KR0157075B1 - Novel pyrimidine derivatives - Google Patents

Abstract

The present invention relates to a novel pyrimidine derivative represented by the following general formula (I) having excellent gastric acid secretion inhibitory effect, or a pharmaceutically acceptable salt thereof, and a preparation method thereof.

Wherein A is 1-substituted-1,2,3,4-tetrahydroisoquinolin-2-yl of formula (II-1) or 7-substituted-4,5,6 of formula (II-2) , 7-tetrahydrothieno [2,3-c] pyridin-6-yl. And R ₁ , R ₂ , R ₆ are hydrogen or C _1-3 alkyl, R ₃ is hydrogen or halogen, R ₄ , R ₅ are the same or different from each other and are hydrogen, C _1-3 alkyl, or ring together To form cyclopentyl or cyclohexyl.

Description

Novel pyrimidine derivatives and preparation methods thereof

The present invention relates to pyrimidine derivatives, and more particularly, to novel pyrimidine derivatives represented by the following general formula (I) excellent in gastric acid secretion inhibitory effect, or a pharmaceutically acceptable salt thereof, and a preparation method thereof.

Wherein A is 1-substituted-1,2,3,4-tetrahydroisoquinolin-2-yl of formula (II-1) or 7-substituted-4,5,6 of formula (II-2) , 7-tetrahydrothieno [2,3-c] pyridin-6-yl. And R ₁ , R ₂ , R ₆ are hydrogen or C _1-3 alkyl, R ₃ is hydrogen or halogen, R ₄ , R ₅ are the same or different from each other and are hydrogen, C _1-3 alkyl, or ring together To form cyclopentyl or cyclohexyl.

Conventional drugs used for the treatment of gastrointestinal ulcers include antacids, anticholinergic drugs, gastric cytoprotective drugs, H ₂ receptor antagonists and proton pump inhibitors. Recently, a proton pump inhibitor omeprazol (Omeprazol) has been introduced to the clinical trials and began to be useful in the treatment of patients with gastroduodenal ulcers, various studies are being conducted based on a unique mechanism of action.

However, since proton pump inhibition of omeprazole is an irreversible mechanism of action, a problem about the possibility of side effects is pointed out, and attempts to develop reversible proton pump inhibition have been actively made. For example, quinazoline derivatives as reversible proton pump inhibitors are known from EP 322133 and EP 404322, in addition to quinoline derivatives (European Patent 259174) and pyrimidine derivatives (International Patent No. 9118887). Is known.

Accordingly, the present inventors have intensively studied to develop a reversible proton pump inhibitor, and the compound of the present invention containing a tetrahydroisoquinoline group or a substituted tetrahydrothienopyridine group substituted at the 4-position of the pyrimidine nucleus is a proton pump. The present invention was completed by finding that the inhibitory effect is excellent as well as the mechanism of action of the reversible proton pump inhibition effect.

It is therefore an object of the present invention to provide novel pyrimidine derivatives or pharmaceutically acceptable salts thereof and methods for their preparation. It is also an object of the present invention to provide a pharmaceutical composition based on such a compound.

Hereinafter, the present invention will be described in detail.

The present invention includes providing a novel pyrimidine derivative represented by the following general formula (I) or a pharmaceutically acceptable salt thereof.

Wherein A is 1-substituted-1,2,3,4-tetrahydroisoquinolin-2-yl of formula (II-1) or 7-substituted-4,5,6 of formula (II-2) , 7-tetrahydrothieno [2,3-c] pyridin-6-yl. And R ₁ , R ₂ , R ₆ are hydrogen or C _1-3 alkyl, R ₃ is hydrogen or halogen, R ₄ , R ₅ are the same or different from each other and are hydrogen, C _1-3 alkyl, or ring together To form cyclopentyl or cyclohexyl.

In particular, R ₁ , R ₂ , R ₆ are hydrogen or methyl, R ₃ is hydrogen or fluoro, and R ₄ , R ₅ are the same or different from each other and are each hydrogen, C _1-3 alkyl, or ring together Pyrimidine derivatives, which are cyclopentyl or cyclohexyl, and pharmaceutically acceptable salts thereof have superior proton pump inhibitory effects than among the compounds of the present invention.

According to the substituent of R ₆ in the compound of the present invention, the carbon atom to which they are bonded becomes an asymmetric center. Such compounds are enantiomers, and the compounds of the present invention represented by general formula (I) also include the enantiomers of each of these compounds and mixtures thereof.

Pharmaceutically acceptable non-toxic salts of the compounds of the present invention represented by general formula (I) may include inorganic acid salts, organic acid salts, and the like, for example: hydrochloric acid, maleic acid, sulfate, phosphoric acid (phosphate), mesylene acid (mesylate), nitric acid (nitrate), tartaric acid (tartrate,), fumarate, citric acid (citrate), acetic acid (acetate). In addition, acid addition salts and the like commonly used in the art of anti-ulcer drugs are included. These acid addition salts can be prepared by conventional techniques.

The present invention also includes providing a pyrimidine derivative represented by the following general formula (I) as an intermediate for preparing a compound of general formula (I).

In formula (III), A, R ₄ , and R ₅ are the same as defined above.

The present invention includes providing a method for producing a compound represented by the general formula (I). The compound of this invention represented by general formula (I) can be manufactured by the manufacturing method described next.

Wherein A, R ₁ , R ₂ , R ₃ , R ₄ , R ₅ , R ₆ are the same as defined above.

In the above reaction scheme, the compound of formula (IV) can be easily prepared by applying a known production method (J. Heteroyclic. Chem., 28,231 (1991) or Org. Synth., Coll. Vol. 638) Compounds of the general formulas (V-1) and (V-2) can be prepared according to known methods (European Patent No. 230871).

As described above, the compound of formula (III) is prepared by reacting the compound of formula (IV) in a suitable solvent and base, and then reacted in a suitable solvent by adding the compound of formula (VI). Compounds can be prepared.

Dichloromethane, acetone, acetonitrile, dimethylformamide, etc. are preferable as a solvent for reacting the compound of Formula (IV) with the compound of Formula (V-1) or (V-2). It is preferable to react for 1-24 hours between 150 ℃. Preferred bases are triethylamine, N, N-dimethylaniline, pyridine and the like.

Dimethylformamide, paradioxane, dimethyl sulfoxide, etc. are preferable as a solvent for preparing the compound of the general formula (I) by reacting the compound of the general formula (III) with the compound of the general formula (IV). It is preferable to react for 2-5 hours between ° C.

Furthermore, this invention includes providing the pharmaceutical composition which has a compound of this invention represented by general formula (I) as a main component. The compounds of the present invention represented by general formula (I) may form a pharmaceutical composition with known pharmaceutical carriers or excipients, which may be formulated by known methods. The compounds of the present invention may also be formulated in the form of suspending agents or emulsifying agents in an oily or aqueous medium, and may contain conventional dispersing, suspending or stabilizing agents. In addition, the compounds of the present invention may be in the form of dry powder which is reconstituted before use with sterile, pyrogen-free water.

The compounds of the present invention can be orally and intraperitoneally administered 0.1-500 mg / day, more preferably 1-100-mg / day, per kilogram of body weight of humans and animals with various gastrointestinal ulcers, in unit dosage form or May be contained in a capacity container.

Hereinafter, the present invention will be described in more detail with reference to Examples and Test Examples. However, the present invention is not limited thereto.

Reference Example 1 Preparation of Substituted 1,2,3,4-Tetrahydroisoquinoline

Reference Example 1-1. Preparation of 1-methyl-1,2,3,4-tetrahydroisoquinoline

Step 1. Preparation of N- (2-phenylethyl) acetamide

Dissolve phenethylamine (37.8ml, 0.3mol) and triethylamine (42ml, 0.3mol) in dichloromethane (200ml), and slowly add dropwise acetyl chloride (20.7ml, 0.3mol) to 0 ℃ or lower at room temperature. After stirring for 10 minutes, the reaction solution was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 42.70 g of the title compound as a white solid.

Step 2. Preparation of 1-methyl-3,4-dihydroisoquinoline

The compound (25.30 g, 154.8 mmol) prepared in step 1 was added to polyphosphoric acid (250 g), followed by reaction at 160 ° C. for 1.5 hours with stirring, and then the reaction solution was poured into iced water and neutralized with ammonia water and ethyl. After extracting with acetate, the residue obtained by drying with magnesium sulfate and concentrated under reduced pressure was purified by silica gel column chromatography using methanol dichloromethane (1:20) mixed solution as a developing solvent to prepare 19.50 g of an oily title compound.

Step 3. Preparation of 1-methyl-1,2,3,4-tetrahydroisoquinoline

Sodium borohydride (5.28g, 138mmol) was suspended in ethanol (200ml), the compound prepared in step 2 (19.4g, 133.8mmol) was added and stirred at room temperature for 1 hour, and then the temperature of the reaction solution was 5 After cooling to less than ℃, it was acidified with dilute hydrochloric acid and then made basic with aqueous sodium hydroxide solution and extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous forget-me-not and concentrated under reduced pressure to give 18.50 g of an oily title compound.

Reference Example 1-2. Preparation of (R) -1-methyl-1,2,3,4-tetrahydroisoquinoline

Step 1. Preparation of (R) -1-methyl-4-methylthio-1,2,3,4-tetrahydroisoquinolin-3-one

(R) -1-phenylethylamine (27.85ml, 0.21mol) and triethylamine (30ml, 0.21mol) were dissolved in dichloromethane (200ml) and cooled to 0 ° C., followed by α-chloro-α- (methylthio ) -Acetylchloride (37.8 g, 0.21 mol) was added dropwise at 0 ° C. and stirred at room temperature for 30 minutes, followed by addition of tin (IV) chloride, followed by stirring at room temperature for 30 minutes. The reaction solution was added to ice water, washed with water, and then the organic layer was dehydrated and concentrated to prepare 32.5 g of the title compound as a solid.

Step 2. Preparation of (R) -1-methyl-1,2,3,4-tetrahydroisoquinolin-3-one

Raney-nickel (150 g) was suspended in ethanol (300 ml), and the compound (32.5 g, 0.16 mol) prepared in step 1 was added thereto, followed by stirring at room temperature for 3 days. Raney-nickel was filtered off and the filtrate was concentrated to afford 20 g of the title compound as a solid.

Step 3. Preparation of (R) -1-methyl-1,2,3,4-tetrahydroisoquinoline

Borane-dimethyl sulfide was added dropwise while refluxing the mixed solution of the compound prepared in step 2 (10.0 g, 62 mmol) and tetrahydrofuran (20 ml), followed by heating and refluxing for 1 hour. 6N-HCl (10 ml) was added to the residue to destroy residual borane-dimethyl sulfide, followed by neutralization by addition of 10% -NaOH, followed by extraction with ethyl acetate. The extract was dehydrated and concentrated to give 8.8 g of oily title compound.

Reference Example 1-3. Preparation of (S) -1-methyl-1,2,3,4-tetrahydroisoquinoline

(S) -1-phenylethylamine (25.6 ml, 0.20 mol) and α-chloro-α- (methylthio) -acetyl chloride (34.8 g, 0.22 mol) were used as starting materials. The reaction was carried out in the same manner to obtain 8.5 g of the title compound in the oil phase.

Reference Example 2. Preparation of 7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridine

Step 1. Preparation of 2- (3-thienyl) chloroethane

Thionyl chloride (17 ml, 0.23 mol) was added dropwise to a mixed solution of 2- (3-thienyl) ethanol (22.4 ml, 0.2 mol) and chloroform (60 ml) at a temperature of 10 ° C. or lower, and stirred at room temperature for 1 hour. The residue was concentrated under reduced pressure and concentrated to give 24 g of the title compound by vacuum distillation.

Yield: 81.5%

Step 2.7-Preparation of methyl-6,7-dihydrothieno [2,3-c] pyridine

To the mixed solution of 2- (3-thienyl) chloroethane (20 g, 0.136 mol) and anhydrous acetonitrile (350 ml) prepared in Step 1, tin (IV) chloride (20 ml, 0.17 mol) was added at room temperature for 16 hours. After refluxing and cooling, water was added to destroy the remaining tin (IV) chloride and washed with dichloromethane. The aqueous layer was separated, added with potassium carbonate aqueous solution under ice-cooling to make basic, extracted with dichloromethane, dehydrated and concentrated to give 10.56 g of the title compound.

Yield: 51%

Step 3. Preparation of 7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridine

Sodium borohydride (4.4 g, 116 mmol) in a mixed solution of 7-methyl-6,7-dihydrothieno [2,3-c] pyridine (10.5 g, 69.4 mmol) and ethanol (100 ml) prepared in step 2 ) Was added in small portions at room temperature, stirred for 1 hour, and water was added to the reaction solution, which was then extracted using dichloromethane. The dichloromethane layer was separated, dehydrated and concentrated to give 10.34 g of the title compound.

Yield: 97%

Reference Example 3. Preparation of 2,4-dichloro-6-ethylpyrimidine

Step 1. Preparation of 2-mercapto-6-ethylpyrimidin-4-one

Thiourea (15.22g, 0.2mol) and methyl propionyl acetate (25.1ml, 0.2mol) were added to a mixed solution of sodium methoxide (24g, 0.44mol) and ethanol (180ml), and then methanol was slowly distilled off completely. Water (200 ml) was added to reflux for 30 minutes. Activated charcoal was added to the reaction solution, the mixture was stirred for 5 minutes, filtered, the filtrate was cooled to room temperature, glacial acetic acid was added, and the resulting solid was filtered and dried to obtain 29 g of the title compound.

Yield: 93%

Step 2. Preparation of 2,4-dihydroxy-6-ethylpyrimidine

The mixed solution of 2-mercapto-6-ethylpyrimidin-4-one (29 g, 0.186 mol), chloroacetic acid (33.3 g, 0.352 mol) and water (400 ml) synthesized in Step 1 was refluxed for 14 hours, followed by room temperature. After cooling down, concentrated hydrochloric acid (95 ml) was added to reflux for one day. The reaction solution was cooled to room temperature, concentrated under reduced pressure, and water (500 ml) was added to the residue. The mixture was stirred for 2 hours, filtered, and dried to obtain 11.16 g of the title compound.

Yield: 43%

Step 3. Preparation of 2,4-dichloro-6-ethylpyrimidine

A mixed solution of 2,4-dihydroxy-6-ethylpyrimidine (11.12 g, 79.3 mmol) synthesized in step 2, phosphorus oxychloride (43 ml) and N, N-dimethylaniline (6.6 ml) was mixed for 6 hours. After refluxing, the mixture was cooled to room temperature and then diluted with dichloromethane. Diluted solution was slowly added to ice water not exceeding 0 ° C., extracted with dichloromethane, dehydrated and concentrated to give 13.10 g of an oily title compound.

Yield: 93.3%

Reference Example 4. Preparation of 2,4-dichloro-6-propylpyrimidine

Reaction in the same manner as in Reference Example 3 using sodium methoxide (24 g, 0.44 mol), thiourea (15.22 g, 0.2 mol), ethyl butyryl acetate (31.6 ml, 0.2 mol) and ethanol (180 ml) as starting materials 10.5 g of an oily title compound was obtained.

Reference Example 5. Preparation of 2,4-dichloro-5-methyl-6-ethylpyrimidine

Sodium methoxide (24 g, 0.44 mol), thiourea (15.22 g, 0.2 mol), ethyl 2-propionylpropionate (31.6 ml, 0.2 mol) and ethanol (180 ml) were used as starting materials. The reaction was carried out in the same manner to obtain 16.5 g of an oily title compound.

Example 1

Preparation of 2- (2-methyl-4-fluorophenylamino) -4 (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Step 1. Preparation of 4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

2,4-dichloropyrimidine (3-0 g, 20 mmol), 1-methyl-1,2,3,4-tetrahydroisoquinoline (3.3 g, 22 mmol) prepared in Reference Example 1-1, triethylamine ( 3.4 ml, 24.4 mmol) and a mixture of N, N-dimethylformamide (20 ml) were stirred at room temperature for 5 hours, and then the reaction solution was diluted with dichloromethane and washed several times with water. The dichloromethane layer was separated, dehydrated using anhydrous forget-me-not, concentrated under reduced pressure, and the residue was separated and purified using a silica gel column to obtain 1.5 g of the title compound.

Yield: 28.9%

Step 2. Preparation of 2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

2- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.5 g, 5.8 mmol) and dimethylformamide (10 ml) in a mixed solution of 2- After adding methyl-4-fluoroaniline (1.1 ml, 10.2 mmol), the mixture was stirred for 3 hours at a temperature between 110-120 ° C., the reaction solution was cooled to room temperature, diluted with dichloromethane, and washed with water. The dichloromethane layer was separated, added with sodium hydroxide aqueous solution to make basic, washed with water, and then concentrated by dehydration. The residue was purified by silica gel column and dissolved in ethyl ether. Filtration gave 1,2g of the title compound.

Example 2

Preparation of 6-methyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Step 1. Preparation of 6-methyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

6-methyl-2,4-dichloropyrimidine (6.52g, 40mmol), 1-methyl-1,2,3,4-tetrahydroisoquinoline (6.6g, 44mmol) prepared in Reference Example 1-1, tri Ethylamine (6.8 ml, 48.8 mmol) and N, N-dimethylformamide (30 ml) were used as starting materials and reacted in the same manner as in Step 1 of Example 1 to obtain 5.5 g of the title compound.

Yield: 50.2%

Step 2. 6-Methyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochlor Manufacture of lead

Mixture of 6-methyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.5 g, 5.5 mmol) with dimethylformamide (10 ml) 2-methyl-4-fluoroaniline (1.1 ml, 10.2 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 1.2 g of the title compound.

Example 3

Preparation of 6-methyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2- (4-fluorophenylamino) pyrimidine hydrochloride

Mixture of 6-methyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.5 g, 5.5 mmol) with dimethylformamide (10 ml) 4-fluoroaniline (0.8 ml, 8.4 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 1.5 g of the title compound.

Example 4

Preparation of 6-methyl-2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Mixture of 6-methyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.5 g, 5.5 mmol) with dimethylformamide (10 ml) N-methylaniline (0.9 ml, 8.4 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 1.2 g of the title compound.

Example 5

Preparation of 6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Step 1. Preparation of 6-ethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

6-ethyl-2,4-dichloropyrimidine (4.9 g, 27.7 mmol) prepared in Reference Example 3, 1-methyl-1,2,3,4-tetrahydroisoquinoline prepared in Reference Example 1-1 ( 4.1 g, 27.8 mmol), triethylamine (4.7 ml, 33.7 mmol) and N, N-dimethylformamide (20 ml) were reacted in the same manner as Step 1 of Example 1, using 5.58 g of the title. The compound was obtained.

Yield: 70%

Step 2. 6-Ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochlor Manufacture of lead

Mixture of 6-ethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.0 g, 3.47 mmol) with dimethylformamide (5 ml) 2-Methyl-4-fluoroaniline (0.77ml, 6.93mmol) was added to the solution, followed by reaction as in Step 2 of Example 1 to obtain 0.92g of the title compound.

Example 6

Preparation of 6-ethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Mixture of 6-ethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.57 g, 1.98 mmol) with dimethylformamide (5 ml) 4-fluoroaniline (0.38 ml, 4.01 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.17 g of the title compound.

Example 7

Preparation of 6-ethyl-2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

6-ethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.61 g, 2.12 mmol) and dimethylformamide (5 ml) N-methylaniline (0.46 ml, 4.25 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.50 g of the title compound.

Example 8

Preparation of 6-ethyl-2- (2: methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

6-ethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.61 g, 2.12 mmol) and dimethylformamide (5 ml) 2-methylaniline (0.46 ml, 4.31 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.52 g of the title compound.

Example 9

Preparation of 2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propylpyrimidine hydrochloride

Step 1. Preparation of 4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propyl-2-chloropyrimidine

2,4-dichloro-6-propylpyrimidine (1.8 g, 9.4 mmol) prepared in Reference Example 4, 1-methyl-1,2,3,4-tetrahydroisoquinoline prepared in Reference Example 1-1 ( 1.6 g, 10.9 mmol), triethylamine (1.6 ml, 11.5 mmol) and N, N-dimethylformamide (20 ml) were reacted in the same manner as in Step 1 of Example 1, using 1.6 g of the title. The compound was obtained.

Yield: 56.4%

Step 2. 2- (2-Methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propylpyrimidine hydrochloro Manufacture of lead

Mixture of 4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propyl-2-chloropyrimidine (0.5 g, 1.66 mmol) with dimethylformamide (5 ml) 4-fluoro-2-methylaniline (0.35 ml, 3.15 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.2 g of the title compound.

Example 10

Preparation of 4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propyl-2- (4-fluorophenylamino) pyrimidine hydrochloride

Mixture of 4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propyl-2-chloropyrimidine (0.5 g, 1.66 mmol) with dimethylformamide (5 ml) 4-fluoroaniline (0.27 ml, 2.85 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.3 g of the title compound.

Example 11

Preparation of 2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propylpyrimidine hydrochloride

Mixture of 4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propyl-2-chloropyrimidine (0.5 g, 1.66 mmol) with dimethylformamide (5 ml) N-methylaniline (0.27ml, 2.49mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.5g of the title compound.

Example 12

5,6-dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride Manufacture

Step 1. Preparation of 5,6-dimethyl-2,4-dichloropyrimidine

A mixed solution of 5,6-dimethyl-2,4-dihydroxypyrimidine (72 g, 0.51 mol), phosphorus oxcyclolide (250 ml) and N, N-dimethylaniline (41 ml) was refluxed for 3 hours. The reaction solution was slowly added to ice water, and the resulting solid was filtered and then recrystallized from dichloromethane to give 54.3 g of the title compound.

Yield: 60%

Step 2. Preparation of 5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

Start 5,6-dimethyl-2,4-dichloropyrimidine (4.3 g, 24 mmol) and 1-methyl-1,2,3,4-tetrahydroisoquinoline (3.9 g, 26.4 mmol) prepared in step 1 4.17 g of the title compound was obtained by reacting in the same manner as Step 1 of Example 1 as a material.

Yield: 60.4%

Step 3. 5,6-Dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine Preparation of Hydrochloride

5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.4 g, 4.8 mmol) prepared in step 2, 2 -Methyl-4-fluoroaniline (1.1ml, 9.9mmol) was added and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 1.35 g of the title compound.

Example 13

(R) -5,6-dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyridine Preparation of Midine Hydrochloride

Step 1. Preparation of (R) -5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

(R) -1-methyl-1,2,3,4-tetrahydroisoquinoline (3.9 g, 26.4 mmol) and 5,6-dimethyl-2,4-dichloropyridine (4.3) synthesized in Reference Example 1-2 g, 24 mmol) was reacted in the same manner as Step 1 of Example 1 to obtain 4.35 g of the title compound.

Yield: 63%

Step 2. (R) -5,6-Dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinoline-2- (1) Preparation of pyrimidine hydrochloride

(R) -5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine prepared in Step 1 (1.4 g, 4.8 mmol) and 2-methyl-4-fluoroaniline (1.1 ml, 9.9 mmol) were added and reacted in the same manner as in Step 2 of Example 1, to obtain 1.10 g of the title compound.

Example 14

(S) -5,6-dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyridine Preparation of Midine Hydrochloride

Step 1. Preparation of (S) -5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

(S) -1-methyl-1,2,3,4-tetrahydroisoquinoline (3.9 g, 26.4 mmol) and 5,6-dimethyl-2,4-dichloropyridine (4.3) synthesized in Reference Example 1-2 g, 24 mmol) was reacted in the same manner as Step 1 of Example 1 to obtain 4.2 g of the title compound.

Yield: 60.8%

Step 2. (S) -5,6-Dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinoline-2- (1) Preparation of pyrimidine hydrochloride

(S) -5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine prepared in step 1 (1.4 g, 4.8 mmol) and 2-methyl-4-fluoroaniline (1.1 ml, 9.9 mmol) were added and reacted in the same manner as in Step 2 of Example 1, to obtain 0.90 g of the title compound.

Example 15

Preparation of 5,6-dimethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.4 g, 4.8 mmol) and dimethylformamide (10 ml) 4-fluoroaniline (1.0 ml, 10 mmol) was added to the mixed solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 1.32 g of the title compound.

Example 16

(R) -5,6-dimethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride Manufacture

(R) -5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.4 g, 4.8 mmol) and dimethylform 4-fluoroaniline (1 ml, 10 mmol) was added to the mixed solution of amide (10 ml), and the reaction was carried out in the same manner as in Step 2 of Example 1, to obtain 1.20 g of the title compound.

Example 17

(S) -5,6-dimethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride Manufacture

(S) -5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.4 g, 4.8 mmol) with dimethylform 4-fluoroaniline (1 ml, 10 mmol) was added to the mixed solution of amide (10 ml), and the reaction was carried out in the same manner as in Step 2 of Example 1, to obtain 1.50 g of the title compound.

Example 18

Preparation of 5,6-dimethyl-2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1,9 g, 6.6 mmol) with dimethylformamide (10 ml N-methylaniline (1.5ml, 14mmol) was added to the mixed solution, and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.25 g of the title compound.

Example 19

Preparation of (R) -5,6-dimethyl-2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

(R) -5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.4 g, 4.8 mmol) and dimethylform N-methylaniline (1.04ml, 9.6mmol) was added to the mixed solution of amide (10ml), and the reaction was carried out in the same manner as in Step 2 of Example 1, to obtain 0.55g of the title compound.

Example 20

Preparation of (S) -5,6-dimethyl-2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

(S) -5,6-dimethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.4 g, 4.8 mmol) with dimethylform N-methylaniline (1.04ml, 9.6mmol) was added to the mixed solution of amide (10ml), and the reaction was carried out in the same manner as in Step 2 of Example 1, to obtain 0.70g of the title compound.

Example 21

5-methyl-6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydro Preparation of Chloride

Step 1. Preparation of 5-methyl-6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

2,4-dichloro-5-methyl-6-ethylpyrimidine (2.7 g, 14.1 mmol) prepared in Reference Example 5 and methyl-1,2,3,4-tetrahydroisoisode prepared in Reference Example 1-1 Using quinoline (2.3 g, 15.6 mmol) as a starting material, the reaction was carried out in the same manner as in Step 1 of Example 1, to obtain 2.3 g of the title compound.

Yield: 54%

Step 2. 5-Methyl-6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) Preparation of Pyrimidine Hydrochloride

Mixture of 5-methyl-6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.80 g, 2.65 mmol) with dimethylformamide (5 ml) 4-fluoro-2-methylaniline (0.55ml, 4.95mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.25 g of the title compound.

Example 22

Preparation of 5-methyl-6-ethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

5-methyl-6-ethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.80 g, 2.65 mmol) and dimethylformamide ( 4-fluoroaniline (0.50ml, 5.28mmol) was added to the mixed solution of 5ml) and reacted in the same manner as in Step 2 of Example 1, to obtain 0.55g of the title compound.

Example 23

Preparation of 5-methyl-6-ethyl-2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

5-methyl-6-ethyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.80 g, 2.65 mmol) and dimethylformamide ( N-methylaniline (0.44ml, 4.06mmol) was added to the mixed solution of 5ml), and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.60g of the title compound.

Example 24

2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] pyrimidinehydrochloride Produce

Step 1. Preparation of 2-amino-4-hydroxycyclopenta [d] pyrimidine

To a mixed solution of sodium methoxide (83.2 g, 0.44 mol) and N, N-dimethylformamide (80 ml), 2-ethoxycarbonyl cyclopentanone (114 ml, 0.77 mol) was added to N, N-dimethylformamide (40 ml The solution dissolved in) is slowly added at 0 ° C or lower. To the reaction solution, a solution of guanidine hydrochloride (81 g, 0.85 mol) dissolved in methanol (127 ml) was added, refluxed for 14 hours, neutralized with concentrated hydrochloric acid, and the resulting solid was filtered and dried to obtain 20.69 g of the title compound. Got.

Yield: 18%

Step 2. Preparation of 2,4-dihydroxycyclopenta [d] pyrimidine

Sodium nitrite (19.4 g) was dissolved in water in a mixed solution of 2-amino-4-hydroxycyclopenta [d] pyrimidine (20.6 g, 0.136 mol) and 20% hydrochloric acid (62 ml) synthesized in step 1 The mixture was slowly added over 4 hours while maintaining at 70 ° C, and then cooled to 0 ° C. The resulting solid was filtered and dried to obtain 15.43 g of the title compound.

Yield: 74.6%

Step 3. Preparation of 2,4-dichlorocyclopenta [d] pyrimidine

Mixed solution of 2,4-dihydroxycyclopenta [d] pyrimidine (15.4 g, 0.1 mol) synthesized in Step 2, phosphoroxoxcyclolide (49 ml) and N, N-dimethylaniline (8.0 ml) Was refluxed for 3 hours, then cooled to room temperature and diluted with dichloromethane. The diluent was slowly added to ice at 10 ° C., extracted with dichloromethane, dehydrated and concentrated to give 2.8 g of the oily title compound.

Yield: 15%

Step 4. Preparation of 4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chlorocyclopenta [d] pyrimidine

2,4-dichlorocyclopenta [d] pyrimidine (2.0 g, 10.5 mmol) prepared in step 3 and 1-methyl-1,2,3,4-tetrahydroisoquinoline prepared in Reference Example 1-1 ( 1.7g, 11.55mmol) was used as a starting material and reacted in the same manner as in Step 1 of Example 1, to obtain 1.95g of the title compound.

Yield: 62%

Step 5. 2- (2-Methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] pyrimidine hydro Preparation of Chloride

4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chlorocyclopenta [d] pyrimidine (0.50 g, 1.70 mmol) and dimethylformamide (5 ml) 4-Fluoro-2-methylaniline (0.40ml, 3.60 mmol) was added to the mixed solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.15 g of the title compound.

Example 25

Preparation of 2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] pyrimidine hydrochloride

4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chlorocyclopenta [d] pyrimidine (0.60 g, 2.0 mmol) and dimethylformamide (5 ml) 4-fluoroaniline (0.40ml, 4.2mmol) was added to the mixed solution, and the reaction was carried out in the same manner as in Step 2 of Example 1, to obtain 0.11 g of the title compound.

Example 26

Preparation of 2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] pyrimidine hydrochloride

4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chlorocyclopenta [d] pyrimidine (0.51 g, 1.70 mmol) and dimethylformamide (5 ml) N-methylaniline (0.20ml, 1.90mmol) was added to the mixed solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.20g of the title compound.

Example 27

2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydro Preparation of quinazoline hydrochloride

Step 1. Preparation of 2,4-dihydroxy-5,6,7,8-tetrahydroquinazoline

Hydrogen was added to a mixed solution of 2,4-dihydroxyquinazolin (39.2 g, 0.24 mol), platinum oxide (4 g), and trifluoroacetic acid (300 mL) for 2 hours, followed by filtration of platinum oxide. The filtrate was concentrated under reduced pressure, and the resulting residue was diluted with water, made basic with 1N aqueous caustic soda solution, and the resulting solid was filtered and dried to yield 13.76 g of the title compound.

Yield: 34.5%

Step 2. Preparation of 2,4-dichloro-5,6,7,8-tetrahydroquinazoline

2,4-dihydroxy-5,6,7,8-tetrahydroquinazolin (3.4 g, 20 mmol) synthesized in step 1 was replaced with phosphorous oxcyclolide (10 mL) and N, N-dimethylaniline (0.8 mL). The mixture was suspended in), refluxed for 3 hours, and the reaction solution was slowly added dropwise to ice water. The resulting solid was filtered and dried to yield 3.26 g of the title compound.

Yield: 80%

Step 3. Preparation of 4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloro-5,6,7,8-tetrahydroquinazoline

2,4-dichloro-5,6,7,8-tetrahydroquinazoline (3.2 g, 15.8 mmol) synthesized in step 2, 1-methyl-1,2,3,4 prepared in Reference Example 1-1 A mixture of tetrahydroisoquinoline (2.6 g, 17.4 mmol), triethylamine (2.8 mL) and N, N-dimethylformamide (20 mL) was stirred at 80 ° C. for 3 hours, and then the reaction solution was cooled. After dilution with ethyl acetate, the mixture was washed with water, and then the organic layer was separated, dehydrated and concentrated. The resulting residue was separated using silica gel column chromatography to obtain 3.1 g of the title compound.

Yield: 62.5%

Step 4. 2- (2-Methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8 Preparation of Tetrahydroquinazoline Hydrochloride

4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloro-5,6,7,8-tetrahydroquinazoline (0.75 g, 2.40 mmol) and dimethyl 4-fluoro-2-methylaniline (0.60 ml, 5.4 mmol) was added to the mixed solution of formamide (5 ml), and the reaction was carried out in the same manner as in Step 2 of Example 1, to obtain 0.58 g of the title compound.

Example 28

2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydroquinazoline hydrochloride Produce

4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloro-5,6,7,8-tetrahydroquinazoline (0.75 g, 2.40 mmol) and dimethyl N-methylaniline (0.50 ml, 4.8 mmol) was added to the mixed solution of formamide (5 ml), and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.26 g of the title compound.

Example 29

Preparation of 6-methyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Step 1. Preparation of 6-methyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

6-methyl-2,4-dichloropyrimidine (3.26 g, 20 mmol), 1,2,3,4-tetrahydroisoquinoline (2.6 ml, 20.5 mmol), triethylamine (3.4 ml, 24.4 mmol) and N , N-dimethylformamide (10 ml) was used as a starting material and reacted in the same manner as in Step 1 of Example 1, to obtain 3.1 g of the title compound.

Yield: 59.7%

Step 2. Preparation of 6-methyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

To a mixed solution of 6-methyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.0 g, 3.8 mmol) and dimethylformamide (10 ml), 2- Methyl-4-fluoroaniline (0.8 ml, 7.2 mmol) was added, followed by the same procedure as in Step 2 of Example 1 to obtain 0.85 g of the title compound.

Example 30

Preparation of 6-methyl-2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

To a mixed solution of 6-methyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.0 g, 3.8 mmol) and dimethylformamide (10 ml), 4- Fluoroaniline (0.7 ml, 7.4 mmol) was added and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.6 g of the title compound.

Example 31

Preparation of 6-methyl-2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

N- in a mixed solution of 6-methyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.95 g, 3.65 mmol) and dimethylformamide (10 ml) Methyl aniline (0.61ml, 5.48mmol) was added and reacted in the same manner as in Step 2 of Example 1 to obtain 0.7g of the title compound.

Example 32

Preparation of 6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Step 1. Preparation of 6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

6-ethyl-2,4-dichloropyrimidine (4.9g, 27.7mmol) prepared in Reference Example 3, 1,2,3,4-tetrahydroisoquinoline (3.5ml, 28mmol), triethylamine (3.9ml , 28 mmol) and N, N-dimethylformamide (20 ml) were reacted in the same manner as in Step 1 of Example 1 to obtain 5.0 g of the title compound.

Yield: 66%

Step 2. Preparation of 6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

To a mixed solution of 6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.7 g, 2.56 mmol) and dimethylformamide (5 ml), 2- Methyl-4-fluoroaniline (0.57ml, 5.13mmol) was added and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.55g of the title compound.

Example 33

Preparation of 6-ethyl-2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

To a mixed solution of 6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.7 g, 2.56 mmol) and dimethylformamide (5 ml), 4- Fluoroaniline (0.50 ml, 5.28 mmol) was added and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.41 g of the title compound.

Example 34

Preparation of 6-ethyl-2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.7 g, 2.56 mmol) and dimethylformamide (5 ml) in a mixed solution of N- Methyl aniline (0.54 ml, 5.15 mmol) was added and reacted in the same manner as in Step 2 of Example 1 to obtain 0.56 g of the title compound.

Example 35

Preparation of 6-ethyl-2- (2-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

To a mixed solution of 6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.7 g, 2.56 mmol) and dimethylformamide (5 ml), 2- Methyl aniline (0.55ml, 5.15mmol) was added and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.23 g of the title compound.

Example 36

Preparation of 5,6-dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Step 1. Preparation of 5,6-dimethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

5,6-dimethyl-2,4-dichloropyrimidine (3.8 g, 21 mmol) and 1,2,3,4-tetrahydroisoquinoline (2.9 g, 23 mmol) prepared in Step 1 of Example 12 were used as starting materials. The reaction was carried out in the same manner as in Step 1 of Example 1, to obtain 3.95 g of the title compound.

Yield: 68.7%

Step 2. 5,6-Dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride Produce

To a mixed solution of 5,6-dimethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.0 g, 3.6 mmol) and dimethylformamide (10 ml) 4-Fluoro-2-methylaniline (0.8 ml, 7 mmol) was added and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.58 g of the title compound.

Example 37

Preparation of 5,6-dimethyl-2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

To a mixed solution of 5,6-dimethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.0 g, 3.6 mmol) and dimethylformamide (5 ml) 4-fluoroaniline (0.7 ml, 7.4 mmol) was added thereto, and the reaction was carried out in the same manner as in Step 2 of Example 1, obtaining 0.67 g of the title compound.

Example 38

Preparation of 5,6-dimethyl-2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

To a mixed solution of 5,6-dimethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (1.0 g, 3.6 mmol) and dimethylformamide (5 ml) N-methylaniline (0.84ml, 7.8mmol) was added and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.55g of the title compound.

Example 39

Preparation of 5-methyl-6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

step. Preparation of 5-methyl-6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine

2,4-dichloro-5-methyl-6-ethylpyrimidine (4.9 g, 27.7 mmol) and 1,2,3,4-tetrahydroisoquinoline (3.5 ml, 28 mmol) prepared in Reference Example 5 were used as starting materials. The reaction was carried out in the same manner as in Step 1 of Example 1, to obtain 5.0 g of the title compound.

Yield: 66%

Step 2. 5-Methyl-6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochlor Manufacture of lead

Mixture of 5-methyl-6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.7 g, 2.4 mmol) with dimethylformamide (5 ml) 4-fluoro-2-methylaniline (0.5 ml, 3.6 mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.53 g of the title compound.

Example 40

Preparation of 5-methyl-6-ethyl-2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Mixture of 5-methyl-6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.7 g, 2.4 mmol) with dimethylformamide (5 ml) 4-fluoroaniline (0.45ml, 3.6mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.50g of the title compound.

Example 41

Preparation of 5-methyl-6-ethyl-2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine hydrochloride

Mixture of 5-methyl-6-ethyl-4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloropyrimidine (0.7 g, 2.4 mmol) with dimethylformamide (5 ml) N-methylaniline (0.40ml, 3.6mmol) was added to the solution, followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.50g of the title compound.

Example 42

Preparation of 2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] pyrimidine hydrochloride

Step 1. Preparation of 4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chlorocyclopenta [d] pyrimidine.

2,4-dichlorocyclopenta [d] pyrimidine (0.79 g, 4 mmol) and 1,2,3,4-tetrahydroisoquinoline (0.5 ml, 4 mmol) prepared in Step 3 of Example 24 were used as starting materials. The reaction was carried out in the same manner as in Step 1 of Example 1, to obtain 0.58 g of the title compound.

Yield: 51%

Step 2. Preparation of 2- (2-methyl-4-fluorophenylamino) -2- (1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] pyrimidine hydrochloride

To a mixed solution of 4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -4-chlorocyclopenta [d] pyrimidine (0.58 g, 2.0 mmol) and dimethylformamide (5 ml), add 4 -Fluoro-2-methylaniline (0.25ml, 2.20mmol) was added thereto and reacted in the same manner as in Step 2 of Example 1, obtaining 0.34 g of the title compound.

Example 43

2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydrquinazoline hydrochlor Manufacture of lead

Step 1. Preparation of 4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloro-5,6,7,8-tetrahydroquinazolin hydrochloride

2,4-dichloro-5,6,7,8-tetrahydroquinazoline (4.0 g, 20 mmol) synthesized in step 2 of Example 27, 1,2,3,4-tetrahydroisoquinoline (2.8 ml, 22 mmol), triethylamine (3.4 mL, 24 mmol) and N, N-dimethylformamide (10 mL) were used for the reaction in the same manner as in Example 1, Step 1 to obtain 4.7 g of the title compound.

Yield: 78.4%

Step 2. 2- (2-Methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydroquina Preparation of Sleepy Hydrochloride

4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloro-5,6,7,8-tetrahydroquinazolin (0.90 g, 3.0 mmol) with dimethylformamide (5 ml 4-fluoro-2-methylaniline (0.75 ml, 6.6 mmol) was added to the mixed solution, and the resulting mixture was reacted in the same manner as in Step 2 of Example 1, obtaining 0.36 g of the title compound.

Example 44

Preparation of 2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydroquinazoline hydrochloride

4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloro-5,6,7,8-tetrahydroquinazolin (0.90 g, 3.0 mmol) with dimethylformamide (5 ml 4-fluoroaniline (0.60 ml, 6.3 mmol) was added to the mixed solution, and the resulting mixture was reacted in the same manner as in Step 2 of Example 1, obtaining 0.62 g of the title compound.

Example 45

Preparation of 2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydroquinazoline hydrochloride

4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloro-5,6,7,8-tetrahydroquinazolin (0.90 g, 3.0 mmol) with dimethylformamide (5 ml N-methylaniline (0.70ml, 6.3mmol) was added to the mixed solution, and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.48g of the title compound.

Example 46

Preparation of 2- (2-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydroquinazoline hydrochloride

4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -2-chloro-5,6,7,8-tetrahydroquinazolin (0.75 g, 2.5 mmol) with dimethylformamide (5 ml 2-methylaniline (0.30ml, 2.7mmol) was added to the mixed solution, and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.50g of the title compound.

Example 47

6-methyl-2- (2-methyl-4-fluorophenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl Preparation of Pyrimidine Hydrochloride

Step 1. Preparation of 6-Methyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -2-chloropyrimidine

2,4-dichloro-6-methylpyrimidine (3.1 g, 19 mmol), 7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridine (2.9 synthesized in Reference Example 2) g, 19 mmol) was used as a starting material, and the reaction was carried out in the same manner as in Step 1 of Example 1, to obtain 2.2 g of the title compound as white crystals.

Yield: 41%

Step 2. 6-Methyl-2- (2-methyl-4-fluorophenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridine- Preparation of 6-yl) pyrimidine hydrochloride

6-methyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -2-chloropyrimidine (0.7 g, 2.5 mmol) and 4-fluoro-2-methylaniline (0.5 ml, 4.6 mmol) was added to the mixed solution of dimethylformamide (10 ml), and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.45 g of the title compound.

Example 48

6-methyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -2- (4-fluorophenylamino) pyrimidine hydro Preparation of Chloride

6-methyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -2-chloropyrimidine (0.7 g, 2.5 mmol) and 4-fluoroaniline (0.4 ml, 3.7 mmol) was added to the mixed solution of dimethylformamide (10 ml), followed by reaction in the same manner as in Step 2 of Example 1 to obtain 0.7 g of the title compound.

Example 49

6-methyl-2- (N-methylphenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) pyrimidine hydrochloride Manufacture

6-methyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -2-chloropyrimidine (0.75 g, 2.7 mmol) and N-methylaniline (0.45ml, 4.05mmol) was added to the mixed solution of dimethylformamide (10ml) and the reaction was carried out in the same manner as in Step 2 of Example 1 to obtain 0.52g of the title compound.

Example 50

5,6-dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridine-6 Preparation of -yl) pyrimidine hydrochloride

Step 1. Preparation of 5,6-dimethyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -2-chloropyrimidine

5,6-dimethyl-2,4-dichloropyrimidine (2.8 g, 16 mmol) prepared in Step 1 of Example 12, 7-methyl-4,5,6,7-tetrahydrothier prepared in Reference Example 2 Method as in Step 1 of Example 1 using no [2,3-c] pyridine (2.7 g, 17.6 mmol), triethylamine (2.7 ml) and N, N-dimethylformamide (20 ml) as starting materials Reaction yielded 1.85 g of the title compound.

Yield: 39.4%

Step 2. 5,6-Dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] Preparation of Pyridin-6-yl) pyrimidine hydrochloride

5,6-dimethyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -2-chloropyrimidine (0.68 g, 2.3 mmol ) And 4-fluoro-2-methylaniline (0.5 ml, 4.6 mmol) were added to the mixed solution of dimethylformamide (5 ml), and the reaction was carried out in the same manner as in Step 2 of Example 1, to obtain 0.12 g of the title compound. .

Example 51

5-methyl-2- (2-methyl-4-fluorophenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl ) -6-ethylpyrimidine hydrochloride

Step 1. 5-Methyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -6-ethyl-2-chloropyrimidine Produce

2,4-dichloro-5-methyl-6-ethylpyrimidine (2.7 g, 14.1 mmol) prepared in Reference Example 5, 7-methyl-4,5,6,7-tetrahydrothier prepared in Reference Example 2 Method as in Step 1 of Example 1 using no [2,3-c] pyridine (2.4 g, 15.7 mmol), triethylamine (2.2 ml) and N, N-dimethylformamide (20 ml) as starting materials Reaction to obtain 2.23 g of the title compound.

Yield: 51.3%

Step 2. 5-Methyl-2- (2-methyl-4-fluorophenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridine- Preparation of 6-yl) -6-ethylpyrimidine hydrochloride

5-methyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -6-ethyl-2-chloropyrimidine (0.74 g, 2.4 mmol) and 4-fluoro-2-methylaniline (0.51 ml, 4.59 mmol) were added to the mixed solution of dimethylformamide (5 ml), followed by reaction in the same manner as in Step 2 of Example 1 to 0.15 g of the title compound. Got.

Test Example 1. Inhibitory Effect of Proton Pump (H ⁺ / K ⁺ ATPase)

1-1 Preparation of Proton Pump Enzyme Source

Newzealand white rabbits were killed and the stomachs were excised to collect wall cells of the lining of the stomach and homogenized with Teflon glass homogenizer on 0.25M sucrose buffer. Centrifuge the homogenate at 10,000 g for 30 minutes and supernatant again at 100,000 g for 1 hour at ultrafast centrifugation (Beckman Ultracentrifuge 18-80 model sw28 Tirotor) to discard the supernatant, and settle the pellet to pH 6.4. After suspension in 50 mM Tris hydrochloric acid buffer solution, 1 ml each was dispensed into tubes and frozen in liquid nitrogen. The whole process was carried out at 4 ℃. This microsome was used as an enzyme source for performing in vitro enzyme reaction studies of proton pumps.

1-2 proton pump activity measurement

The inhibitory effect of proton pump activity on the compounds of the present invention was determined by an in vitro enzyme reaction study. That is, the compounds of the present invention were treated with magnesium ion (Mg ⁺⁺ ) stimulated proton pump activity as negative control group and magnesium ion (Mg ⁺⁺ ) and potassium ion (K ⁺ ) stimulated proton pump activity as positive control group. The degree of proton pump inhibition was measured. Omeprazole was used as a comparative drug.

The test tube was divided into four groups, the first group was negative control group (n = 3), the second group was positive control group (n = 3), the third group was the test substance administration group (n = 5x2), and the fourth group was compared. It was set as the compound administration group (n = 5x2). Herein, groups 3 and 4 were dissolved in dimethyl sulfoxide (DMSO) and the compound prepared in Example and omeprazole, respectively, were prepared at five concentrations to measure the inhibitory effect of proton pump activity.

100 μl of 4 mM magnesium chloride and 100 μl of the enzyme source prepared in Test Example 1-1 were added to the 1, 2, 3, and 4 groups, respectively, and 50 mM of each of the 2, 3, and 4 groups except the first group. 50 [mu] l of potassium chloride and 6 mM ammonium chloride were added. 10 μl of dimethyl sulfoxide was added to the first and second groups, and the solution prepared in Example 5 was dissolved in dimethyl sulfoxide, and 10 μl of the solution prepared in five concentrations was used for each of the third group. 2 each) to each of the test group. In addition, a solution of five concentrations (37.6, 21.4, 12.1, 7.0, and 4.0 μM) prepared by dissolving omeprazole in dimethyl sulfoxide was added to each of four (2 each) test tube subgroups of each concentration of 10 μl. Then 40 mM Tris. Hydrochloric acid buffer solution at pH 6.0 was added to adjust the total volume of the 1,2,3,4 groups to 40 mM. The preparation of each of all reactive components was also made using 40 mM Tris. Hydrochloric acid buffer solution at pH6.0. After the treatment as described above, the test tubes of each group were preincubated for 30 minutes in a 37 ° C. water bath, and then 100 μl of 6.6 mM ATP solution was added so that the final reaction volume was 500 μl. After reacting at 37 ° C. for 30 minutes, the enzyme reaction was stopped by adding 100 µl of cold 25% trichloroacetic acid, and the free inorganic phosphorus was quantified by an automatic analyzer (Express 550, Corning). The difference between the first group and the second group was taken as the activity of the proton pump stimulated with K ⁺ ions, and based on this value, the effect of the activity on the proton pump appearing at each concentration of the third group and the fourth group was%. Calculated by value. The effect of each of the five concentrations in Groups 3 and 4 on proton pump activity was analyzed using the Litchfield-wilcoxon equation (J. Pharmacol. Exp. Ther. (1949) 96, 99). The concentration of the test substance and the comparative substance (IC ₅₀ ) that inhibits the proton pump activity by 50% was calculated, and the ratio of the third group IC ₅₀ to the fourth group is shown in Table 1.

[Test Example 2. Basic gastric acid secretion inhibitory effect]

(Shay's rat model, Shay, H., et al., (1945) Gastroenterology 5,43-61)

200 ± 10g of Sprague-Dawley male rats were divided into three groups (n = 5) and fasted with water for 24 hours. Anesthetized with ether, the abdominal cavity was dissected and ligation was performed. In the first group, 30% polyethylene glycol 400 aqueous solution was administered at 0.5 ml / 200 g as a control, and in the second and third groups, the compound prepared in Example and omeprazole were suspended in 30% polyethylene glycol 400 aqueous solution at 20 mg / kg concentration, respectively. Was injected into the duodenum (0.5 ml / 200 g).

The abdominal cavity was sutured again, and after 5 hours, it was lethal by the cervical thoracotomy. After centrifugation of the obtained gastric liquid at 1,000g for 20 minutes to remove the precipitate, the amount of gastric juice and acidity (acidity) was measured. Relative volume, relative concentration and relative acid output were calculated by the following equation and the results are shown in Table 2.

* Relative volume fraction of test substance (Equation I)

= (Average gastric juice in group 1-average gastric juice in group 2) / (average gastric juice in group 1-average gastric juice in group 3)

* Relative acid concentration rate of test substance (Equation II)

= (Average pH of group 1-average acidity of group 2) / (average pH of group 1-average acidity of group 3)

* Relative total gastric acid secretion rate of the test substance (Equation III)

= (Total gastric acid secretion in group 1-total gastric acid secretion in group 2) / (Total gastric acid secretion in group 1-total gastric acid secretion in group 1)

Test Example 3 Reversibility Test

3-1 Preparation of Gastric vesicles

Gastric vesicles are described by Saccomani et al. (Saccomani, G. Sach, G. cha racterization of gastric mucosal membranes, VIII.The localization of peptides by iodination and phosphorylation. J. Biol. , 1975). The prepared gastric vesicles were lyophilized to be lyophilized vesicles (Lyophilized vesicle) and stored at -70 ° C. Protein quantification was performed according to the Lowry method, and bovine serum albumin was used as a reference (Lowry, OH, Rosebrough, NJ and Randall, RJ protein measurement with the folin phenol reagent. J. Biol. Chem. 193,265-275,1951.)

3-2. Reversibility of inhibition

The inhibitory mechanism for the proton pump activity of the compounds of the present invention is based on the Dilution Washout method (D.J. keeling, R.C. Malcolm, S.M.Laing, R.J.Ife SKF96067 is a reversible, lumenally acting inhibitor of the gastric (H / K ) -ATPase, Biochemical Phamacol., 42 (1) 123-130,1991).

That is, the test tubes were divided into non-diluting groups and dilution groups to evaluate reversibility, and the two groups were divided into four subgroups. 90 ml of 5 mM pipes / tris buffer solution and 10 ml of DMSO were added to the first and second subgroups of the diluted and undiluted groups, and 90 ml of 5 mM pipes / tris buffer solution was added to the third and fourth subgroups. 10 μl of the compound prepared in 50 μM Example 38 was added, and lyophilized vesicles prepared in Test Example 4-1 were prepared at 100 μg protein / ml in all groups, and 100 μl was added for 15 minutes. Preincubation was performed in a 37 ° C. incubator. After 15 minutes, 2mM MgCl was treated in the 1st and 3rd subgroups of the undiluted group, 2mM MgCl and 10mM KCl were added to the 2nd and 4th subgroups, and 3mM ATP was added to all 4 subgroups to adjust the final reaction volume to 500 μl. Of the compound prepared in Example 38 in an undiluted state by incubation for 30 minutes (H , K The degree of inhibition of ATPase activity was measured. The dilution group was diluted 50 times in 4 groups with 5 mM pipes / tris buffer solution after 15 minutes of pre-reaction, and then the supernatant was discarded after 60 minutes at 4 ° C (Beckman Ultracentrifuge, model L8-80). After washing out with 10 ml of 5 mM pipes / tris buffer, the pellet is filled with 200 µl of 5 mM pipes / tris buffer to the same volume as the pre-reaction, suspended and 2 mM in each subgroup as in the undiluted group. After treatment with MgCl, 10mM KCl, 3mMATP and adjusting the final reaction volume to 500µl incubated in a 37 ℃ thermostat for 30 minutes (H) , K ) -ATPase activity inhibition was measured. H before and after dilution washout / K The degree of inhibition of ATPase activity is shown in Table 3 below.

As can be seen in Table 3 above, the test substance showed 62% inhibition of enzymatic activity before dilution washout, but almost no inhibition of enzymatic activity after dilution washout.

Claims (5)

A pyrimidine derivative represented by the following general formula (I) or a pharmaceutically acceptable salt thereof. Wherein A is 1-substituted-1,2,3,4-tetrahydroisoquinolin-2-yl of formula (II-1) or 7-substituted-4,5,6 of formula (II-2) , 7-tetrahydrothieno [2,3-c] pyridin-6-yl. And R ₁ , R ₂ , R ₆ are hydrogen or C _1-3 alkyl, R ₃ is hydrogen or halogen, R ₄ , R ₅ are the same or different from each other and are hydrogen, C _1-3 alkyl, or ring together To form cyclopentyl or cyclohexyl. 2. 2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 6- Methyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 6-methyl-4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -2- (4-fluorophenylamino) pyrimidine, 6-methyl-2- (N-methylphenylamino) -4 -(1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1- Methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 6-ethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3, 4-tetrahydroisoquinolin-2-yl) pyrimidine, 6-ethyl-2- (N-methylphenylamino) -4- (1-methyl-1,2,3,41tetrahydroisoquinolin-2-yl) Pyrimidine, 6-ethyl-2- (2-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 2- (2-methyl- 4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) -6-propylpyrimidine, 4- (1-methyl-1,2,3,4-tetrahydroiso Quinolin-2-yl) -6-propyl-2- (4-fluorophenylamino) pyrimidine, 2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydro Isoquinolin-2-yl) -6-propylpyrimidine, 5,6-dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4- Tetrahydroisoquinolin-2-yl) pyrimidine, (R) -5,6-dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3, 4-tetrahydroisoquinolin-2-yl) pyrimidine, (S) -5,6-dimethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2, 3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 5,6-dimethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydro Isoquinolin-2-yl) pyrimidine, (R) -5,6-dimethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinoline -2-yl) pyrimidine, (S) -5,6-dimethyl-2- (4-flu Rophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 5,6-dimethyl-2- (N-methylphenylamino) -4- ( 1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, (R) -5,6-dimethyl-2- (N-methylphenylamino) -4- (1-methyl- 1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, (S) -5,6-dimethyl-2- (N-methylphenylamino) -4- (1-methyl-1,2, 3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 5-methyl-6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2, 3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 5-methyl-6-ethyl-2- (4-fluorophenylamino) -4- (1-methyl-1,2,3,4- Tetrahydroisoquinolin-2-yl) pyrimidine, 5-methyl-6-ethyl-2- (N-methylphenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinoline-2 -Yl) pyrimidine, 2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] Pyrimidine, 2- (4-fluorophenylamidine ) -2- (1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] pyrimidine, 2- (N-methylphenylamino) -4- (1-methyl- 1,2,3,4-tetrahydroisoquinolin-2-yl) cyclopenta [d] pyrimidine, 2- (2-methyl-4-fluorophenylamino) -4- (1-methyl-1,2 , 3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydroquinazolin, 2- (N-methylphenylamino) -4- (1-methyl-1,2,3, 4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydroquinazolin, 6-methyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2 , 3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 6-methyl-2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinoline-2- Yl) pyrimidine, 6-methyl-2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 6-ethyl-2- (2- Methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 6-ethyl-2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahi Leuisoquinolin-2-yl) pyrimidine, 6-ethyl-2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 6-ethyl -2- (2-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 5,6-dimethyl-2- (2-methyl-4-fluoro Phenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 5,6-dimethyl-2- (4-fluorophenylamino) -4- (1,2 , 3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 5,6-dimethyl-2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinoline-2- Yl) pyrimidine, 5-methyl-6-ethyl-2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine , 5-methyl-6-ethyl-2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 5-methyl-6-ethyl -2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) pyrimidine, 2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tet Lahydroisoquinolin-2-yl) cyclopenta [d] pyrimidine, 2- (2-methyl-4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinoline-2- Il) -5,6,7,8-tetrahydrquinazolin, 2- (4-fluorophenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -5, 6,7,8-tetrahydroquinazolin, 2- (N-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetra Hydroquinazolin, 2- (2-methylphenylamino) -4- (1,2,3,4-tetrahydroisoquinolin-2-yl) -5,6,7,8-tetrahydroquinazolin, 6-methyl -2- (2-methyl-4-fluorophenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) pyrimidine , 6-methyl-4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -2- (4-fluorophenylamino) pyrimidine , 6-methyl-2- (N-methylphenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) pyrimidine, 5 , 6-dimethyl-2- (2-methyl-4-fluorophenylami No) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) pyrimidine, 5-methyl-2- (2-methyl-4 -Fluorophenylamino) -4- (7-methyl-4,5,6,7-tetrahydrothieno [2,3-c] pyridin-6-yl) -6-ethylpyrimidine A pyrimidine derivative or a pharmaceutically acceptable salt thereof. A pyrimidine derivative represented by the following general formula (III). Wherein A is 1-substituted-1,2,3,4-tetrahydroisoquinolin-2-yl of formula (II-1) or 7-substituted-4,5,6 of formula (II-2) , 7-tetrahydrothieno [2,3-c] pyridin-6-yl. And R ₆ is hydrogen or C _1-3 alkyl, R ₃ is hydrogen or halogen, R ₄ , R ₅ are the same or different from each other and are hydrogen, C _1-3 alkyl, or ring together to form cyclopentyl or cyclo Hexyl may be formed. A compound represented by the general formula (III) is prepared by reacting a compound represented by the general formula (IV) with a compound represented by the general formula (V-1) or (V-2), and then, A method for producing a compound represented by formula (I), wherein the compound represented by the reaction is reacted. Wherein A is 1-substituted-1,2,3,4-tetrahydroisoquinolin-2-yl of formula (II-1) or 7-substituted-4,5,6 of formula (II-2) , 7-tetrahydrothieno [2,3-c] pyridin-6-yl. And R ₁ , R ₂ , R ₆ are hydrogen or C _1-3 alkyl, R ₃ is hydrogen or halogen, R ₄ , R ₅ are the same or different from each other and are hydrogen, C _1-3 alkyl, or ring together To form cyclopentyl or cyclohexyl. An antiulcer composition comprising a pyrimidine derivative represented by the following general formula (I) or a pharmaceutically acceptable salt thereof as a main component and a pharmaceutically acceptable carrier. Wherein A is 1-substituted-1,2,3,4-tetrahydroisoquinolin-2-yl of formula (II-1) or 7-substituted-4,5,6 of formula (II-2) , 7-tetrahydrothieno [2,3-c] pyridin-6-yl. And R ₁ , R ₂ , R ₆ are hydrogen or C _1-3 alkyl, R ₃ is hydrogen or halogen, R ₄ , R ₅ are the same or different from each other and are hydrogen, C _1-3 alkyl, or ring together To form cyclopentyl or cyclohexyl.