C, 59.23; H, 5.07; N, 19.60. C ₁₉ H ₂₀ N ₆ .l, 05 (C ₂ H ₂ O ₄ ) requires C, 59.36; H, 5. 22; N, 19.68%); δ (360MHZ, D ₂ O) 3.09 (2H, t, J * 6.9Hz, CH ₂ ); 3.29 (2H, t, J 6.9 Hz, CH ₂ ); 4.30 (2H, s, CH ₂ ); 5.77 (2H, s, CH ₂ ); 7.11 (1H, dd, J = 1.6 and 8.4H, Ar-H); 7.28 (1H, s, Ar-H); 7.32-7.34 and 7.39.7.41 (5H, m, Ar-H); 7.43 (1H, d, J = 8.4Hz, Ar-H); 7.51 (1H, s, Ar-H).

EXAMPLE 2

2- (5- (1-Benzyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethylamine hydrochloride. 1 / 2hydrate

The hydrochloride semihydrate salt was prepared; m.p. 210-213 ° C; (Found: C, 60.39; H, 5.88; N, 22.14. C ₁₉ H _2O N ₆ .HC1.1 / 2H ₂ O requires C, 60.39; H, 5.87; N, 22.24%); δ (250MHz, D ₂ O) 3.02 (2H, t, J = 68 Hz, CH ₂ ); 3.19 (2H, t, J = 6.8 Hz, CH ₂ ); 4.44 (2H, s, CH ₂ ); 5.60 (2H, s, CH ₂ ); 6.95-7.02 (3H, m, Ar-H); 7.16-7.25 (4H, m, Ar-H); 7.28 (1H, s, Ar-H); 7.40 (1H, d, J = 8.4Hz, Ar-H).

EXAMPLE 3

N, N-Diraethyl-2- C5- (2-methyltetrazol-5-ylmethyl) -1H-indol-3-yl Ethylamine, oxalate

1. H-tert-butyloxycarbonyl-2- [5- (2-methyltetrazo 1-5ylmethyl) 1H-indol-3-yl) ethyl amine and N-tert-butyloxycarbonyl-2- (5- (1-methyltetrazole) -5i It has yl-1H- and ndo 1-3-yl] ethyl amine

Tetrazole solution from step 4, Example 1 (0.95 g, 2.78 mmol) and triethylamine (0.56 g, 5.5 mmol) in dry acetonitrile (15 ml) were added methyl iodide (0.44 g) while stirring. , 3.1 mmol). After 10 hours, a further equivalent of methyl iodide was added and stirred for another 16 hours. The solvent was removed in vacuo and the residue was chromatographed on silica gel with CH ₂ Cl ₂ / MeOH eluent (97: 3) to give the title mixture of 1- and 2-methyltetrazoles 0.6 g, 61%); δ (360MHz, COC1 ₃ ) 1.43 (9H, m, 3 of CH ₃ ); 2.89-2-92 (2H, m, CH ₂ ); 3.38-3.48 (2H, m, CH ₂ ); 3.83 (2H, s, CH ₂ ); 4.28 and 4.40 (total 3H, s, CK ₃ ); 6.98 and 7.17 (total 1H, d, J = 8.4Hz, Ar-H); 7.02 and 7.06 (total 1H, s, Ar-H); 7.30 and 7.31 (total 1H, d, J = 8.4Hz, Ar-H); 7.43 and 7.54 (total 1H, s, Ar-H); 8.00 and 8.10 (total 1H, br s, NH).

2. 2- [5- (2-Methyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethylamine and 2 [5- (1-methyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethyl ami n

It was prepared from the previous methyltetrazoles using the procedure described in Step 6, Example 1. The crude product was chromatographed on silica gel with CH ₂ Cl ₂ / EtOH / NH ₃ eluent (40: 8: 1) to give 2 separate components. The less polar product (0.1 g, 24%) was identified as 2methyltetrazole; δ (360 MHz, COC1 _3, 1.38 (9H, s, 3 of CH _3), 2.88 (2H, t, J = 6.6 Hz, CH _2); 3.00 (2H, t, J = 6 , 6Hz, CH ₂ ); 4.28 (3H, s, CH ₃ ); 4.33 (2H, s,

CH ₂ ); 7.00 (1H, d, J = 8.4Hz, Ar-H); 7.06 (1H, d, J = 2.1 Hz, Ar-H); 7.17 (1H, cT, J = 8.4Hz, Ar-H); 7.56 (1H, s, Ar-H); 8.04 (1H, br s, NH).

The more polar product (0.13 g, 31%) was identified as 1methyltetrazole; δ (360MHz, CDCl ₃ ) 1.38 (9H, s, 3 of CH ₃ ); 2.86 (2H, t, J =

6.6 Hz, CH ₂ ); 3.00 (2H, t, J = 6.6 Hz, CH ₂ ); 3.82 (3H, s, CH ₃ ); 4.40 (2H, s,

CH ₂ ); 6.98 (1H, dd, J = 1.6 and 8.3Hz, Ar-H); 7.06 (1H, d, J = 1.6 Hz, ArH); 7.31 (1H, d, J = 8.3Hz, Ar-H); 7.41 (1H, s, Ar-H); 8.18 (1H, br s, NH).

3. Ν, Ν-dimethyl and 1 -2- [5- (meth and 1 tetrazo 1 -5-imyl) -IH-indol-3-yl] ethyl and 7 aminoxalate

A solution of formaldehyde (80 mg of 30% solution) in methanol (15 ml) was ¹ added to a stirred solution of 2- 5- (2-meti1tetrazol-5-i1 meti1) -lH-indol-3-yl ethylamine (0.1 g, 0, 4 mmol), NaCNBH ₃ (60 mg) and glacial acetate (0.12 g) in methanol (15 ml). The solution was stirred for 2 hours, basified with K ₂ CO ₃ solution and MeOH removed under vacuum. The crude product obtained after extraction with ethyl acetate and solvent removal was chromatographed on silica gel with eluent CH ₂ Cl ₂ / EtOH / NH ₃ (40: 8: 1) to give the desired N, Ndimethyltryptamine (96 mg, 87%). The oxalate salt was prepared: m.p. 185187 ° C (MeOH / Et ₂ O); (found: C, 54.42; H, 5.74; N, 22.53. C ₁₅ H ₂ qN _6. C ₂ H ₂ O ₄ requires C, 54.54; H, 5.92; N, 22 , 45%); δ (360MHz, D ₂ O) 2.91 (6H, s, 2 of CH ₃ ); 3.21 (2H, t, J = 7.4 Hz, CH ₂ ); 4.47 (2H, t, J = 7.4 Hz, CH ₂ ); 4.30 (3H, s, CH ₃ ); 4.34 (2H, s, CH ₂ ); 7.17 (1H, dd, J = 1.5 and 8.4Hz, Ar-H); 7.33 (1H, s, Ar-H); 7.48 (1H, d, J = 8.4Hz, Ar-H); 7.59 (1H s, Ar-H).

EXAMPLE 4

N, N-Diraethyl-2- [5- (1-methyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethylamine oxalate

It was prepared from 2-E5- (1-methyltetrazol-5-ylmethyl) ethyl-indol-3-yl ethylamine (0.125 g, 0.49 mmol) using the procedure described in Step 3, Example 3. The free base obtained was converted to an oxalic acid salt and recrystallized from MeOH / Et ₂ O, m.p. 176-177 ° C; (found: C, 54.21; H, 5.84; N, 22.36. C ₁₅ H ₂₀ N _6. C ₂ H ₂ 0 ₄ requires C, 54.54; H, 5.92; N, 22 , 45%); δ (360MHz, D ₂ 0); 2.91 (6H, s, 2 of CH ₃ ); 3.21 (2H, t, J = 7.4 Hz, CH ₂ ); 3.40 (2H, f, J = 7.4 Hz, CH ₂ ); 4.00 (3H, s, CH ₃ ); 4.43 (2H, s, CH ₂ ); 7.13 (1H, dd, J1.5 and 8.4Hz, Ar-H); 7.35 (1H, s, Ar-H); 7.50 (1H, d, d = 8.4Hz, Ar-H); 7.54 (1H, s, Ar-H).

EXAMPLE 5

N, N-dimethyl-2- [5- (1,2,4-triazol-1-ylraethyl) -1H-indol-3-yl] ethylamine oxalate 1 / 2hydrate

1. 1- (4-Nitrophenyl) aet1-1,2,4-triazole

4-Nitrobenzyl bromide (21.6'g, 0.1 mol) was added while stirring rapidly to a suspension of the 1,2,4-triazole sodium salt (9.1 g, 0.1 mol) in anhydrous DMF (100 ml) and the mixture stirred at room temperature for 16 hours. Ethyl acetate (400 ml) was added followed by water (250 ml) and the layers were separated. The organic phase was washed with water (3 x 250 ml), dried (MgSO4) and evaporated. The residue was chromatographed on silica gel with ethyl acetate as eluent to give the title product (10.6 g, 52%); m.p. 98-100 ° C. δ (360 MHz, CDCl3) 5.47 (2H, s, CH _2); 7.40 (2K, d, J = 9Hz, Ar-H); 8.02 (1H, s, Ar-H); 8.18 (1H, s, Ar-H); 8.23 (2H, d, J = 9 Hz, Ar-H).

2. 1- (4-aninophenyl) ii) ethyl-1,2,4-triazole hydrochloride

A solution of 1- (4-nitrophenyl) methyl-1,2,4-triazole (10.0 g, 49 mmol) in ethanol (50 ml), ethyl acetate (50 ml), 5M HCl (10 ml) and water (10 ml) was hydrogenated over 10% Pd / C (1.0 g) at 40 psi in a Parr apparatus until an increase of 188 psi (approximately 10 minutes) was observed. The catalyst was removed by filtration through a hyphol and the solvent was vacuum-filtered. The residue was azeotroped with ethanol (x 2) to give the title amine hydrochloride (10.6 g, 100%) δ (360MHz, D ₂ O) 5.53 (2H, s, CH ₂ ); 7.37-7.48 (4H, m, Ar-H); 8.12 (1H, s, Ar-H); 8.66 (1H, s, Ar-H).

3. 1- (4-Hydrazenic acid 1) Methyl-1,2,4-triazo 1

To a solution of the precursor amine hydrochloride (10.0 g, 48 mmol) in concentrated HCl (40 ml) was added a solution of sodium nitrite 83.28 g, 48 mmol) in water (20 ml) at such a rate that the temperature did not exceed -10 ° C. After completion of the addition, the solution was stirred at 0 ° C for 0.25 hours and then added to the solution of SnCl ₂ .2H ₂ O (40 g) in concentrated HCl (40 ml) while stirring rapidly. The solution was warmed to room temperature and basified with a 20% aqueous NaOH solution. The solution was extracted with ethyl acetate (3 x 250 ml) and the combined extracts were dried (MgSO4) and filtered through hyflo. The solution was evaporated to dryness to give the desired hydrazine (5.0 g, 56%) of the soil. 109-112 ° C. Δ (360MHz, D ₆ -DMSO) 3.93 (2H, br s, NH ₂ ); 5.20 (2H, with CH ₂ ); 6.73 (2H, d, -J = 8 Hz, Ar-H); 7.08 (2H, d, J = 8 Hz, Ar-H); 7.92 (1H, s, Ar-H); 8.57 (1H, s, Ar-H).

4. 2- [5- (1,2,4-Triazol-1-ylethyl) -1H-indol-3-yl] ethylamine

To a solution of precursor hydrazine (5.0 g, 26.4 mmol) in ethanol / water (5: 1, 180 ml) and 5M HCl (4.5 ml), 4-chlorobutanal dimethylacetal (3.22 g, 21 was added with stirring) , 1 mmol) and the solution was refluxed for hours. The solvents were removed in vacuo and the residue was chromatographed on silica gel eluting with CH ₂ Cl ₂ (EtOH / NH ₃ (30: 8: 1) to give the desired tryptamine (2.4 g, 38%). Δ (360MHz, CDCl ₃ ) 2.90 (2H, t, J = 7Hz, CH ₂ ); 2.99 (2H, t, J = 7Hz, CH ₂ ); 5.43 (2H, s, CH ₂ ); 7.10 (1H, s, Ar-H); 7.11 (1H, d, J = 8, Hz, Ar-H);

7.39 (1H, d, J = 8 Hz, Ar-H); 7.57 (1H, s, Ar-H); 7.94 (1H, s, Ar 1 H); 8.08 (1H, s, Ar-H).

5. N _t N-Diaethyl-2- [5- (l ₁ 2,4-triazol-1-haethyl) -1H-indol-3-yl] ethea.oxalate 1/2 hydrate

Mixtures of pre-tryptamine (0.36 g, 1.5 mmol), NaCNBH ₃ (0.225 g,

3.6 mmol) and glacial acetate (0.45 g) in methanol (10 ml) were added a solution of formaldehyde (37% w / w solution, 0.19 g) in methanol (10 ml). The mixture was stirred at room temperature for 2 hours before saturated K ₂ CO ₃ (50 ml) was added and the methanol was evaporated. The residue was extracted with ethyl acetate (3 x 100 ml) and the combined extracts washed with brine (100 ml), dried (K ₂ CO ₃ ) and evaporated. The crude product was chromatographed on silica gel with CH ₂ Cl ₂ / EtOH / NH ₃ (20: 8: 1) as eluent to give the free base of the title compound (0.21 g, 52%), and an oxalate polyhydrate salt, m.p. . Mp 165-167 ° C (MeOH / Et ₂ O); (found: C, 55.53; H, 6.04; N, 18.59. C ₁₅ H _ig N ₅ .®2 ^ 2θ4 · 0 »55H ₂ O requires C, 55.29; H, 6.03 N, 18.96%; m / e 269 (M +); δ (360MHz, 0 ₂ 0) 2.91 (6H, s, NMe ₂ ); 3.22 (2H, t, J = 7 Hz, CH ₂ ); 3.47 (2H, t, J = 7 Hz, CH ₂ ); 5.52 (2H, s, CH ₂ ); 7.21 (1H, dd, J = 1.6 and 8.4 Hz, Ar-H);

7.36 (1H, s, Ar-H); 8.56 (1H, s, Ar-H).

EXAMPLE 6

N, N-dimethyl-2- [5- (1,2,3,4-tetrazol-2-ylmethyl) -1H-indol-3-yl] ethylamine oxalate r

1. 1- (4-Nitrophenyl) acetyl-1,2,3,4 ~ tetrazole and 2- (4-nitrophenyl) acetyl-1,2,3,4-tetrazole

4-Nitrobenzene (15.42 g, 71.3 mmol) was added to the solution while stirring

N-tetrazole (5.0 g ', 71.3 mmol) and triethylamine (7.9 g, 78.0 mmol) in acetonitrile (100 ml). The mixture was stirred at room temperature for 16 hours, the solvent removed in vacuo and the residue chromatographed on silica gel eluting with dichloromethane to give the 2-isomers. The 2-alkylated product was obtained as the less polar product (2.47 g, 17%); δ (360 MHz, CDCl?) 5.92 (2H, s, CH _2); 7.53 (2H, d, J = 8.7 Hz, Ar-H); 8.25 (2H, d, J = 8.7Hz, ArH), 8.56 (1H, s, Ar-H). The more polar product, the major isomer, was identified as the 1-alkylation product (11 g, 75%); δ (360 MHz, CDCl?) 5.73 (2H, s, CH _2); 7.46 (2H, d, J = 8.7Hz, Ar-H); 8.27 (2H, d, d = 8.7Hz, Ar-H); 8.64 (1H, s, Ar-H).

2. 2- (4-ae / nofen / 77eet77-2,2,3,4-tetrazo 7. hydrochloride

2- (4-Nitrophenyl) methyl-1,2,3,4-tetrazole (2.47 g, 12.1 mmol) was hydrogenated as described in Example 5, Step 2. Product (2.55 g, 100% ) was obtained as the hydrochloride salt; δ (250MHz, 0 ₂ 0) 5.86 (2H, s, CH ₂ );

7.40 (2H, d, J = 8.7 Hz, Ar-H); 7.36 (2H, d, J = 8.7 Hz, Ar-H); 8.74 (1H, s, Ar-H).

3. N, N-dimethyl-2- [5 (1,2,3,4-tetrazol-2-yl-ethyl) -1-H-indol-3-yl] ethylamine. oxalate

The preceding amine was converted to the title compound using the general procedures described in Example 5, steps 3-5. An oxalate salt was prepared and recrystallized from MeOH / Et ₂ O; m.p. Mp 198-199 ° C; (found: C, 53.38; H, 5.55; N, 22.63. C ₁₄ H ₁₈ N _6. C ₂ H ₂ 0 _4. 0.2 (EtOH) requires C, 53.30; H. 5.78; N, 22.74%) δ (360MHz, D ₂ O) 2.91 (6H, s, NMe ₂ ); 3.23 (2H, t, J = 7.4 Hz, CH ₂ ); 3.48 (2H, t, J = 7.4 Hz, Ch ' ₂ ); 6.0 (2H, s, CH ₂ ); 7.30 (1H, dd, J = 1.6 and 8.4Hz, Ar-H); 7.37 (1H, s, Ar-H)); 7.53 (1H, d, J = 8.4Hz, Ar-H); 7.76 (1H, s, Ar-H); 8.74 (1H, s, Ar-H).

EXAMPLE 7

N, N-Diraethyl-2- [5- (1,2,3,4-tetrazol-1-ylmethyl) -1H-indol-3-ylmethylamine. Succinate 1- (4-nitrophenyl) methyl-1,2,3,4-tetrazole was converted to the title compound using the procedures described in Example 5. A succinic acid salt, m.p. 55-56 ° C (isopropyl alcohol); (found: C; 57.08; H, 6.14; N, 23.34. C ^ HgNg. 0.75 (C4H5O4) requires C, 56.89; H, 6.32; N, 23.42% ); δ (360ΜΗζ, D ₂ O) 2.93 (6H, s, NMe ₂ ); 3.23 (2H, t, J = 7.5 Hz, CH ₂ ); 3.48 (2H, t, J = 7.5 Hz, CH ₂ ), 6.81 (2H, s, CH ₂ ); 7.28 (1H, dd, J = 1.7 and 8.4Hz, Ar-H); 7.39 (1H, s, Ar-H); 7.56 (1H, d, J = 8.4 Hz, Ar-H); 7.75 (1H, s, Ar-H); 9.20 (1H, s, Ar-H).

EXAMPLE 8

N, N-dimethyl-2- (5- (1- (1-methyl-1,2,4-triazol-5-ylraethyl) -1H-indol-3-yl) amine bisoxalate

1. Ethyl 3- [2- (dimethyl and 1 aminoethyl HJ-1H-indole-5-methyl and carboxy and dimethyl hydrochloride

A solution of N, N-dimethyl-2- (5-cyanomethyl-1H-indol-3-yl) ethylamine (5 g, 22.01 mmol) in ethanol was saturated with gaseous HCl and stirred at room temperature for 16 hours. The solvent was removed in vacuo to give the title product (6g, 92%); δ (360MHz, Dg-DMSO) 1.29 (3H, t, J = 7.0Hz, CH ₂ ); 2.83 (6H, s, NME ₂ ); 3.13 (2H, t, J = 7.5 Hz, CH ₂ ); 3.31 (2H, m, CH ₂ ); 4.04 (2H, s, CH ₂ ); 4.42 (2H, q, J = 7.0 Hz, CH ₂ ); 7.08 (1H, dd, J = 1.5 and 8.4Hz, Ar-H); 7.27 (1H, s, Ar-H); 7.37 (1H, d, J = 8.4 Hz, Ar-H); 7.48 (1H, br s, NH); 7.71 (1H, s, Ar-H).

.Ν, Ν-dimet i 1 -2- [5- (1 -met i 1 -1,2,4, three azo 1 -5-i Imet i 1) - IH- i ndo 1 -3-i 1] ethylamine. bisoxalate

A mixture of pre-imidate ester (3 g, 10.15 mmol), methylhydrazine (0.8 ml) and triethylamine (3.54 ml) in ethanol (30 ml) was stirred at room temperature for 3 hours. The solvent was removed in vacuo and the resulting product dissolved in formic acid (98%, 3.3 ml) and the solution stirred for 0.5 hours at room temperature and refluxed for 2 hours. The solution was cooled to room temperature, poured into aqueous K ₂ CO ₃ solution (75 ml) and extracted with ethyl acetate (4 x 200 ml). The combined extracts were dried (MgSO ₄ ) and evaporated and the residue was chromatographed on silica gel eluting with CH ₂ Cl ₂ / EtOH / NH ₃ (40: 8: 1) to give 2-components. The less polar isomer was identified as the title 1-methyl-1,2,4-triazole (360 mg). Bisoxalate salt was prepared; m.p. 135-137 ° C; (found: C, 50.91, H, 5.38; N, 13.86; Cj ₆ H ₂ jN ₅ 0.25 (ethanol) requires C, 50.70; H, 5.47; N, 14. 08%); δ (360ΜΗζ, D ₂ 0); 2.91 (6H, s, NMe ₂ ); 3.23 (2H, t, J = 7.3 Hz, CH ₂ ); 3.48 (2H, t, J = 7.3 Hz, CH ₂ ); 3.95 (3H, s, Me); 4.48 (2H, s, CH ₂ ); 7.13 (1H, dd, J = 1.5 and 8.4Hz, Ar-H); 7.37 (1H, s, Ar-H); 7.53 (1H, d, J = 8.4Hz, Ar-H); 7.57 (1H, s, Ar-H); 8.32 (1H, s, Ar-H).

EXAMPLE 9

N, N-dimethyl-2-C5- (1-methyl-1,2,4-triazol-3-ylmethyl) -1H-indol-3-ylethylamine. trichydrochloride

The more polar isomer obtained in Example 8, step 2, was identified as the title triazole (180 mg). The trichydrochloride salt, m.p. <40 ° C (hygroscopic); (found: C, 49.80; H, 6.56; N, 16.96. C ₁₆ H ₂₁ N _5. 3HC1. 0.35 (Et ₂ O) requires C, 49.91; H, 6.62 N, 16.73%; δ (360MHz, D ₂ O) 2.91 (6H, with NMe ₂ ); 3.23 (2H, t, J = 7.4 Hz, CH ₂ );

3.49 (2H, t, J = 7.4 Hz, CH ₂ ); 3.95 (3H, s, Me); 4.27 (2H, s, CH ₂ ); 7.17 (1H, dd, J = 1.5 and 8.5Hz, Ar-H), 7.34 (1H, s, Ar-H); 7.50 (1H, d, J 8.5Hz, Ar-H); 7.60 (1H, s, Ar-H); 8.88 (1H, s, Ar-H).

EXAMPLE 10

N, N-dimethyl-2-C5- (1-methyl-1,2,4-triazol-5-ylmethyl) -1H-indol-3-ylethylamine. bisoxalate

1. 1- (4-Nitrophenyl) tetlethyl-1,2,3-triazole

4-Nitrobenzyl bromide (25.4 g, 0.12 mol) was added to a solution of 1H1,2,3-triazole (8.12 g, 0.12 mol) and triethylamine (11.88 g, 0.12 mol) in anhydrous acetonitrile. The mixture was refluxed for 1 hour, cooled to room temperature, and crossed to wash the wound NEtg. HBr filtered off. The solvent was removed in vacuo and the residue chromatographed through silica gel, eluting with CH ₂ Cl ₂ (100) to CH ₂ Cl ₂ / MeOH (95.5) to give 2-products. The Bd j polar product was determined as the title 1-isomer (13 g, 54%); m.p. 114-116 ° C.

δ (250MHz, CDCl ₃ ) 5.72 (2Η, s, CH ₂ ); 7.38 (2H, d, J = 9 Hz, Ar-H); 7.64 (1H, s, Ar-H); 7, 78 (1H, s, Ar-H); 8.18 (2H, d, J = 9 Hz, Ar-H). the less polar isomer present in a smaller amount was identified as the product

2-alkylation (2.25 g, 9%); m.p. 112-113 ° C. δ (250ΜΗζ, CDCl- _3); 5.72 <2H, s, CH ₂ ); 7.40 {2H, d, J = 9 Hz, Ar-H); 7.66 (2H, s, Ar-H); 8.18 (2H, d, J = 9 Hz, Ar-H).

2. N, N-Diaethyl-2- (5- (1,2,3-triazol-1-ylethyl) -1H-indol-3-ylmethyl) oxalate 1- (4-nitrophenyl) methyl-1,2,3 -triazole was converted to the title indole using the usual procedure described in Example 5. The oxalate salt, mp 210-212 ° C, was prepared (found: C, 55.88; H, 5.75; N, 18.69. C ₁₅ H ₁₉ N ₅ .1.1 (C ₂ H ₂ O ₄ ) .O ₁₅ H ₂ O requires C, 55.67; H, 5.84; N.

18.87%); δ (360MHz, 0 ₂ 0); 2.90 (6H, s, NMe ₂ ); 3.22 (2H, t, J = 7.4 Hz, CH ₂ ); 3.46 (2H, t, J = 7.4 Hz, CH ₂ ); 5.72 (2H, s, CH ₂ ); 7.24 (1H, dd, J =

1.6 and 8.4Hz, Ar-H); 7.36 (1H, s, Ar-H); 7.52 (1H, d, J = 8.4 Hz, Ar-H); 7.66 (1H, s, Ar-H); 7.79 (1H, s, Ar-H); 8.00 (1H, d, J = 1Hz, Ar-H).

EXAMPLE 11

3- (2-Aminoethyl) -5- (2- «ethyltetrazol-5-yl) benzo b thiophene. oxalate

Tier 1

4-bronophenyluercaptopropanone

To a solution of 4-bromothiophenol (5.09 g, 26.9 mmol) in NaOH (1.08 y, 26.9 mmol) and water (32 ml) chloroacetone (2.17 ml, 27.3 mmol) was added with stirring. and the mixture was stirred under nitrogen for 45 minutes before being extracted with ether, washed with water, dried (Na ₂ $ 0 ₄ ) and evaporated in vacuo leaving 6.89 g (100%) of the title compound as a white solid, δ (CDCl ₃ ) 2.27 (3H, s); 3.65 (2H, s); 7.20 (2H, d, J = 8.5Hz); 7.41 (2H, d, J = 8.5 Hz).

Tier 2

5-Brouo-3-uethyl benzo [b] thiophene

A mixture of polyphosphoric (V) acid (4.47 g) and chlorobenzene (100 ml) was added dropwise 4 hours with moderate 4-bromophenylmercaptopropanone (2.24 g, 9.14 mmol) and then heated at reflux for 8 days. . After cooling, the organic phase was decanted and the residue was decomposed with HgO (~ 100 ml), extracted with CHgClg (2 x 75 ml), dried (MgSO4) and combined with the organic phase cast. This was evaporated in vacuo to leave a brown oil. Distillation in a Kugelrohr apparatus yielded 1.83 g (88%) of the hunting compound as a pale yellow liquid, boiling. 110 ° C / 0.35 mbar. δ (CDCl ₃ ) 2.41 (3H, s); 7.10 (1H, s); 7.43 (1H, dd, J = 8.5 and 1.9Hz); 7.69 (1H, d, J = 8.5Hz); 7.64 (1H, d, ύ = 1.9Hz).

Tier 3

5-cyano-3-methyl benzo [b] thiophene

To copper (I) cyanide (0.569 g, 6.35 mmol) was added 5-bromo-3-methyl benzo [b) thiophene (1.179 g, 5.9 mmol) in N-methylpyrrolidinone (10 ml) and the mixture was stirred at 180 -190 ° C 17 hours It was then partitioned between ether (75 ml) and ammonia solution (75 ml). The ether layer was separated, washed with more ammonia solution (2 x 50 ml), dried (Na 2 SO 4) and evaporated in vacuo to leave 0.81 g of faded solids. Flash chromatography on silica eluting with 10% ethyl acetate / petroleum ether gave 0.76 g (85%) of the title compound as a white solid, δ (CDCl ₃ ) 2.47 (3H, s); 7.23 (1H, s); 7.55 (1H, dd, J = 8.3 and 1.5Hz); 7.93 (1H, d, J = 8.4Hz); 8.03 (1H, d, J = 1.4 Hz).

Tier 4

3-methyl-5- (tetrazol-5-yl) benzo [blethiophene

To a solution of 5-cyano-3-methyl benzo [b) thiophene (0.194 g, 1.12 mmol) in Nmethylpyrrolidinone (5 ml) under nitrogen was added triethylamine hydrochloride (0.231 g, 1.68 mmol) followed by sodium azide (0.234 g, 3.59 mmol) and the mixture was extracted with ether (4 x 50 mL). The combined ether extracts were dried (HgSO4) and evaporated in vacuo to leave 0.78 g of a white solid. It was chromatographed on flash silica eluting with CH2Cl2 / MeOH / NH3 (in water) (40: 8.1) to give 0.246 g (100%) of the title product as a white solid. δ (DMSO) 2.46 (3H, s); 7.41 (1H, s); 7.98 (1H, d; J = 8.4Hz); 8.03 (1H, dd, J = 8.4H and 1.5Hz); 8.36 (1H, d, J =

0.9Hz); m / z (C 1 ', NH ₃ ); 215 (MH), 160.

Tier 5

3-methyl 1-5- (2-methyl and 1 tetrazol-5-yl) benzo [b] t iophene and 3-acetyl 1-5- (1aetetetrazol-5-yl) benzo [beta thiophene

To a mixture of 3-methyl-5- (tetrazol-5-yl) benzo [b] thiophene (0.241 g, 1.12 ranol) in acetonitrile (5 ml) was added triethylamine (0.28 ml, 2.01 mmol). then iodomethane (0.486 ml, 7.81 mmol) and then DMF (3 ml) until a clear solution was formed. The solution was stirred overnight under nitrogen before evaporation in vacuo and the residue partitioned between water (50 ml) and ether (25 ml). The aqueous layer was separated and extracted with more ether (2 x 25 mL), the combined ether extracts dried (MgSO4) and evaporated in vacuo to leave 0.241 g of a yellow solid. Flash chromatography on silica eluting with 25-40% ethyl acetate / petroleum ether gave 0.168 g (65%) of 2 isomers of the title product as a white solid, and 0.063 g (24%) of the 1 isomers of the title product as a white solid. 2-isomer δ (CDCl ₃ ) 2.52 (3H, s); 4.42 (3H, s); 7.14 (1H, s); 7.94 (1H, d, J = 8.4Hz); 8.10 (1H, dd, J = 8.4 and 1.5Hz); 8.51 (1H, s), m / z (CI ⁺ 'NH 3); 231 (M + H) ⁺ 1-isomer δ (CdCl3) 2.50 (3H, s); 4.22 (3H, s); 4.22 (3H, s); 7.23 (1H, s); 7.64 (1H, dd, J = 8.3 and 1.5Hz); 8.03 (1H, d, J = 8.4Hz); 8.12 (1H, d, J 1.6 Hz). m / z (CI ⁺ , NH ₃ ); 231 (M + H) &lt; ⁺ &gt;, 202, 172.

Level 6

3-cyanoaet and 1 -5- (2-aet and 1 tetrazol-5-i 1) benzo [bj ti ofen

Mixtures of 3-methyl-5- (2-methyltetrazol-5-yl) benzo [b] thiophene (0.162 g, 0.703 mmol) and benzoyl peroxide (10.6 mg) in carbon tetrachloride (10 ml) illuminated by two table lamps ( 2 x 60W) N-bromosuccinimide (0.126 g, 0.707 mmol) was added in small portions during reflux. After complete addition, the mixture was heated at reflux for a further 90 minutes, then filtered and the filtrate was evaporated in vacuo to leave an oil / solid mixture. Flash chromatography on silica eluting with dichloromethane afforded 0.161 g of crude 3-bromomethyl-5- (2-methyltetrazol-5-yl) benzo [b] thiophene as a colorless oil.

Crude 3-bromomethyl-5- (2-methyltetrazol-5-yl) benzo [b] thiophene (0.145 'g) in DMSO (0.3 ml) was added to a mixture of sodium cyanide (29.9 mg, 0.61 mmol) in OMSO (0.2 ml) and the mixture was stirred at 100 ° C for 2 hours. After cooling, the mixture was poured into water (10 ml) and the brown solid filtered off, washed with water and dried in a vacuum gun to leave 73.5 mg. The filtrate was extracted with dichloromethane (3 x 30 ml) and the combined extracts were dried (Na2SO4) and evaporated in vacuo to leave 44.7 mg. This was combined with the original solid and chromatographed on flash silica eluting with 2050% ethyl acetate / petroleum ether to give 61.5 mg (38%) of the title product as a white solid. δ (CDCl3) 3.99 (2H, s); 4.43 (3H, s); 7.59 (1H, s); 8.00 (1H, d, J = 8.5Hz); 8.19 (1H, dd, J = 8.5 and 1.5Hz); 8.47 (1H, s).

Level 7

3- (2-amyleth and Ί) -5- (2-Bettleth 7-5- / 7) benzo [bj t and ofen. oxalate

To a solution of 3-cyanomethyl-5- (2-methyltetrazol-5-yl) benzo [b '] thiophene (0.434 g, 1.70 mmol) in THF (16 ml), a 1.0 M boron complex was added dropwise under nitrogen. tetrahydrofuran in THF (5.10 ml, 5.10 mmol) and the mixture was refluxed for 6 hours. After being cooled in an ice bath, the mixture was stabilized with 2M HCl (22 ml) and refluxed for 1 hour. THF was then removed in vacuo and the residue basified with 50% sodium hydroxide solution (4 ml) before extraction with dichloromethane (3 x 75 ml). The combined extracts were dried (KgCO2) and evaporated in vacuo to leave 0.45 g. Flash silica chromatography eluting with (^ ΟΙζ / ΜθΟΗ / ΝΗβίν water) (60: 8: 1) afforded 0.383 g (87%) of the title product as a white solid. An oxalate salt was prepared using oxalic acid in methanol / ether to give the title product oxalate, as a white solid, m.p. 204-209 ° C. Analysis determined: C, 47.75; H, 4.28; N, 19.28%. Calculated for C ^ H ^ NgS. 1.1 C2H2O4 *. C, 47.59; H, 4.28; N, 19.54%. δ (DMSO) 3.17-3.21 (4H, m); 4.46 (3H, s); 7.72 (1H, s); 8.06 (1H, dd, J = 8.4 and 1.4Hz); 8.52 (1H, s); m / z (CI ⁺ , NH ₃ ), 260 (M + H) ⁺ , 230.

EXAMPLE 12

3- (2-afliinoethyl) -5- (1-methyltetrazol-5-yl) benzoCb] thiophene. oxalate

Tier 1

3-cyanooethyl 1-5- (1-tetetrazol-5-yl) benzo [b] thiophene

Following the procedure of Example 11, Step 6, 0.666 g (2.89 mmol) of 3-methyl-5- (1-methyltetrazol-5-yl) benzo [beta] thiophene were digested with 0.515 g (2.89 mmol) of N-bromosuccinimide and 38.1 mg of benzoyl peroxide in 30 ml of carbon tetrachloride. The reaction mixture was evaporated in vacuo and chromatographed on flash silica eluting with 0-3% methanol / dichloromethane to give 0.532 g of crude 3-bromo-5- (1-methyltetrazol-5-yl) benzo b thiophene.

Crude 3-bromo-5- (1-methyltetrazol-5-yl) benzo [b) thiophene (0.504 g) was reacted with 97.7 mg (1.99 mmol) of sodium cyanide in 1.5 ml of DMSO at 100 ° C. for 2 hours. After cooling down, the reaction mixture was poured into water (25 ml) and extracted with dichloromethane (6 x 50 ml). The combined extracts were dried (Na2SO4) and evaporated in vacuo to leave 0.37 g. Flash chromatography on silica eluting with 30-60% ethyl acetate / petroleum ether to give 28.0 mg (4%) of the title product, 5 (CDCl ₃ ) 4.00 (2H, s); 4.23 (3H, s); 7.63 (1H, s); 7.73 (1H, dd); 8.08 (1H, d); 8.15 (1H, d).

Tier 2

3- (2-aminoethyl) -5- (1-net and 1-tetrazo 1-5-yl) benzene b) t and ofen. oxa 1 at

Following the procedure of Example 11, step 7, 26.1 mg (0.102 mmol) of 3 cyanomethyl-5- (1-methyltetrazol-5-yl) benzo b thiophene were reacted with 0.36 ml (0.36 mmol) in 2 ml of THF. 1,0M of the boron-tetrahydrofuran complex in THF. Flash chromatography on silica eluting with CHgCl2 / MeOH / NHgiv water (60: 8: 1) gave 17.7 mg (67%) of the title product as a colorless oil. An oxalate salt was prepared using oxalic acid in methanol / ether to give the title product oxalate, as a white solid, m.p. Mp 206-212 ° C. The analysis determined <C, 47.55; H, 4.05; N, 19.65%. Calculated for C ₁₂ H ₁₃ N ₅ S.1.1 C ₂ H ₂ O ₄ : C, 47.59; H, 4.28; N, 19.54%. δ (D ₂ O) 3.32-3.35 (2H, m); 3.40-3.44 (2H, m); 4.22 (3H, s);

7.64 (1H, s); 7.73 (1H, d, J = 8.4Hz); 8.19 (1H, s); 8.22 (1H, d, '8.5Hz).

EXAMPLE 13

3- [2- (N, N-dimethylamino) ethyl] -5- (2-methyltetrazol-5-yl) benzo [b] thiophene.

oxalate

Mixtures of - (2-aminoethyl) -5- (2-methyltetrazol-5-yl) benzo [b] thiophene (0.372 g, 1.43 mmol) and sodium cyanoborohydride (0.136 g, 2.15 mmol) in methanol (3 ml ) and acetic acid (0.247 ml, 4.30 mmol) cooled in an ice bath, 38% w / v formaldehyde solution (0.453 ml, 5.74 mmol) in methanol (3 ml) was added dropwise over 5 minutes. the mixture was stirred at room temperature for 3 hours. After this time, saturated potassium carbonate solution (30 ml) was added and the mixture was extracted with ethyl acetate (3 x 50 ml). The combined extracts were evaporated in vacuo to leave 0.53 g. Flash silica chromatography eluting with 10-30% methanol / dichloromethane gave 0.335 g (81%) of the title product as a colorless oil. The oxalate salt was prepared using oxalic acid in methanol / ether to give the title product oxalate, as a white solid, m.p. 214-218 ° C. Analysis determined: C, 50.58; H, 4.80; N, 18.28%. Calculated for CJ4HJ7N5S. C2H2O4: C, 50.92; H, 5.07; N, 18.56%. δ (DMSO) 2.84 (6H, s); 3.30-3.42 (4H, m); 4.46 (3H, s); 7.69 (1H, s); 8.06 (1H, dd, J = 8.4 and 1.4Hz); 8.20 (1H, d, J = 8.4Hz); 8.56 (1H, s), m / z (CI ⁺ , NH ₃ ) 288 (M + H) ⁺ .

EXAMPLE 14

N, N-Diraethyl-2- [5- (2-methylimidazol-1-yl having 1) -N-indol-3-yl] ethylamine. trisoxalate

1. 1- (4-Nitrophenyl) aeti7-2-aetilian dazo 1

To a solution of 2-methylimidazole (5.0 g, 60.9 mmol) Sodium hydride (2.45 g; 61.0 mmol, 60% dispersion in oil) was added to DMF (100 ml). The mixture was stirred at room temperature for 0.25 hours before 4nitrobenzyl bromide (13.2 g, 61.0 mmol) was added and heated at 110 ° C for 2 hours, then stirred at room temperature for 16 hours. Water (200 ml) and ethyl acetate (500 ml) were added, the aqueous phase separated, and extracted with ethyl acetate (2 x 250 ml). The combined extracts were washed with water (3 x 250 ml), dried (MgSO ₄ ) and evaporated. The crude product was chromatographed on silica gel, eluting with CHgClg / MeOH (4%) to give the title product (1.85 g, 10.5%); δ (360MHz, CDCl ₃ ) 2.34 (3H, s, Me); 5.16 (2H, s, CH ₂ ); 6.67 (1H, d, J =

1.3Hz, Ar-H); 7.03 (1H, d, J = 1.3 Hz, Ar-H); 7.19 (2H, d, J = 9.5Hz, ArH); 8.22 (2H, d, J = 9.5 Hz, Ar-H).

2. N, N -diethyl and 1 -2- [5- (2-aethanol or 1-yl-ethyl) -1H-indol-3-yl] ethylamine. trisoxalate

It was prepared from the previous 4-nitrobenzyl imidazole using the general procedure described in Example 5. The trisoxalate salt, m.p. 160-163 ° C (ΜβΟΗ / Εΐ2θ); (found: C, 50.57; H, 5.25; N, 10.60. C ₁₇ H ₂₂ N _4. 2.8 (C ₂ H ₂ 0 ₄ ) requires C, 50.79; H, 5. 21; N, 10.48%; m / e 282 (M ⁺ ); δ (360MHz, D ₂ O) 2.65 (3H, s, Me); 2.92 (6H, s, NMe ₂ ); 3.25 (2H, t, J = 7.3 Hz, CH ₂ ); 3.50 (2H, t, J = 7.3 Hz, CH ₂ ); 5.42 (2H, s, CH ₂ ); 7.18 (1H, d, J = 8.4Hz, Ar-H); 7.31-7.40 (2H, m, Ar-H); 7.40 (1H, s, ArH); 7.56 (1H, d, J = 8.4Hz, Ar-H); 7.66 (1H, s, Ar-H),

EXAMPLE 15

N, N-dimethyl-2- [5- (imidazol-1-ylmethyl) -1H-indol-3-yl] ethylamine.

bisoxalate

It was prepared from imidazole and 4-nitrobenzyl bromide using the procedure described in Example 5. The bisoxalate salt, m.p. T65-166 ° C (MrOH / Et ₂ O); (found: C, 53.30; H, 5.34; N, 12.18.

^c 16 ^H 20 ^N 4- ² » ⁰⁵ ( ^C 2 ^H 2 ° 4) ^{2requires C '53} » ³⁰ ? 5.36, N, 12.37%); δ (360MHz,

D ₂ O) 2.92 (6H, s, NMe ₂ ); 3.24 (2H, t, J = 7.7 Hz, CH ₂ ); 3.48 (2H, t, J = 7.7 Hz, CH ₂ ); 5.50 (2H, s, CH ₂ ); 7.27 (1H, dd, J = 1.5 and 8.4Hz, Ar-H);

7.37 (1h, s, Ar-H); 7.45 (1H, s, Ar-H); 7.49 (1H, s, Ar-H); 7.56 (1H, d, J = 8.4 Hz, Ar-H); 7.75 (1H, s, Ar-H); 8.78 (1H, s, Ar-H).

EXAMPLE 16

N, N-d and meth and 1-2- [5- (2-meth and 1 and ar dazol -1 - i 1) - 1H-i ndol-3 - i 1} et i 1 ami n. sesquioxalate

1- (4-Nitrophenyl) -2-methylimidazole

To a solution of 2-methyl 1 imidazole a (10 g, 122.0 mmol) in DMF (100 ml) was added sodium hydride (4.87 g, 122.0 mmol, 60% dispersion in oil) and stirred at 0.25 hours at room temperature. 1-Fluoro-4nitrobenzene (17.8 g, 122.0 mmol) was added to the reaction mixture and stirred at room temperature for 16 hours. Water (150 ml) and ethyl acetate (250 ml) were added, the aqueous layer was separated and extracted with ethyl acetate (3 x 150 ml). The combined extracts were washed with water (3 x 150 ml), dried (NagSO4) and evaporated to give the desired product (11.5 g, 47%); δ (360 MHz, CDC1 ₃₎ 2.24 (3H, s, Me); 7.06 (1H, d, J = 1.5 Hz, Ar-H); 7.10 (1H, d, J = 1.5 Hz, Ar-H); 7.50 (2H, d, J = 9.5Hz, ArH); 8.38 (2H, d, J = 9.5 Hz, Ar-H).

2. Ν, d-diaethyl and 1 -2- [5- (2-methyl-1-imidazol-1-yl) -IH-indol-3-yl] ethyl and lamin, sesquioxalate

It was prepared from the previous 4-nitrophenyl imidazole using the procedure described in Example 5. The sesquioxalate salt, m.p. 185-186 ° C (iPA / MeOH); (found: C, 56.17; H, 5.99; N, 13 46. ^c 16 ^H 20 ^N 4- ^{1 '55} ( ^c 2 ^H 2 ° 4) - °' ^1Et0H requires C, 56.19; H , 5.79; N, 13.58%). δ (360MHz, D ₂ O) 2.55 (3H, s, Me); 2.93 (6H, s, NMe ₂ ); 3.26 (2H, t, - J = 7.4 Hz, CH ₂ ); 3.51 (2H, t, J = 7.4 Hz, CH ₂ ); 7.30 (1H, dd, J = 2.0 and 8.7Hz, Ar-H); 7.48 (1H, d, J = 2.1 Hz, Ar-H); 7.51-7.53 (2H, m, Ar-H); 7.70 (1H, d, J = 8.7Hz, Ar-H); 7.79 (1H, d, J = 2.0 Hz, Ar-H);

EXAMPLE 17

N, N-dimethyl-2- [5- (1,2,4-triazol-1-ylethyl) -1H-indol-3-yl] ethylamine. succinate. Procedure B

A solution of 1- (4-hydrazinophenyl) methyl-1,2,4-triazole dihydrochloride (2 g, 7.6 mmol, Example 5, step 3) and 4-N, N-dimethylaminobutanal dimethylacetal (1.8 g, 11, 2 mmol) in 4% aqueous sulfuric acid (70 ml) was heated at reflux for 2 hours. After the reaction mixture was cooled to room temperature, ethyl acetate (200 ml) was added and the aqueous phase was basified with K ₂ CO ₃ . The aqueous layer was separated and further extracted with ethyl acetate (2 x 150 ml). The combined organic extracts were dried (NagSO4) and evaporated, and the residue was chromatographed on silica gel eluting with OHgCl2 / EtOH / NH3 (30: 8: 1) to give the title triazole (610 mg, 30%). A succinate salt was prepared by adding a solution of succinic acid (0.27 g, 2.3 mmol) in methanol (3 ml) to a solution of triazole (0.61 g, 2.3 mmol) in methanol (5 ml). The solvent was removed in vacuo and the resulting product recrystallized from isopropyl alcohol a, m.p. 118-120 ° C; (found: C, 58.76; H, 6.27; N, 17.79. C ₁₅ H ₁₉ N ₃ C ₄ H ₆ O ₄ requires C, 58.90; H, 6.27; N, 18. 08%.

EXAMPLE 18

N, N-dimethyl-2- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-yl] ethylamine.

benzoate

The benzoate salt of N, N-dimethyl-2- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3ylethylamine was prepared by adding a solution of benzoic acid in diethyl ether to a free base solution in ethanol / diethyl ether (1: 4). The precipitated salt was recrystallized from ethanol, m.p. 178-180 ° C; (found: C, 67.28; H, 6.55; N, 17.66. C ₁₅ H ₁₉ N _3. C ₆ H ₅ C0 ₂ requires C, 67.50; H, 6.44; N, 17 , 89%; ^} H NMR (360MHz, D ₂ O) δ 2.92 (6H, s, NMe ₂ ); 3.22 (2H, t, J = 7.3 Hz, CH ₂ ); 3.46 (2H , t, J * 7.3Hz, CH ₂ ); 5.52 (2H, s, CH ₂ ); 7.22 (1H, dd, J = 1.6 and 8.4Hz, Ar-H); 7, 36 (1H, s, Ar-H); 7.44-7.58 (4H, m Ar-H);

7.65 (1H, S, Ar-H); 7.87-7.91 (2H, m, Ar-H); 8.06 (1H, s, Ar-H), 8.54 (1H, s, Ar-H).

EXAMPLE 19

N, N-dimethyl-2- [5- (2-ethyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethylamine. oxalate

It was prepared as described in Example 3 using ethyl iodide. Oxalate salt, m.p. 140-14 ° C; (found ·: C, 55.71; H, 6.26; N, 21.35. C ₁₆ H ₂₂ N _6. C ₂ H ₂ O ₄ requires C, 55.66; H, 6.23; N. 21.64%);

NMR (360MHz, D ₂ O) δ 1.54 (3H, t, J = 7.4Hz, CH ₃ ); 2.91 (6H, s, NMe ₂ ); 3.21 (2H, t, J = 7.4 Hz, CH ₂ ); 3.47 (2H, t, J = 7.4 Hz, CH ₂ ); 4.34 (2H, s, CH ₂ ); 4.64 (2H, q, J = 7.4 Hz, CH ₂ CH ₃ ); 7.17 (1H, dd, J = 1.5 and 8.4Hz, Ar48

H); 7.33 (1H, s, Ar-H); 7.48 (1H, d, J = 8.4Hz, Ar-H); 7.59 (1H, s, Ar-H).

EXAMPLE 20

N, N-dimethyl-2- (5- (1-ethyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethylamine, oxalate

It was prepared according to the procedure described in Example 4 using ethyl iodide. Oxalate salt, m.p. 170 ° C (MeOH / Et ₂ O); (found: C, 55.59; H, 6.23; N, 21.49; C ₁₆ H ₂₂ Ng. C ₂ H ₂ O ₄ requires C, 5.66; H, 6.23; N, 21. 64%); ¹ H NMR (360MHz, D ₂ O) δ 1.32 (3H, t, J = 7.4Hz, CH ₃ ); 2.90 (6H, s, NMe ₂ ); 3.21 (2H, t, J = 7.4 Hz, CH ₂ ); 3.46 (t, 2H, J »7.4 Hz, CH _2); 4.38 (2H, q, J = 7.4 Hz, CH ₂ ); 4.47 (2H, s, CH ₂ ); 7.14 (1H, dd, J = 1.5 and 8.4Hz, Ar-H); 7.35 (1H, s, Ar-H); 7.50 (1H, d, J = 8.4 Hz, Ar-H); 7.53 (1H, s, Ar-H).

EXAMPLE 21

N, N-dimethyl-2- [5- (1,2,4-triazol-1-yl) -1H-indol-3-yl] ethylamine.

bisoxalate

It was prepared as described in Example 16 from the sodium derivative of 1,2,4-triazole and 1-fluoro-4-nitrobenzene. Bisoxalate salt, m.p. 210 ° C (MeOH / Et ₂ O); (found: C, 50.11; H, 4.78; N, 16.35 .'- C ₁₄ H ₁₇ N ₅ .1.9 (C ₂ H ₂ O ₄ ) requires C, 50.14; H. 4.92; N, 16.43%; ^! H NMR (360MHz, 0 ₂ 0); Δ 2.92 (5H, s, NMe ₂ ); 3.25 (2H, t, J = 7.4 Hz, CH ₂ );

3.50 (2H, t, J = 7.4 Hz, CH ₂ ); 7.44 (1H, s, Ar-H); 7.47 (1H, dd, J = 2.0 and 8.7Hz, Ar-H); 7.63 (1H, d, J = 8.7Hz, Ar-H); 7.88 (1H, d, J = 2.0 Hz, ArH); 8.36 (1H, s, Ar-H); 9.05 (1H, s, Ar-H).

EXAMPLE 22

4- [5- (2-Methylimidazol-1-yl) -1H-indol-3-yl] -N-methylpiperidine.

bisoxalate sesquihydrate

A solution of N-methyl-4- (form 1methyl) piperidine (0.25 g, 1.8 mmol) and 4- (2methylimidazolyl) phenyl hydrazine hydrochloride (0.48 g, 2.1 mmol) in 4% H ₂ SO ₄ (25 ml) was refluxed for 16 hours. The mixture was cooled to room temperature, basified with K ₂ CO ₃ solution and extracted with CH ₂ Cl ₂ (3 x 75 ml). The combined extracts were dried (Na ₂ SO ₄ ) and evaporated, and the residue was purified by chromatography on silica gel eluting with CH ₂ Cl ₂ / EtOH / NH ₃ (60: 8: 1) to give the title compound (0, 12 g). Bioxalate sesquihydrate salt, m.p. 65-70 ° (hygroscopic); (found: C, 52.97; H, 5.51; N, 11.07. C ₁₈ H ₂₂ N ₄ .2 (C ₂ H ₂ O ₄ ) 1.5H ₂ O requires C, 52 _a 69; H , 5.83; N, 11.17%; NMR (360MHz, D ₂ O); Δ 1.96-2.08 (2H, m, CH ₂ ); 2,312.40 (2H, m, CH ₂ ); 2.56 (3H, s, CH ₃ ); 2.95 (3H, s, CH ₃ ); 3.20-3.27 (3H, m, CH and CH ₂ ); 3.64-3.68 (2H, m, CH ₂ ); 7.28 (1H, dd, J = 2 and 8.7Hz, ArH); 7.44 (1H, s, Ar-H); 7.48 (1H, d, J = 2 Hz, Ar-H); 7.53 (1H, d, J = 2 Hz, Ar-H); 7.69 (1H, d, J = 8.7Hz, Ar-H); 7.81 (1H, d, J = 2 Hz, Ar-H).

EXAMPLE 23

4- [5- (1,2,4-Triazol-1-ylmethyl) -1H-indol-3-yl-N-methyl piperidine. oxalate

A solution of N-methyl-4- (formylmethyl) piperidine (0.1 g, 0.71 mmol) and 4 (1,2,4-triazolylmethyl) phenyl hydrazine dihydrochloride (0.185 g, 0.71 mmol) in 4% H ₂ S0 ₄ was heated at reflux for 2 hours. The mixture was cooled to room temperature, basified with K ₂ CO ₃ solution and extracted with CHgCl ₂ / EtOH / NH ₃ (40: 8: 1) to give the title compound (60 mg). The oxalate salt, mp 218-220 ° C, was prepared. (found: C, 58.61; H, 6.03; N, 17.94.- C ₁₇ H ₂₁ N _5.1 , O2 (C ₂ H ₂ O ₄ ) requires C, 58.96; H, 6 , 38; N, 17.56%); ¹ H NMR (360MHz, D ₂ O); Δ 1.88-2.02 (2H, m, -CH ₂ ); 2.20-2.34 (2H, m, CH ₂ ); 2.92 (3H, s, CH ₃ ); 3.10-3.24 (3H, m, CH and CH ₂ ); 3.60-3.64 (2H, m, CH ₂ ); 5.51 (2H, s, CH ₂ ); 7.21 (1H, dd, J = 1.5 and 8.4Hz, Ar-H); 7.26 (1H, s, Ar-H);

7.51 (1H, d, J = 8.4Hz, Ar-H); 7.69 (1H, s, Ar-H); 8.05 (1H, s, Ar-H);

8.55 (1H, s, Ar-H).

EXAMPLE 24

1H-4-1- (Z-methylimidazol-1-yl) -N-indol-3-yl piperidine. bisoxalate dihydrate

1. 4- [5- (2-Net and 1-diazol-1-yl) -1H-indol-1-yl] -N-benzylpiperidine;

It was prepared from N-benzyl-4- (formylmethyl) piperidine using the procedure described in Example 22; NMR (360 MHz, CDC1 ₃₎ δ 1,80l, 94 (2H, m, CH _2); 1.98-2.06 (2H, m, CH ₂ ); 2.14-2.24 (2H, m, CH ₂ ); 2.33 (3H, s, CH ₃ ); 2.76-2.85 (1H, m, CH); 3.02-3.08 (2H, m, CH ₂ ); 3.60 (2H, s, CH ₂ ); 7.03-7.10 (4H, m, Ar-H); 7.26-7.38 (5H, m, Ar-H); 7.41 (1H, d, J = 8.5 Hz, Ar-H); 7.52 (1H, d, J = 1.8 Hz, Ar-H); 8.30 (1H, br s, NH).

2. 1H-4- [5- (2-Methylinidazol-1-H) -1H-indol-3-yl] piperidine. bisoxalate dihydrate

Ammonium formate solutions (0.32 g, 5.07 mmol) and 4- (5- (2-methylimidazol-1-yl) -1H-indol-3-yl] -N-benzylpiperidine (0.4 g, 1, 08 mmol) in methanol (40 ml) was added Pd / C (10%; 0.4 g) and the mixture was stirred at 60 ° C for 3 hours. The catalyst was removed by filtration through celite and the solvent was removed in vacuo. The residue was taken up in H ₂ O (30 ml), basified with NH ₃ solution and extracted with ethyl acetate (3 x 100 ml). The combined extracts were dried (Na ₂ SO ₄ ) and evaporated, and the residue was chromatographed on silica gel eluting with CH ₂ Cl ₂ / MeOH / NH ₃ (30: 8: 1) to give the desired piperidine (0.2 g). Bisoxalate dihydrate salt, m.p. 80 ° C (hygroscopic); (found: C, 50.53; H, 5.54; N, 10.87. Ci ₇ H ₂₀ N ₄ .2 (C ₂ H ₂ O ₄ ) .2.2H ₂ O requires 50.43; H. 5.72; N, 11.20%; ¹ H NMR (360MHz, D ₂ O); δ 1.91-2.03 (2H, m, CH ₂ ); 2.30-2.34 (2H, m, CH ₂ ); 2.55 (3H, s, CH ₃ ); 3.19-3.36 (3H, m, CH and CH ₂ ); 3.55-3.62 (2H, m, CH ₂ ); 7.28 (1H, dd, J = 1.2 and 8.6Hz, Ar-H); 7.44 (1H, s, Ar-H); 7.47 (1H, d, J = 2.0Hz, Ar-H); 7.52 (1H, d, J = 2.0 Hz, Ar-H) - 7.69 (1H, d, J = 8.6 Hz, Ar-H); 7.82 (1H, d, J = 1.2 Hz, Ar-H).

EXAMPLE 25

1H-4- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-yl] piperidine. oxalate

It was prepared from N-benzyl-4- (formylmethyl) piperidine and 4- (1,2,4 triazolylmethyl) phenyl hydrazine dihydrochloride using the procedures described in Examples 23 and 24. Oxalate salt, m.p. ° C; (found: C, 58.27; H, 5.56; N, 18.79. C ₁₆ H ₁₉ N ₅ .C ₂ H ₂ O ₄ requires

C, 58.21; Ή, 5.70; N, 18.86%); NMR (360MHz, D ₂ O); δ 1.86-1.98 (2H, m,

CH ₂ ); 2.24-2.28 (2H, m, CH ₂ ); 3.15-3.36 (3H, m, CH and CH ₂ ); 3.52-3.56 (2H, m, CH ₂ ); 5.51 (2H, s, CH ₂ ); 7.21 81H, dd, J = 1.6 and 8.5Hz, Ar-H); 7.27 (1H, s, Ar-H); 7.52 (1H, d, J = 8.5 Hz, Ar-H); 7.70 (1H, d, J = 1.6 Hz, ArH); 8.09 (1H, s, Ar-H); 8.60 (1H, s, Ar-H).

EXAMPLE 26 1H-3- [5- (2-Methylimidazol-1-yl) -1H-indol-3-yl] pyrrolidine. bisoxalate

1. 3- [5- (2-Net i-iidazo-1-yl) -1H-indo-3-i] -N-benzyl pyrrolidine

It was prepared from N-benzyl-3- (formylmethyl) pyrrolidine and 4- (2-methylimidazolyl) phenyl hydrazine hydrochloride as described in Example 22;

NMR (360 MHz, CDC1 _3); 51.98-2.06 (1H, m, CH of CH ₂ ); 2.34 (3H, s, CH3); 2,34-2,44 (2H, m, 2 from CH from CH ₂ ); 2.71 (1H, t, J = 7.4Hz, CH from CH ₂ ); 2.80 (1H, t, J = 6.9Hz, CH from CH ₂ ); 3.05 (1H, t, J = 8.7Hz, CH from CH ₂ ); 3.61-3.73 (1H, m, CH); 3.72 (2H, ABq, J = 1.3 Hz, CH ₂ ); 6.95-7.14 (4H, m, Ar-H); 7.22-7.41 (5H, m, Ar-H); 7.40 (1H, d, J = 8.5 Hz, Ar-H); 7.66 (1H, s, Ar-H); 8.30 (1H, br s, NH).

2. 1H-3- [5- (2-Ethylimidazol-1-yl) -1H-indol-3-yl] pyrrolidine. bisoxalate

It was prepared from the preceding N-benzylpyrrolidone using the procedure described in Example 24. A bisoxalate salt, m.p. 210-213 ° C (methanol / ether); (Found: C, 53.93; H, 5.22; N, 12.50. ^C 16 ^H 18 ^N 4 * ² ( ^C 2 ^H 2 ° 4) requires C, 53.81; H, 4.97; N, 12.55%); ¹ H NMR (360MHz, D ₂ O); Δ 2.91-2.30 (1H, m, CH from CH ₂ ); 2.55 (3H, s, CH ₃ ); 2,552.60 (1H, m, CH of CH ₂ ); 3.35-3.64 (3H, m, CH and CH ₂ ); 3.80-3.90 (2H, m,

CH ₂ ); 7.30 (1H, dd, J = 2 and 8.6Hz, Ar-H); 7.47 (H, d, J = 2 Hz, Ar-H);

7.50 (1H, s, Ar-H); 7.53 (1H, d, J = 2 Hz, Ar-H); 7.70 81H, d, J - 8.6Hz,

Ar-H); 7.80 (1H, d, J = 2 Hz, Ar-H).

EXAMPLE 27

N-methyl-3-5- (2-methylimidazol-1-yl) -1H-indol-3-yl] pyrrolidine. bisoxalate

Cooled (0 ° C) mixtures of 1H-3- [5- (2-methyl and 1-imidazol-1-yl) -1H-indol-3-yl} pyrrolidine (0.12 g, 0.45 mmol ), acetic acid (0.136 g, 2.3 mmol) and NaCNBH ₃ (71 mg, 1.1 mmol) in methanol (15 ml) were added dropwise a formaldehyde solution (89 mg 38% w / w solution in Η £ θ, 1, mmol) in methanol (10 ml). The mixture was stirred at 0 ° C for 0.1 hour before being warmed to room temperature and stirred for another 1.5 hours. A saturated solution of l <2 CO ₃ (10 ml) was added and the solvent was removed in vacuo. The residue was extracted with ethyl acetate (3 x 100 ml) and the combined extracts were dried (^ SO ^) and evaporated. The crude product was chromatographed on silica gel, eluting with CH ₂ C12 / MeOH / NH ₃ (60: 8: 1) to give the title product (0.1 g). Bisoxalate salt, m.p. 191-1994 ° C (MeOH / Et 2 O). (Found: C, 54.39; H, 5.30; N, 11.87; C ₁₇ H ₂ oN ₄ .2 (C ₂ H ₂ O ₄ ) .O, 2H ₂ O requires C, 54.36; H, 5.30; N, 12.07%; ^! H NMR (360MHz, D ₂ °); δ 2.26-2.45 (1H, m, CH of CH ₂ ); 2.55 (3H, s, Me); 2.62-2.75 (1H, m, CH of CHn); 3.02 and 3.03 (total 3H, s, Me); 3.23-3.45 (2H, m, CH ₂ ); 3.60-3.68, 3.77-4.1 and 4.12-4.15 (total 3H, each m, CH and CH2); 7.30 (1H, d, J = 8.9 Hz, Ar-H); 7.48 (1H, d, J = 2.2 Hz, Ar-H); 7.52 (1H, s, Ar-H); 7.53 (1H, d, J = 2.2 Hz, Ar-H);

7.70 (1H, d, J = 8.9Hz, Ar-H); 7.78 (1H, s, Ar-H).

EXAMPLE 28

- 1H-4- [5- (imidazol-1-yl) -1H-indol-3-yl] piperidine. bisoxalate

It was prepared from N-benzyl-4- (formylmethyl) piperidine and 4 (imidazoyl) phenyl 1 hydrazine hydrochloride using the procedures described in Examples 22 and 23. The bisoxalate salt, m.p. 155157 ° C. (found: C, 54.32; H, 5.50; N, 11.66. ^c 16 ^H 18 ^N 4- ² ( ^c 2 ^H 2 ° 4) ' ⁰ ' ³ and ^Et 2 °) requires C, - 54.33; H, 5.38; N, 11.96%). ^X H NMR (360MHz, D ₂ O); δ 1.90-2.04 (2H, m, CH ₂ ); 2.32 (2H, br d, J = 1.3 Hz »CH ₂ ); 3.00-3.32 (3H, m, CH and CH- ₂ ); 3.55-3.60 (2H, m, CH ₂ ); 7.41-7.44 (2H, m, Ar-H); 7.64 (1H, s, Ar-H); 7.68 (1H, d, J = 8.7Hz, Ar-H); 7.85 (1H, s, Ar-H); 7.92 (1H, d, J = 2Hz, Ar-H); 9.06 (1H, s, Ar-H). .

EXAMPLE 29

N-4- [5- (1,2,3-triazol-1-yl) -N-indol-3-yl] piperidine. 1/2 oxalate

It was prepared from N-benzyl-4- (formylmethyl) piperidine and 4- (1,2,3triazolyl) phenyl 1 hydrazine hydrochloride using the procedures described in Examples 22 and 24. A hemioxalate salt, m.p. 278 ° C (MeOH / Et ₂ O). (Found: C, 61.84; H, 6.10; N, 22.21; C ₁₅ h ₁₇ N ₅ .0.5 (C ₂ H ₂ 0 ₄ ) requires C, 61.53; H, 5. 81; N, 22.42%); ^! H NMR (360MMHz, D ₆ -DMS0); δ 1.66-1.82 (2H, m, CH ₂ ); 1.98-2.06 (2H, m, CH ₂ ); 2.83-2.89 (2H, m, CH ₂ ); 2.98-3.08 (1H, m CH); 3.21 (2H, br d, J = 12.5 Hz, CH ₂ ); 7.28 (1H, s, Ar-H); 7.51-7.56 (2H, m, Ar-H); 7.93 (1H, s, Ar-H); 8.05 (1H, s, Ar-H);

8.73 (1H, s, Ar-H).

EXAMPLE 30

N-methyl-4- [5- (imidazol-1-yl) -1H-indol-3-yl] piperidine. sesquioxalate

It was prepared from N-methyl-4- (formylmethyl) piperidine and 4 (imidazolyl) phenyl hydrazine hydrochloride as described in Example 22. A sesquioxalate salt, mp 217 ° C; (Found: C, 57.41; H. 5.83; N, 13.30. C ₁₇ H ₂₀ N ₄ .l, 5 (C ₂ H ₂ O ₄ ) .0.14 (CH ₃ OH) z-claim C, 57.61; H, 5. 66; N, ^13.34%).}; H NMR (360 MHz, D ₂ O) δ 1.94 to 2.06 (2H, m, CH _2); 2,342,38 (m, 2H, CH ₂₎ 2 , 94 (3H, s, CH ₃ ); 3.20-3.27 (3H, m, CH and CH ₂ ); 3,633.67 (2H, m, CH ₂ ); 7.40-7.43 (2H , m, Ar-H); 7.64- (1H, s, Ar-H); 7.68 (1H, d, J = 8.7Hz, Ar-H); 7.84 (1H, s, Ar -H); 7.90 (1H, d, J = 1.3 Hz, Ar-H); 9.07 (1H, s, Ar-H).

EXAMPLE 31

N-methyl-4- [5- (1,2,3-triazol-1-yl) -1H-indol-3-yl] piperidine.

It was prepared from N-methyl-4- (formylmethyl) piperidine and 4- (1,2,3triazolyl) phenyl hydrazine hydrochloride as described in Example 22. The hemioxalate salt, m.p. 251-254 ° C (MeOH / Et ₂ O). .- (Found: C, 62.21; H, 6.49; N, 21.21. C ₁₆ H ₁₉ N ₅ .0.5 (C ₂ H ₂ O ₄ ) .0.1 H ₂ 0 requires C , 62.22; H, ¹ 6.20; N, 21.34%). ¹ H NMR (360MHz, D ₂ O); δ 1,692.01 (2H, m, CH ₂ ); 2.25-2.31 (2H, m, CH ₂ ); 2.94 (3H, s, CH ₃ ); 3.04-3.20 (3H, m, CH and CH ₂ ); 3.61-3.65 (2H, m, CH ₂ ); 7.32 (1H, s, Ar-H); 7.44 (1H, dd, J = 1.9 and 8.7Hz, Ar-H); 7.58 (1H, d, J = 8.7Hz, Ar-H); 7.86 (1H, d, J = 1.8 Hz, Ar-H); 7.94 (1H, s, Ar-H); 8.29 (1H, s, Ar-H).

EXAMPLE 32

N-methyl-3- [5- (1,2,3-triazol-1-yl) -1H-indol-3-yl] pyrrolidine. oxalate

It was prepared from N-benzyl-3- (formylmethyl) pyrrolidine and 4- (1,2,3triazolyl) phenyl hydrazine hydrochloride as described in Examples 26 and 27. The oxalate salt, m.p. 154-156 ° C (MeOH / Et ₂ O). (Found: C, 57.06; H, 5.39; N, 19.43. C ₁₅ H ₁₇ N _5. C ₂ H ₂ O _{4 found} C, 57.14; H, 5.36; N, 19 , 60%). 1 H NMR (360MHz, D ₂ O); δ 2.23-2.38 (1H, m, CH of CH ₂ ); 2.55-2.69 (1H, m, CH of CH ₂ ); 3.01 (3H, s, Me); 3.13-3.42 and 3.55-3.60 (total 2H, each m, CH ₂ ); 3.70-4.09 (3H, m, CH and CH ₂ ); 7.39 (1H, d, J = 8.7Hz, Ar-H); 7.42-7.46 (1H, m, Ar-H); 7.58 (1H, d, J = 8.7Hz, Ar-H); 7.62 (1H, s, ArH); 7.93 (1H, s, Ar-H); 8.30 (1H, s, Ar-H).

EXAMPLE 33

N-methyl-3- [5- (2-methylimidazol-1-yl) -1H-indol-3-yl] pyrrolidine. bisoxalate

It was prepared from N-benzyl-3- (formylmethyl) pyrrolidone and 4- (2 (methyl) imidazol-1-ylmethyl 1) phenyl hydrazine hydrochloride as described in Examples 26 and 27. The bisoxalate salt, m.p. Mp 152-153 ° C. (Found: C, 55.41; H, 5.51; N, 11.61. CjqH ₂₂ N _4. (C ₂ H ₂ O ₄ ) requires C, 55.69; H, 5.52; N, 11 , 81%). ¹ H NMR (360MHz, D ₂ O); δ 2.22-2.46 (1H, m, CH of CH ₂ ); 2.58-2.76 (1H, m, CH of CH ₂ ); 2.65 (3H, s, Me); 3.02 and 3.03 (total 3H, s, Me); 3.21-3.44, 3.60-3.67, 3.75-3.95 and 4.09-4.14 (total 5H, each m, CH and 2 of CH ₂ ); 5.42 (2H, s, CH ₂ ); 7 ^ .17-7.19 (1H, m, Ar-H); 7.32 (2H, s, Ar-H); 7.39 (1H, d, J = 8.4Hz, Ar-H); 7.56 (1H, d, J = 8.4 Hz, Ar-H); 7.67 (1H, s, Ar-H).

EXAMPLE 34

N-methyl-3- [5- (imidazol-1-yl) -1H-indol-3-yl] pyrrolidine. bisoxalate

It was prepared from N-benzyl-3- (formylmethyl) pyrrolidine and 4 (imidazolyl) phenyl hydrazine hydrochloride using the procedures described in Examples 26 and 27. Bisoxalate salt, m.p. 173175 ° C (MeOH / Et ₂ O). (Found: C, 53.94; H, 5.07; N, 12.51. Ci6 ^H 18 ^N 4-2 ( ^c 2 ^H 2 ° 4) ^requires in ^ac >53.81; ^H ' ⁴ ' ⁹⁷ ? ^N , 12.55%). ₁ H NMR (360MHz, D ₂ O); δ 2.26-2.45 and 2.60-2.78 (each 1H, each m, CH ₂ ); 3.02 and 3.03 (total 3H, each s, Me); 3.23-3.45, 3.61-3.66, 3.78-3.95 and 4.114.16 (total 5H, each m, 2 from CH ₂ and CH); 7.42 and 7.45 (total 1H, each s, Ar-H); 7.49 (1H, d, J = 9.2 Hz, Ar-H); 7.65 (1H, s, Ar-H); 7.69 (1H, d, J = 9.2 Hz, Ar-H); 7.86-7.89 (2H, m, Ar-H); 9.09 (1H, s, Ar-H).

EXAMPLE 35

N-methyl-3- [5- (1,2,4-triazol-1-yl) ethyl) -1H-indol-3-yl] pyrrolidine. sesquioxalate. 1/2 hydrate

It was prepared from N-benzyl-3- (formylmethyl) pyrrolidine and 4- (1,2,4 triazolylmethyl) phenyl 1 hydrazine dihydrochloride as described in Examples 26 and 27. The sesquioxalate hemihydrate salt, m.p. 59-61 ° C (isopropyl alcohol / Et ₂ O). (Found: C, 55.10; H, 5.79; N, 16.99.

^C 16 ^H 19 ^N 5- ¹ ' ³ ( ^C 2 ^H 2 ° 4) - °' ^4H 2 ° ^{requires c} »55.08; H, 5.57; N, 17.27%). ¹ H NMR (360MHz, D ₂ O); δ 2.20-2.42 and 2.54-2.72 (each 1H, each m, CH ₂ ); 3.00 and 3.02 (total 3H, each, s, Me); 3.16-3.42, 3.56-3.62, 3.72, 3.73, 3.82-3.94 and 3.98-4.10 (total 5H, each m, 2 from CH ₂ and CH), 5.52 (2H, s, CH ₂ ); 7.22 and 7.24 (total 1H, each s, Ar-H); 7.34 (1H, d, J = 8.6 Hz, ArH); 7.52 (1H, d, J = 8.6 Hz, Ar-H); 7.66 (1H, s, Ar-H); 8.06 (1H, s, Ar-H); 8.58 (1H, s, Ar-H).

EXAMPLE 36

N-Flethyl-3- [5- (imidazol-1-ylraethyl) -1H-indol-3-yl] pyrrolidine. oxalate 1/2 hydrate

It was prepared from N-benzyl-3- (formylmethyl) pyrrolidine and 4 (imidazol-1-ylmethyl 1) phenyl 1 hydrazine hydrochloride as described in Examples 26 and 27. An oxalate hemihydrate salt (found: C, 59, was prepared). 51; H, 6.35; N, 14.54. C ₁₇ H ₂₀ N ₄ .C ₂ H ₂ 0 _4. -0.6H ₂ 0.0, l ( ^and PrOH) requires C, 59.86; H, 6 , 5; N, 14.47%). NMR (360MHz, D ₂ O); Δ 2.26-2.42 (1H, m, CH of CH ₂ ); 2.60-2.74 (1H, m, CH of CH ₂ ); 3.03 (3H, s, Me); 3.16-4.12 (5H, br m, 2 from CH ₂ and CH); 5.45 (3H, s, Me); 7.27 (1H, dd, J = 1.6 and 8.5Hz, ArH); 7.31 (1H, s, Ar-H); 7.38-7.40 (2H, m, Ar-H); 7.58 (1H, d, J = 8.5 Hz, Ar-H); 7.70 (1H, s, Ar-H); 8.39 (1H, s, Ar-H).

EXAMPLE 37

N, N-dimethyl-2 ~ [5- (2-aminoimidazol-1-yl) -1H-indol-3-yl) ethyl amine. bisoxalate

It was prepared from 2-aminoimidazole and 4-fluoronitrobenzep as described in Example 16. In order to prevent the reaction of aminoimidazole with sodium nitrite under diazotization conditions, the amino group was protected as acetamide, with Ac ₂ O / AcOH, before hydrogenation and hydration. on. The Fischer reaction of 4- 2- (methylcarbonylamino) imidazol-1-yl phenyl hydrazine with N, N-dimethylaminobutanal dimethylacetal gave the title product. Bisoxalate salt, m.p. 199-200 ° C (MeOH / Et ₂ O); (Found: C, 50.35; H, 5.06; N, 15.05. C ₅ H ₅ N _ig .2,1 (C ₂ H ₂ 0 ₄ ) requires C, 50.31; H, 5.10; N, 15.28%. ¹ H NMR (360MHz, D ₂ O); δ 2.91 (6H, s, (NMe) ₂ ); 3.27 (2H, t, J = 7.4 Hz, CH ₂ ); 3.50 (2H, t, J = 7.4 Hz, CH ₂ ); 6.97 (2H, s, ar-H); 7.29 (1H, dd, J = 1.8 and 8.7Hz, Ar-H); 7.48 (1H, s, Ar-H); 7.67 (1H, d, J = 8.7Hz, Ar-H); 7.78 (1H, d, J = 1.8 Hz, Ar-H).

EXAMPLE 38

N, N-dimethyl-2- [5- (2-aminoinridazol-1-ylmethyl) -1H-indol-3-yl] ethylamine.

sesquioxalate

1. 4-cyanophenylhydrazine. hydrochloride

Cooled (-15 ° C) and a mixed suspension of 4-aminobenzonitrile (50 g, 423 mmol) in concentrated hydrochloric acid (550 ml) was added dropwise a solution of sodium nitrite (31.5 g, 457 mmol) in water (200 ml). at such a rate that the temperature was maintained below -10 ° C. When the addition was complete, the reaction mixture was quickly filtered to remove solids, and the filtrate was added portionwise to cooled (-20 ° C) and mixed solution of tin (II) chloride dihydrate (477 g, 2.1 mol) in concentrated hydrochloric acid (370 ml) at such a rate that the temperature was maintained below -10 ° C. After a further 15 minutes at -10 to 0 ° C, a white precipitate was collected by filtration, washed with diethyl ether (4 x 250 mL) and dried to give 56 g (78%) of the title compound; m.p. 235-237 ° C (ethanol / water 1: 1); ^! H NMR (250MHz, DMSO-d5) δ 10.50 (3H, br s, -N ⁺ H3); 9.10 (1H, br s, -NH-),

7.71 (2H, d, J = 8.8 Hz, Ar-H); 7.03 (2H, d, J = 8.8 Hz, Ar-H); m / z (CI) 132 (M ⁺ -1).

2. 2- [5-cyano-1H-indol-3-yl] ethylamine. hydrochloride

To a stirred suspension of 4-cyanophenylhydrazine (50 g) in a mixture of ethanol and water (5: 1; 21) was added 4-chlorobutanal dimethylacetal (45 g) and the resulting mixture was refluxed for 18 hours. The solvents were removed in vacuo and the residue azeotroped with toluene to give a brown solid. Crystallization of this crude material from methanol (150 ml) gave 23 g (35%) of the title compound as a yellow solid; m.p. 270-274 ° C. ¹ H NMR (250MHz, DMSO-d6); δ 11.60 (1H, br s, indole NH); 8.17 (1H, d, J = 1.1 Hz, Ar-H); 7.97 (3H, br s - N ⁺ H 3); 7.54 (1H, d, J = 8.5 Hz, Ar-H); 7.46 (1H, s, Ar-H); 7.44 (1H, dd, J = 8.5 and 1.1Hz, Ar-H); 3.05 (4H, br s, -CH ₂ CH ₂ N-); m / z (CI) 184 (M ⁺ -1).

3. N-tert-butyloxycarbonyl-2- [5-cyano-N-indol-3-yl] ethyl

The title compound was obtained from the previous tryptamine in 58% yield using the conditions described in Example 1 (step 4); a white solid was obtained; m.p. 132-134 ° C (hexane-ethyl acetate). 1 H NMR (250MHz, CDCl ₃ ); δ 8.42 (1H, br s, indole NH); 7.93 (1H, s, Ar-H); 7.41 (2H, s, Ar-H); 7.12 (1H, d, J = 2.2 Hz, Ar-H); 4.71 (1H, br with -NH-); 3.44 (2H, q, J = 6.9 Hz, -CH ₂ NH-); 2.94 (2H, t, J = 6.9 Hz, Ar-CH ₂ -); 1.45 (9H, s, t-Bu); m / z (CI) 286 (M ⁺ + 1).

4. N-tert-butyloxycarbonyl-2- [5-aminoaethyl-1-H-indol-3-yl] ethylamine

A solution of the product from the previous step (11.3 g) in a mixture of absolute ethanol (750 ml) and chloroform (22 ml) was hydrogenated at 50 psi over platinum (IV) oxide (1 g) for 28 hours. The catalyst was removed by filtration and the solvents were removed in vacuo. Flash chromatography of the residue (silica gel, dichloromethane-methanol-ammonia 90: 10: 1) gave 9.5 g (82%) of the title compound as a white solid; m.p. 147-149 ° C. NMR (360MHz, COC1 ₃ ); δ 8.04 (1H, br s, indole NH); 7.52 (1H, s, Ar-H); 7.33 (1H, d, J = 8.4 Hz, Ar-H); 7.16 (1H, d, J = 8.4Hz, Ar-H). 7.03 (1H, s, Ar-H); 4.61 (1H, br s, -NHBOC); 3.96 (2H, s, Ar-CH ₂ NH ₂ ); 3.45 (2H, br q, -CH ₂ NHBOC); 2.95 (2H, t, J = 6.8 Hz, Ar-CH ₂ -); 1.43 (9H, s, t-Bu); m / z (CI) 288 (M + -1).

5. N-tert-butyloxy carbonyl-2- [5-dinethyl aainonetyl-1-H-indole-3-yl ethylamine

The title compound was prepared from the previous step product in 71% yield using the conditions described in Example 3 (step 2); a colorless rare oil was obtained; 1 H NMR (250MHz, CDCl 3); δ 8.07 (1H, br s, indole NH); 7.50 (1H, s, Ar-H); 7.31 (1H, d, J = 8.3 Hz, Ar-H); 7.16 (1H, d, J = 8.3 Hz, Ar-H); 7.02 (1H, s, Ar-H); 4.61 (1H, br s, -NH-); 3.54 (2H, s, Ar-CH ₂ N-); 3.45 (2H, q, J = 6.2 Hz, -CH ₂ NH-); 2.94 (2H, t, J = 6.2 Hz, Ar-CH ₂ -); 2.27 (6H, s, -NMe ₂ ); 1.43 (9H, s, t-Bu).

6. N-tert-butyloxycarbonyl-2- [5-triethylammonium nethyl-1H-indol-3-yl] ethylamine. iodide

A solution of the product of step 5 (2.9 g) in a mixture of anhydrous diethyl ether (170 ml) and iodomethane (36 ml) was allowed to stand for 16 hours in the dark at room temperature. The white solid was collected by filtration, washed with diethyl ether and dried over phosphorus pentoxide at 50 ° C under vacuum to give 4.2 g (100%) of the title compound; m.p. 199-202 ° C (decomposition); 1 H NMR (360MHz m DMSO-d ₆ ); δ 11.09 (1H, br s, indole NH); 7.69 (1H, s, Ar-H); 7.44 (1H, d, J = 8.3 Hz, Ar-H); 7.26 (1H, s, Ar-H); 7.19 (1H, d, J = 8.3Hz, arH); 6.89 (1H, br, t-NH-); 4.57 (2H, s, Ar-CH ₂ -); 3.23 (2H, q, J = 7.6Hz,

-CH ₂ NH-); 3.01 (9H, s, N ⁺ Me ₃ ); 2.83 (2H, t, J = 7.6 Hz, Ar-CH ₂ -); 1.37 (9H, ^E s, t-Bu); m / z (FAB) 332. (Found: C, 49.30; H, 6.55; N, 8.79.

^c 19 ^ 30 ^ 3 ⁼ 2 ^for bteva: C, 49.68; H, 6.58; N, 9.15%).

7. N-tert-Bot Iloxy Carbonyl 1 -2- [5- (2-Nitroaidazo 1-1-yl) and 1) 1H-indol-3-yl] ethylamine

To a solution of 2-nitroimidazole (1.61 g, 14.2 mmol) in DMF (65 ml) was added sodium hydride (0.6 g 60% dispersion in oil) while stirring at room temperature. After 0.5 hours, a solution of the previous methiodide (3.26 g, 7.1 mmol) in DMF (40 ml) was added and the mixture was refluxed for 2 hours and then stirred at room temperature for 18 hours. Treatment with water followed by flash chromatography of the crude product afforded the title compound (2.6 g);

NMR (360 MHz, CDC1 _3); δ 1.43 (9H, s, t-Bu); 2.94 (2H, t, J = 7.0 Hz, CH ₂ ); 3.40-3.48 (2H, m, CH ₂ ); 5.69 (2H, s, CH ₂ ); 7.01 (1H, s, Ar-H); 7.09 (1H, d, J = 8.4Hz, Ar-H); 7.10 (2H, s, Ar-H); 7.37 (1H, d, J = 8.4 Hz, Ar-H); 7.54 (1H, s, Ar-H); 8.12 (1H, s, indoi-NH).

8. 2- [5- (2-Thienoidazol-1-yl-1-yl) -1H-indol-3- and 1] ethyl lanine

A solution of the previous imidazole (2.6 g, 6.7 mmol) in 90% HCO ₂ H (150 ml) was stirred at room temperature for 1.25 hours. The reaction was quenched by the addition of MeOH and the solvents were removed in vacuo. The crude product was purified by flash chromatography on silica gel, eluting with CH ₂ Cl ₂ / EtOH / NH ₃ (30: 8: 1). The product (0.73 g) was obtained as a yellow oil. ^! H NMR (360MHz, D ₄ -MeOH) δ 2.87-2.94 (4H, m, 2 from CH ₂ ); 5.71 (2H, s, CH ₂ ); 7.05 (1H, d, J = 8.4Hz, Ar-H); 7.11 (1H, s, Ar-H); 7.12 (1H, s, ArH); 7.35 (1H, d, J = 8.4Hz, Ar-H); 7.39 (1H, s, Ar-H); 7.55 (1H, s, Ar-H).

9. Ν, Ν-diaet and 1 -2- [5- (2-nitro iaidazo 1-1-imetyl) - 1 H- and ndo 1 3-yl] ethylamine

It was prepared from pre-tryptamine using the conditions described in Example 3 (step 3); 1 H NMR (250MHz, CDCl ₃ ) δ 2.33 (6H, s, N (Me) ₂ ); 2.62 (2H, t, J = 7.4 Hz, CH ₂ ); 2.92 (2H, t, J - 7.4Hz,

CH ₂ ); 5.68 (2H, s, CH ₂ ); 7.00 (1H, d, J = 1.0 Hz, Ar-H); 7.07 (1H, dd, J =

1.0 and 8.2Hz, Ar-h); 7.09 (1H, d, J = 2.4 Hz, Ar-H); 7.0 81H, d, J = 2.4Hz,

Ar-H); 7.35 (1H, d, J = 8.2 Hz, Ar-H); 7.53 (1H, s, Ar-H); 8.19 (1H, br s, indole-NH).

10. N-dimethyl N-2- [5- (2-aanoidazo] -1-imethyl) -1H-indol-3-H] ethylamine. sesquioxalate

The title compound was prepared from a Step 9 product using the conditions described in Example 5 (Step 2). The sesquioxalate salt, m.p. 211-212 ° C (MeOH / Et 2 O); (Found: C, 54.46; H, 6.08; N, 16.53. C ₁₆ H ₂₁ N _5. 1.5 (C ₂ H ₂ O ₄ ) .06 (MeOH) requires C, 54 , 46; H, 5.81; N, 16.66%. 1 H NMR (360MHz, 0 ₂ 0) δ 2.91 (6H, s, N (Me) ₂ ); 3.25 (2H, t, J = 7.4 Hz, CH ₂ ); 3.49 (2H, t, J = 7.4 Hz, CH ₂ ); 5.16 (2H, s, CH ₂ ); 6.77 (1H, d, J = 2.3 Hz, Ar-H); 6.83 (1H, d, J = 2.3 Hz, Ar-H); 7.19 (1H, dd, J =

1.5 and 8.5Hz, Ar-H); 7.39 (1H, s, Ar-H); 7.56 (1H, d, J = 8.5 Hz, Ar-H); 7.61 (1H, s, Ar-H).

EXAMPLE 39

N-methyl-2- [5- (1,2,4-triazol-1-ylethyl) -1H-indole-3-lamine. oxalate

1. N-benzyl Ί -2- [5- (1,2,4-tri azo 1-1-i Imet ί 1) -1H-indo 1-3-i 1] eth and lamin

To a solution of 2- [5- (1,2,4-triazol-1-i Have 1) -IH-indol-3-yl] ethylamine (1.5 g, 6.2 mmol) in EtOH (30 ml) was added freshly distilled benzaldehyde (0.66 g, 6.2 mmol) and the solution was stirred at room temperature for 21 hours. NaBH ₄ (0.24 g, 6.3 mmol) was added portionwise over 10 minutes at room temperature, and the resulting mixture was stirred for 0.5 h before the solvent was removed in vacuo. The resulting residue was collected with water (10 ml) and acidified with IM HCl (15 ml). The mixture was then basified with 2M NaoH and extracted with EtOAc (4 x 50 mL). The combined organic phases were washed with brine (30 ml), dried and concentrated. Chromatography of the residue on silica gel, eluting with

CH ₂ C! ₂ / MeOH (85:15) gave the title product (1.38 g, 67%); NMR (360 MHz, CDC1 ₃₎ δ 2.94 (4H, s, 2 of CH _2); 3.80 (2H, s, CH ₂ ); 5.38 (2H, s, CH ₂ ); 7.04 (1H, d, J = 2 Hz, Ar-H); 7.08 (1H, dd, J = 1.5 and 8.4Hz, ArH); 7.18-7.30 (5H, m, Ar-H); 7.32 (1H, d, J = 8.4 Hz, Ar-H); 7.54 (1H, s,

Ar-H); 7.94 (1H, d, J = 2 Hz, Ar-H); 8.17 (1H, br s, indole-NH).

2. N-benzyl 1-N-aet and 1 -2- [5- (1,2,4-triazol-1-yl) and 1) -IH-indole-3-tetanylanine

To a solution of the precursor amine (1.14 g, 3.4 mmol) in anhydrous DMF (45 ml), K ₂ CO ₃ (0.89 g, 6.4 mmol) and dimethyl sulfate (0.46 g, 3) were added with stirring. , 7 mmol). The mixture was stirred at room temperature for 3.5 hours before H ₂ O (90 ml) was added and extracted with EtOAc (2 x 100 ml). The combined organic solutions were washed with brine (40 ml), dried and concentrated. The residue was chromatographed on silica gel, eluting with CH ₂ Cl ₂ / MeOH (90:10) to give the desired product (0.69 g). 1 H NMR (360MHz, CDCl ₃ ) _Z S 2.34 (3H, s, CH ₃ ); 2.70-2.76 (2H, m, CH ₂ ); 2.94-3.00 (2H, m, CH ₂ ); 3.60 (2H, s, CH ₂ ); 5.38 (2H, s, CH ₂ ); 7.04 (1H, d, J = 2 Hz, Ar-H); 7.08 (1H, dd, J = 2 and 8.4Hz, Ar-H); 7.20-7.36 (6H, m, Ar-H); 7.44 (1H, s, Ar-H); 7.94 (1H, s, Ar-H); 7, 96 (1H, s, Ar-H); 8.18 (1H, br s, indole-NH).

3. N-Nethyl-2- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-yl] ethylamine. oxalate

A solution of previous benzylamine (0.69 g, 2.0 mmol) in ethanol (100 ml) and 2m HCl (2 ml) was hydrogenated at 30 psi over 10% Pd / C (0.6 g) for 4 hours. The catalyst was removed by filtration through hyfl, the solvent removed in vacuo and the residue chromatographed on silica gel eluting with CH ₂ Cl ₂ / EtOH / NH ₃ (40: 8.1) to afford the title N-methylamine (0.34 g, 68 %). an oxalate salt was prepared and recrystallized from isopropyl alcohol; m.p. 149-150 ° C; (found: C, 55.42; H, 5.72; N, 19.55. ^C 14 ^H 17 ^N 5 · ^c 2 ^h 2 ° 4- ° » ¹⁵ ( ^iPA ) requires C, 55.72; H. 5.75; N, 19.76%). ^! H NMR (360MHz, D ₂ ) δ 2.44 (3H, s, CH ₃ ); 2.87-2.98 (4H, m, 2 of CH ₂ ); 5.41 (2H, s, CH ₂ ); 7.05 (1H, s, Ar-H); 7.09 (1H, dd, J = 1.6 and 8.4Hz, Ar-H);

7.31 (1H, d, J = 8.4Hz, Ar-H); 7.57 (1H, s, Ar-H); 7.96 (1H, S, Ar-H); 7.99 (1H, s, Ar-H).

EXAMPLE 40

Preparation of tablets

Tablets containing 1.0, 2.0, 25.0 26.0 50.0 and 100.0 mg of the following compounds are prepared as illustrated below:

N, N-dimethyl-2- [5- (2-methyltetrazol-5-ylmethyl) -1H-indol-3-yl ethylamine oxalate

N, N-dimethyl-2- [5- (1,2,3-triazol-1-ylmethyl) -1H-indol-3-yl] ethylaminobenzoate

N, N-dimethyl-2-C 5- (1,2,3,4-tetrazol-1-ylmethyl) -1H-indol-3-yl ethylamino succinate

N-methyl-4- [5- (2-imidazol-1-yl-1H-indol-3-yl] piperidine.sessioxalate

N-methyl-3- [5- (1,2,3-triazol-1-yl) -1H-indol-3-yl] pyrrolidine and n.oxalate

DOSAGE TABLE CONTAINING 1 TO 25 MG OF ACTIVE COMPOUNDS

Amount - mg

The active compound 1.0 2.0 · 25,0 Microcrystalline cellulose 49.25 48.75 37,25 Modified food cereal starch 49.25 48.75 37,25 Magnesium stearate 0.50 0.50 ¹ 0.50

TABLE IA DOSES CONTAINING 26 TO 100 MG OF ACTIVE COMPOUNDS

Amount - mg

The active compound

Microcrystalline Cellulose Modified Food Grain Starch Magnesium stearate

26,0

52,0

2.21

0.39

50.0

100,0

4.25

0.75

100,0

200,0

8.5

1.5

Mix all the active compound, cellulose and part of the cereal starch and granulate up to 10% of the cereal starch paste. The resulting granulation is sieved, dried and milled with a residue of cereal starch and magnesium stearate. The resulting granulation is then compressed into tablets containing 1.0 mg, 2.0 mg, 25.0 mg, 26.0 mg, 50.0 mg and 100 g of active ingredient per tablet.

Claims (9)

PATENT APPLICATIONS A compound of formula I, or a salt or prodrug thereof: (I) in which the dashed circle means two non-adjacent double bonds at any position of the five-membered ring; two, three or four of V, W, X, Y and Z represent nitrogen and the rest carbon if, when two of V, W, X, Y and Z represent nitrogen and the remaining carbon, said nitrogen atoms in non-adjacent positions in a five-member ring; A * represents hydrogen, hydrocarbon, heterocyclic group, halogen, cyano, trifluoromethyl, -O R ^x , -SR ^X , -NR ^x R ^y , -NR ^x CO ₂ R ^y or -NR ^with CTNR ^x R ^y ; A ^ represents an unbound electron pair when four of V, W, X, Y, and Z represent nitrogen and the other represents carbon; or, when two or three of V, W, X, Y and Z are nitrogen and the rest are carbon, A ^ represents hydrogen, hydrocarbon, heterocyclic group, halogen, cyano, trifluoromethyl, -OR ^x , -SR ^X , -NR ^x R ^y , -NR ^x COR ^y , -NR ^x CO2R ^y , -NR ^x SO2R ^y or NR ^with CTNR ^x R ^y ; E represents a bond or a straight or branched alkylene chain containing 1 to 4 carbon atoms; F represents a group of formula Oh U represents nitrogen or C-R; Ο Β means oxygen, sulfur or N-R, R1 stands for -CHjj.CHR ^ .NR ^ R? or a group of formula wherein the broken line represents any chemical bond; R ³ , R ³ , R ^, r5, r6 and R? independently represent hydrogen or C1-8 alkyl; ^{R * x} and R ^y independently represent hydrogen, hydrocarbon or a heterocyclic group, or R ^x and R ^y together represent a C ₂ _g alkylene group; R ^z represents hydrogen, hydrocarbon or heterocyclic group; T represents oxygen, sulfur or a group of formula = N.G; and G represents a hydrocarbon, heterocyclic group or electron-attracting group. Compound according to claim 1, characterized in that it is represented by formula IIA, and salts or prodrugs thereof: (HA) in which χΐ represents nitrogen or A ^ -C; n is zero, 1, 2 or 3; means oxygen, sulfur or NR * ³ ; A ¹¹ and independently represent Cj_g alkyl, C ₂ .G alkenyl, C ₂ _g alkynyl, C3-7 cycloalkyl, aryl, aryl (Cj_g) alkyl, Cg.j heterooikloalkil, heteroaryl or heteroaryl (Cj_g) alkyl, each of which groups can be po66 i Optionally substituted; or hydrogen, halogen, cyano, trifluoromethyl, Cj_ ₆ alkoxy, Cj_g alkylthio or -NR ^X R ^; r? 2, R ^3, βΐθ and R ⁷ independently represent hydrogen or Cj_g alkyl; and ^{R * x} and y independently represent hydrogen, hydrocarbon or a heterocyclic group, or R ^x and R ^y together represent a C ₂ .G alkylene group. Compound according to claim 1, characterized in that it is represented by formula IIB, and salts and prodrugs thereof: A / N, (θΗ ₂ ) _η nr ²⁶ r ²⁷ (IIB) in which Y * represents nitrogen or A ^ -C; n is zero, 1, 2 or 3; B ^z represents oxygen, sulfur or NR ³³ ; pl pp A ^x and A ^FCC independently Cj_g alkyl, C ₂ _g alkenyl, C ₂ _g alkynyl, C3-7 cycloalkyl, aryl, aryl (Cjg) alkyl, Cg_ ₇ heterocycloalkyl, heteroaryl or heteroaryl (Cj.g) alkyl, each of groups may be optionally substituted; or hydrogen, halogen, cyano, trifluoromethyl, C1-6 alkoxy, C1-6 alkylthio or -NR ^X R4. R ^Z3 , R ^ _? r26 i _n r27 _neoc j _V i _sno mean hydrogen or C1-8 alkyl; and ^Rx and Ry independently represent hydrogen, hydrocarbon or a heterocyclic group, or R ^x and R ^y together represent a C ₂ _g alkylene group. Compound according to claim 1, characterized in that it is represented by formula IIC, and salts or prodrugs thereof: (HC) in which Y ² represents nitrogen or A ³² -C; Z * represents nitrogen or CH; n is zero, 1, 2 or 3; B ³ represents oxygen, sulfur or NR ³³ ; A ³ ^ and A ³² independently represent Cj_g alkyl, C ₂ _g alkenyl, C ₂ "g alkynyl, C ₃ _ ₇ cycloalkyl, aryl, aryl (Cj.g) alkyl, C ₃ _ ₇ heterocycloalkyl 1, heteroaryl or heteroaryl (C .g) alkyl, each of which may be optionally substituted; or hydrogen, halogen, cyano, trifluoromethyl, C1-8 alkoxy, C1-8 alkylthio or -NR ^x R ^y . R ³ is -CH ₂ .CHR ³⁴ .NR ³ ®R ³ 7 or a group of formula R ³² , R ³³ , R ³⁴ , R ³ ^, R ³⁵ and R ³ ? independently represent hydrogen or C 1-6 alkyl; and R ^x and R ^x independently represent hydrogen, hydrocarbon or a heterocyclic group, or R ^x and R ^x together represent C ₂ alkylene group .G. Compound according to claim 1, characterized in that it is represented by the formula IID, and salts or prodrugs thereof: (I I D) in which M ¹ represents nitrogen or CA ⁴² ; n is zero, 1, 2 or 3; B ⁴ represents oxygen, sulfur or NR ⁴³ ; A ⁴¹ and A ⁴² independently represent a Cj.g alkyl, C ₂ _g alkenyl, C ₂ _g alkynyl, C3-7 cycloalkyl, aryl, aryl (Cpgjalkil, heterocycloalkyl, heteroaryl or heteroaryl (Cj_g) alkyl, any of which groups may be optionally substituted; or hydrogen, halogen, cyano, trifluoromethyl, C1-6 alkoxy, C1-6 alkylthio or -NR ^X R4. R ⁴¹ is -CH ₂ .CHR ⁴⁴ .NR ⁴ ®R ⁴ ^ or a group of the formula R ⁴² , R ⁴³ , R ⁴⁴ , R ⁴⁵ , R ⁴ ® and R ⁴ ? independently represent hydrogen or C1-8 alkyl; and R ^x and R ^y independently represent hydrogen, hydrocarbon or a heterocyclic group, or R ^x and R ^ together represent a C ₂ _g alkylene group. A compound according to claim 1, characterized in that it is selected from: 2- [5- (2-Benzyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethyl amine; 2- [5- (1-Benzyltetrazol-5-ylmethyl) -1H-indol-3-yl] ethylamine; N, N-dimethyl-2- [5- (1-methyl tetrazol-5-yl having 1) -IH-indol-3-ylethylamine; N, N-dimethyl-2- (5- (2-methyltetrazol-5-ylmethyl) -1H-indol-3-ylethylamine; N, N-dimethyl-2- (5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-ylethylamine; N, N-dimethyl-2- (5- (tetrazol-2-ylmethyl) -1H-indol-3-ylethylamine; N, N-dimethyl-2- (5- (tetrazol-1-ylmethyl) -1H-indol-3-ylethylamine; N, N-dimethyl-2- (5- (1-methyl-1,2,2-triazol-5-ylmethyl) -1H-indol-3-ylethylamine Ν, d-diraethyl-2- (5- (1 -methyl-1,2,2-triazol-3-ylmethyl) -1H-indol-3-ylethylamine N, N-dimethyl-2- (5- (1,2,3-triazol-1-ylmethyl) -1H- indol-3-ylamine lamin ;. 3- (2-aminoethyl) -5- (1-methyltetrazol-5-yl) -benzoibenzothiophene; 3- (2-amphnoethyl) -5- (2-methyltetrazol-5-yl) -benzo (b] thiophene; 3- t2- (N, N-dimethylamino) ethyl-5- (2-methyltetrazol-5-yl) benzo (b) thiophene; N, N-dimethyl-2-L5- (2-methylimidazol-1-yl having 1) -IH-indole · -3-ylethylamine; N, N-dimethyl-2- (5- (imidazol-1-ylmethyl) -1H-indol-3-ylethyl amine; N, N-dimethyl-2- (5- (2-methylimidazol-1-yl) -1H-indol-3-ylmethylamine; N, N-dimethyl-2- [5- (2-ethyltetrazol-5-ylmethyl) -1H-indol-3-ylethyl amine; N, N-dimethyl-2- [5- (1-ethyltetrazol-5-ylmethyl) -1H-indol-3-yl] lamine; N, N-dimethyl-2- (5- (1,2,4-triazol-1-yl) -1H-indol-3-ylethylamine; 1-methyl 1-4- (5- (2-methylimidazol-1-yl) -1H-indol-3-ylpiperidine; 1-methyl-4- (5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-ylpiperidine; 4- (5- (2-methylimidazol-1-yl) -1H-indol-3-ylpiperidine; 4- (5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-yl] piperidine; 3- (5- (2-methylimidazol-1-yl) -1H-indol-3-yl pyrrolidine; 1-Methyl 1-3- (5- (2-methylimidazol-1-yl) -1H-indol-3-yl pyrrolidine; 4- (5- (imidazol-1-yl) -1H-indol-3-ylpiperidine; 4- (5- (1,2,3-triazol-1-yl) -1H-indol-3-ylpiperidine; 1-methyl-4- [5- (imidazol-1-yl) -1H-indol-3-ylpiperidine; 1-methyl · -4- [5- (1,2,3-triazol-1-yl) -1H-indol-3-yl] piperidine; 1-methyl-3- [5- (1,2,3-triazol-1-yl) -1H-indol-3-ylpyrrolidine; 1-methyl-3- (5- (2-methylimidazol-1-ylmethyl) -1H-indol-3-yl] pyrrolidine; 1-Methyl 1-3- (5- (imidazol-1-yl) -1H-indol-3-ylpyrrolidine; 1-Methyl 1-3- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-ylpyrrolidine; 1-methyl-3- [5- (imidazol-1-ylmethyl) -1H-indol-3-ylpyrrolidine; N, N-dimethyl-2- [5- (2-aminoimidazol-1-yl) -1H-indol-3-ylethylamine n; N, N-dimethyl-2- (5- (2-aminimidazol-1-ylmethyl) -1H-indol-3-yl) lamine; N-methyl-2- [5- (1,2,4-triazol-1-ylmethyl) -1H-indol-3-yl] lamine; 1n their salts and prodrugs. A pharmaceutical composition comprising a compound according to any one of the preceding claims, together with a pharmaceutically acceptable carrier or excipient. A compound according to any one of claims 1 to 6 for use in therapy. Use of a compound according to any one of claims 1 to 6 for the manufacture of a medicament for the treatment and / or prevention of clinical conditions for which 5-HT 1 -like racaptors are indicated. MERCK SHARP & DOHME LIMITED United Kingdom For: OOVE1 NINA RSM LJUBLJANA Τβΐ33 n rc a EC ¹ SELIH k, Risova 24 -238 Summary DERIVATIVES OF IMIDAZOLE, TRIAZOLE AND TETRAZOLE A group of substituted imidazole, triazole and tetrazole derivatives are selective agonists of 5-HT1-like receptors and are therefore useful in the treatment of clinical conditions, in particular migraine and related conditions, for which selective agonists of these receptors are indicated.