KR101478140B1 - Precursor of １８f-labeled pet radiopharmaceuticlas and preparation method thereof - Google Patents

Abstract

The invention positron emission tomography as (PET) on the precursor, the production process and application of the radiopharmaceutical for, and more particularly 4 as a precursor, a method of manufacturing the same and a single step by using this, having an organic salt of departure ¹⁸ F To a method for producing a desired PET radiopharmaceutical in a high radiochemical yield within a short production time. The precursor comprising the quaternary organic salt leaving group of the present invention can simplify the conventional multi-step complex radioactive pharmaceutical preparation to a single step, can reduce the production cost by eliminating the need for an excessive phase transfer catalyst, And the reaction speed is fast. This feature is suitable for mass production of PET radiopharmaceuticals by automated synthesis systems.

Description

TECHNICAL FIELD [0001] The present invention relates to a precursor of a 18F-labeled PET radiopharmaceutical and a method of producing the precursor of the 18F-labeled PET radiopharmaceutical,

The present invention is a ¹⁸ F in a single step by positron emission tomography (PET) relates to a precursor, a method of manufacturing and application of the radiopharmaceutical, and more particularly 4 precursor having an organic salt of departure, a method of manufacturing and using this To produce a desired ¹⁸ F-labeled PET radiopharmaceutical within a short production time with high radiochemical yield.

Positron Emission Tomography (PET), a nuclear medicine molecular imaging technique that real-time images the human body, is an effective human imaging technique that can detect biochemical and physiological changes in the human body at the early stage of disease. It is showing steep growth. Early PET medicines research on new diseases uses the positron-emitting radioisotope, ¹¹ C, because it has the advantage of being relatively easy to label and carbon, the basic skeleton of organic matter. However, ¹¹ C has a short half-life of 20 minutes, which is not suitable for commercial use.

On the other hand, other radioactive isotopes such as ¹⁸ F can be easily mass-produced from cyclotrons. In particular, they have recently attracted attention as commercially available radionuclides because of their relatively long half-lives of 110 minutes. Since usefulness of ¹⁸ F, the ¹¹ C-labeled compounds developed to replace existing or newly developed disease with ¹⁸ F- labeled compounds - introducing profile functional as a way to introduce ¹⁸ F in the target compound as a ^[18 F] fluoro Is generally used. However, radiopharmaceuticals in which [ ¹⁸ F] fluoropropyl groups are introduced show a tendency to decrease the binding force to the target substance, increase the lipophilicity, increase the intake in some tissues, decrease the selectivity by increasing nonspecific binding There is a problem that the image becomes worse. ^[18 F] can be solved if such a problem by introducing a methyl group to a propyl functionality instead of ^[11 C] ^[18 F] fluoro similar to the methyl group and structural fluoro.

A conventional method of introducing [ ¹⁸ F] fluoromethyl groups is to use [ ¹⁸ F] fluoromethylation reagents. These reagents can generally be obtained by labeling ¹⁸ F with a methane compound having two or more leaving groups. This is followed by a nucleophilic substitution reaction with the precursor to produce the radiopharmaceutical into which the desired [ ¹⁸ F] fluoromethyl group is introduced. However, the above method requires a two-step synthesis process on the ¹⁸ F mark, and thus has a disadvantage in that the process is complicated and the manufacturing time is long. The complexity of the manufacturing process makes it difficult to implement an automated synthesis system, which is essential for commercialization.

It is an object of the present invention to provide a quaternary organic salt precursor for the manufacture of ¹⁸ F-labeled PET radiopharmaceuticals.

It is another object of the present invention to provide a process for preparing a tetravalent organic salt precursor for the production of ¹⁸ F-labeled PET radiopharmaceuticals.

It is another object of the present invention to provide a nucleophilic fluorination reaction using tetravalent organic salt precursors.

Yet another object of the present invention is to provide ¹⁸ F-labeled PET radiopharmaceuticals prepared through nucleophilic fluorination of quaternary organic salt precursors.

In order to accomplish the above object, the present invention provides a precursor comprising a tetravalent organic salt leaving group represented by the following formula (1).

In Formula 1,

R ₁ is -X-CH ₂ at the ¹⁸ F radiotracer the cover - as a portion other than the portions ¹⁸ F, C ₁ -C ₁₀₀₀ and a hydrocarbon group, the group is a C ₁ carbon of the main chain hydrocarbon -C oxygen _1000, May be substituted or unsubstituted with nitrogen, sulfur, phosphorus, or a combination thereof, and hydrogen in the main chain may be substituted or unsubstituted with halogen,

X is oxygen, sulfur, or -C (O) -,

The leaving group is a substituted or unsubstituted C ₂ -C ₅₀ quaternary ammonium salt.

Preferably, in formula (1)

R ₁ is a C ₁ -C ₂₀₀ hydrocarbon group, and the C ₁ -C ₂₀₀ hydrocarbon group may be substituted or unsubstituted with oxygen, nitrogen, sulfur, phosphorus, or a combination thereof in the main chain, Which may be substituted or unsubstituted with halogen,

X is oxygen, sulfur, or -C (O) -,

이고, 상기 이탈기에서, The leaving group

And in said leaving group,

A, B, C, D and E independently of one another are nitrogen, oxygen, sulfur or carbon,

(i) hydrogen of each carbon may be substituted or unsubstituted with R ₂ or R ₃ ,

(ii) for each nitrogen, R < _{2 >} or R < ₃ > may be substituted or unsubstituted,

R ₂ and R ₃ are each independently a C ₁ -C ₂₀ hydrocarbon group, and the carbon of the main chain may be substituted or unsubstituted with oxygen, nitrogen, sulfur, or a combination thereof, Lt; / RTI >

Y is selected from the group consisting of a halogen anion, a sulfonate anion, BF ₄ ^- , PF ₆ ^- , SbF ₆ ^- , N (SO ₂ CF ₃ ) ₂ ^- and N (CN) ₂ ^-

n is 0 or 1;

Preferably, in formula (1)

R ₁ is a C ₁ -C ₁₀₀ hydrocarbon group, and the hydrocarbon group of the C ₁ -C ₁₀₀ hydrocarbon group may be substituted or unsubstituted with oxygen, nitrogen, sulfur, phosphorus, or a combination thereof in the main chain, Which may be substituted or unsubstituted with halogen,

X is oxygen, sulfur, or -C (O) -,

The leaving group

또는

중에서 선택되는 4가 양이온; 및 (ii) Y인 음이온으로 구성되는 염이고, (i)

or

A tetravalent cation selected from the group consisting of: And (ii) a salt consisting of an anion Y,

One nitrogen in the ring of the tetravalent cation is substituted by R ₃ , each carbon may be independently substituted or unsubstituted with R ₂ ,

R ₂ and R ₃ are C ₁ -C ₂₀ hydrocarbon groups in which the carbon of the main chain may be substituted or unsubstituted with oxygen, nitrogen, sulfur or a combination thereof, and hydrogen in the main chain may be substituted or unsubstituted with halogen ,

Y is independently selected from the group consisting of trifluoromethane sulfonate (CF ₃ SO ₃ ^- ), paratoluene sulfonate, methane sulfonate and para-nitrobenzenesulfonate.

Preferably, in formula (1)

,

,

,

,

,

,

,

,

,

,

및

로 이루어지는 군으로부터 선택되고,R ₁ is

,

,

,

,

,

,

,

,

,

,

And

, ≪ / RTI >

X is oxygen, sulfur, or -C (O) -,

The leaving group

또는

중에서 선택되는 4가 양이온; 및 (ii) Y인 음이온으로 구성되는 염이고, (i)

or

A tetravalent cation selected from the group consisting of: And (ii) a salt consisting of an anion Y,

,

, 및

로 이루어지는 군으로부터 선택되고, 4 is a nitrogen in a ring of the cation substituted with R ₃ each carbon may be unsubstituted or substituted by R ₂ independently from each other, R ₂ and R ₃ are independently C _{1 -4} straight or branched chain alkyl groups each , Such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl,

,

, And

, ≪ / RTI >

Y is independently selected from the group consisting of trifluoromethane sulfonate (CF ₃ SO ₃ ^- ), paratoluene sulfonate, methane sulfonate and para-nitrobenzenesulfonate.

Preferably, the precursor represented by the general formula (1)

4-tert-butyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate;

4-methoxycarbonyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate;

4- [3,5-di (trifluoromethyl) phenyl] -3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate;

4- (4-methoxyphenyl) -3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate;

3-methyl-4-phenyl-1- (2-phenylethen-2-one-1-yl) -1,2,3-triazolium trifluoromethanesulfonate;

4-tert-butyl-3-methyl-1 - [(phenylthio) methyl] -1,2,3-triazolium trifluoromethanesulfonate;

3-methyl-1 - ((2-naphthoxy) methyl) -4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

3-methyl-1- [3- (2-naphthoxy) -n -propyl] oxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

1- [1-methylsulfonyloxy-3- (2-naphthyl) -2-oxypropyl] oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

3-Methyl- (2-naphthyl) methyloxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

3-methyl-1 - ((2-naphthoxy) methyl) -4-phenylimidazolium trifluoromethanesulfonate;

(S) -1- (4- (2-BOC-amino-2- (t-butoxycarbonyl) ethyl) phenyloxymethyl) -4-phenyl-1,2,3- triazolium trifluoromethanesulfo Nate;

1- (4-biphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

1- (4-bromo-2-methylphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

1- (3,4-dimethoxyphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

3-methyl-1- (4-nitrophenyl) oxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

1- (4-acetylaminophenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;

1- (3- O -estrone) methyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate; And

3-acetonaphthyl-1-methylimidazolium. ≪ / RTI >

The present invention also provides a process for preparing a precursor comprising a quaternary organic salt leaving group represented by the general formula (1) according to the sub-concept of the general formula (1), and specifically, .

Method 1:

Specifically, as shown in Reaction Scheme 1 below,

Synthesizing an azido compound of formula (3) from a compound of formula (2) (step 1);

Synthesizing the compound of Chemical Formula 5 through a [3 + 2] cyclization addition reaction between the azido compound of Chemical Formula 3 and the alkene compound of Chemical Formula 4 obtained in Step 1 (Step 2);

A step of synthesizing the organic salt of formula (I-a) using the alkylating reagent of formula (6) obtained in step (2).

[Reaction Scheme 1]

In the above Reaction Scheme 1, R ₁ , R ₂ , R ₃ and Y are as defined above, and Z is chlorine, bromine, iodine or R ₄ SO ₃ ^- . Wherein R ₄ is a C ₁ -C ₂₀ hydrocarbon group, and the carbon of the main chain may be substituted or unsubstituted with oxygen, nitrogen, sulfur, or a combination thereof, and hydrogen in the main chain may be substituted or unsubstituted with halogen.

In the process for producing a precursor comprising a quaternary organic salt leaving group of the present invention, step 1 of Scheme 1 is a step of synthesizing an azide compound of formula (3) from a compound represented by formula (2) The solvent can be any organic chemical reaction that is conventionally applied. Step 2 of the above Reaction Scheme 1 is a step for carrying out an alkyne / azide [3 + 2] cyclization addition reaction (Copper (I) - ) -catalyzed Alkyne / Azide [3 + 2] Cycloaddition, CuAAC), wherein the compounds of formulas (2) and (3) are commercially available or can be synthesized by conventional methods , And the reaction solvent used may be a solvent commonly used in the alkyne / azide [3 + 2] cyclization addition reaction of copper (I) -catalyst between an azido compound and an alkyne compound. Step 3 of Scheme 1 is a step of synthesizing an organic salt of formula (I-a) using 1,2,3-triazole compound of formula (5) obtained in step 2 using an alkylating reagent represented by formula (6) Is a commercially available compound or a compound which can be synthesized by a conventional method. The reaction solvent used may be a solvent commonly used in an organic salt production reaction.

Recipe 2 :

Specifically, as shown in Reaction Scheme 2 below,

Synthesizing a compound of formula (5) through a nucleophilic substitution reaction between a compound represented by formula (7) and a compound represented by formula (8) (step 1); And

(B) synthesizing an organic salt of formula (1-b) using the alkylating reagent of formula (6) obtained in step (1).

[Reaction Scheme 2]

Wherein R ₁ , R ₂ , R ₃ , A, B, C, D, E, X, Y and n are as defined above and Z is as defined in Production Method 1 above.

In the process for the preparation of the precursor compound of formula (I) wherein the quaternary organic salt leaving group of the present invention comprises the quaternary organic salt leaving group, Step 1 of Scheme 2 can be carried out by a nucleophilic substitution reaction between the compound of formula (7) Wherein the compound represented by the general formulas (7) and (8) is a commercially available compound or a compound which can be synthesized by a conventional method, and the reaction solvent to be used is a solvent commonly used in the nucleophilic substitution reaction Can be used. Step 2 of Scheme 2 is a step of synthesizing the organic salt of formula (1-b) using the alkylation reagent of formula (6) obtained in step 1, wherein the compound represented by formula (6) Or a compound which can be synthesized by a conventional method. The reaction solvent used may be a solvent which is usually used in an organic salt production reaction.

Method 3:

Specifically, as shown in the following Reaction Scheme 3,

(B) synthesizing a compound of the formula (I-b) through a nucleophilic substitution reaction between a compound represented by the formula (7) and a compound represented by the formula (9).

[Reaction Scheme 3]

Wherein R ₁ , R ₂ , R ₃ , A, B, C, D, E, X, Y and n are as defined above and Z is as defined in Preparation Method 1.

In the process for the preparation of the precursor compound of formula (I) wherein the quaternary organic salt leaving group is of the present invention, step 1 of Scheme 3 can be carried out by a nucleophilic substitution reaction between the compound of formula (7) Wherein the compound represented by the formula (7) is a commercially available compound or a compound that can be synthesized by a conventional method, and the compound represented by the formula (9) is a compound represented by the formula With an alkylating reagent represented by the general formula (6). The reaction solvent used in Step 1 may be a solvent commonly used in an organic salt preparation reaction.

Method 4 :

Specifically, as shown in Reaction Scheme 4 below,

(B) synthesizing a compound of the formula (I-b) through a nucleophilic substitution reaction between the compound represented by the formula (10) and the compound represented by the formula (11).

[Reaction Scheme 4]

R ₁ , R ₂ , R ₃ , A, B, C, D, E, X, Y and n are as defined above.

In the process for the preparation of the precursor compound of formula (I) wherein the quaternary organic salt leaving group of the present invention comprises the quaternary organic salt leaving group, step 1 of Scheme 4 is carried out by a nucleophilic substitution reaction between the compound of formula (10) 1-b, wherein the compounds represented by formulas (10) and (11) are commercially available or can be synthesized by a conventional method. The reaction solvent to be used is usually a compound A solvent to be used may be used.

The present invention also relates to a process for producing an ¹⁸ F-labeled compound, which comprises reacting a compound containing a quaternary organic salt leaving group represented by the above formula (1) with a fluorine salt represented by the formula MF Nucleophilic fluorination reaction) and an ¹⁸ F-labeled compound represented by formula (12).

[Reaction Scheme 5]

In the above Reaction Scheme 5, R ₁ , X and the leaving group are the same as defined in Formula 1, M is a metal cation selected from the group consisting of Li, Na, K, Rb, and Cs; Tetravalent ammonium cation; Or a tetravalent phosphonium cation, and F is ¹⁸ F.

Compounds containing a quaternary organic salt leaving group of Formula 1 according to the present invention may be used as precursors in nucleophilic fluorination reactions with fluoride anions in the form of various metal salts or organic salts, as shown in FIG. In Figure 1, the intermediate compound is formed by the interaction of the quaternary organic salt precursor with a fluoride anion in the form of a metal salt or an organic salt, resulting in anion exchange, which results in the fast F- Is converted to a labeled compound. Wherein the nucleophilic fluorination reaction (where F is ¹⁸ F) can be carried out under commonly used reaction conditions.

Further, the present invention provides the product of Scheme 5, ¹⁸ F-labeled compound.

The precursor of the present invention can introduce the ¹⁸ F-fluoromethyl group into the radiopharmaceuticals in a simple stepwise manner. In addition, the present invention has the effect of simplifying the conventional multistage complex synthesis by introducing a quaternary organic salt into an activated leaving group into a precursor to produce an ¹⁸ F-fluoromethyl group in a one-step process. In addition, since the tetravalent organic salt included in the leaving group of the precursor serves as a phase transfer catalyst, it is possible to reduce the production cost by eliminating the need for an additional excessive phase transfer catalyst required for a general nucleophilic [ ¹⁸ F] fluorination reaction, There is an advantage that separation is easy. The catalytic action of the quaternary organic salt in the precursors induces a nucleophilic fluorination reaction in the molecule, which is advantageous in that the reaction rate is much higher than that of a general intramolecular nucleophilic fluorination reaction. This feature is suitable for mass production of [ ¹⁸ F] radiopharmaceuticals by automated synthesis systems.

1 is a reaction scheme for preparing ¹⁸ F-labeled compounds in a single step using a precursor having a quaternary organic salt leaving group of the present invention.

Hereinafter, the present invention will be described in more detail with reference to Production Examples and Examples. However, the following examples are illustrative of the present invention, and the present invention is not limited thereto.

Preparation Example 1: Preparation of 2- (azidomethoxy) naphthalene ( 3a )

Step 1:

After dissolving 2-naphthol ( 7a , 1.15 g, 8.0 mmol) in hexamethylphosphoramide (HMPA, 40 mL), sodium hydride (NaH, 352 mg, 8.8 mmol) And chloromethyl-methylsulfide (0.737 mL, 8.8 mmol) was added, followed by stirring at room temperature for 16 hours. Water was added to terminate the reaction, and the organic compound was extracted with ethyl acetate. The extracted ethyl acetate solution was treated with anhydrous sodium sulfate and subjected to column chromatography (20% ethyl acetate / n -hexane) to obtain a sulfide intermediate ( 13 , 410 mg, 25%).

^{1 H NMR (500 MHz, CDCl} 3) δ 2.26 (s, 3H), 5.22 (s, 2H), 7.20-7.16 (m, 2H), 7.34 (t, J = 7.6 Hz, 1H), 7.43 (t, J = 7.6 Hz, 1 H), 7.73 (m, 3 H).

Step 2:

The sulfide compound ( 13 , 410 mg, 2.0 mmol) obtained in Step 1 was dissolved in dichloromethane, and then sulfuryl chloride (1.0 M SO ₂ Cl ₂ / CH ₂ Cl ₂ 2.4 mL, 2.4 mmol) was slowly added to the solution, stirred for 30 minutes, and then the solvent and the reaction residue were removed under reduced pressure. The remaining organics were redissolved in dimethylformamide (DMF), sodium azide (NaN ₃ , 650 mg, 10 mmol) was added and the mixture was stirred for 12 hours. Water was added to terminate the reaction, and the organic compound was extracted with ethyl acetate. The resulting ethyl acetate solution was treated with anhydrous sodium sulfate and subjected to column chromatography (10% ethyl acetate / n -hexane) to obtain the target compound, 2- (azidomethoxy) naphthalene ( 3a , 279 mg, 70% .

^{1 H NMR (500 MHz, CDCl} 3) δ 5.27 (s, 2H), 7.21 (dd, J = 9.0 Hz, J = 2.5 Hz, 2H), 7.30 (d, J = 2.5 Hz, 1H), 7.40-7.37 (m, 1H), 7.48-7.45 (m, 2H), 7.75 (d, J = 8.0 Hz, 1H), 7.79 (d, J = 9.0 Hz, 2H).

Production Example 2: Preparation of 2 -azidopropionate ( 3b )

2-Bromo-collection Seto benzophenone (10a, 1.97 g, 10.0 mmol ) into the sodium azide _{(NaN 3, 650 mg, 11.0} mmol) was dissolved in acetonitrile (40 mL) was stirred for 12 hours. Water was added to terminate the reaction, and the organic compound was extracted with dichloromethane. The extracted dichloromethane solution was treated with anhydrous sodium sulfate and subjected to column chromatography (10% ethyl acetate / n -hexane) to obtain the target compound, 2-azidopropionone ( 3b , 2.11 g, 100%).

^{1 H NMR (500 MHz, CDCl} 3) δ 4.56 (s, 2H), 7.49 (t, J = 6.2 Hz, 2H), 7.62 (t, J = 6.0 Hz, 1H), 7.90 (d, J = 7.6 Hz , 2H).

Preparation Example 3: Preparation of azidomethylphenylsulfide ( 3c )

( 10b , 1.58 g, 10.0 mmol) was dissolved in dimethylformamide (40 mL), sodium azide (NaN ₃ , 1.3 g, 20.0 mmol) was added thereto, and the mixture was stirred for 12 hours. Water was added to terminate the reaction, and the organic compound was extracted with ethyl acetate. The extracted ethyl acetate solution was treated with anhydrous sodium sulfate and subjected to column chromatography (1% ethyl acetate / n -hexane) to obtain aziridinium methylphenylsulfide ( 3c , 1.62 g, 98%) as a target compound.

^{1 H NMR (500 MHz, CDCl} 3) δ 4.54 (s, 2H), 7.37-7.25 (m, 3H), 7.45 (d, J = 8.0 Hz, 2H).

Example  1: 4- tert -Butyl-3- methyl -1 - ((2- Naphthoxy ) methyl ) -1,2,3- Triazolium Trifluoromethanesulfonate  (1a)

Step 1:

The compound 2- (azidomethoxy) naphthalene ( 3a , 390 mg, 2.0 mmol) and 3,3-dimethyl-1-butyne ( 4a , 246 mg, 3.0 mmol) obtained in Step 2 of Preparation Example 1 were dissolved in acetone (77 mg, 0.4 mmol) and triethylamine (0.056 mL, 0.4 mmol) were added to the solution. The mixture was stirred at room temperature for 2 hours, concentrated under reduced pressure, and then subjected to column chromatography (1% methanol / Dichloromethane) yielded the desired compound 4-tert-butyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazole ( 5a , 477 mg, 85%).

^{1 H NMR (500 MHz, CDCl} 3) δ 1.35 (s, 9H), 6.30 (s, 2H), 7.19 (dd, J = 9.0 Hz, J = 2.5 Hz, 1H), 7.40-7.38 (m, 1H) , 7.46-7.44 (m, 2H), 7.51 (s, 1H), 7.76 (t, J = 8.0 Hz, 3H);

¹³ C NMR (125 MHz, CDCl ₃ )? 158.8, 154.3, 134.3, 130.14, 130.05, 127.8, 127.5, 126.9, 124.9, 118.7, 118.6, 109.9, 76.2, 31.0, 30.4.

Step 2:

( 5a , 477 mg, 1.69 mmol) obtained in Step 1 was dissolved in acetonitrile (7.0 mL), and methyltri (2-naphthoxy) fluoro-sulfonate (6a, MeOTf, 0.278 mL, 2.5 mmol) was added to the back, behind which at 0 ℃ stirred for 30 minutes, the solvent was removed under reduced pressure to give the desired compound 4-tert- butyl-3-methyl-1- ( (2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1a , 580 mg, 77%).

^{1 H NMR (500 MHz, CDCl} 3) δ 1.46 (s, 9H), 4.35 (s, 3H), 6.60 (s, 2H), 7.22 (dd, J = 9.0, 2.5 Hz, 1H), 7.42-7.39 ( m, 1H), 7.49-7.45 (m, 2H), 7.77 (d, J = 8.0 Hz, 1H), 7.80 (t, J = 8.5 Hz, 2H), 8.60

^{13 C NMR (125 MHz, CDCl} 3) d 153.1, 152.3, 134.1, 130.6, 130.4, 128.4, 127.8, 127.6, 127.2, 125.4, 120.8 (q, J = 319 Hz), 118.0, 110.2, 79.2, 40.9, 31.6 , 28.4.

Example  2: 4- Methoxycarbonyl -3- methyl -1 - ((2- Naphthoxy ) methyl ) -1,2,3- Triazolium  Preparation of trifluoromethanesulfonate (1b)

Step 1:

( 4b , 252 mg, 3.0 mmol) was used instead of 3,3-dimethyl-1-butyne ( 4a ) used in the step 1 of Example 1 to obtain 4- Methoxycarbonyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazole ( 5b , 346 mg, 61%).

^{1 H NMR (500 MHz, CDCl} 3) δ 3.94 (s, 3H), 6.41 (s, 2H), 7.17 (dd, J = 9.0 Hz, J = 2.5 Hz, 1H), 7.36 (d, J = 2.5 Hz , 1 H), 7.42-7.39 (m , 1H), 7.49-7.45 (m, 1H), 7.73 (d, J = 8.0 Hz, 1H), 7.79-7.77 (m, 2H), 8.34 (s, 1H) ;

¹³ C NMR (125 MHz, CDCl ₃ )? 161.0, 153.6, 141.0, 134.1, 130.5, 130.3, 127.9, 127.6, 127.4, 127.1, 125.2, 118.3, 110.2, 76.7, 52.5.

Step 2:

Example 1 4-tert- butyl used in step 2 of l - ((2-naphthyl) methyl) in place of 1, 2,3-triazole (5a) 4- methoxycarbonyl-1 - (( (2-naphthoxy) methyl) -1,2,3-triazole ( 5b , 346 mg, 1.22 mmol) was used in place of 4-methoxycarbonyl- ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1b , 513 mg, 94%).

^{1 H NMR (500 MHz, CDCl} 3) δ 3.96 (s, 3H), 4.35 (s, 3H), 6.70 (s, 2H), 7.22 (dd, J = 9.0 Hz, 2.5 Hz, 1H), 7.41 (td , J = 7.8, 1.2 Hz, 1H), 7.47 (td, J = 7.3, 1.3 Hz, 1H), 7.51 (d, J = 2.5 Hz, 1H), 7.76 (d, J = 8.0 Hz, 1H), 7.80 (t, J = 9.0 Hz, 2H), 9.26 (s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) δ 155.4, 152.9, 134.1, 133.8, 133.3, 130.8, 130.7, 127.8, 127.7, 127.3, 125.6, 120.7 (t, J = 318 Hz), 118.0, 110.9, 80.3, 54.3 , 41.5.

Example  3: 4- [3,5-di ( Trifluoromethyl ) Phenyl ] -3- methyl -1 - ((2- Naphthoxy ) methyl ) -1,2,3- Triazolium Trifluoromethanesulfonate  (1c)

Step 1:

Ethynyl-3, 5-bis (trifluoromethyl) benzene ( 4c , 530 L, 3.0 mmol) was used instead of the 3,3-dimethyl-1-butyne ( 4a ) used in step 1 of Example 1 (Trifluoromethyl) phenyl] -1 - ((2-naphthoxy) methyl) -1,2,3-triazole ( 5c , 700 mg, 80%).

^{1 H NMR (500 MHz, CDCl} 3) δ 6.45 (s, 2H), 7.20 (dd, J = 9.0 Hz, J = 2.5 Hz, 1H), 7.41-7.38 (m, 1H), 7.43 (d, J = 2.5 Hz, 1H), 7.49-7.45 (m, 1H), 7.80-7.75 (m, 3H), 7.83 (s, 1H), 8.19 (s, 1H);

¹³ C NMR (125 MHz, CDCl ₃ )? 134.2, 132.6, 132.4, 132.3, 130.4, 130.2, 127.9, 127.4, 127.1, 125.9, 125.2, 124.4, 122.2, 122.1, 120.7, 118.4, 109.9, 76.5.

Step 2:

(3-tert-butyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazole ( 5a ) used in step 2 of Example 1 was replaced with 4- [ Methyl] phenyl] -1 - ((2-naphthoxy) methyl) -1,2,3-triazole ( 5c , 700 mg, 1.60 mmol) (Trifluoromethyl) phenyl] -3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3- triazolium trifluoromethanesulfonate ( 1c , 860 mg, 89%).

^{1 H NMR (500 MHz, MeOD} ) δ 4.36 (s, 3H), 6.81 (s, 2H), 7.35 (dd J = 9.0 Hz, 2.5 Hz, 1H), 7.43 (td, J = 7.0 Hz, 1.0 Hz, 1H), 7.50 (td, J = 7.0 Hz, 1.0 Hz, 1H), 7.64 (d, J = 2.5 Hz, 1H), 7.85 (t, J = 7.0 Hz, 2H), 7.73 (d, J = 9.0 Hz , ≪ / RTI > 1H), 8.33 (s, 1H), 8.36 (s, 2H);

^{13 C NMR (125 MHz, MeOD} ) δ 153.2, 141.2, 134.2, 132.7 (q, J = 34 Hz), 130.6, 130.4 (d, J = 3 Hz), 130.2, 127.4, 127.1, 126.7, 125.4 (q, J = 4 Hz), 125.0, 124.9, 123.9, 121.8, 120.4 (q, J = 317 Hz), 117.8, 110.7, 79.8, 38.4.

Example  4: 4- (4- Methoxyphenyl ) -3- methyl -1 - ((2- Naphthoxy ) methyl ) -1,2,3- Triazolium  Preparation of trifluoromethanesulfonate (1d)

Step 1:

( 4d , 252 mg, 3.0 mmol) was used instead of 3,3-dimethyl-1-butyne ( 4a ) used in step 1 of Example 1 To obtain 4- (4-methoxyphenyl) -1 - ((2-naphthoxy) methyl) -1,2,3-triazole ( 5d , 391 mg, 59%).

^{1 H NMR (500 MHz, CDCl} 3) δ 3.83 (s, 3H), 6.39 (s, 2H), 7.00-6.93 (m, 2H), 7.20 (dd, J = 9.0 Hz, J = 2.5 Hz, 1H) , 7.27 (d, J = 9.0 Hz, 1H), 7.40-7.37 (m, 1H), 7.47-7.44 (m, 2H), 7.78-7.72 (m, 5H), 7.93 (s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) δ 134.3, 133.9, 130.3, 130.2, 129.9, 127.8, 127.5, 127.4, 127.3, 127.0, 125.0, 123.0, 118.7, 118.6, 114.5, 110.1, 76.5, 55.5.

Step 2:

(4-methoxyphenyl) -1- (2-naphthoxy) methyl) -1,2,3-triazole ( 5a ) used in Step 2 of Example 1 instead of 4-tert- - (2-naphthoxy) methyl) -1,2,3-triazole ( 5d , 391 mg, 1.18 mmol) 3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1d , 521 mg, 89%).

^{1 H NMR (500 MHz, CDCl} 3) δ 3.82 (s, 3H), 4.25 (s, 3H), 6.65 (s, 2H), 7.03-7.00 (m, 2H), 7.25 (dd, J = 9.0, 2.5 J = 8.5 Hz, 1H), 7.83 (d, J = 9.0 Hz, 1H), 7.42 (td, J = 7.5, 1.0 Hz, 1H), 7.53-7.47 ), 8.76 (s, 1 H);

^{13 C NMR (125 MHz, CDCl} 3) δ 162.7, 153.1, 144.1, 134.2, 131.3, 130.8, 130.6, 128.5, 127.8, 127.7, 118.0, 115.5, 113.5, 110.5, 79.6, 55.7, 38.9.

Example  5: 3- methyl -4- Phenyl -1- (2- Phenyl ethane One-1-yl) -1,2,3- Triazolium Trifluoromethanesulfonate  (1e)

Step 1:

2-O map acetophenone (3b, 322 mg, 2.0 mmol ) and phenylacetylene (4e, 225 mg, 2.2 mmol ) was dissolved in acetonitrile (8 mL) and copper iodide (77 mg, 0.4 mmol) and triethylamine (0.056 mL, 0.4 mmol) was added and the mixture was stirred at room temperature for 2 hours. The mixture was concentrated under reduced pressure and then subjected to column chromatography (1% methanol / dichloromethane) 2-one-1-yl) -1,2,3-triazole ( 5e , 520 mg, 83%).

^{1 H NMR (500 MHz, CDCl} 3) δ 5.90 (s, 2H), 7.35 (t, J = 7.4 Hz, 1H), 7.44 (t, J = 7.4 Hz, 2H), 7.55 (t, J = 7.8Hz 2H), 7.68 (t, J = 7.4 Hz, 1H), 7.87 (d, J = 8.4 Hz, 2H), 7.95 (s, 1H), 8.03 (t, J = 8.4 Hz, 2H).

Step 2:

( 5e , 520 mg, 1.67 mmol) obtained in Step 1 was dissolved in acetonitrile (7.0 mL), and the mixture was stirred at room temperature for 2 hours. Methyltrifluoromethanesulfonate ( 6a , MeOH, 0.278 mL, 2.5 mmol) was added to the mixture, and the mixture was stirred at 0 ° C for 30 minutes. The solvent was distilled off under reduced pressure to obtain the target compound 3-methyl- 1-yl) -1,2,3-triazolium trifluoromethanesulfonate ( 1e , 694 mg, 87%).

^{1 H NMR (500 MHz, CDCl} 3) δ 4.31 (s, 3H), 6.43 (s, 2H), 7.55-7.72 (m, 8H), 8.04 (d, J = 6.0 Hz, 2H), 8.76 (s, 1H).

Example  6: 4- tert -Butyl-3- methyl -One-[( Phenylthio ) methyl ] -1,2,3- Triazolium Trifluoromethanesulfonate  (1f)

Step 1:

( 3c , 330 mg, 2.0 mmol) and 3,3-dimethyl-1-butyne ( 4a , 246 mg, 3.0 mmol) obtained in Preparation Example 3 were dissolved in acetonitrile After adding copper iodide (77 mg, 0.4 mmol) and triethylamine (0.056 mL, 0.4 mmol), the mixture was stirred at room temperature for 2 hours, concentrated under reduced pressure, and then subjected to column chromatography (1% methanol / dichloromethane) The objective compound 4-tert-butyl-1 - [(phenylthio) methyl] -1,2,3-triazole ( 5f , 411 mg, 83%) was obtained.

¹ H NMR (500 MHz, CDCl ₃ )? 1.23 (s, 9H), 5.90 (s, 2H), 7.45-7.34 (m, 5H), 7.76 (s, 1H).

Step 2:

Tert-butyl-1 - [(phenylthio) methyl] -1,2,3-triazole ( 5f , 411 mg, 1.66 mmol) obtained in Step 1 was dissolved in acetonitrile Romero burnt sulfonate (6a, MeOTf, 0.278 mL, 2.5 mmol) was added to the back, behind which at 0 ℃ stirred for 30 minutes under reduced pressure of the solvent the desired compound 4-tert- butyl-3-methyl-1 - [(phenyl Im Methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1f , 615 mg, 90%).

¹ H NMR (500 MHz, CDCl ₃ )? 1.46 (s, 9H), 4.28 (s, 3H), 5.93 (s, 2H), 7.43-7.38 (m, 5H), 8.17

Example  7: 3- methyl -1 - ((2- Naphthoxy ) methyl )-4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1 g)

Step 1:

After dissolving 2-naphthol ( 7a , 720 mg, 5.0 mmol) and potassium carbonate (2.07 g, 15 mmol) in acetonitrile (20 mL), 1- (chloromethyl) Triazole ( 8a , 1.45 g, 7.5 mmol) was added thereto, followed by stirring at 80 ° C for 5 hours. Water was added to terminate the reaction, and the organic compound was extracted with ethyl acetate. The extracted ethyl acetate solution was treated with anhydrous sodium sulfate and then subjected to column chromatography (30% ethyl acetate / n -hexane) to obtain 4-phenyl-1 - ((2-naphthoxy) methyl) -Triazole ( 5 g , 1.13 g, 75%).

^{1 H NMR (500 MHz, CDCl} 3) δ 6.40 (s, 2H), 7.20 (dd, J = 9.0 Hz, J = 2.5 Hz, 1H), 7.26 (d, J = 9.5 Hz, 1H), 7.47-7.31 (m, 6H), 7.79-7.76 (m, 3H), 7.83-7.81 (m, 2H), 8.01 (s, 1H);

¹³ C NMR (125 MHz, CDCl ₃ )? 134.2, 133.9, 130.3, 130.2, 129.9, 129.0, 128.6, 127.8, 127.5, 127.0, 126.03, 125.94, 125.0, 119.6, 118.5, 110.1, 76.5.

Step 2:

( 5 g , 1.13 g, 3.75 mmol) obtained in Step 1 was dissolved in acetonitrile (15.0 mL), methyltrifluoroacetate Methanesulfonate ( 6a , MeOTf, 0.618 mL, 5.63 mmol) was added, the mixture was stirred at 0 ° C for 30 minutes and then the solvent was removed under reduced pressure to obtain the objective compound 4-phenyl- Methoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1 g , 1.68 g, 96%).

^{1 H NMR (500 MHz, CDCl} 3) d 3.81 (s, 3H), 6.35 (s, 2H), 7.22 (dd, J = 9. 0 Hz, 2. 0 Hz, 1H), 7.40-7.35 (m, J = 8.0 Hz, 1H), 7.78 (d, J = 9.0 Hz, 1H), 7.85 (t, J = 8.5 Hz, 1H), 9.63 s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) d 152.8, 138.3, 136.6, 134.3, 131.1, 130.6, 130.4, 129.64, 129.60, 127.7, 127.2, 125.3, 124.5, 120.9 (d, J = 319 Hz), 118.4, 118.1 , 110.3, 76.0, 35.1.

Example  8: 3- methyl -1- [3- (2- Naphthoxy ) - n -profile] Oxymethyl -4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1h)

Step 1:

Was dissolved butoxide (1.69 g, 15 mmol) in tetrahydrofuran (20 mL), 1- (chloromethyl) - 3- (2-naphthoxy) propanol (7b, 1.01 g, 5.0 mmol ) and potassium-tert Phenyl-1,2,3-triazole ( 8a , 1.16 g, 6.0 mmol) was added and the mixture was stirred at room temperature for 3 hours. Water was added to terminate the reaction, and organic compounds were extracted with dichloromethane. By performing 1-The extracted dichloromethane solution was after column chromatography (hexane to 30% ethyl acetate / n) treated with anhydrous sodium sulfate, [3- (2-naphthoxy) - n - propyl] oxy-4- Phenyl-1,2,3-triazole ( 5h , 1.25 g, 70%).

^{1 H NMR (500 MHz, CDCl} 3) δ 2.10 (q, J = 6.0 Hz, 2H), 3.79 (t, J = 6.3 Hz, 2H), 4.12 (t, J = 6.3 Hz, 2H), 5.74 (s 2H), 7.05 (dd, J = 9.0 Hz, J = 2.5 Hz, 1H), 7.09 (d, J = 2.5 Hz, 1H), 7.38-7.31 (m, 4H), 7.44-7.41 , 7.65 (d, J = 8.5 Hz, 1H), 7.68 (d, J = 8.5 Hz, 1H), 7.76-7.73 (m, 3H), 7.87 (s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) δ 156.9, 148.9, 134.7, 130.4, 129.6, 129.2, 129.0, 128.5, 127.8, 126.9, 126.5, 126.0, 123.8, 119.3, 118.9, 106.8, 79.3, 66.5, 64.2, 29.3 .

Step 2:

1 obtained in step 1 of [3- (2-naphthoxy) - - n propyl] oxy-4-phenyl-1,2,3-triazole (5h, 1.25 mg, 3.5 mmol ) in acetonitrile (14.0 mL Methyltrifluoromethanesulfonate ( 6a , MeOTf, 0.57 mL, 5.25 mmol) was added to the mixture, and the mixture was stirred at 0 ° C for 30 minutes. The solvent was then removed under reduced pressure to obtain the target compound 3-methyl-1- [3 - (2-naphthoxy) -n -propyl] oxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1h , 1.4 g, 76%).

^{1 H NMR (500 MHz, CDCl} 3) d 2.11 (q, J = 5.8 Hz, 2H), 4.01-3.99 (m, 5H), 4.08 (t, J = 5.5 Hz, 2H), 5.95 (s, 2H) , 7.01 (dd, J = 9.0 , 2.5 Hz, 1H), 7.07 (d, J = 2.5 Hz, 1H), 7.44-7.26 (m, 7H), 7.51-7.48 (m, 1H), 7.62 (d, J = 9.0 Hz, 1H), 7.67 (d, J = 8.0 Hz, 1H), 7.71 (d, J = 8.0 Hz, 1H), 8.68

^{13 C NMR (125 MHz, CDCl} 3) d 156.7, 143.8, 134.7, 132.0, 129.71, 129.66, 129.5, 129.1, 128.3, 127.8, 126.9, 126.8, 12.0, 121.7, 120.8 (d, J = 318 Hz), 118.6 , 106.8, 83.6, 68.2, 63.7, 38.7, 29.1

Example  9: 1- [1- Methylsulfonyloxy -3- (2- Naphthyl )-2- Oxypropyl ] Oxymethyl -3- methyl -4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1i)

Instead of Example 8 3- (2-naphthoxy) propanol (7b) used in the use of 2-hydroxy-3- (naphthalene-2-yloxy) propyl methane sulfonate (7c, 889 mg, 3.0 mmol ) Methyl-4-phenyl-1,2,3-triazin-2-yl) ( 1i , 1.39 g, 75%) was obtained in the form of a white solid.

^{1 H NMR (500 MHz, CDCl} 3) δ 2.99 (s, 3H), 4.15 (s, 3H), 4.31-4.22 (m, 2H), 4.43 (d, J = 5.5 Hz, 2H), 4.69-4.67 ( m, 1H), 6.22 (q , J = 9.3 Hz, 2H), 7.07 (dd, J = 8.8, 2.8 Hz, 1H), 7.13 (d, J = 2.5 Hz, 1H), 7.43 (td, J = 7.5 J = 8.0 Hz, 2H), 7.23 (t, J = 8.0 Hz, 2H), 7.52-7.48 (m, 4H), 7.57-7.54 8.91 (s, 1 H);

^{13 C NMR (125 MHz, CDCl} 3) δ 155.9, 143.9, 134.5, 132.1, 129.9, 129.8, 129.6, 129.5, 128.8, 127.8, 127.2, 126.9, 124.4, 122.0, 120.9 (d, J = 319 Hz), 118.3 , 107.5, 82.8, 78.5, 69.7, 67.2, 38.8, 37.4.

Example  10: 3- methyl -(2- Naphthyl ) Methyloxymethyl -4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1j)

Except that naphthalene methanol ( 7d , 475 mg, 3.0 mmol) was used instead of 3- (2-naphthoxy) propanol ( 7b ) used in Example 8 to obtain 3-methyl- Yl) methyloxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1j , 1.09 g, 76%).

^{1 H NMR (500 MHz, CDCl} 3) δ 3.96 (s, 3H), 4.88 (s, 2H), 5.94 (s, 2H), 7.24 (d, J = 7.5 Hz, 2H), 7.45-7.32 (m, 6H), 7.68 (d, J = 8.5 Hz, 1H), 7.76-7.71 (m, 3H), 8.48 (s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) δ 143.39, 143.38, 133.1, 132.9, 131.8, 129.5, 129.3, 128.3, 128.2, 128.1, 127.69, 127.67, 126.61, 126.55, 125.9, 124.6, 121.59, 121.58, 120.8 (q , J = 319 Hz), 82.7, 73.9, 38.5.

Example  11: (S) -1- (4- (2- BOC -Amino-2- (t- Butoxycarbonyl )ethyl) Phenyloxymethyl ) -4-phenyl-1,2,3- Triazolium Trifluoromethanesulfonate  (1k)

Step 1:

N-BOC-L-tyrosine tert-butyl ester ( 7e, 0.79 g, 2.35 mmol) was dissolved in acetone (23 mL) and cesium carbonate (2.00 g, 5.87 mmol) -1,2,3-triazole ( 8a , 0.46 g, 2.59 mmol) were added in this order, and the mixture was stirred at 50 ° C for 6 hours. The reaction mixture is distilled under reduced pressure, diluted with ethyl acetate, and filtered. The filtrate is washed with 1.0 normal aqueous hydrochloric acid solution, water and saturated aqueous sodium chloride solution. After drying the washed organic layer over anhydrous sodium sulfate and concentrated was purified by column chromatography (SiO _2, 20% ethyl acetate / hexane) to conduct a white solid compound (S) -1- (4- (2 -BOC- amino-2- (t-butoxycarbonyl) ethyl) phenyloxymethyl) -4-phenyl-1,2,3-triazole ( 5k , 1.07 g, 2.16 mmol, 92%).

^{1 H NMR (400 MHz, CDCl} 3) δ 1.38 (s, 18H), 2.99 (s, 2H), 4.39 (d, J = 6.4 Hz, 1H), 5.03 (d, J = 8 Hz, 1H), 6.23 (s, 3H), 7.09 ( d, J = 8 Hz, 2H), 7.33 (d, J = 6.4 Hz, 1H), 7.41 (t, J = 7.6 Hz, 1H), 7.82 (d, J = 7.6 Hz , ≪ / RTI > 2H), 7.97 (s, 1H)

Step 2:

(S) -1- (4- (2-BOC-amino-2- (t-butoxycarbonyl) ethyl) phenyloxymethyl) -4-phenyl-1,2,3-triazole ( 5k , 0.47 g, 0.96 mmol) was dissolved in acetonitrile (2.5 mL), methyltrifluoromethane sulfonate ( 6a , 53 μl, 0.48 mmol) was added and the mixture was stirred at room temperature for 90 minutes. The reaction mixture was concentrated and then subjected to column chromatography (SiO _2, 5% methanol / dichloromethane) to obtain the desired compound (S) -1- (4- (2-BOC- ) Ethyl) phenyloxymethyl) -3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1k , 0.22 g, 0.34 mmol, 70%).

^{1 H NMR (400 MHz, CDCl} 3) δ 1.40 (s, 18H), 3.04-2.98 (m, 2H), 4.30 (s, 3H) 4.37 (d, J = 6.0 Hz, 1H), 5.00 (d, J = 8.0 Hz, 1H), 6.54 (s, 2H), 7.03 (d, J = 8.8 Hz, 1H), 7.14 (d, J = 8.4 Hz, 2H), 7.61-7.54 , 1H).

Example  12: 3- methyl -1 - ((2- Naphthoxy ) methyl )-4- Phenyl imidazolium Trifluoromethanesulfonate  (1)

Step 1:

2-naphthol (7a, 720 mg, 5.0 mmol ) and potassium carbonate (2.07 g, 15 mmol) was dissolved in acetonitrile (20 mL), 1- (chloromethyl) -4-phenyl-imidazole (8b, 1.44 g, 7.5 mmol), and the mixture was stirred at 80 ° C for 5 hours. Water was added to terminate the reaction, and the organic compound was extracted with ethyl acetate. By performing the 4-phenyl-1 - the extracted ethyl acetate solution after column chromatography (hexane to 20% ethyl acetate / n) - treated with anhydrous sodium sulfate ((2-naphthyl) methyl) imidazole (5l, 931 mg, 62%).

^{1 H NMR (500 MHz, CDCl} 3) δ 5.94 (s, 2H), 7.13 (dd, J = 9.2 Hz, J = 2.4 Hz, 1H), 7.28-7.24 (m, 2H), 7.43-7.36 (m, 4H), 7.48 (td, J = 7.4 Hz, J = 1.2 Hz, 1H), 7.71 (d, J = 1.2 HZ, 1H), 7.74 (d, J = 8.0 Hz, 1H), 7.81-7.77 (m, 4H).

Step 2:

( 5 l , 931 mg, 3.10 mmol) obtained in Step 1 was dissolved in acetonitrile (15.0 mL), methyltrifluoromethanesulfonate ( 6a , MeOTf (2-naphthoxy) , 0.51 mL, 4.65 mmol) and the mixture was stirred at 0 ° C for 30 minutes. The solvent was then removed under reduced pressure to obtain the title compound 4-phenyl-3-methyl-1- ( Trifluoromethanesulfonate ( 1 l , 734 mg, 51%) was obtained.

^{1 H NMR (500 MHz, CDCl} 3) d 3.78 (s, 3H), 6.33 (s, 2H), 7.21 (dd, J = 8.8, 2.3 Hz, 1H), 7.38-7.34 (m, 3H), 7.52- 8.0 Hz, 1H), 7.41 (m, 6H), 7.73 (d, J = 8.0 Hz, 1H), 7.76 (d, J = 9.0 Hz, 1H), 7.84 (d, J = 8.0 Hz, 1H)

^{13 C NMR (125 MHz, CDCl} 3) d 152.9, 138.1, 136.5, 134.3, 131.0, 130.6, 130.3, 129.6, 129.5, 127.72, 127.69, 127.1, 125.2, 124.5, 120.9 (q, J = 319 Hz), 118.5 , 118.2, 110.3, 76.0, 35.1.

Example  13: 3- methyl -1 - ((2- Naphthoxy ) methyl )-4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1 g)

2-Naphthol ( 7a , 288 mg, 2.0 mmol) and potassium carbonate (829 mg, 6.0 mmol) were dissolved in acetonitrile (8 mL) 2,3-triazolium trifluoromethanesulfonate ( 9a , 858 mg, 2.4 mmol) was added and the mixture was stirred at 80 ° C for 5 hours. Water was added to terminate the reaction, and organic compounds were extracted with dichloromethane. The obtained dichloromethane solution was treated with anhydrous sodium sulfate and subjected to column chromatography (5% methanol / dichloromethane) to obtain the target compound 4-phenyl-3-methyl- Methoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1 g , 577 mg, 62%).

^{1 H NMR (500 MHz, CDCl} 3) d 3.81 (s, 3H), 6.35 (s, 2H), 7.22 (dd, J = 9. 0 Hz, 2. 0 Hz, 1H), 7.40-7.35 (m, J = 8.0 Hz, 1H), 7.78 (d, J = 9.0 Hz, 1H), 7.85 (t, J = 8.5 Hz, 1H), 9.63 s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) d 152.8, 138.3, 136.6, 134.3, 131.1, 130.6, 130.4, 129.64, 129.60, 127.7, 127.2, 125.3, 124.5, 120.9 (d, J = 319), 118.4, 118.1, 110.3, 76.0, 35.1.

Example  14: 1- (4- Biphenyl ) Oxymethyl -3- methyl -4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1 m)

( 7f , 510 mg, 3.0 mmol) was used instead of 2-naphthol ( 7a ) used in Example 12 to obtain 1- (4-biphenyl) Methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1m , 1.28 g, 87%).

^{1 H NMR (500 MHz, CDCl} 3) δ 4.26 (s, 3H), 6.56 (s, 2H), 7.19 (q, J = 5.0 Hz, 1H), 7.19 (d, J = 9.0 Hz, 1H), 7.32 (td, J = 7.5, 1.3 Hz, 1H), 7.41 (t, J = 7.8 Hz, 2H), 7.61-7.50 (m, 9H), 7.80 (t, J = 8.5 Hz, 2H), 8.79 (s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) δ 154.8, 144.0, 140.0, 137.4, 132.3, 129.9, 129.7, 129.0, 128.9, 128.8, 127., 121.7, 120.8 (q, J = 319 Hz), 116.6, 79.7, 39.1.

Example  15: 1- (4- Bromo -2- Methylphenyl ) Oxymethyl -3- methyl -4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1n)

The procedure of Example 12 was repeated except for using 4-bromo-2-methylphenol ( 7 g , 561 mg, 3.0 mmol) instead of 2-naphthol ( 7a ) ) Oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1n , 1.14 g, 75%).

^{1 H NMR (500 MHz, CDCl} 3) δ 2.20 (s, 3H), 4.28 (s, 3H), 7.04 (d, J = 9.5 Hz, 2H), 7.31-7.27 (m, 2H), 7.61-7.53 ( m, 5 H), 8.83 (s, 1 H);

^{13 C NMR (125 MHz, CDCl} 3) δ 152.8, 144.0, 134.5, 132.3, 130.5, 130.4, 129.9, 129.7, 128.9, 121.7, 120.7 (q, J = 319 Hz), 116.6, 115.3, 79.6, 39.1, 16.1 .

Example  16: 1- (3,4- Dimethoxyphenyl ) Oxymethyl -3- methyl -4- Phenyl -1,2,3- Triazolium  Preparation of trifluoromethanesulfonate (1o)

( 7h , 462 mg, 3.0 mmol) was used instead of 2-naphthol ( 7a ) used in Example 12 to obtain 1- (3,4-dimethoxy phenyl) oxy-3-methyl-4-phenyl-1,2,3-triazole methane sulfonate (1o, 927 mg, yield 65%) as an imidazolium trifluoroacetate.

^{1 H NMR (500 MHz, CDCl} 3) δ 3.79 (s, 3H), 3.82 (s, 3H), 4.24 (s, 3H), 6.43 (s, 2H), 6.62 (dd, J = 8.5, 2.8 Hz, 1H), 6.68 (s, 1H), 6.76 (d, J = 8.5 Hz, 1H), 7.58-7.48 (m, 5H), 8.72 (s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) δ 105.2, 149.4, 146.0, 143.8, 132.2, 129.8, 129.5, 128.6, 121.7, 120.7 (q, J = 319 Hz), 111.7, 106.8, 102.4, 80.6, 56.3, 56.2 , 39.0.

Example  17: 3- methyl -1- (4- Nitrophenyl ) Oxymethyl -4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1p)

The same procedure was followed except that 4-nitrophenol ( 7i , 417 mg, 3.0 mmol) was used instead of 2-naphthol ( 7a ) used in Example 12 to give 3-methyl-1- (4-nitrophenyl) Oximethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1p , 898 mg, 65%).

^{1 H NMR (500 MHz, CDCl} 3) δ 4.36 (s, 3H), 6.79 (s, 2H), 7.41 (d, J = 9.5 Hz, 2H), 7.72-7.64 (m, 5H), 8.30 (d, J = 9.5 Hz, 2H);

^{13 C NMR (125 MHz, CDCl} 3) δ 160.1, 144.2, 143.8, 131.8, 129.4, 129.2, 125.7, 122.1, 120.4 (d, J = 317 Hz, only two peaks of quartet of CF 3 -C were shown), 116.3, 78.5, 38.3.

Example  18: 1- (4- Acetylaminophenyl ) Oxymethyl -3- methyl -4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1q)

The same procedure was followed except that 3-acetaminophenol ( 7j , 453 mg, 3.0 mmol) was used instead of 2-naphthol ( 7a ) used in Example 12 to obtain 1- (4-acetylaminophenyl) oxymethyl -3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1q , 1.08 g, 76%).

^{1 H NMR (500 MHz, CDCl} 3) δ 2.09 (s, 3H), 6.41 (s, 2H) 4.26 (s, 3H), 6.72 (dd, J = 8.3, 2.3 Hz, 1H), 7.20-7.15 (m , 2H), 7.63-7.49 (m, 5H), 7.66 (d, J = 8.0 Hz, 1H), 8.70 (s, 1H), 8.93 (s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) δ 170.0, 155.4, 144.1, 140.9, 132.5, 130.8, 130.0, 129.7, 128.3, 121.7, 120.7 (q, J = 318 Hz), 116.0, 112.5, 106.6, 80.1, 39.2 , 24.5.

Example  19: 1- (3- O - Estronyl ) methyl -3- methyl -4- Phenyl -1,2,3- Triazolium Trifluoromethanesulfonate  (1r)

Except that 2-naphthol ( 7a ) used in Example 12 was replaced by estrone ( 7k , 811 mg, 3.0 mmol) to give 1- (3- O -estrone) methyl- Methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate (1 r , 1.26 g, 71%).

¹ H NMR (500 MHz, CDCl ₃ )? 0.89 (s, 3H), 1.64-1.39 (m, 6H), 1.95-1.93 , 1H), 2.37-2.35 (m, 1H), 2.49 (dd, J = 19.0, 8.5 Hz, 2H), 2.92-2.90 (m, 2H), 4.27 (s, 3H), 6.50 (s, 2H), 6.88-6.87 (m, 2H), 7.24 (d, J = 9.5 Hz, 1H), 7.62-7.55 (m, 5H), 8.70 (s, 1H);

^{13 C NMR (125 MHz, CDCl} 3) δ 220.7, 153.5, 144.0, 139.3, 136.1, 132.3, 129.9, 129.7, 128.7, 127.2, 121.8, 120.8 (q, J = 319 Hz), 116.3, 113.5, 80.0, 50.6 , 48.1, 44.2, 39.0, 38.3, 36.0, 31.7, 29.6, 26.5, 26.0, 21.7, 14.0.

Example  20: 3- Acetanaphthyl -One- Methylimidazolium  (1s)

( 10a , 2.49 g, 10 mmol) was dissolved in acetonitrile (50 mL), methylimidazole ( 11a , 0.836 mL, 10.5 mmol) Lt; / RTI > for 12 hours. After the reaction was completed, the reaction solvent was removed under reduced pressure, and then column chromatography (10% methanol / dichloromethane) was conducted to obtain the desired compound 3-acetanaphthyl-1-methylimidazolium ( 1s , 3.08 g, 93% .

^{1 H NMR (500 MHz, CDCl} 3) δ 4.02 (s, 3H), 6.15 (s, 2H), 7.68 (m, 4H), 7.99 (m, 4H), 8.74 (s, 1H), 9.01 (s, 1H);

¹³ C NMR (125 MHz, CDCl ₃ ) δ 191.3, 139.5, 137.7, 134.0, 132.5, 130.9, 130.5, 130.0, 129.4, 129.0, 128.7, 125.4, 124.6, 124.3, 56.3, 36.8.

Example  21: Nucleophilic  Fluorination reaction

Methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1a , 0.5 mmol) obtained in Example 1 and tetra Butylammonium fluoride (TBAF, 0.75 mmol) was added to the reaction vessel, and acetonitrile (2.0 mL) was added to dissolve it. The mixture was stirred at 80 ° C for 1 hour. Water was added to terminate the reaction, and organic compounds were extracted with dichloromethane. The extracted dichloromethane solution was treated with anhydrous sodium sulfate and subjected to column chromatography (2% ethyl acetate / hexane) to obtain the target compound, 2-fluoromethoxynaphthalene ( 12a , 78 mg, 89%).

^{1 H NMR (500 MHz, CDCl} 3) δ 5.85 (d, J = 55.0 Hz, 2H), 7.29 (dd, J = 9.0, 2.5 Hz, 1H), 7.44 (t, J = 7.3 Hz, 1H), 7.52 -7.49 (m, 2H), 7.81 (d, J = 8.5 Hz, 1H), 7.83 (d, J = 9.0 Hz, 2H);

^{13 C NMR (125 MHz, CDCl} 3) [delta] 154.9, 134.5, 130.5, 130.1, 128.0, 127.6, 126.9, 125.1, 118.8, 111.4, 101.1 (d, J = 218 Hz).

Example  22: Fluorination reaction under various organic solvent conditions

Methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1a , 0.5 mmol) obtained in Example 1 and tetra (TBAF, 196 mg, 0.75 mmol) and using various organic solvents (2.0 mL) such as tert-butanol, tetrahydrofuran and dimethylformamide instead of acetonitrile as in Example 20 The fluorination reaction was carried out. For each reaction, the reaction time was checked and the amount of 2-fluoromethoxynaphthalene, the product of the fluorination reaction, was determined. The measured results are shown in Table 1 below.

menstruum Time (minutes) Yield (%) MeCN 60 89 t-BuOH 60 81 THF 40 85 DMF 20 79

Example  22: Various Fluorination  Reaction with reagents

(4-tert-butyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1a , 0.5 mmol) obtained in Example 1 was used And the fluorination reaction was carried out in the same manner as in Example 21 using cesium fluoride instead of tetrabutylammonium fluoride as the fluorination reagent. For each reaction, the reaction time was checked and the amount of 2-fluoromethoxynaphthalene, the product of the fluorination reaction, was determined. The measured results are shown in Table 2 below.

MF (equivalent) time Yield (%) CsF (3.0) 24 hours 38 TBAF (1.5) 60 minutes 89

Example  24: 2- (3- Fluoromethoxy - n - Propoxy ) Preparation of naphthalene 12b

Methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1a ) used in Example 21 instead of 4-tert- butyl- ( 1h , 262 mg, 0.5 mmol) was used in place of 1- [3- (2-naphthoxy) -n -propyl] oxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate (3-Fluoromethoxy- n -propoxy) naphthalene ( 12b , 90 mg, 77%) was obtained.

^{1 H NMR (500 MHz, CDCl} 3) δ 2.19 (q, J = 6.1 Hz, 2H), 3.98 (td, J = 6.3, 2.0 Hz, 2H), 4.21 (t, J = 6.0 Hz, 2H), 5.30 (d, J = 56.0 Hz, 2H), 7.16-7.14 (m, 2H), 7.34 (td, J = 7.5, 1.2 Hz, 1H), 7.45 (td, J = 7.5, 2.0 Hz, 1H), 7.78- 7.72 (m, 3 H);

^{13 C NMR (125 MHz, CDCl} 3) [delta] 154.9, 134.5, 130.5, 130.1, 128.0, 127.6, 126.9, 125.1, 118.8, 111.4, 101.1 (d, J = 218 Hz).

Example  25: 2- (2- Fluoromethoxy -3- Methanesulfonyloxy - n - Propoxy ) Preparation of naphthalene 12c

Except that 1 - [(2-naphthoxy) methyl] -1,2,3-triazolium trifluoromethanesulfonate ( 1a ) was used in place of 4-tert- butyl- -3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1i , 310 mg, , 0.5 mmol) in the same manner as in Example 1 to give 2- (2-fluoromethoxy-3-methanesulfonyloxy- n -propoxy) naphthalene ( 12c , 110 mg, 67%).

^{1 H NMR (500 MHz, CDCl} 3) δ 3.06 (s, 3H), 4.37-4.23 (m, 3H), 4.58-4.49 (m, 2H), 5.46 (ddd, J = 55.8, 17.5, 3.0 Hz, 2H ), 7.16-7.14 (m, 2H) , 7.37 (td, J = 8.0, 1.0 Hz, 1H), 7.47 (td, J = 8.3, 1.3 Hz, 1H), 7.76 (q, J = 9.00 Hz, 3H) ;

^{13 C NMR (125 MHz, CDCl} 3) [delta] 156.1, 134.6, 130.0, 129.5, 127.9, 127.1, 126.9, 124.4, 118.7, 107.2, 103.8 (d, J = 216 Hz), 69.1, 67.0, 37.8.

Example  26: (2- Fluoromethoxy ) -2-methylnaphthalene (12d)

Methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1a ) used in Example 21 instead of 4-tert- butyl- (2-naphthyl) methyloxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1j , 240 mg, 0.5 mmol) 2-fluoromethoxy) -2-methylnaphthalene ( 12d , 75 mg, 79%).

^{1 H NMR (500 MHz, CDCl} 3) δ 4.95 (s, 2H), 5.40 (d, J = 56.4 Hz, 2H), 7.75 Hz, 2H), 7.51-7.47 (m, 3H), 7.87-7.83 (m , 4H);

^{13 C NMR (125 MHz, CDCl} 3) [delta] 134.0, 133.4, 133.3, 128.6, 128.1, 127.9, 127.2, 126.5, 126.4, 125.9, 102.9 (d, J = 213 Hz)

Example  27: O- Fluoromethyl -N- BOC -L-tyrosine- tert - < / RTI > butyl ester (12e)

(S) - (2-naphthyl) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1a ) instead of 4-tert- butyl- Methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfoate was prepared by reacting 1- (4- (2-BOC-amino-2- (t- butoxycarbonyl) carbonate (1k, 0.22g, 0.36 mmol), and proceeds to a fluoromethyl O- -N-BOC-L- tyrosine -tert- butyl ester (12e, 75 mg, 60% ) in the same manner but using the .

^{1 H NMR (400 MHz, CDCl} 3) δ 1.42 (d, J = 4.0 Hz, 18H), 3.01-3.04 (m, 2H), 4.42 (d, J = 6.8 Hz, 1H), 4.98 (d, J = 6.8 (s, 1H), 7.00 (d, J = 8.4 Hz, 2H), 7.13 (d, J = 8.4 Hz, 2H).

Example  28: 4- Fluoromethoxybiphenyl  (12e)

(4-tert-butyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3- triazolium trifluoromethanesulfonate ( 1a ) -Biphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1m , 246 mg, 0.5 mmol) To obtain 4-fluoromethoxybiphenyl ( 12f , 74 mg, 73%).

^{1 H NMR (500 MHz, CDCl} 3) δ 5.78 (d, J = 55.0 Hz, 2H), 7.21 (d, J = 9.0 Hz, 2H), 7.39 (td, J = 7.5, 1.0 Hz, 1H), 7.49 (t, J = 7.8 Hz, 2H), 7.61 (d, J = 8.5 Hz, 4H);

^{13 C NMR (125 MHz, CDCl} 3) [delta] 156.59, 156.57, 140.7, 136.9, 129.1, 128.7, 127.4, 127.2, 117.23, 117.22, 101.0 (d, J = 218 Hz).

Example  29: 5- Bromo -2- Fluoromethoxy toluene  (12 g)

(4-tert-butyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3- triazolium trifluoromethanesulfonate ( 1a ) Methylphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1n , 254 mg, 0.5 mmol) To give 5-bromo-2-fluoromethoxy toluene ( 12 g , 91 mg, 83%).

^{1 H NMR (500 MHz, CDCl} 3) δ 2.24 (s, 3H), 5.70 (d, J = 54.5 Hz, 2H), 6.95 (d, J = 8.5 Hz, 1H) 7.31 (m, 2H);

^{13 C NMR (125 MHz, CDCl} 3) [delta] 154.4, 133.9, 130.5, 130.0, 116.6, 116.0, 101.0 (d, J = 218 Hz), 16.2.

Example  30: 4- Fluoromethoxy -1,2- Dimethoxybenzene  (12h)

(3-tert-butyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3- triazolium trifluoromethanesulfonate ( 1a ) (4-dimethoxyphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1o , 238 mg, 0.5 mmol) To yield 4-fluoromethoxy-1,2-dimethoxybenzene ( 12h , 70 mg, 75%).

^{1 H NMR (500 MHz, CDCl} 3) δ 3.84 (s, 3H), 3.85 (s, 3H), 5.64 (d, J = 55.0 Hz, 2H), 6.65-6.61 (m, 2H), 6.78 (d, J = 8.5 Hz, 1 H);

^{13 C NMR (125 MHz, CDCl} 3) [delta] 151.3, 149.8, 145.5, 111.6, 107.6, 102.6, 101.8 (d, J = 217 Hz), 56.4, 56.0.

Example  31: 4- Fluoromethoxy -1-nitrobenzene (12i)

Methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate ( 1a ) used in Example 21 instead of 4-tert- butyl- The same procedure was followed except that 1- (4-nitrophenyl) oxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1p , 230 mg, 0.5 mmol) was used To obtain 4-fluoromethoxy-1-nitrobenzene ( 12i , 62 mg, 72%).

^{1 H NMR (500 MHz, CDCl} 3) δ 5.79 (d, J = 53.0 Hz, 2H), 7.18-7.17 (m, 2H), 8.26-8.24 (m, 2H);

^{13 C NMR (125 MHz, CDCl} 3) [delta] 161.3, 143.7, 126.1, 116.6, 99.8 (d, J = 221 Hz).

Example  32: N - (3- Fluoromethoxyphenyl ) Acetamide  (12j)

(4-tert-butyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3- triazolium trifluoromethanesulfonate ( 1a ) -Acetylaminophenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate ( 1q , 236 mg, 0.5 mmol) To obtain N - (3-fluoromethoxyphenyl) acetamide ( 12j , 70 mg, 76%).

^{1 H NMR (500 MHz, CDCl} 3) δ 2.20 (s, 3H), 5.72 (d, J = 54.5 Hz, 2H), 6.85 (d, J = 7.0 Hz, 1H), 7.20 (d, J = 7.5 Hz , ≪ / RTI > 1H), 7.29-7.26 (m, 1H), 7.41 (s, 1H), 7.46 (bs, 1H);

^{13 C NMR (125 MHz, CDCl} 3) [delta] 168.7, 157.4, 139.5, 130.2, 115.0, 112.5, 108.7, 100.9 (d, J = 218 Hz), 24.9.

Example  33: 3 -O- Fluoromethylestrone  (12j)

(3-tert-butyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3- triazolium trifluoromethanesulfonate ( 1a ) -O -estrone) Methyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate (1 r , 296 mg, 0.5 mmol) To give 3- O- fluoromethylestrone ( 12k , 125 mg, 83%).

¹ H NMR (500 MHz, CDCl ₃ )? 0.89 (s, 3H), 1.66-1.39 (m, 7H), 2.16-1.93 (m, 5H), 2.25-2.20 , 1H), 2.48 (dd, J = 19.0, 8.5 Hz, 1H), 2.89 (t, J = 4.3 Hz, 2H), 5.66 (d, J = 55.0 Hz, 2H), 6.81 (d, J = 2.5 Hz , 1H), 6.86 (dd, J = 8.5, 2.5 Hz, 1H), 7.22 (d, J = 8.5 Hz, 4H);

^{13 C NMR (125 MHz, CDCl} 3) (d, J = 217 Hz), 50.6, 48.2, 44.2, 38.4, 36.1, 31.8, 29.8, 26.7, 21.8, 14.1.

Example  34: 3 -O- [ ¹⁸ F] - Fluoromethylestrone  ([ ¹⁸ F] 12k)

Distilled water (2.0 mL) and 0.2 M sodium methanesulfonate aqueous solution (2.0 mL) were sequentially poured into Chromafix (R) and washed again with distilled water (2.0 mL). The [ ¹⁸ F] fluoride [ ¹⁸ O] H ₂ O solution (1-10 mCi) produced in the cyclotron was slowly poured off and washed with distilled water (2.0 mL). Methanol (2.0 mL) was poured into the [ ¹⁸ F] fluoride-containing cartridge to remove water and elute the [ ¹⁸ F] fluoride ion by flowing a 0.1 M tetrabutylammonium methanesulfonate solution (0.5 mL). After heating to 100 ^° C, nitrogen was blown off to remove the solvent and then 1- (3- O -estrone) methyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate 1r , 5 mg) was dissolved in acetonitrile or t-amyl alcohol, potassium carbonate (3 mg) was added, and the mixture was stirred at 120 ° C for 20 minutes. The yield of each reaction was measured using Radio-TLC, and it is shown in Table 3 below.

Acetonitrile t-amyl alcohol Radio-TLC (%) 100 82

Claims (11)

delete delete delete A compound represented by the following formula (1).
[Chemical Formula 1]

In Formula 1,
R ₁ is

,

,

,

,

,

,

,

,

,

,

And

, ≪ / RTI >
X is oxygen, sulfur, or -C (O) -,
The leaving group

or

≪ / RTI > and < RTI ID =
Y is an anion,
The tetravalent and nitrogen within a ring of the cation substituted with R ₃ may be unsubstituted or substituted on each carbon is independently R ₂ together, R ₂ and R ₃ are independently a C _1-4 straight-chain or branched-chain one another Alkyl group, phenyl,

,

, And

≪ / RTI > is selected from the group consisting of
Y is independently selected from the group consisting of trifluoromethane sulfonate (CF ₃ SO ₃ ^- ), paratoluene sulfonate, methane sulfonate and para-nitrobenzenesulfonate.
5. The method of claim 4,
The compound represented by the general formula (1)
4-tert-butyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate;
4-methoxycarbonyl-3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate;
4- [3,5-di (trifluoromethyl) phenyl] -3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate;
4- (4-methoxyphenyl) -3-methyl-1 - ((2-naphthoxy) methyl) -1,2,3-triazolium trifluoromethanesulfonate;
3-methyl-4-phenyl-1- (2-phenylethen-2-one-1-yl) -1,2,3-triazolium trifluoromethanesulfonate;
4-tert-butyl-3-methyl-1 - [(phenylthio) methyl] -1,2,3-triazolium trifluoromethanesulfonate;
3-methyl-1 - ((2-naphthoxy) methyl) -4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
3-methyl-1- [3- (2-naphthoxy) -n -propyl] oxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
1- [1-methylsulfonyloxy-3- (2-naphthyl) -2-oxypropyl] oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
3-Methyl- (2-naphthyl) methyloxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
3-methyl-1 - ((2-naphthoxy) methyl) -4-phenylimidazolium trifluoromethanesulfonate;
(S) -1- (4- (2-BOC-amino-2- (t-butoxycarbonyl) ethyl) phenyloxymethyl) -4-phenyl-1,2,3- triazolium trifluoromethanesulfo Nate;
1- (4-biphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
1- (4-bromo-2-methylphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
1- (3,4-dimethoxyphenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
3-methyl-1- (4-nitrophenyl) oxymethyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
1- (4-acetylaminophenyl) oxymethyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate;
1- (3- O -estrone) methyl-3-methyl-4-phenyl-1,2,3-triazolium trifluoromethanesulfonate; And
3-acetonaphthyl-1-methylimidazolium. ≪ / RTI >
As shown in Scheme 1 below,
Synthesizing an azido compound of formula (3) from a compound represented by formula (2) (step 1);
Synthesizing the compound of Chemical Formula 5 through a [3 + 2] cyclization addition reaction between the azido compound of Chemical Formula 3 and the alkene compound of Chemical Formula 4 obtained in Step 1 (Step 2); And
A step of synthesizing the organic salt of formula (I-a) using the alkylating reagent represented by formula (6) obtained in step (2) (step 3).
[Reaction Scheme 1]

In the above Reaction Scheme 1,
R ₁ is

,

,

,

,

,

,

,

,

,

,

And

, ≪ / RTI >
R ₂ and R ₃ independently of one another are C _1-4 linear or branched alkyl groups,

,

, And

, ≪ / RTI >
X is oxygen, sulfur, or -C (O) -,
Y is selected from the group consisting of trifluoromethane sulphonate (CF ₃ SO ₃ ^- ), para toluene sulphonate, methane sulphonate, and para-nitrobenzenesulphonate,
Z is chlorine, bromine, iodine, R ₄ SO ₃ ^- . Wherein R ₄ is a C ₁ -C ₂₀ hydrocarbon group, and the carbon of the main chain may be substituted or unsubstituted with oxygen, nitrogen, sulfur, or a combination thereof, and hydrogen in the main chain may be substituted or unsubstituted with halogen.
delete delete delete As shown in Reaction Scheme 5 below,
A process for preparing an ¹⁸ F-labeled compound represented by the formula (12) through a nucleophilic fluorination reaction between a compound represented by the formula (1) and a fluorine salt represented by the formula (MF).
[Reaction Scheme 5]

In the above Reaction Scheme 5,
R ₁ is

,

,

,

,

,

,

,

,

,

,

And

, ≪ / RTI >
X is oxygen, sulfur, or -C (O) -,
The leaving group

or

≪ / RTI > and < RTI ID =
Y is an anion,
The tetravalent and nitrogen within a ring of the cation substituted with R ₃ may be unsubstituted or substituted on each carbon is independently R ₂ together, R ₂ and R ₃ are independently a C _1-4 straight-chain or branched-chain one another Alkyl group, phenyl,

,

, And

, ≪ / RTI >
Y is independently selected from the group consisting of trifluoromethane sulfonate (CF ₃ SO ₃ ^- ), paratoluene sulfonate, methane sulfonate and para-nitrobenzenesulfonate,
M is a metal cation selected from the group consisting of Li, Na, K, Rb, and Cs; Tetravalent ammonium cations; Or a tetravalent phosphonium cation,
F is ¹⁸ F.
delete

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