The method for preparing the novel compounds of the general formula (III) will be described below in detail.

Initially, the starting material represented by the above general formula (VI) is reacted with readily available amine (VII) and paraformaldehyde

wherein

R ₁ and R ₂ are same or different and independently selected from the group consisting of hydrogen, lower alkyl of from 1 to 4 carbon atoms, substituted or unsubstituted phenyl-C _1-4 alkyl or R ₁ and R ₂ are fused with nitrogen atom to form cyclic group which has 4 to 7 carbon atoms;

to synthesize 1,3-aminoketone compound represented by the general formula (VIII).

wherein

A, R ₁ and R ₂ are the same as defined above.

The compound of formula (VIII) is followed by the treatment with sodium borohydride in methanol to yield the corresponding 1,3-diaminoalchol compound represented by the general formula (IX).

The compound of formula (IX) is reacted with triphenylphosphine, diisopropyl azodicarboxylate and azole compounds such as imidazole, triazole, tetrazole, 5-methyltetrazole, 5-phenyltetrazole, benzotriazole represented by the structural formula (II) to give the compound represented by the general formula (III).

wherein

A and B _{are the same as defined above.}

R ₁ and R ₂ are same and different and independently selected from the group consisting of hydrogen, lower alkyl of from 1 to 4 carbon atoms, substituted or unsubstituted phenyl-C _1-4 alkyl or R ₁ and R ₂ are fused to form cyclic group with nitrogen atom;

This procedure is summarized as set forth in Reaction Scheme I below.

Reaction Scheme I

Details of the reaction condition described in reaction scheme I are as follows.

In the first step, the concentration of the starting material (VI) is about to 0.005 to 3 moles with paraformaldehyde ranging from about 3.0 to 5.0 equivalents, amine (VII) ranging from about 3.0 to 5.0 equivalents and aq. HCl. The reaction is carried out at temperature about 90?. For the conversion of the compound (VIII) to the compound (IX), sodium borohydride ranging from about 1.0 to 2.5 equivalents is used in methanol. The resulting compound is treated with 1.5 equivalents of PPh3, diisopropyl azodicarboxylate and azole compound to give the compound (III).

Additionally, the compounds of formula (III) may be converted into pharmaceutically acceptable salts (X) by treating the compound (III) with acid as described in the reaction scheme I. In the reaction scheme I, HX represents an acid capable of forming a pharmacologically useful salt with the basic nitrogen atom. Specific examples of the anhydrous acid used for the preparation of the compound (X) from the compound (III) include hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, acetic acid, benzoic acid, carbonic acid, citric acid, malonic acid, salicylic acid, malic acid, fumaric acid, oxalic acid, succinic acid, tartaric acid, lactic acid, gluconic acid, ascorbic acid, maleic acid, aspartic acid, camphorsulfonic acid, p-toluenesulfonic acid, benzene sulfonic acid, methane sulfonic acid, ethane sulfonic acid, hydroxymethane sulfonic acid and hydroxyethane sulfonic acid and the like. Additional acids can refer to "Pharmaceutical Salts", J. Pharm. Sci., 1977; 66(1): 1-19. This preparation is executed in a reaction media which can be exemplified by an ethereal solvent such as THF, an alcoholic solvent such as methanol, an ester solvent such as ethyl acetate, and aromatic solvent, and any compositional mixture thereof. An ethereal solvent is recommended as an addition solution, including ethyl ether, propyl ether, isopropyl ether, butyl ether, isobutyl ether. The concentration of the compound (III) is on the order of about 0.01 to 5 moles.

The methods for preparing the compounds of the general formula (III) in which R ₁ is hydrogen and R ₂ is methyl, i.e. the compounds of the general formular (XI), will be described below.

The compounds of general formula (III) wherein R ₁ and R ₂ are methyl is treated with ethyl chloroformate, sodium bicarbonate and potassium hydroxide to yield the monomethyl amine compound represented by the structural formula (XI).

Wherein

A and B _{are the same as defined above.}

The compound of formula (XI) may be converted into pharmaceutically acceptable salt (XII) as described above.

This procedure of preparing the compounds of general formula (XI) and pharmaceutically acceptable salts thereof is summarized as set forth in Reaction Scheme II below.

Reaction Scheme II

Details of the reaction condition described in reaction scheme II are as follows. For the conversion of compound(III) in which R ₁ and R ₂ are methyl, to the compound (XI), ethyl chloroformate ranging from 10 to 15 equivalents, sodium bicarbonate ranging from 20 to 25 equivalents and similar amount of potassium hydroxide are used at temperature about 100℃.

In reaction scheme II, HX represents an acid capable of forming a pharmacologically useful salt with the basic nitrogen atom as described above.

Enantiomeric isomers represented by the structural formula (IV) and (V) are obtained from racemic mixture (III) by means of chiral preparative Liquid Chromatography ("Prep-LC"). The methods for preparing the general formula (IV) and (V) will be described below.

The racemic mixture (III) is dissolved in a small amount of isopropylalcohol and separated by chiral preparative Liquid Chromatography. Separation is performed by using a CHIRALPACK OD-H column (manufactured by Daicel Chemical Industries, Ltd.) as the Prep-LC column, at a column temperature of 25℃, with n-hexane / isopropylalcohol including 0.1% triethylamine (90:10) as the eluent. Enantiomeric isomers represented by the structural formula (IV) and (V) can be obtained in the ratio of 1:1 from the racemic mixture (III).

This procedure is summarized as set forth in reaction scheme III below.

Reaction Scheme III

In reaction scheme III, HX represents an acid capable of forming a pharmacologically useful salt with the basic nitrogen atom as described above.

The compounds of formula (IV) and (V) may be converted into pharmaceutically acceptable salts (XIII) and (XIV) as described above.

The compounds prepared according to the above methods include the following compounds.

[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

S-[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl -amine

[3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-dime thyl-amine

Dimethyl-(3-naphthalen-2-yl-3-[1,2,3]triazol-2-yl-propyl) -amine

Dimethyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine

(3-Benzotriazol-2-yl-3-naphthalen-2-yl-propyl)-dimethyl-a mine

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-pr opyl]-amine

[3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-1-yl-propyl]-dim ethyl-amine

Dimethyl-[3-(4-phenoxy-phenyl)-3-tetrazol-2-yl-propyl]-am ine

Dimethyl-[3-(4-phenoxy-phenyl)-3-tetrazol-1-yl-propyl]-am ine

[3-(6-Chloro-naphthalen-2-yl)-3-[1,2,3]triazol-2-yl-propy l]-dimethyl-amine

[3-(6-Chloro-naphthalen-2-yl)-3-[1,2,3]triazol-1-yl-propy l]-dimethyl-amine

[3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dim ethyl-amine

[3-(4-Methoxy-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimet hyl-amine

(3-Biphenyl-3-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine

[3-(4-Benzyloxy-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl- amine

(3-Biphenyl-4-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine

Dimethyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-pr opyl]-amine

Dimethyl-[3-(6-methyl-naphthalen-2-yl)-3-tetrazol-2-yl-pr opyl]-amine

[3-(6-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-di methyl-amine

[3-(6-Methoxy-naphthalen-2-yl)-3-[1,2,3]triazol-2-yl-prop yl]-dimethyl-amine

[3-Benzotriazol-1-yl-3-(3,4-dichloro-phenyl)-propyl]-dime thyl-amine

2-[1-(3,4-Dichloro-phenyl)-3-pyrrolidin-1-yl-propyl]-2H-[ 1,2,3]triazole

[3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-di ethyl-amine

[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-diethyl- amine

2-[1-(3,4-Dichloro-phenyl)-3-pyrrolidin-1-yl-propyl]-2H-t etrazole

Dimethyl-(3-naphthalen-1-yl-3-tetrazol-2-yl-propyl)-amine

Dimethyl-(3-naphthalen-1-yl-3-[1,2,3]triazol-2-yl-propyl) -amine

[3-(3,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

[3-(3,4-Dichloro-phenyl)-3-(5-phenyl-tetrazol-2-yl)-propy l]-dimethyl-amine

[3-(3,4-Difluoro-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl -amine

[3-(3,4-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

[3-(3,4-Difluoro-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-di methyl-amine

[3-(3,4-Difluoro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-di methyl-amine

[3-(3,4-Dimethyl-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-di methyl-amine

[3-(3,4-Dimethyl-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-di methyl-amine

[3-(3,4-Dimethyl-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl -amine

[3-(3,4-Dimethyl-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

[3-(4-Chloro-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl-ami ne

[3-(4-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-ami ne

Dimethyl-(3-phenyl-3-[1,2,3]triazol-1-yl-propyl)-amine

Dimethyl-(3-phenyl-3-[1,2,3]triazol-2-yl-propyl)-amine

[3-(4-Chloro-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-dimeth yl-amine

[3-(4-Chloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimeth yl-amine

[3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-di methyl-amine

[3-(3,4-Dichloro-phenyl)-3-imidazol-1-yl-propyl]-dimethyl -amine

[3-(3-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-di methyl-amine

[3-(3-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl) -propyl]-dimethyl-amine

[3-(6-Fluoro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dim ethyl-amine

[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)- propyl]-dimethyl-amine

[3-(1,4-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl ]-dimethyl-amine

[3-(1,4-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-dimethyl-amine

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl ]-dimethyl-amine

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-dimethyl-amine

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-1-yl-propyl ]-dimethyl-amine

Dimethyl-[3-(4-methyl-naphthalen-1-yl)-3-tetrazol-2-yl-pr opyl]-amine

Dimethyl-[3-(4-methyl-naphthalen-1-yl)-3-(5-methyl-tetraz ol-2-yl)-propyl]-amine

[3-(4-Fluoro-naphthalen-1-yl)-3-tetrazol-2-yl-propyl]-dim ethyl-amine

[3-(4-Fluoro-naphthalen-1-yl)-3-(5-methyl-tetrazol-2-yl)- propyl]-dimethyl-amine

(3-Isoquinolin-1-yl-3-tetrazol-2-yl-propyl)-dimethyl-amin e

[3-Isoquinolin-1-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-di methyl-amine

(3-Benzo[1,3]dioxol-5-yl-3-tetrazol-2-yl-propyl)-dimethyl -amine

[3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

[3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-1-yl)-propy l]-dimethyl-amine

[3-(3,4-Dimethoxy-phenyl)-3-tetrazol-2-yl-propyl]-dimethy l-amine

[3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-tetrazol-2-yl-pr opyl]-dimethyl-amine

[3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-(5-methyl-tetraz ol-2-yl)-propyl]-dimethyl-amine

Dimethyl-(3-quinolin-2-yl-3-tetrazol-2-yl-propyl)-amine

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-quinolin-2-yl-prop yl]-amine

Dimethyl-[3-(1-methyl-1H-indol-2-yl)-3-tetrazol-2-yl-prop yl]-amine

Dimethyl-[3-(1-methyl-1H-indol-2-yl)-3-(5-methyl-tetrazol -2-yl)-propyl]-amine

Dimethyl-[3-(1,2,3,4-tetrahydro-naphthalen-2-yl)-3-tetraz ol-2-yl-propyl]-amine

[3-(6-Chloro-pyridin-3-yl)-3-tetrazol-2-yl-propyl]-dimeth yl-amine

(3-Benzo[b]thiophen-2-yl-3-tetrazol-2-yl-propyl)-dimethyl -amine

[3-Benzo[b]thiophen-2-yl-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

(3-Benzofuran-2-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine

[3-Benzofuran-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-dim ethyl-amine

(3-Benzofuran-2-yl-3-tetrazol-1-yl-propyl)-dimethyl-amine

[3-(3,4-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

Dimethyl-[3-tetrazol-2-yl-3-(2,4,5-trifluoro-phenyl)-prop yl]-amine

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,4,5-trifluoro-p henyl)-propyl]-amine

[3-(3-Bromo-4-fluoro-phenyl)-3-tetrazol-2-yl-propyl]-dime thyl-amine

[3-(3-Bromo-4-fluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-p ropyl]-dimethyl-amine

[3-(6-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl) -propyl]-dimethyl-amine

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-phenoxy-phenyl) -propyl]-amine

[3-(4-Bromo-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amin e

[3-(4-Bromo-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-di methyl-amine

Dimethyl-[3-tetrazol-2-yl-3-(4-trifluoromethyl-phenyl)-pr opyl]-amine

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethyl -phenyl)-propyl]-amine

Dimethyl-[3-tetrazol-2-yl-3-(2,3,4-trichloro-phenyl)-prop yl]-amine

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,3,4-trichloro-p henyl)-propyl]-amine

[3-(3-Chloro-4-methoxy-phenyl)-3-tetrazol-2-yl-propyl]-di methyl-amine

[3-(3-Chloro-4-methoxy-phenyl)-3-(5-methyl-tetrazol-2-yl) -propyl]-dimethyl-amine

[3-(4-tert-Butyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

[3-(2,5-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

[3-(2,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

[3-(3-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-d imethyl-amine

[3-(2-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-d imethyl-amine

[3-(2,5-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

[3-(2,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

[3-(3-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-ami ne

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethox y-phenyl)-propyl]-amine

[3-(3-Bromo-4-methyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-p ropyl]-dimethyl-amine

Dimethyl-[3-tetrazol-2-yl-3-(4-trifluoromethoxy-phenyl)-p ropyl]-amine

[3-(4-Bromo-3-methyl-phenyl)-3-tetrazol-2-yl-propyl]-dime thyl-amine

[3-(4-Methanesulfonyl-phenyl)-3-(5-methyl-tetrazol-2-yl)- propyl]-dimethyl-amine

[3-(4-Isopropyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl ]-dimethyl-amine

[3-(9H-Fluoren-2-yl)-3-(5-methyl-tetrazol-2-yl)-propyl]-d imethyl-amine

Methyl-(3-naphthalen-2-yl-3-[1,2,3]triazol-2-yl-propyl)-a mine

[3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-meth yl-amine

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-prop yl]-amine

(3-Benzotriazol-2-yl-3-naphthalen-2-yl-propyl)-methyl-ami ne

(3-Biphenyl-4-yl-3-tetrazol-2-yl-propyl)-methyl-amine

[3-(3,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

[3-(4-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine

[3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-me thyl-amine

[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

Methyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine

[3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-met hyl-amine

Methyl-(3-naphthalen-1-yl-3-tetrazol-2-yl-propyl)-amine

Methyl-[3-(6-methyl-naphthalen-2-yl)-3-tetrazol-2-yl-prop yl]-amine

Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-prop yl]-amine

(3 S )-3-(3,4-dichlorophenyl)- N -methyl-3-(2 H -tetrazol-2-yl)propan-1-amine

(3 R )-3-(3,4-dichlorophenyl)- N -methyl-3-(2 H -tetrazol-2-yl)propan-1-amine

(3 S )-3-(2 H -benzotriazol-2-yl)-3-(3,4-dichlorophenyl)- N -methylpropan-1-amine

(3 R )-3-(2 H -benzotriazol-2-yl)-3-(3,4-dichlorophenyl)- N -methylpropan-1-amine

(3 S )-3-(3,4-dichlorophenyl)- N -methyl-3-(2 H -1,2,3-triazol-2-yl)propan-1-amine

(3 S )-3-(3,4-dichlorophenyl)- N -methyl-3-(5-methyl-2 H -tetrazol-2-yl)propan-1-amine

(3 R )-3-(3,4-dichlorophenyl)- N -methyl-3-(5-methyl-2 H -tetrazol-2-yl)propan-1-amine

(3 R )-3-(3,4-dichlorophenyl)- N -methyl-3-(2 H -1,2,3-triazol-2-yl)propan-1-amine

(3 R )- N -methyl-3-(2-naphthyl)-3-(2 H -tetrazol-2-yl)propan-1-amine

(3 S )- N -methyl-3-(2-naphthyl)-3-(2 H -tetrazol-2-yl)propan-1-amine

[3-(3-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-me thyl-amine

[3-(3-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl) -propyl]-methyl-amine

[3-(6-Fluoro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-met hyl-amine

[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)- propyl]-methyl-amine

[3-(1,4-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl ]-methyl-amine

[3-(1,4-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-methyl-amine

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl ]-methyl-amine

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-methyl-amine

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-1-yl-propyl ]-methyl-amine

Methyl-[3-(4-methyl-naphthalen-1-yl)-3-tetrazol-2-yl-prop yl]-amine

Methyl-[3-(4-methyl-naphthalen-1-yl)-3-(5-methyl-tetrazol -2-yl)-propyl]-amine

[3-(4-Fluoro-naphthalen-1-yl)-3-tetrazol-2-yl-propyl]-met hyl-amine

[3-(4-Fluoro-naphthalen-1-yl)-3-(5-methyl-tetrazol-2-yl)- propyl]-methyl-amine

(3-Benzo[1,3]dioxol-5-yl-3-tetrazol-2-yl-propyl)-methyl-a mine

[3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

[3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-1-yl)-propy l]-methyl-amine

[3-(3,4-Dimethoxy-phenyl)-3-tetrazol-2-yl-propyl]-methyl- amine

[3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-tetrazol-2-yl-pr opyl]-methyl-amine

[3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-(5-methyl-tetraz ol-2-yl)-propyl]-methyl-amine

Methyl-[3-(1,2,3,4-tetrahydro-naphthalen-2-yl)-3-tetrazol -2-yl-propyl]-amine

[3-(6-Chloro-pyridin-3-yl)-3-tetrazol-2-yl-propyl]-methyl -amine

(3-Benzo[b]thiophen-2-yl-3-tetrazol-2-yl-propyl)-methyl-a mine

[3-Benzo[b]thiophen-2-yl-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

(3-Benzofuran-2-yl-3-tetrazol-2-yl-propyl)-methyl-amine

[3-Benzofuran-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-met hyl-amine

(3-Benzofuran-2-yl-3-tetrazol-1-yl-propyl)-methyl-amine

[3-(3,4-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

[3-(3,4-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

Methyl-[3-tetrazol-2-yl-3-(2,4,5-trifluoro-phenyl)-propyl ]-amine

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,4,5-trifluoro-phe nyl)-propyl]-amine

[3-(3-Bromo-4-fluoro-phenyl)-3-tetrazol-2-yl-propyl]-meth yl-amine

[3-(3-Bromo-4-fluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-p ropyl]-methyl-amine

[3-(6-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-me thyl-amine

[3-(6-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl) -propyl]-methyl-amine

Methyl-[3-(4-phenoxy-phenyl)-3-tetrazol-2-yl-propyl]-amin e

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-phenoxy-phenyl)-p ropyl]-amine

[3-(4-Bromo-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine

[3-(4-Bromo-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-me thyl-amine

Methyl-[3-tetrazol-2-yl-3-(4-trifluoromethyl-phenyl)-prop yl]-amine

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethyl-p henyl)-propyl]-amine

Methyl-[3-tetrazol-2-yl-3-(2,3,4-trichloro-phenyl)-propyl ]-amine

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,3,4-trichloro-phe nyl)-propyl]-amine

[3-(3-Chloro-4-methoxy-phenyl)-3-tetrazol-2-yl-propyl]-me thyl-amine

[3-(3-Chloro-4-methoxy-phenyl)-3-(5-methyl-tetrazol-2-yl) -propyl]-methyl-amine

[3-(2-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-m ethyl-amine

[3-(3-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-m ethyl-amine

[3-(2,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

[3-(2,5-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

[3-(3-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine

[3-(2,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

[3-(2,5-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

[3-(4-Methanesulfonyl-phenyl)-3-(5-methyl-tetrazol-2-yl)- propyl]-methyl-amine

[3-(4-Isopropyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl ]-methyl-amine

[3-(9H-Fluoren-2-yl)-3-(5-methyl-tetrazol-2-yl)-propyl]-m ethyl-amine

(3S)-Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl -propyl]-amine

(3S)-Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl) -propyl]-amine

(3R)-Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl -propyl]-amine

(3R)-Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl) -propyl]-amine

(3R)-[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-methyl-amine

(3S)-[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-methyl-amine

The compound or pharmaceutically acceptable salt thereof according to the present invention can be used for treating CNS disorders such as depression, anxiety and pain disorder.

In therapeutic use as agents for various CNS disorders such as depression, anxiety and pain disorder, the compounds of the present invention, alone or in combination with pharmaceutically acceptable carrier, are administered to patients at a dosage of from 0.7 to 7,000mg per day. For a normal human adult with a body weight of approximately 70kg, the administration amount is translated into a daily dose of 0.01 to 100mg per kg of body weight. The specific dosage employed, however, may vary depending upon the requirements of the patient, the severity of patient's condition and the activity of the compound. The determination of optimum dosages for a particular situation must clinically be done and is within the skill of the art.

In utilizing the compounds of the present invention for the central nervous system, the compounds represented by general structural formula (I), (III), (IV) and (V) can be administered in any form or mode which makes the compound bioavailable in effective amounts, including the oral, rectal, transdermal, subcutaneous, intravenous, intramuscular or intranasal routs. However it is preferred to administer the compounds orally. Since the compounds absorb well orally, it usually will not be necessary to resort to parenteral administration. For oral administration, the compounds having the general formula (I), (III), (IV) and (V) is preferably combined with a pharmaceutical carrier. The ratio of the carrier to the compound of structural formula (I), (III), (IV) and (V) is not critical to express the effects of the medicine on the central nervous system, and they can vary considerably depending on whether the composition is to be filled into capsules or formed into tablets. In tableting, various edible pharmaceutical carriers or the mixture thereof can be used. A suitable carriers, for example, are a mixture of lactose, diabasic calcium phosphate and/or corn starch. Other pharmaceutically acceptable ingredients can be further added, including lubricants such as magnesium stearate.

The present invention includes methods of treating depression, anxiety and pain disorder in a mammal which comprises administering the composition of the compound of structural formula (I), (III), (IV) and (V) to a mammal in need of therapy.

A better understanding of the present invention may be obtained in light of following examples which are set forth to illustrate, but are not to be construed to limit, the present invention.

Example 1

[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

To a solution of 3,4-dichloroacetophenone(2mmol) in ethanol was added dimethylamine (5 equiv.), paraformaldehyde (5 equiv.) and aq. HCl. After 12h, the solvent was removed and ethyl acetate and 1N NaOH were added and organic layer was extracted 3 times. It was dried over MgSO ₄ , filtered, evaporated and the filtrate was concentrated at reduced pressure. The residue was purified by column chromatography eluting with ethyl acetate and hexane. The product was dissolved in methanol and added NaBH ₄ (2 equiv.). After 2h, sat. NaHCO ₃ and ethyl acetate were added and the organic layer was extracted 3 times with ethyl acetate. It was dried over MgSO ₄ , filtered, evaporated and the filtrate was concentrated at reduced pressure. The residue was purified by column chromatography eluting with ethyl acetate and methanol. The resulting residue was dissolved in THF and was added 1 H -tetrazole (1.5equiv.), triphenylphosphine (1.5equiv.) and diisopropyl azodicarboxylate (1.5equiv.) dropwise at 0℃ and warmed to room temperature. After 2h, the solvent was removed and the residue was purified by column chromatography eluting with ethyl acetate and methanol. : Yield 35%

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.6(m, 2H), 6.0(t, 1H), 7.2(dd, 1H), 7.4(dd, 1H), 7.5(d, 1H), 8.5(s, 1H)

Example 2

[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

To a solution of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine(2mmol) in chloroform was added ethylchloroformate(>10 equiv.) and NaHCO ₃ (>20 equiv.) and this solution was refluxed for 3h. After that, chloroform was evaporated and ethyl acetate was added and then this organic layer was washed with water 3 times. It was dried over MgSO ₄ , filtered, evaporated and the filtrate was concentrated at reduced pressure. The residue was dissolved in ethanol and potassium hydroxide(>20 equiv.) dissolved in water was added and refluxed for 3 days. After that, ethyl acetate and sat. NaHCO3 were added and the organic layer was extracted. It was dried over MgSO ₄ , filtered, evaporated and the filtrate was concentrated at reduced pressure. The residue was purified by column chromatography eluting with ethyl acetate and methanol. : Yield 80%

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H), 8.5(s, 1H)

Example 3

S-[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl -amine

S-[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl -amine was obtained from the [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e using a CHIRALPACK OD-H column(manufactured by Daicel Chemical Industries, Ltd.) as the Prep-LC column, at a column temperature of 25℃, with n-hexane/isopropylalcohol including 0.1% triethylamine(90:10) as the eluent.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H), 8.5(s, 1H)

Example 4

[3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-dime thyl-amine

The procedure given in Example 1 was followed using benzotriazole as a reactant, instead of tetrazole, to give [3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-dimethy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.1(m, 1H), 7.4(m, 4H), 7.6(t, 1H), 7.9(m, 2H)

Example 5

Dimethyl-(3-naphthalen-2-yl-3-[1,2,3]triazol-2-yl-propyl) -amine

The procedure given in Example 1 was followed using 2-acetonaphthone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-(3-naphthalen-2-yl-3-[1,2,3]triazol-2-yl-propyl)-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.1(m, 1H), 7.4(m, 3H), 7.6(d, 2H), 7.8(m, 5H)

Example 6

Dimethyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine

The procedure given in Example 1 was followed using 2-acetonaphthone as a reactant, instead of 3,4-dichloroacetophenone, to give Dimethyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.1(m, 1H), 7.5(m, 3H), 7.8(m,4H), 8.5(s, 1H)

Example 7

(3-Benzotriazol-2-yl-3-naphthalen-2-yl-propyl)-dimethyl-a mine

The procedure given in Example 1 was followed using 2-acetonaphthone and benzotriazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give (3-Benzotriazol-2-yl-3-naphthalen-2-yl-propyl)-dimethyl-amin e.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.1(m, 1H), 7.4(m, 5H), 7.5(d, 1H), 7.8(m, 6H)

Example 8

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-pr opyl]-amine

The procedure given in Example 1 was followed using 2-acetonaphthone and 5-methyl-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-propy l]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.1(m, 4H), 7.5(d, 3H), 7.8(d, 4H)

Example 9

[3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-1-yl-propyl]-dim ethyl-amine

The procedure given in Example 1 was followed using 6-Chloro-2-acetonaphthone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-1-yl-propyl]-dimeth yl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.7(m, 1H), 7.5(m, 3H), 7.8(dd, 2H), 8.1(s, 1H), 8.6(s, 1H)

Example 10

Dimethyl-[3-(4-phenoxy-phenyl)-3-tetrazol-2-yl-propyl]-am ine

The procedure given in Example 1 was followed using 4-phenoxyacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-(4-phenoxy-phenyl)-3-tetrazol-2-yl-propyl]-amine .

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.1(m,1H), 6.9(m, 4H), 7.1(m, 1H), 7.4(m, 4H), 8.5(s, 1H)

Example 11

Dimethyl-[3-(4-phenoxy-phenyl)-3-tetrazol-1-yl-propyl]-am ine

The procedure given in Example 1 was followed using 4-phenoxyacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-(4-phenoxy-phenyl)-3-tetrazol-1-yl-propyl]-amine .

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 5.8(m,1H), 6.9(m, 4H), 7.1(m, 1H), 7.4(m, 4H), 8.5(s, 1H)

Example 12

[3-(6-Chloro-naphthalen-2-yl)-3-[1,2,3]triazol-2-yl-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 6-Chloro-2-acetonaphthone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(6-Chloro-naphthalen-2-yl)-3-[1,2,3]triazol-2-yl-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.7(m,1H), 7.4(m, 3H), 7.6(m, 2H), 7.8(m, 2H), 8.4(s, 1H)

Example 13

[3-(6-Chloro-naphthalen-2-yl)-3-[1,2,3]triazol-1-yl-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 6-Chloro-2-acetonaphthone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(6-Chloro-naphthalen-2-yl)-3-[1,2,3]triazol-1-yl-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.7(m,1H), 7.4(m, 3H), 7.6(m, 2H), 7.8(m, 2H), 8.2(s, 1H)

Example 14

[3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dim ethyl-amine

The procedure given in Example 1 was followed using 6-Chloro-2-acetonaphthone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dimeth yl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.7(m, 1H), 7.5(m, 3H), 7.8(dd, 2H), 8.3(s, 1H), 8.5(s, 1H)

Example 15

[3-(4-Methoxy-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimet hyl-amine

The procedure given in Example 1 was followed using 4-methoxyacetophenone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(4-Methoxy-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimethyl -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 2H), 2.8(m, 1H), 5.7(m, 1H), 6.8(dd, 2H), 7.3(dd, 2H), 7.6(s, 2H)

Example 16

(3-Biphenyl-3-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine

The procedure given in Example 1 was followed using 3-phenylacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give (3-Biphenyl-3-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.5(m, 9H), 8.5(s, 1H)

Example 17

[3-(4-Benzyloxy-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl- amine

The procedure given in Example 1 was followed using 4-benzyloxyacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(4-Benzyloxy-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-ami ne.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 5.0(s, 2H), 6.1(m, 1H), 7.0(m, 2H), 7.4(m, 7H), 8.5(s, 1H)

Example 18

(3-Biphenyl-4-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine

The procedure given in Example 1 was followed using 4-phenylacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give (3-Biphenyl-4-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.1(m, 1H), 7.4(m, 9H), 8.5(s, 1H)

Example 19

Dimethyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-pr opyl]-amine

The procedure given in Example 1 was followed using 2-acetonaphthone and 5-Methyl-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-propy l]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.1(m, 1H), 7.5(m, 5H), 7.6(m, 1H), 7.8(m, 3H), 8.0(s, 1H), 8.2(m, 2H)

Example 20

Dimethyl-[3-(6-methyl-naphthalen-2-yl)-3-tetrazol-2-yl-pr opyl]-amine

The procedure given in Example 1 was followed using 6-Methylacetonaphthone as a reactant, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-(6-methyl-naphthalen-2-yl)-3-(5-methyl-tetrazol- 2-yl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 3H), 2.8(m, 1H), 6.1(m, 1H), 7.3(dd, 1H), 7.5(m, 2H), 7.7(dd, 2H), 7.9(s, 1H), 8.5(s, 1H)

Example 21

[3-(6-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 6-Methoxyacetonaphthone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(6-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 3.9(s, 3H), 6.1(m, 1H), 7.3(dd, 1H), 7.5(m, 2H), 7.7(dd, 2H), 7.9(s, 1H), 8.5(s, 1H)

Example 22

[3-(6-Methoxy-naphthalen-2-yl)-3-[1,2,3]triazol-2-yl-prop yl]-dimethyl-amine

The procedure given in Example 1 was followed using 6-Methoxyacetonaphthone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(6-Methoxy-naphthalen-2-yl)-3-[1,2,3]triazol-2-yl-propyl] -dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 3.9(s, 3H), 6.1(m, 1H), 7.3(dd, 1H), 7.5(m, 2H), 7.7(dd, 2H), 7.9(s, 1H), 8.5(s, 2H)

Example 23

[3-Benzotriazol-1-yl-3-(3,4-dichloro-phenyl)-propyl]-dime thyl-amine

The procedure given in Example 1 was followed using benzotriazole as a reactant, instead of 1 H -tetrazole, to give [3-Benzotriazol-1-yl-3-(3,4-dichloro-phenyl)-propyl]-dimethy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(m, 1H), 2.8(m, 1H), 6.0(m, 1H), 7.4(m, 6H), 8.0(t, 1H)

Example 24

2-[1-(3,4-Dichloro-phenyl)-3-pyrrolidin-1-yl-propyl]-2H-[ 1,2,3]triazole

The procedure given in Example 1 was followed using pyrrolidine and 1 H -1,2,3-triazole as reactants, instead of dimethylamine and 1 H -tetrazole, to give 2-[1-(3,4-Dichloro-phenyl)-3-pyrrolidin-1-yl-propyl]-2H-[1,2 ,3]triazole.

1H-NMR(CDCl3, 200MHz) δ1.84(m, 4H), 2.2(m, 7H), 2.7(m, 1H), 6.0(m, 1H), 7.2(m, 3H), 7.6(m, 2H)

Example 25

[3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-di ethyl-amine

The procedure given in Example 1 was followed using diethylamine and 1 H -1,2,3-triazole as reactants, instead of dimethylamine and 1 H -tetrazole, to give [3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dieth yl-amine.

1H-NMR(CDCl3, 200MHz) δ1.0(m, 6H), 2.3(m, 7H), 2.6(m, 1H), 6.0(m, 1H), 7.2(m, 3H), 7.6(m, 2H)

Example 26

[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-diethyl- amine

The procedure given in Example 1 was followed using diethylamine as a reactant, instead of dimethylamine, to give [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-diethyl-ami ne.

1H-NMR(CDCl3, 200MHz) δ1.0(m, 6H), 2.3(m, 7H), 2.6(m, 1H), 6.0(m, 1H), 7.2(dd, 1H), 7.4(dd, 1H), 7.6(t, 1H), 8.5(s, 1H)

Example 27

2-[1-(3,4-Dichloro-phenyl)-3-pyrrolidin-1-yl-propyl]-2H-t etrazole

The procedure given in Example 1 was followed using pyrrolidine as a reactant, instead of dimethylamine, to give 2-[1-(3,4-Dichloro-phenyl)-3-pyrrolidin-1-yl-propyl]-2H-tetr azole.

1H-NMR(CDCl3, 200MHz) δ1.8(m, 4H), 2.4(m, 7H), 2.8(m, 1H), 6.1(m, 1H), 7.2(dd, 1H), 7.4(dd, 1H), 7.6(t, 1H), 8.5(s, 1H)

Example 28

Dimethyl-(3-naphthalen-1-yl-3-tetrazol-2-yl-propyl)-amine

The procedure given in Example 1 was followed using 1-acetonaphthone as a reactant, instead of 3,4-dichloroacetophenone, to give Dimethyl-(3-naphthalen-1-yl-3-tetrazol-2-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 8H), 2.6(m, 1H), 2.9(m, 1H), 7.0(m, 1H), 7.5(m, 4H), 7.9(t, 2H), 8.3(d, 1H), 8.5(s, 1H)

Example 29

Dimethyl-(3-naphthalen-1-yl-3-[1,2,3]triazol-2-yl-propyl) -amine

The procedure given in Example 1 was followed using 1-acetonaphthone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-(3-naphthalen-1-yl-3-[1,2,3]triazol-2-yl-propyl)-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 8H), 2.6(m, 1H), 2.9(m, 1H), 7.0(m, 1H), 7.5(m, 4H), 7.9(t, 2H), 8.3(d, 1H)

Example 30

[3-(3,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 5-methyl-1 H -tetrazole e as a reactant, instead of 1 H -tetrazole, to give [3-(3,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.6(m, 3H), 2.9(m, 3H), 6.0(t, 1H), 7.2(dd, 1H), 7.4(dd, 1H), 7.5(s, 1H)

Example 31

[3-(3,4-Dichloro-phenyl)-3-(5-phenyl-tetrazol-2-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 5-phenyl-1 H -tetrazole as a reactant, instead of 1 H -tetrazole, to give [3-(3,4-Dichloro-phenyl)-3-(5-phenyl-tetrazol-2-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.6(m, 3H), 2.9(m, 3H), 6.0(t, 1H), 7.4(m, 5H), 8.1(m, 2H)

Example 32

[3-(3,4-Difluoro-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl -amine

The procedure given in Example 1 was followed using 3,4-difluoroacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(3,4-Difluoro-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 8H), 2.6(m, 2H), 2.9(m, 1H), 6.0(t, 1H), 7.4(m, 4H), 8.7(s, 1H)

Example 33

[3-(3,4-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

The procedure given in Example 1 was followed using 3,4-difluoroacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(3,4-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 8H), 2.6(m, 2H), 2.9(m, 1H), 6.0(t, 1H), 7.4(m, 4H), 8.4(s, 1H)

Example 34

[3-(3,4-Difluoro-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 3,4-difluoroacetophenone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3,4-Difluoro-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 8H), 2.6(m, 2H), 2.9(m, 1H), 6.0(t, 1H), 7.4(m, 3H),7.5(s, 1H), 7.7(s, 1H)

Example 35

[3-(3,4-Difluoro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 3,4-difluoroacetophenone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3,4-Difluoro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 8H), 2.6(m, 2H), 2.9(m, 1H), 6.0(t, 1H), 7.4(m, 3H),7.6(s, 2H)

Example 36

[3-(3,4-Dimethyl-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 3,4-dimethylacetophenone and 1 H -1,2,3-triazole as reactant, instead of 3,4-dichloroacetophenone, and 1 H -tetrazole to give [3-(3,4-Dimethyl-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 14H), 2.6(m, 2H), 2.9(m, 2H), 6.0(t, 1H), 7.4(m, 3H), 7.5(s, 1H), 7.7(s, 1H)

Example 37

[3-(3,4-Dimethyl-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 3,4-dimethylacetophenone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3,4-Dimethyl-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 14H), 2.6(m, 2H), 2.9(m, 2H), 6.0(t, 1H), 7.4(m, 3H), 7.5(t, 2H)

Example 38

[3-(3,4-Dimethyl-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl -amine

The procedure given in Example 1 was followed using 3,4-dimethylacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(3,4-Dimethyl-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 14H), 2.6(m, 2H), 2.9(m, 2H), 6.0(t, 1H), 7.4(m, 3H), 8.5(s, 1H)

Example 39

[3-(3,4-Dimethyl-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

The procedure given in Example 1 was followed using 3,4-dimethylacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(3,4-Dimethyl-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 14H), 2.6(m, 2H), 2.9(m, 2H), 6.0(t, 1H), 7.4(m, 3H), 8.3(s, 1H)

Example 40

[3-(4-Chloro-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl-ami ne

The procedure given in Example 1 was followed using 4-chloroacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(4-Chloro-phenyl)-3-tetrazol-1-yl-propyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.6(m, 2H), 2.9(m, 2H), 6.0(t, 1H), 7.4(m, 4H), 8.7(s, 1H)

Example 41

[3-(4-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-ami ne

The procedure given in Example 1 was followed using 4-chloroacetophenone as a reactant, instead of 3,4-dichloroacetophenone, to give [3-(4-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.6(m, 2H), 2.9(m, 2H), 6.0(t, 1H), 7.4(m, 4H), 8.7(s, 1H)

Example 42

Dimethyl-(3-phenyl-3-[1,2,3]triazol-1-yl-propyl)-amine

The procedure given in Example 1 was followed using acetophenone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-(3-phenyl-3-[1,2,3]triazol-1-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.6(m, 2H), 2.9(m, 2H), 6.0(t, 1H), 7.2(m, 5H), 7.4(s, 1H), 7.6(s, 1H)

Example 43

Dimethyl-(3-phenyl-3-[1,2,3]triazol-2-yl-propyl)-amine

The procedure given in Example 1 was followed using acetophenone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-(3-phenyl-3-[1,2,3]triazol-2-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.6(m, 2H), 6.0(t, 1H), 7.2(m, 5H), 7.4(s, 2H)

Example 44

[3-(4-Chloro-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-dimeth yl-amine

The procedure given in Example 1 was followed using 4-chloroacetophenone and 1 H -1,2,3-triazole as reactant, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(4-Chloro-phenyl)-3-[1,2,3]triazol-1-yl-propyl]-dimethyl- amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.6(m, 2H), 6.0(t, 1H), 7.2(m, 4H), 7.5(s, 1H), 7.7(s, 1H)

Example 45

[3-(4-Chloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimeth yl-amine

The procedure given in Example 1 was followed using 4-chloroacetophenone and 1 H -1,2,3-triazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(4-Chloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimethyl- amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.6(m, 2H), 6.0(t, 1H), 7.2(m, 4H), 7.6(s, 2H)

Example 46

[3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 1 H -1,2,3-triazole as a reactant, instead of 1 H -tetrazole, to give [3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.4(m, 2H), 2.6(m, 2H), 6.0(t, 1H), 7.2(dd, 1H), 7.4(dd, 2H), 7.6(s, 2H)

Example 47

[3-(3,4-Dichloro-phenyl)-3-imidazol-1-yl-propyl]-dimethyl -amine

The procedure given in Example 1 was followed using imidazole as a reactant, instead of 1 H -tetrazole, to give [3-(3,4-Dichloro-phenyl)-3-imidazol-1-yl-propyl]-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(br, 10H), 5.3(t, 1H), 7.2(dd, 1H), 7.4(dd, 2H), 7.6(s, 2H)

Example 48

[3-(3-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 1-(3-Methoxy-naphthalen-2-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(3-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 13H), 6.2(m, 1H), 7.5(m, 3H), 7.8(m, 4H), 8.5(s, 1H)

Example 49

[3-(3-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl) -propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(3-Methoxy-naphthalen-2-yl)-ethanone and 5-Methyl-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 5H), 2.8(m, 1H), 4.0(s, 3H), 6.6(m, 1H), 7.5(m, 3H), 7.8(m, 4H)

Example 50

[3-(6-Fluoro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dim ethyl-amine

The procedure given in Example 1 was followed using 1-(6-Fluoro-naphthalen-2-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(6-Fluoro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dimeth yl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 12H), 2.5(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(m, 1H), 7.8(m, 3H), 8.5(s, 1H)

Example 51

[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)- propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(6-Fluoro-naphthalen-2-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 4H), 2.8(m, 1H), 6.2(t, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(m, 1H), 7.8(m, 3H)

Example 52

[3-(1,4-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl ]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(1,4-Dimethoxy-naphthalen-2-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(1,4-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-d imethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 12H), 2.5(m, 1H), 2.8(m, 1H), 4.0(d, 6H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(m, 1H), 7.8(m, 2H), 8.5(s, 1H)

Example 53

[3-(1,4-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(1,4-Dimethoxy-naphthalen-2-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(1,4-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl )-propyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 12H), 2.5(m, 1H), 2.8(m, 1H), 4.0(d, 6H), 6.2(m, 1H), 6.9(s, 1H), 7.5(m, 2H), 8.0(s, 1H), 8.2(d, 1H)

Example 54

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl ]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(3,5-Dimethoxy-naphthalen-2-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-d imethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 12H), 2.5(m, 1H), 2.8(m, 1H), 4.0(m, 6H), 6.8(m, 1H), 7.3(s, 6H), 7.5(m, 2H), 8.5(s, 1H)

Example 55

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(3,5-Dimethoxy-naphthalen-2-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl )-propyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 4H), 2.8(m, 1H), 4.0(m, 6H), 6.6(m, 1H), 6.8(m, 1H), 7.2(s, 3H), 7.5(s, 1H), 7.7(s, 1H)

Example 56

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-1-yl-propyl ]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(3,5-Dimethoxy-naphthalen-2-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-1-yl-propyl]-d imethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 12H), 2.5(m, 1H), 2.8(m, 1H), 4.0(m, 6H), 6.6(m, 1H), 6.8(m, 1H), 7.2(s, 3H), 7.5(s, 1H), 7.7(s, 1H), 8.7(s, 1H)

Example 57

Dimethyl-[3-(4-methyl-naphthalen-1-yl)-3-tetrazol-2-yl-pr opyl]-amine

The procedure given in Example 1 was followed using 1-(4-Methyl-naphthalen-1-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-(4-methyl-naphthalen-1-yl)-3-tetrazol-2-yl-propy l]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.4(m, 1H), 2.8(m, 4H), 3.0(m, 1H), 7.0(m, 1H), 7.2(m, 1H), 7.5(m, 4H), 8.0(m, 1H), 8.3(m, 1H), 8.5(s, 1H)

Example 58

Dimethyl-[3-(4-methyl-naphthalen-1-yl)-3-(5-methyl-tetraz ol-2-yl)-propyl]-amine

The procedure given in Example 1 was followed using 1-(4-Methyl-naphthalen-1-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(4-methyl-naphthalen-1-yl)-3-(5-methyl-tetrazol- 2-yl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.4(m, 3H), 2.8(m, 3H), 3.0(m, 1H), 7.0(m, 1H), 7.2(m, 1H), 7.5(m, 4H), 8.0(m, 1H), 8.3(m, 1H)

Example 59

[3-(4-Fluoro-naphthalen-1-yl)-3-tetrazol-2-yl-propyl]-dim ethyl-amine

The procedure given in Example 1 was followed using 1-(4-Fluoro-naphthalen-1-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(4-Fluoro-naphthalen-1-yl)-3-tetrazol-2-yl-propyl]-dimeth yl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 12H), 2.4(m, 1H), 2.8(m, 1H), 7.0(m, 1H), 7.2(m, 1H), 7.5(m, 4H), 8.0(m, 1H), 8.3(m, 1H), 8.5(s, 1H)

Example 60

[3-(4-Fluoro-naphthalen-1-yl)-3-(5-methyl-tetrazol-2-yl)- propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(4-Methyl-naphthalen-1-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(4-Fluoro-naphthalen-1-yl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.4(m, 4H), 2.8(m, 1H), 7.0(m, 1H), 7.2(m, 1H), 7.5(m, 3H), 8.1(m, 1H), 8.3(m, 1H)

Example 61

(3-Isoquinolin-1-yl-3-tetrazol-2-yl-propyl)-dimethyl-amin e

The procedure given in Example 1 was followed using 1-Isoquinolin-1-yl-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give (3-Isoquinolin-1-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.4(m, 1H), 2.8(m, 1H), 7.2(m, 1H), 7.6(m, 2H), 7.8(m, 2H), 8.4(m, 1H), 8.5(m, 1H), 9.1(s, 1H)

Example 62

[3-Isoquinolin-1-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 1-Isoquinolin-1-yl-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-Isoquinolin-1-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.5(m, 3H), 2.8(m, 3H), 7.2(m, 1H), 7.6(m, 2H), 7.8(m, 2H), 8.4(m, 1H), 8.5(m, 1H)

Example 63

(3-Benzo[1,3]dioxol-5-yl-3-tetrazol-2-yl-propyl)-dimethyl -amine

The procedure given in Example 1 was followed using 1-Benzo[1,3]dioxol-5-yl-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give (3-Benzo[1,3]dioxol-5-yl-3-tetrazol-2-yl-propyl)-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.5(m, 1H), 2.8(m, 1H), 6.0(s, 2H), 6.1(m, 1H), 6.8(d, 1H), 7.0(d, 2H), 8.5(m, 1H)

Example 64

[3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 1-Benzo[1,3]dioxol-5-yl-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 15H), 2.8(m, 1H), 6.0(s, 2H), 6.1(m, 1H), 6.8(d, 1H), 7.0(d, 2H), 8.5(m, 1H)

Example 65

[3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-1-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 1-Benzo[1,3]dioxol-5-yl-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-1-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.4(m, 1H), 2.5(s, 3H), 2.8(m, 1H), 5.5(t, 2H), 6.1(s, 2H), 6.8(m, 3H)

Example 66

[3-(3,4-Dimethoxy-phenyl)-3-tetrazol-2-yl-propyl]-dimethy l-amine

The procedure given in Example 1 was followed using 1-(3,4-Dimethoxy-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(3,4-Dimethoxy-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-a mine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 12H), 2.4(m, 1H), 2.8(m, 1H), 4.0(s, 6H), 6.1(s, 2H), 6.8(d, 1H), 7.0(d, 2H), 8.5(s, 1H)

Example 67

[3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-tetrazol-2-yl-pr opyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-tetrazol-2-yl-propy l]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 12H), 2.4(m, 3H), 3.8(m, 1H), 4.6(m, 1H), 5.4(m, 1H), 7.0(s, 5H), 8.5(s, 1H)

Example 68

[3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-(5-methyl-tetraz ol-2-yl)-propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-(5-methyl-tetrazol- 2-yl)-propyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 10H), 2.4(m, 3H), 2.8(m, 4H), 3.8(m, 1H), 4.0(m, 1H), 4.8(m, 1H), 5.3(m, 1H), 7.0(s, 4H)

Example 69

Dimethyl-(3-quinolin-2-yl-3-tetrazol-2-yl-propyl)-amine

The procedure given in Example 1 was followed using 1-Quinolin-2-yl-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give Dimethyl-(3-quinolin-2-yl-3-tetrazol-2-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 10H), 2.8(m, 2H), 6.5(t, 1H), 7.3(m, 2H), 7.5(m, 1H), 7.8(m, 2H), 8.0(t, 2H), 8.5(s, 1H)

Example 70

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-quinolin-2-yl-prop yl]-amine

The procedure given in Example 1 was followed using 1-Quinolin-2-yl-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-quinolin-2-yl-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 10H), 2.5(s, 3H), 2.8(m, 2H), 6.5(t, 1H), 7.3(m, 2H), 7.5(m, 1H), 7.8(m, 2H), 8.0(t, 2H), 8.5(s, 1H)

Example 71

Dimethyl-[3-(1-methyl-1H-indol-2-yl)-3-tetrazol-2-yl-prop yl]-amine

The procedure given in Example 1 was followed using 1-(1-Methyl-1H-indol-2-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-(1-methyl-1H-indol-2-yl)-3-tetrazol-2-yl-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 10H), 2.5(s, 3H), 2.8(m, 2H), 6.5(t, 1H), 7.3(m, 2H), 7.5(m, 1H), 7.8(m, 2H), 8.0(t, 2H), 8.5(s, 1H)

Example 72

Dimethyl-[3-(1-methyl-1H-indol-2-yl)-3-(5-methyl-tetrazol -2-yl)-propyl]-amine

The procedure given in Example 1 was followed using 1-(1-Methyl-1H-indol-2-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(1-methyl-1H-indol-2-yl)-3-(5-methyl-tetrazol-2- yl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.5(s, 3H), 2.8(m, 2H), 3.8(s, 2H), 6.5(t, 1H), 6.8(s, 1H), 7.3(m, 1H), 7.5(m, 2H), 7.8(m, 2H)

Example 73

Dimethyl-[3-(1,2,3,4-tetrahydro-naphthalen-2-yl)-3-tetraz ol-2-yl-propyl]-amine

The procedure given in Example 1 was followed using 1-(1,2,3,4-Tetrahydro-naphthalen-2-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-(1,2,3,4-tetrahydro-naphthalen-2-yl)-3-tetrazol- 2-yl-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 11H), 2.8(m, 8H), 5.0(m, 1H), 7.0(m, 4H), 8.5(s, 1H)

Example 74

[3-(6-Chloro-pyridin-3-yl)-3-tetrazol-2-yl-propyl]-dimeth yl-amine

The procedure given in Example 1 was followed using 1-(6-Chloro-pyridin-3-yl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(6-Chloro-pyridin-3-yl)-3-tetrazol-2-yl-propyl]-dimethyl- amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.5(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.8(m, 1H), 8.5(s, 1H)

Example 75

(3-Benzo[b]thiophen-2-yl-3-tetrazol-2-yl-propyl)-dimethyl -amine

The procedure given in Example 1 was followed using 1-Benzo[b]thiophen-2-yl-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give (3-Benzo[b]thiophen-2-yl-3-tetrazol-2-yl-propyl)-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.8(m, 1H), 6.5(m, 1H), 7.4(m, 3H), 7.8(m, 2H), 8.5(s, 1H)

Example 76

[3-Benzo[b]thiophen-2-yl-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 1-Benzo[b]thiophen-2-yl-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-Benzo[b]thiophen-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.8(m, 5H), 6.5(m, 1H), 7.4(m, 3H), 7.8(m, 2H)

Example 77

(3-Benzofuran-2-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine

The procedure given in Example 1 was followed using 1-Benzofuran-2-yl-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give (3-Benzofuran-2-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.8(m, 2H), 6.5(m, 1H), 7.4(m, 3H), 7.8(m, 2H), 8.5(s, 1H)

Example 78

[3-Benzofuran-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-dim ethyl-amine

The procedure given in Example 1 was followed using 1-Benzofuran-2-yl-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-Benzofuran-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-dimeth yl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.8(m, 2H), 6.5(m, 1H), 7.4(m, 3H), 7.8(m, 2H)

Example 79

(3-Benzofuran-2-yl-3-tetrazol-1-yl-propyl)-dimethyl-amine

The procedure given in Example 1 was followed using 1-Benzofuran-2-yl-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give (3-Benzofuran-2-yl-3-tetrazol-1-yl-propyl)-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.8(m, 2H), 6.2(m, 1H), 7.4(m, 3H), 7.8(m, 2H)

Example 80

[3-(3,4-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 1-Benzofuran-2-yl-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3,4-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.8(m, 4H), 6.2(m, 1H), 7.4(m, 4H)

Example 81

Dimethyl-[3-tetrazol-2-yl-3-(2,4,5-trifluoro-phenyl)-prop yl]-amine

The procedure given in Example 1 was followed using 1-(2,4,5-Trifluoro-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-tetrazol-2-yl-3-(2,4,5-trifluoro-phenyl)-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 12H), 2.8(m, 2H), 6.5(m, 1H), 7.0(m, 1H), 7.4(m, 1H), 8.6(s, 1H)

Example 82

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,4,5-trifluoro-p henyl)-propyl]-amine

The procedure given in Example 1 was followed using 1-(2,4,5-Trifluoro-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,4,5-trifluoro-phen yl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 12H), 2.8(m, 4H), 6.5(m, 1H), 7.0(m, 1H), 7.4(m, 1H)

Example 83

[3-(3-Bromo-4-fluoro-phenyl)-3-tetrazol-2-yl-propyl]-dime thyl-amine

The procedure given in Example 1 was followed using 1-(3-Bromo-4-fluoro-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(3-Bromo-4-fluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.4(m, 2H), 2.8(m, 1H), 6.5(m, 1H), 7.0(m, 1H), 7.4(m, 1H), 7.8(m, 1H), 8.5(s, 1H)

Example 84

[3-(3-Bromo-4-fluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-p ropyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(3-Bromo-4-fluoro-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3-Bromo-4-fluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-prop yl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.4(m, 2H), 2.8(m, 1H), 6.5(m, 1H), 7.0(m, 1H), 7.4(m, 1H), 7.8(m, 1H)

Example 85

[3-(6-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl) -propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(6-Methoxy-naphthalen-2-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(6-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 11H), 2.4(m, 2H), 2.8(m, 1H), 4.0(s, 3H), 6.3(m, 1H), 7.1(m, 3H), 7.4(m, 1H), 7.8(m, 1H)

Example 86

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-phenoxy-phenyl) -propyl]-amine

The procedure given in Example 1 was followed using 1-(4-Phenoxy-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-phenoxy-phenyl)-pr opyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 8H), 2.4(m, 6H), 2.8(m, 1H), 6.2(m, 1H), 7.1(m, 4H), 7.4(m, 4H)

Example 87

[3-(4-Bromo-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amin e

The procedure given in Example 1 was followed using 1-(4-Bromo-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(4-Bromo-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.4(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.3(m, 2H), 7.5(m, 2H), 8.5(s, 1H)

Example 88

[3-(4-Bromo-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 1-(4-Bromo-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(4-Bromo-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 1H), 2.5(s, 3H), 2.8(m, 1H), 6.0(m, 1H), 7.3(m, 2H), 7.5(m, 2H)

Example 89

Dimethyl-[3-tetrazol-2-yl-3-(4-trifluoromethyl-phenyl)-pr opyl]-amine

The procedure given in Example 1 was followed using 1-(4-Trifluoromethyl-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-tetrazol-2-yl-3-(4-trifluoromethyl-phenyl)-propy l]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.3(m, 2H), 7.5(m, 2H), 8.5(s, 1H)

Example 90

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethyl -phenyl)-propyl]-amine

The procedure given in Example 1 was followed using 1-(4-Trifluoromethyl-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethyl-ph enyl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 1H), 2.5(s, 3H), 2.8(m, 1H), 6.0(m, 1H), 7.6(m, 4H)

Example 91

Dimethyl-[3-tetrazol-2-yl-3-(2,3,4-trichloro-phenyl)-prop yl]-amine

The procedure given in Example 1 was followed using 1-(2,3,4-Trichloro-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-tetrazol-2-yl-3-(2,3,4-trichloro-phenyl)-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.3(m, 3H), 8.5(s, 1H)

Example 92

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,3,4-trichloro-p henyl)-propyl]-amine

The procedure given in Example 1 was followed using 1-(2,3,4-Trichloro-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,3,4-trichloro-phen yl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 1H), 2.5(s, 3H), 2.8(m, 1H), 6.0(m, 1H), 7.2(m, 2H)

Example 93

[3-(3-Chloro-4-methoxy-phenyl)-3-tetrazol-2-yl-propyl]-di methyl-amine

The procedure given in Example 1 was followed using 1-(3-Chloro-4-methoxy-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(3-Chloro-4-methoxy-phenyl)-3-tetrazol-2-yl-propyl]-dimet hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.3(m, 1H), 2.8(m, 1H), 4.0(s, 3H), 6.1(m, 1H), 6.9(d, 1H), 7.3(d, 1H), 7.5(s, 1H), 8.5(s, 1H)

Example 94

[3-(3-Chloro-4-methoxy-phenyl)-3-(5-methyl-tetrazol-2-yl) -propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(3-Chloro-4-methoxy-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3-Chloro-4-methoxy-phenyl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 10H), 2.3(m, 1H), 2.8(m, 1H), 4.0(s, 3H), 6.1(m, 1H), 6.9(d, 1H), 7.3(d, 1H), 7.5(s, 1H)

Example 95

[3-(4-tert-Butyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(4-tert-Butyl-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(4-tert-Butyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ1.2(s, 9H), 2.4(m, 3H), 2.5(m, 6H), 2.7(m, 1H), 6.2(m, 1H), 7.4(m, 4H)

Example 96

[3-(2,5-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(2,5-Difluoro-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(2,5-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 3H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 3H)

Example 97

[3-(2,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(2,4-Dichloro-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(2,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 3H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 3H)

Example 98

[3-(3-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-d imethyl-amine

The procedure given in Example 1 was followed using 1-(3-Chloro-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-dime thyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 3H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 4H)

Example 99

[3-(2-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-d imethyl-amine

The procedure given in Example 1 was followed using 1-(2-Chloro-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(2-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-dime thyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 3H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 4H)

Example 100

[3-(2,5-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

The procedure given in Example 1 was followed using 1-(2,5-Difluoro-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(2-5-difluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 1H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 3H), 8.5(s, 1H)

Example 101

[3-(2,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl -amine

The procedure given in Example 1 was followed using 1-(2,4-Dichloro-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(2,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 1H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 3H), 8.5(s, 1H)

Example 102

[3-(3-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-ami ne

The procedure given in Example 1 was followed using 1-(3-Chloro-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(3-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 1H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 4H), 8.5(s, 1H)

Example 103

Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethox y-phenyl)-propyl]-amine

The procedure given in Example 1 was followed using 1-(4-Trifluoromethoxy-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethoxy-p henyl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 3H), 2.7(m, 1H), 6.4(m, 1H), 7.2(m, 2H),7.4(m, 2H)

Example 104

[3-(3-Bromo-4-methyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-p ropyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(3-Bromo-4-methyl-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(3-Bromo-4-methyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-prop yl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 3H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 3H)

Example 105

Dimethyl-[3-tetrazol-2-yl-3-(4-trifluoromethoxy-phenyl)-p ropyl]-amine

The procedure given in Example 1 was followed using 1-(4-Trifluoromethoxy-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give Dimethyl-[3-tetrazol-2-yl-3-(4-trifluoromethoxy-phenyl)-prop yl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 1H), 2.7(m, 1H), 6.4(m, 1H), 7.2(m, 2H),7.4(m, 2H), 8.5(s, 1H)

Example 106

[3-(4-Bromo-3-methyl-phenyl)-3-tetrazol-2-yl-propyl]-dime thyl-amine

The procedure given in Example 1 was followed using 1-(3-Bromo-4-methyl-phenyl)-ethanone as reactants, instead of 3,4-dichloroacetophenone, to give [3-(4-Bromo-3-methyl-phenyl)-3-tetrazol-2-yl-propyl]-dimethy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 1H), 2.7(m, 1H), 6.4(m, 1H), 7.4(m, 3H), 8.5(s, 1H)

Example 107

[3-(4-Methanesulfonyl-phenyl)-3-(5-methyl-tetrazol-2-yl)- propyl]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(4-Methanesulfonyl-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(4-Methanesulfonyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-dimethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 3H), 2.7(m, 1H), 3.0(m, 3H), 6.4(m, 1H), 7.2(m, 2H),7.4(m, 2H)

Example 108

[3-(4-Isopropyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl ]-dimethyl-amine

The procedure given in Example 1 was followed using 1-(4-Isopropyl-phenyl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(4-Isopropyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-d imethyl-amine.

1H-NMR(CDCl3, 200MHz) δ1.0(s, 6H), 2.4(m, 10H), 2.7(m, 1H), 3.0(m, 3H), 6.4(m, 1H), 7.2(m, 2H),7.4(m, 2H)

Example 109

[3-(9H-Fluoren-2-yl)-3-(5-methyl-tetrazol-2-yl)-propyl]-d imethyl-amine

The procedure given in Example 1 was followed using 1-(9H-Fluoren-2-yl)-ethanone and 5-Me-1 H -tetrazole as reactants, instead of 3,4-dichloroacetophenone and 1 H -tetrazole, to give [3-(9H-Fluoren-2-yl)-3-(5-methyl-tetrazol-2-yl)-propyl]-dime thyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10H), 2.5(m, 3H), 2.7(m, 1H), 4.0(m, 3H), 6.4(m, 1H), 7.2(m, 2H),7.4(m, 2H)

Example 110

Methyl-(3-naphthalen-2-yl-3-[1,2,3]triazol-2-yl-propyl)-a mine

The procedure given in Example 2 was followed using dimethyl-(3-naphthalen-2-yl-3-[1,2,3]triazol-2-yl-propyl)-am ine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-(3-naphthalen-2-yl-3-[1,2,3]triazol-2-yl-propyl)-amin e.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 6H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 3H), 7.6(d, 2H), 7.8(m, 4H)

Example 111

[3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-meth yl-amine

The procedure given in Example 2 was followed using [3-benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-dimethy l-amineas a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-methyl- amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 4H), 7.6(s, 1H), 7.9(m, 2H)

Example 112

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-prop yl]-amine

The procedure given in Example 2 was followed using [dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-prop yl]-amine a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.4(s, 1H), 2.6(m, 6H), 2.8(m, 1H), 6.2(m, 1H), 7.5(m, 3H), 7.8(m, 4H)

Example 113

(3-Benzotriazol-2-yl-3-naphthalen-2-yl-propyl)-methyl-ami ne

The procedure given in Example 2 was followed using (3-benzotriazol-2-yl-3-naphthalen-2-yl-propyl)-dimethyl-amin e as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give (3-benzotriazol-2-yl-3-naphthalen-2-yl-propyl)-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(s, 1H), 2.6(m, 6H), 2.8(m, 1H), 6.2(m, 1H), 7.4(m, 4H), 7.6(d, 1H), 7.9(m, 6H)

Example 114

(3-Biphenyl-4-yl-3-tetrazol-2-yl-propyl)-methyl-amine

The procedure given in Example 2 was followed using (3-biphenyl-4-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give (3-Biphenyl-4-yl-3-tetrazol-2-yl-propyl)-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(s, 1H), 2.6(m, 6H), 2.8(m, 1H), 6.2(m, 1H), 7.4(m 9H), 8.5(s, 1H)

Example 115

[3-(3,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

The procedure given in Example 2 was followed using [3-(3,4-dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,4-dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 6H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H)

Example 116

[3-(4-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine

The procedure given in Example 2 was followed using [3-(4-chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(4-chloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 6H), 2.7(m, 1H), 6.2(m, 1H), 7.3(m, 4H), 8.5(s, 1H)

Example 117

[3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-me thyl-amine

The procedure given in Example 2 was followed using [3-(3,4-dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-dimet hyl-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,4-dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-methy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H), 7.6(d, 2H)

Example 118

[3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

The procedure given in Example 2 was followed using [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H), 8.5(s, 1H)

Example 119

Methyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine

The procedure given in Example 2 was followed using dimethyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give methyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.5(m, 3H), 7.8(m, 4H), 8.5(s, 1H)

Example 120

[3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-met hyl-amine

The procedure given in Example 2 was followed using [3-(6-chloro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dimeth yl-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(6-Chloro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-methyl -amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 7.0(m, 1H), 7.5(m, 3H), 7.8(m, 2H), 8.3(s, 1H), 8.5(s, 1H)

Example 121

Methyl-(3-naphthalen-1-yl-3-tetrazol-2-yl-propyl)-amine

The procedure given in Example 2 was followed using Dimethyl-(3-naphthalen-1-yl-3-tetrazol-2-yl-propyl)-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give methyl-(3-naphthalen-1-yl-3-tetrazol-2-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 7.5(m, 4H), 7.9(t, 2H), 8.3(d, 1H), 8.5(s, 1H)

Example 122

Methyl-[3-(6-methyl-naphthalen-2-yl)-3-tetrazol-2-yl-prop yl]-amine

The procedure given in Example 2 was followed using Dimethyl-[3-(6-methyl-naphthalen-2-yl)-3-tetrazol-2-yl-propy l]-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give methyl-[3-(6-methyl-naphthalen-2-yl)-3-tetrazol-2-yl-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.4(s, 3H), 2.5(m, 6H), 2.8(m, 1H), 6.3(m,1H), 7.3(dd, 1H), 7.5(m, 2H), 7.7(dd, 2H), 7.8(s, 1H), 8.5(s, 1H)

Example 123

Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-prop yl]-amine

The procedure given in Example 2 was followed using Dimethyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-propy l]-amine as a reactant, instead of [3-(3,4-dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.3(m, 1H), 7.5(m, 5H), 7.6(dd, 1H), 7.8(m, 3H), 7.9(s, 1H), 8.2(m, 2H)

Example 124

(3 S )-3-(3,4-dichlorophenyl)- N -methyl-3-(2 H -tetrazol-2-yl)propan-1-amine

The procedure given in Example 3 was followed using [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give (3S)-3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl- amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H), 8.5(s, 1H)

Example 125

(3 R )-3-(3,4-dichlorophenyl)- N -methyl-3-(2 H -tetrazol-2-yl)propan-1-amine

The procedure given in Example 3 was followed using [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give 3R-3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H), 8.5(s, 1H)

Example 126

(3 S )-3-(2 H -benzotriazol-2-yl)-3-(3,4-dichlorophenyl)- N -methylpropan-1-amine

The procedure given in Example 3 was followed using [3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-methyl- amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give S-[3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-methy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 4H), 7.6(s, 1H), 7.9(m, 2H)

Example 127

(3 R )-3-(2 H -benzotriazol-2-yl)-3-(3,4-dichlorophenyl)- N -methylpropan-1-amine

The procedure given in Example 3 was followed using [3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-methyl- amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give R-[3-Benzotriazol-2-yl-3-(3,4-dichloro-phenyl)-propyl]-methy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 4H), 7.6(s, 1H), 7.9(m, 2H)

Example 128

(3 S )-3-(3,4-dichlorophenyl)- N -methyl-3-(2 H -1,2,3-triazol-2-yl)propan-1-amine

The procedure given in Example 3 was followed using [3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-methy l-amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give S-[3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-met hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H), 7.6(d, 2H)

Example 129

(3 S )-3-(3,4-dichlorophenyl)- N -methyl-3-(5-methyl-2 H -tetrazol-2-yl)propan-1-amine

The procedure given in Example 3 was followed using [3-(3,4-Dichloro-phenyl)-3-(4-methyl-[1,2,3]triazol-2-yl)-pr opyl]-methyl-amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give S-[3-(3,4-Dichloro-phenyl)-3-(4-methyl-[1,2,3]triazol-2-yl)- propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 6H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H)

Example 130

(3 R )-3-(3,4-dichlorophenyl)- N -methyl-3-(5-methyl-2 H -tetrazol-2-yl)propan-1-amine

The procedure given in Example 3 was followed using [3-(3,4-Dichloro-phenyl)-3-(4-methyl-[1,2,3]triazol-2-yl)-pr opyl]-methyl-amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give R-[3-(3,4-Dichloro-phenyl)-3-(4-methyl-[1,2,3]triazol-2-yl)- propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 6H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H)

Example 131

(3 R )-3-(3,4-dichlorophenyl)- N -methyl-3-(2 H -1,2,3-triazol-2-yl)propan-1-amine

The procedure given in Example 3 was followed using [3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-methy l-amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give R-[3-(3,4-Dichloro-phenyl)-3-[1,2,3]triazol-2-yl-propyl]-met hyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(s, 1H), 7.6(d, 2H)

Example 132

(3 R )- N -methyl-3-(2-naphthyl)-3-(2 H -tetrazol-2-yl)propan-1-amine

The procedure given in Example 3 was followed using Methyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give R-Methyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.5(m, 3H), 7.8(m, 4H), 8.5(s, 1H)

Example 133

(3 S )- N -methyl-3-(2-naphthyl)-3-(2 H -tetrazol-2-yl)propan-1-amine

The procedure given in Example 3 was followed using Methyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give S-Methyl-(3-naphthalen-2-yl-3-tetrazol-2-yl-propyl)-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 3H), 2.5(m, 3H), 2.7(m, 1H), 6.2(m, 1H), 7.5(m, 3H), 7.8(m, 4H), 8.5(s, 1H)

Example 134

[3-(3-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-me thyl-amine

The procedure given in Example 2 was followed using [3-(3-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dimet hyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-methy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 10),6.2(m, 1H), 7.5(m, 3H), 7.8(m, 4H), 8.5(s, 1H)

Example 135

[3-(3-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl) -propyl]-methyl-amine

The procedure given in Example 2 was followed using [3-(3-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 5H), 2.8(m, 1H), 4.0(s, 3H), 6.6(m, 1H), 7.5(m, 3H), 7.8(m, 4H)

Example 136

[3-(6-Fluoro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-met hyl-amine

The procedure given in Example 2 was followed using [3-(6-Fluoro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dimeth yl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(6-Fluoro-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-methyl -amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(m, 1H), 7.8(m, 3H), 8.5(s, 1H)

Example 137

[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)- propyl]-methyl-amine

The procedure given in Example 2 was followed using [3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 6H), 2.5(m, 2H), 2.8(m, 1H), 6.2(t, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(m, 1H), 7.8(m, 3H)

Example 138

[3-(1,4-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl ]-methyl-amine

The procedure given in Example 2 was followed using [3-(1,4-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-d imethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(1,4-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-m ethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 1H), 2.8(m, 1H), 4.0(d, 6H), 6.2(m, 1H), 7.2(m, 1H), 7.4(m, 1H), 7.5(m, 1H), 7.8(m, 2H), 8.5(s, 1H)

Example 139

[3-(1,4-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-methyl-amine

The procedure given in Example 2 was followed using [3-(1,4-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl )-propyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(1,4-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl )-propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 1H), 2.8(m, 1H), 4.0(d, 6H), 6.2(m, 1H), 6.9(s, 1H), 7.5(m, 2H), 8.0(s, 1H), 8.2(d, 1H)

Example 140

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl ]-methyl-amine

The procedure given in Example 2 was followed using [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-d imethyl-amineas a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-m ethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 1H), 2.8(m, 1H), 4.0(m, 6H), 6.8(m, 1H), 7.3(s, 6H), 7.5(m, 2H), 8.5(s, 1H)

Example 141

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-methyl-amine

The procedure given in Example 2 was followed using [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl )-propyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl )-propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.0(s, 6H), 2.4(m, 6H), 2.5(m, 2H), 2.8(m, 1H), 4.0(m, 6H), 6.6(m, 1H), 6.8(m, 1H), 7.2(s, 3H), 7.7(d, 2H)

Example 142

[3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-1-yl-propyl ]-methyl-amine

The procedure given in Example 2 was followed [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-1-yl-propyl]-d imethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,5-Dimethoxy-naphthalen-2-yl)-3-tetrazol-1-yl-propyl]-m ethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.4(m, 9H), 2.5(m, 4H), 2.8(m, 1H), 4.0(m, 6H), 6.6(m, 1H), 6.8(m, 1H), 7.2(s, 3H), 7.5(s, 1H), 7.7(s, 1H), 8.7(s, 1H)

Example 143

Methyl-[3-(4-methyl-naphthalen-1-yl)-3-tetrazol-2-yl-prop yl]-amine

The procedure given in Example 2 was followed Dimethyl-[3-(4-methyl-naphthalen-1-yl)-3-tetrazol-2-yl-propy l]-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-(4-methyl-naphthalen-1-yl)-3-tetrazol-2-yl-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.4(m, 1H), 2.8(m, 4H), 3.0(m, 1H), 7.0(m, 1H), 7.2(m, 1H), 7.5(m, 4H), 8.0(m, 1H), 8.3(m, 1H), 8.5(s, 1H)

Example 144

Methyl-[3-(4-methyl-naphthalen-1-yl)-3-(5-methyl-tetrazol -2-yl)-propyl]-amine

The procedure given in Example 2 was followed Dimethyl-[3-(4-methyl-naphthalen-1-yl)-3-(5-methyl-tetrazol- 2-yl)-propyl]-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-(4-methyl-naphthalen-1-yl)-3-(5-methyl-tetrazol-2- yl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.4(m, 3H), 2.8(m, 3H), 3.0(m, 1H), 7.0(m, 1H), 7.2(m, 1H), 7.5(m, 4H), 8.0(m, 1H), 8.3(m, 1H)

Example 145

[3-(4-Fluoro-naphthalen-1-yl)-3-tetrazol-2-yl-propyl]-met hyl-amine

The procedure given in Example 2 was followed [3-(4-Fluoro-naphthalen-1-yl)-3-tetrazol-2-yl-propyl]-dimeth yl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(4-Fluoro-naphthalen-1-yl)-3-tetrazol-2-yl-propyl]-methyl -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.4(m, 1H), 2.8(m, 1H), 7.0(m, 1H), 7.2(m, 1H), 7.5(m, 4H), 8.0(m, 1H), 8.3(m, 1H), 8.5(s, 1H)

Example 146

[3-(4-Fluoro-naphthalen-1-yl)-3-(5-methyl-tetrazol-2-yl)- propyl]-methyl-amine

The procedure given in Example 2 was followed [3-(4-Fluoro-naphthalen-1-yl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(4-Fluoro-naphthalen-1-yl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 4H), 2.4(m, 6H), 2.8(m, 1H), 7.0(m, 1H), 7.2(m, 1H), 7.5(m, 3H), 8.1(m, 1H), 8.3(m, 1H)

Example 147

(3-Benzo[1,3]dioxol-5-yl-3-tetrazol-2-yl-propyl)-methyl-a mine

The procedure given in Example 2 was followed (3-Benzo[1,3]dioxol-5-yl-3-tetrazol-2-yl-propyl)-dimethyl-am ine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give (3-Benzo[1,3]dioxol-5-yl-3-tetrazol-2-yl-propyl)-methyl-amin e.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.5(m, 1H), 2.8(m, 1H), 6.0(s, 2H), 6.1(m, 1H), 6.8(d, 1H), 7.0(d, 2H), 8.5(m, 1H)

Example 148

[3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

The procedure given in Example 2 was followed [3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-2-yl)-propyl]- methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 12H), 2.8(m, 1H), 6.0(s, 2H), 6.1(m, 1H), 6.8(d, 1H), 7.0(d, 2H), 8.5(m, 1H)

Example 149

[3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-1-yl)-propy l]-methyl-amine

The procedure given in Example 2 was followed [3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-1-yl)-propyl]- dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-Benzo[1,3]dioxol-5-yl-3-(5-methyl-tetrazol-1-yl)-propyl]- methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.4(m, 1H), 2.5(s, 3H), 2.8(m, 1H), 5.5(t, 2H), 6.1(s, 2H), 6.8(m, 3H)

Example 150

[3-(3,4-Dimethoxy-phenyl)-3-tetrazol-2-yl-propyl]-methyl- amine

The procedure given in Example 2 was followed [3-(3,4-Dimethoxy-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-a mine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,4-Dimethoxy-phenyl)-3-tetrazol-2-yl-propyl]-methyl-ami ne.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 9H), 2.4(m, 1H), 2.8(m, 1H), 4.0(s, 6H), 6.1(s, 2H), 6.8(d, 1H), 7.0(d, 2H), 8.5(s, 1H)

Example 151

[3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-tetrazol-2-yl-pr opyl]-methyl-amine

The procedure given in Example 2 was followed [3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-tetrazol-2-yl-propy l]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-tetrazol-2-yl-propy l]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 9H), 2.4(m, 3H), 3.8(m, 1H), 4.6(m, 1H), 5.4(m, 1H), 7.0(s, 5H), 8.5(s, 1H)

Example 152

[3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-(5-methyl-tetraz ol-2-yl)-propyl]-methyl-amine

The procedure given in Example 2 was followed [3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-(5-methyl-tetrazol- 2-yl)-propyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(2,3-Dihydro-benzo[1,4]dioxin-2-yl)-3-(5-methyl-tetrazol- 2-yl)-propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 7H), 2.4(m, 3H), 2.8(m, 4H), 3.8(m, 1H), 4.0(m, 1H), 4.8(m, 1H), 5.3(m, 1H), 7.0(s, 4H)

Example 153

Methyl-[3-(1,2,3,4-tetrahydro-naphthalen-2-yl)-3-tetrazol -2-yl-propyl]-amine

The procedure given in Example 2 was followed Dimethyl-[3-(1,2,3,4-tetrahydro-naphthalen-2-yl)-3-tetrazol- 2-yl-propyl]-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-(1,2,3,4-tetrahydro-naphthalen-2-yl)-3-tetrazol-2- yl-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(s, 8H), 2.8(m, 8H), 5.0(m, 1H), 7.0(m, 4H), 8.5(s, 1H)

Example 154

[3-(6-Chloro-pyridin-3-yl)-3-tetrazol-2-yl-propyl]-methyl -amine

The procedure given in Example 2 was followed [3-(6-Chloro-pyridin-3-yl)-3-tetrazol-2-yl-propyl]-dimethyl- amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(6-Chloro-pyridin-3-yl)-3-tetrazol-2-yl-propyl]-methyl-am ine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.5(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.2(m, 1H), 7.8(m, 1H), 8.5(s, 1H)

Example 155

(3-Benzo[b]thiophen-2-yl-3-tetrazol-2-yl-propyl)-methyl-a mine

The procedure given in Example 2 was (3-Benzo[b]thiophen-2-yl-3-tetrazol-2-yl-propyl)-dimethyl-am ine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give (3-Benzo[b]thiophen-2-yl-3-tetrazol-2-yl-propyl)-methyl-amin e.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.8(m, 1H), 6.5(m, 1H), 7.4(m, 3H), 7.8(m, 2H), 8.5(s, 1H)

Example 156

[3-Benzo[b]thiophen-2-yl-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

The procedure given in Example 2 was [3-Benzo[b]thiophen-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-Benzo[b]thiophen-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]- methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.8(m, 5H), 6.5(m, 1H), 7.4(m, 3H), 7.8(m, 2H)

Example 157

(3-Benzofuran-2-yl-3-tetrazol-2-yl-propyl)-methyl-amine

The procedure given in Example 2 was (3-Benzofuran-2-yl-3-tetrazol-2-yl-propyl)-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give (3-Benzofuran-2-yl-3-tetrazol-2-yl-propyl)-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.8(m, 2H), 6.5(m, 1H), 7.4(m, 3H), 7.8(m, 2H), 8.5(s, 1H)

Example 158

[3-Benzofuran-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-met hyl-amine

The procedure given in Example 2 was [3-Benzofuran-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-dimeth yl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-Benzofuran-2-yl-3-(5-methyl-tetrazol-2-yl)-propyl]-methyl -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.8(m, 2H), 6.5(m, 1H), 7.4(m, 3H), 7.8(m, 2H)

Example 159

(3-Benzofuran-2-yl-3-tetrazol-1-yl-propyl)-methyl-amine

The procedure given in Example 2 was (3-Benzofuran-2-yl-3-tetrazol-1-yl-propyl)-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give (3-Benzofuran-2-yl-3-tetrazol-1-yl-propyl)-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.8(m, 2H), 6.2(m, 1H), 7.4(m, 3H), 7.8(m, 2H)

Example 160

[3-(3,4-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

The procedure given in Example 2 was [3-(3,4-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,4-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 12H), 6.2(m, 1H), 7.4(m, 4H), 8.5(s, 1H)

Example 161

[3-(3,4-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

The procedure given in Example 2 was [3-(3,4-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3,4-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.8(m, 4H), 6.2(m, 1H), 7.4(m, 4H)

Example 162

Methyl-[3-tetrazol-2-yl-3-(2,4,5-trifluoro-phenyl)-propyl ]-amine

The procedure given in Example 2 was Dimethyl-[3-tetrazol-2-yl-3-(2,4,5-trifluoro-phenyl)-propyl] -amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-tetrazol-2-yl-3-(2,4,5-trifluoro-phenyl)-propyl]-a mine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.8(m, 2H), 6.5(m, 1H), 7.0(m, 1H), 7.4(m, 1H), 8.6(s, 1H)

Example 163

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,4,5-trifluoro-phe nyl)-propyl]-amine

The procedure given in Example 2 was Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,4,5-trifluoro-phen yl)-propyl]-amineas a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,4,5-trifluoro-phenyl )-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 12H), 6.4(m, 1H), 7.0(m, 1H), 7.4(m, 1H)

Example 164

[3-(3-Bromo-4-fluoro-phenyl)-3-tetrazol-2-yl-propyl]-meth yl-amine

The procedure given in Example 2 was [3-(3-Bromo-4-fluoro-phenyl)-3-tetrazol-2-yl-propyl]-dimethy l-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3-Bromo-4-fluoro-phenyl)-3-tetrazol-2-yl-propyl]-methyl- amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.4(m, 2H), 2.8(m, 1H), 6.5(m, 1H), 7.0(m, 1H), 7.4(m, 1H), 7.8(m, 1H), 8.5(s, 1H)

Example 165

[3-(3-Bromo-4-fluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-p ropyl]-methyl-amine

The procedure given in Example 2 was [3-(3-Bromo-4-fluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-prop yl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3-Bromo-4-fluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-prop yl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.4(m, 2H), 2.8(m, 1H), 6.5(m, 1H), 7.0(m, 1H), 7.4(m, 1H), 7.8(m, 1H)

Example 166

[3-(6-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-me thyl-amine

The procedure given in Example 2 was [3-(6-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-dimet hyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(6-Methoxy-naphthalen-2-yl)-3-tetrazol-2-yl-propyl]-methy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 5H), 2.4(m, 2H), 2.8(m, 1H), 4.0(s, 3H), 6.3(m, 1H), 7.1(m, 3H), 7.4(m, 1H), 7.8(m, 1H), 8.5(s, 1H)

Example 167

[3-(6-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl) -propyl]-methyl-amine

The procedure given in Example 2 was [3-(6-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(6-Methoxy-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 8H), 2.4(m, 2H), 2.8(m, 1H), 4.0(s, 3H), 6.3(m, 1H), 7.1(m, 3H), 7.4(m, 1H), 7.8(m, 1H)

Example 168

Methyl-[3-(4-phenoxy-phenyl)-3-tetrazol-2-yl-propyl]-amin e

The procedure given in Example 2 was Dimethyl-[3-(4-phenoxy-phenyl)-3-tetrazol-2-yl-propyl]-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-(4-phenoxy-phenyl)-3-tetrazol-2-yl-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.4(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.1(m, 3H), 7.4(m, 1H), 7.6(m, 4H), 8.5(s, 1H)

Example 169

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-phenoxy-phenyl)-p ropyl]-amine

The procedure given in Example 2 was Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-phenoxy-phenyl)-pr opyl]-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-phenoxy-phenyl)-prop yl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 5H), 2.4(m, 6H), 2.8(m, 1H), 6.2(m, 1H), 7.1(m, 4H), 7.4(m, 4H)

Example 170

[3-(4-Bromo-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine

The procedure given in Example 2 was [3-(4-Bromo-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(4-Bromo-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.4(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.3(m, 2H), 7.5(m, 2H), 8.5(s, 1H)

Example 171

[3-(4-Bromo-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-me thyl-amine

The procedure given in Example 2 was [3-(4-Bromo-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-dimet hyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(4-Bromo-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-methy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 1H), 2.5(s, 3H), 2.8(m, 1H), 6.0(m, 1H), 7.3(m, 2H), 7.5(m, 2H)

Example 172

Methyl-[3-tetrazol-2-yl-3-(4-trifluoromethyl-phenyl)-prop yl]-amine

The procedure given in Example 2 was Dimethyl-[3-tetrazol-2-yl-3-(4-trifluoromethyl-phenyl)-propy l]-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-tetrazol-2-yl-3-(4-trifluoromethyl-phenyl)-propyl] -amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.3(m, 2H), 7.5(m, 2H), 8.5(s, 1H)

Example 173

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethyl-p henyl)-propyl]-amine

The procedure given in Example 2 was Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethyl-ph enyl)-propyl]-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(4-trifluoromethyl-phen yl)-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 1H), 2.5(s, 3H), 2.8(m, 1H), 6.0(m, 1H), 7.6(m, 4H)

Example 174

Methyl-[3-tetrazol-2-yl-3-(2,3,4-trichloro-phenyl)-propyl ]-amine

The procedure given in Example 2 was Dimethyl-[3-tetrazol-2-yl-3-(2,3,4-trichloro-phenyl)-propyl] -amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-tetrazol-2-yl-3-(2,3,4-trichloro-phenyl)-propyl]-a mine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 1H), 2.8(m, 1H), 6.2(m, 1H), 7.3(m, 2H), 8.5(s, 1H)

Example 175

Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,3,4-trichloro-phe nyl)-propyl]-amine

The procedure given in Example 2 was Dimethyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,3,4-trichloro-phen yl)-propyl]-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give Methyl-[3-(5-methyl-tetrazol-2-yl)-3-(2,3,4-trichloro-phenyl )-propyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 1H), 2.5(s, 3H), 2.8(m, 1H), 6.0(m, 1H), 7.2(m, 2H)

Example 176

[3-(3-Chloro-4-methoxy-phenyl)-3-tetrazol-2-yl-propyl]-me thyl-amine

The procedure given in Example 2 was [3-(3-Chloro-4-methoxy-phenyl)-3-tetrazol-2-yl-propyl]-dimet hyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3-Chloro-4-methoxy-phenyl)-3-tetrazol-2-yl-propyl]-methy l-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.3(m, 1H), 2.8(m, 1H), 4.0(s, 3H), 6.1(m, 1H), 6.9(d, 1H), 7.3(d, 1H), 7.5(s, 1H), 8.5(s, 1H)

Example 177

[3-(3-Chloro-4-methoxy-phenyl)-3-(5-methyl-tetrazol-2-yl) -propyl]-methyl-amine

The procedure given in Example 2 was [3-(3-Chloro-4-methoxy-phenyl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3-Chloro-4-methoxy-phenyl)-3-(5-methyl-tetrazol-2-yl)-pr opyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 7H), 2.3(m, 1H), 2.8(m, 1H), 4.0(s, 3H), 6.1(m, 1H), 6.9(d, 1H), 7.3(d, 1H), 7.5(s, 1H)

Example 178

[3-(2-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-m ethyl-amine

The procedure given in Example 2 was [3-(2-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-dime thyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(2-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-meth yl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 7.2(m, 2H), 7.4(m, 2H)

Example 179

[3-(3-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-m ethyl-amine

The procedure given in Example 2 was [3-(3-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-dime thyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3-Chloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-meth yl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 7.2(m, 2H), 7.4(m, 2H)

Example 180

[3-(2,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

The procedure given in Example 2 was [3-(2,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(2,4-Dichloro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 7.2(m, 3H)

Example 181

[3-(2,5-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propy l]-methyl-amine

The procedure given in Example 2 was [3-(2,5-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(2,5-Difluoro-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]- methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 7.2(m, 3H)

Example 182

[3-(3-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine

The procedure given in Example 2 was [3-(3-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(3-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.5(m, 1H), 2.8(m, 1H), 7.2(m, 2H), 7.4(m, 2H)

Example 183

[3-(2,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

The procedure given in Example 2 was [3-(2,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(2,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 7.2(m, 3H)

Example 184

[3-(2,5-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-a mine

The procedure given in Example 2 was [3-(2-Chloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(2,5-Difluoro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 7.2(m, 3H)

Example 185

[3-(4-Methanesulfonyl-phenyl)-3-(5-methyl-tetrazol-2-yl)- propyl]-methyl-amine

The procedure given in Example 2 was [3-(4-Methanesulfonyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-dimethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(4-Methanesulfonyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 3.0(s, 3H), 7.2(m, 3H)

Example 186

[3-(4-Isopropyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl ]-methyl-amine

The procedure given in Example 2 was [3-(4-Isopropyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-d imethyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(4-Isopropyl-phenyl)-3-(5-methyl-tetrazol-2-yl)-propyl]-m ethyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 4.0(s, 6H), 7.2(m, 3H)

Example 187

[3-(9H-Fluoren-2-yl)-3-(5-methyl-tetrazol-2-yl)-propyl]-m ethyl-amine

The procedure given in Example 2 was [3-(9H-Fluoren-2-yl)-3-(5-methyl-tetrazol-2-yl)-propyl]-dime thyl-amine as a reactant, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-dimethyl-am ine, to give [3-(9H-Fluoren-2-yl)-3-(5-methyl-tetrazol-2-yl)-propyl]-meth yl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 6H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 4.2(s, 2H), 7.2(m, 3H)

Example 188

(3S)-Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl -propyl]-amine

The procedure given in Example 3 was followed using Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-propyl] -amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give (3S)-Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-pr opyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 4.2(s, 2H), 7.4(m, 3H), 7.8(m, 4H)

Example 189

(3S)-Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl) -propyl]-amine

The procedure given in Example 3 was followed using Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-propyl] -amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give (3S)-Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-pr opyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 4.2(s, 2H), 7.4(m, 10H), 7.8(m, 4H)

Example 190

(3R)-Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl -propyl]-amine

The procedure given in Example 3 was followed using Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-propyl] -amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give (3R)-Methyl-[3-(5-methyl-tetrazol-2-yl)-3-naphthalen-2-yl-pr opyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 4.2(s, 2H), 7.4(m, 3H), 7.8(m, 4H)

Example 191

(3R)-Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl) -propyl]-amine

The procedure given in Example 3 was followed using Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-propyl] -amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give (3R)-Methyl-[3-naphthalen-2-yl-3-(5-phenyl-tetrazol-2-yl)-pr opyl]-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 4.2(s, 2H), 7.4(m, 10H), 7.8(m, 4H)

Example 192

(3R)-[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-methyl-amine

The procedure given in Example 3 was followed using [3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-methyl-amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give (3R)-[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl )-propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 4.2(s, 2H), 7.4(m, 3H), 7.8(m, 4H)

Example 193

(3S)-[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2 -yl)-propyl]-methyl-amine

The procedure given in Example 3 was followed using [3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl)-pro pyl]-methyl-amine, instead of [3-(3,4-Dichloro-phenyl)-3-tetrazol-2-yl-propyl]-methyl-amin e, to give (3S)-[3-(6-Fluoro-naphthalen-2-yl)-3-(5-methyl-tetrazol-2-yl )-propyl]-methyl-amine.

1H-NMR(CDCl3, 200MHz) δ2.2(m, 9H), 2.3(m, 3H), 2.5(m, 1H), 2.8(m, 1H), 4.2(s, 2H), 7.4(m, 3H), 7.8(m, 4H)

Serotonin transporter reuptake inhibition assay

The method to test the ability of compounds to inhibit transporters from reuptake of serotonin followed Gu H. et al., J Biol Chem., 1994, 269, p7214~7130.

The recombinant HEK-293 cells with human serotonin transporter were plated. Test compounds described in table 1 were pre-incubated with cells (2 x 10 ⁵ /ml) in modified Tris-HEPES buffer pH 7.1 for 20 minutes at 25℃ and then they were incubated for additional 10 minutes after 65 nM of [ ³ H]Serotonin was added. Bound cells were filtered and counted to determine [ ³ H]Serotonin uptake. Reduction of [ ³ H]Serotonin uptake by 50 percent or more (≥50%) relative to 10μM fluoxetine indicates significant inhibitory activity. Compounds were screened at 10, 1, 0.1, 0.01 and 0.001μM for IC50s.

Norepinephrine transporter reuptake inhibition assay

Norepinephrine transporter reuptake inhibition assay used the method described by Galli A. et al., J Exp Biol.,1995, 198, p2197~2212.

MDCK cells with stably expressed human recombinant norepinephrine transporter were plated one day. Test compounds were pre-incubated with cells (2 x 10 ⁵ /ml) in modified Tris-HEPES buffer pH 7.1 for 20 minutes at 25℃ and then they were incubated for additional 10 minutes after 25 nM of [ ³ H]Norepinephrine was added. A lysate was obtained from solubilized cells and the filtered lysate was counted to determine [ ³ H]Norepinephrine uptake. Reduction of [ ³ H]Norepinephrine uptake by 50 percent or more (≥50%) relative to 10μM desipramine indicates significant inhibitory activity. Compounds were screened at 10, 1, 0.1, 0.01 and 0.001μM to determine their IC50s.

Dopamine transporter reuptake inhibition assay

The assay followed the method modified from Pristupa Z.B. et al., Mol Pharmacol., 1994, p125~135.

CHO-K1 cells with human recombinant dopamine transporter were plated. Test compounds were pre-incubated with cells (4 x 10 ⁵ /ml) in modified Tris-HEPES buffer pH 7.1 for 20 minutes at 25℃ and then they were incubated for additional 10 minutes after 50 nM of [ ³ H]Dopamine was added. A lysate is obtained from solubilized cells and counted to determine [ ³ H]Dopamine uptake. Reduction of [ ³ H]Dopamine uptake by 50 percent or more (≥50%) relative to 10 mM nomifensine indicates significant inhibitory activity. Compounds were tested at 10, 1, 0.1, 0.01 and 0.001μM for IC50s.

The results obtained by testing compounds of the invention are given in the following table 1:

[Table 1]

The data in Table 1 show that racemic or enantiomerically enriched 3-substituted propanamine derivatives, the compounds of the invention have a significantly high inhibition potency of the serotonin, norepinephrine, dopamine transporter reuptake. This inhibition of serotonin, norepinephrine, dopamine transporter reuptake has been associated with the treatment of one or more of the CNS disorders such as depression, anxiety and pain disorder.

Forced swimming test in mice(FST)

The Forced swimming test is an animal model based on the rodent's behavioral repertoire for screening drugs with potential antidepressant activity. As in several other models used for this goal, an uncontrollable stress stimulus produces behavioral changes that are sensitive to antidepressant treatment.

The mice were intraperitoneally treated with the test compound with an injection volume of 10 mg/kg. The group treated with 30% PEG400 served as a control group. Thirty minutes following administration, mice were individually forced to swim in a transparent glass vessel (14 cm high, 11.5 cm in diameter) filled with 10 cm of water at 25℃. The total duration of immobility (second) was measured during the last 4 minutes of a single 6-min test session. Mice were considered immobile when they made no further attempts to escape other than the movements necessary to keep their heads above the water. The potent ability of the compounds was determined as percent value of reduction in the duration of immobility comparing to the control group.

The results obtained by testing compounds of the invention are given in the following table 2 :

[Table 2]

Specially the results of forced swimming test(FST) in mice as noted in Table 2 show the compounds of the invention are related to the treatment of depression.

Marble burying test

The Marble burying test is a screening tool for putative anxiolytics. In this test, control mice naturally bury glass marbles in the cage bedding and the administration of anxiolytic compounds, including Diazepam, reduces the number of buried marbles. Positive compounds in the marble burying test including selective serotonin reuptake inhibitor may be especially beneficial to obsessive-compulsive disorder.

A group of mice was intraperitoneally treated with test compound dissolved in 30% PEG400 with an injection volume of 10 ml/kg. The group treated with only 30% PEG400 served as a control group. Thirty minutes after the treatment, the animals were individually placed in a polycarbonate cage which was same as used for animal housing with an open top located within a quiet room. Each cage consisted of 1/8 inch corn bedding 5 cm deep. Twenty four clean glass marbles (15 mm diameter) were evenly spaced in four rows of six on top of the bedding. Each mouse was left in the cage for 30 minutes and the number of marbles buried (buried more than 1/2 or 2/3) was counted. The potent ability of the compounds was determined as percent value of reduction in the number of marbles buried comparing to the control group.

The results obtained by testing compounds of the invention are given in the following table 3 :

[Table 3]

Specially the results of Marble burying test(MB) in mice as noted in Table 3 show the compounds of the invention are related to the treatment of anxiety.

Acetic acid induced writhing test (AA writhing test)

The Acetic acid-induced writhing test is a well-established nociceptive test using a chemical stimulus. Although several animal models of nociceptive tests have been developed to examine and compare the anti-nociceptive effects of different drugs, the anti-nociceptive effects of antidepressants appear to be test-dependent. Indeed, the acetic acid-induced writhing test is more sensitive to antidepressants than other tests using thermal, mechanical or electrical stimuli.

The animals were subcutaneously treated with the test compound with an injection volume of 10 ml/kg. The group treated with 30% PEG400 or saline served as a control group. Thirty minutes later, the mice were intraperitoneally treated with 0.8 %(v/v) acetic acid. Each mouse was then placed in a cage for individual observation. The writhing numbers for 10 minutes were counted. The writhe is operationally defined as a contraction of the abdomen followed by stretching of the hind limbs. The potent ability of the compounds was determined as percent value of reduction in the number of writhing comparing to the control group.

The results obtained by testing compounds of the invention are given in the following table 4 :

[Table 4]

Specially the results of Acetic acid induced writhing test(AA writhing test) in mice as noted in Table 4 show the compounds of the invention are related to the treatment of pain.