Category: 762240-92-6

Related Products of 762240-92-6, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride belongs to pyrazines compound, it is a common compound, a new synthetic route is introduced below.

N,N-dimethylformamide (96.0 L) to (3R)-3-[N-(tert-butoxycarbonyl)amino]-4-(2,4,5-trifluorophenyl)butanoic acid (12.00 kg) and 3-(trifluoromethyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-alpha]pyrazine hydrochloride (9.05 kg) was added, stirring and the temperature was cooled to -5 C to 0 C. N-methylmorpholine (4.01 kg) and 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride (8.28 kg) were added, After stirring for 1 hour at -5 C to 0 C and warmed to 20 C to 25 C and stirred for 3 hours. Ethyl acetate (192.0 L) and purified water (96.0 L) were added to the reaction mixture, which was then stirred for 10 minutes. The organic layer was separated, and the separated water layer was extracted with ethyl acetate (48.0 L) once more for 10 minutes to collect the organic layers. The combined organic layer was washed successively with 5% aqueous sodium carbonate solution and washed with a (sodium carbonate: 96.0 L: 4.8 kg, purified water). Dehydrated with anhydrous magnesium sulfate (12.0 kg) for 10 minutes, filtered and washed with ethyl acetate (24.0 L) and concentrated under reduced pressure. cyclohexane (240.0 L) was put into the obtained residue, and it stirred at 70 degreeC-72 degreeC for 5 minutes. After cooling to 20 to 25 stirred for 1 hour, filtered and washed with cyclohexane (36.0 L). Vacuum drying at 40 C to 45 C. the desired compound 7-[(3R)-3-[(N-tert-butoxycarbonyl)amino]-4-(2,4,5-trifluorophenyl)butanoyl]-3-(trifluoromethyl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-alpha]pyrazine (15.70 kg, yield : 85.9%) was obtained.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; Most Medicine Co., Ltd.; Hong Seung-min; Shin So-yeong; Kang Seok-won; (10 pag.)KR2019/60235; (2019); A;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Synthetic Route of 762240-92-6, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, This compound has unique chemical properties. The synthetic route is as follows.

589 mg (1 mmol) of the compound of the formula (2-1), 457 mg (2 mmol) of the compound of the formula (3) and 3 mL of triethylamine were dissolved in 10 mL of dichloroethane, and the mixture was stirred at 70C for 48 hours. Then, the mixture was extracted with water and dichloromethane, and then the organic solvent was collected and water was removed in the presence of sodium sulfate (Na2SO4). The filtrate obtained through the Celite filter was removed under reduced pressure, and the first citric acid complex intermediate of formula (1-1) was obtained in a yield of 91% by column chromatography.

The chemical industry reduces the impact on the environment during synthesis 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride. I believe this compound will play a more active role in future production and life.

Reference:
Patent; Sungkyunkwan University Industry-Academic Cooperation Foundation; Song, Chung Uii; Bae, Han Yong; (22 pag.)KR2017/93021; (2017); A;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

In the chemical reaction process, reaction time, type of solvent, can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product. An updated downstream synthesis route of 762240-92-6 as follows. name: 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride

At room temperature, compound I22.8g (100mmol), bromoacetyl chloride 31.2g (200mmol) and cesium carbonate 65.2g (200mmol) were added to the flask in 100mL DMF and stirred for 3h at room temperature; after the reaction was completed, ethyl acetate was extracted The organic phase was concentrated, washed with water, and then recrystallized from ethanol, and dried to obtain 28.4 g of compound II in a yield of 91%.

According to the analysis of related databases, 762240-92-6, the application of this compound in the production field has become more and more popular.

Reference:
Patent; Nanjing Qike Pharmaceutical Co., Ltd.; Yang Bo; Chen Yao; (11 pag.)CN110577542; (2019); A;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Application of 762240-92-6, A common heterocyclic compound, 762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, molecular formula is C6H8ClF3N4, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

To the 1 OOgm(3R)-3- [(1,1 -dimethyl ethoxy carbonyl)amino}-4-(2,4,5-trifluorophenyl butanoic acid charged 700m1 methylenedichioride and 67gm triethylamineandstirred for 10 minutes.Added 68gmNN?-Dicyclohexylcarbodiimide, 44.6 gm of anhydrous 1 – hydroxylbenzotriazole and maintained for about 10-20 minutes.Added75.5gm 3- trifluromentyl 5,6,7,8-tetrahydro (1 ,2,4) triazolo[4,3-a] pyrazineHCl and heated to 25- 30C and maintained for 4 hours. After completion of reaction,filtered the reaction mass and filtrate was washed with 2x350m1 2.5%sodium bicarbonate solutionandwashed with 2x500m1 of water.MDC layer was taken without purification and Cooled to 0-10C.400m1 1 6%Methanolic HCI added and raised the temperature to 25-30C and Stirred for 4 hours.After completion of the reaction added 1000m1 water and separatedlayers.ExtractedtheMDClayer with 2x300m1 DM water.Aqueous layer was washed with 300m1 MDC and pH of the aqueous layer was adjusted to 10-1 1%with 1 0%sodium hydroxide solution. 1 000m1 MDC charged and Stirred for I 0mm. The organic layer separated and the Aq layer was extracted twice with 300 ml MDC. The organic layer was separated and washed with 300 ml of water followed by 300m1 5% NaCl; and driedthe organic layer with anhydrous sodium sulfate. The organic layer separated and the solvent was distilled out under vacuum. 1 OOm1IPA was added to residue and again distilled under vacuum followed by addition of 800m1 heptane. Filtered the crystallized Material and dried under vacuum at 50C for 12-15 hours to get 96.5% titled compound.BPLC purity:99-99.9% Chiral purity: 99.9%

The synthetic route of 762240-92-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; HARMAN FINOCHEM LIMITED; KADAM, Vijay, Trimbak; SARANAPU, Nareesh; SINGAMPALLI, Sri, Hari; MINHAS, Harpreet, Singh; MINHAS, Gurpreet, Singh; (16 pag.)WO2017/6335; (2017); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, belongs to pyrazines compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows. SDS of cas: 762240-92-6

Azetidinone lla’ (0.5 g, 2.32 mmol, ee 99.5 %), 3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1 ,2,4]triazolo[4,3-a] pyrazine hydrochloride (Ill’, 1.06 g, 4.65 mmol), Et3N (0.28 g, 4.65 mmol) and 2-ethylhexanoic acid (0.17 g, 1.16 mmol) were suspended in THF (1 0 ml). The resulting suspensionwas stirred at 75C for 72 h. After cooling the mixture to 0C, the excess of the compound Ill’ wasfiltered off and the solvent was removed in vacuo. To the remaining oil was added water (1 0 ml) andthe product was extracted with dichloromethane (3 x10 ml). The organic phases were combined,dried over magnesium sulfate and concentrated in vacuo to give 0.90 g of sitagliptin (IV”) (95%, ee99.5 %) as dark yellow oil.

The synthetic route of 762240-92-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; LEK PHARMACEUTICALS D.D.; STARCEVIC, Stefan; MRAK, Peter; KOPITAR, Gregor; WO2013/186326; (2013); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Electric Literature of 762240-92-6, A common heterocyclic compound, 762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, molecular formula is C6H8ClF3N4, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

Example 4-16-Propyl-4-(3-trifluoromethyl-5,6-dihydro-8H-[1,2,4]triazolo[4,3-a]pyrazin-7-yl)thieno[2,3-d]pyrimidine-2-carboxylic acid ethyl ester The compound obtained from Preparation Example 4-1-3 (2.04 g, 7.71 mmol) and the compound obtained from Preparation Example 1-1-2 (1.80 g, 7.87 mmol) were diluted with N,N-dimethylformamide (20 mL), then triethylamine (2.34 g, 23.1 mmol) was added thereto at 0 C. and stirred at room temperature for 16 hours. The resulting mixture was distilled under reduced pressure, then diluted with ethyl acetate and washed with water and salt water. Organic layer was dried with anhydrous magnesium sulfate, distilled under reduced pressure and then purified by column chromatography with the 1:1 mixture of hexane and ethyl acetate to give the title compound (2.56 g, 81%).1H NMR (500 MHz, CDCl3); delta 7.11 (1H, s), 5.37 (2H, s), 4.50 (2H, q), 4.43 (4H, s), 2.93 (2H, t), 1.80 (2H, m), 1.45 (3H, t), 1.02 (3H, t)

The synthetic route of 762240-92-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; LG LIFE SCIENCES LTD.; US2011/166121; (2011); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Related Products of 762240-92-6, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, This compound has unique chemical properties. The synthetic route is as follows.

General procedure: A solution of 3-(trifluoromethyl)-5,6,7,8-tetrahydro [1,2,4]triazolo[4,3-a]pyrazine hydrochloride salt (1.0 eq.) in dimethylformamide(DMF, 2-3 mL)was added potassium carbonate (2.5eq.) at and stirred for 15 min at room temperature. To this, N-(benzo[d]thiazol-2-yl)-2-chloroacetamide derivatives (1.0 eq.) in DMF was added to the reaction mixture at room temperature. The resulting reaction mixturewas heated at 70 C for 18 h. The completion of the reaction was monitored on TLC (using 10% MeOH: DCM and ammonia as a modifier as mobile phase) which confirmed that the reaction got completed after 18 h. The reaction mixture was pouredinto ice-cold water and extracted with ethyl acetate (2 x 30 mL).Organic layers were combined and the combined organic layer was dried over sodium sulfate and concentrated under reduced pressure to afford crude desired product and crystallized it from methanol to get N-(benzo[d]thiazol-2-yl)-2-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo [4,3-a]pyrazin-7 (8H)-yl)acetamide derivatives(12a-12e) in good practical yield.

The chemical industry reduces the impact on the environment during synthesis 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride. I believe this compound will play a more active role in future production and life.

Reference:
Article; Jethava, Divya J.; Acharya, Prachi T.; Vasava, Mahesh S.; Bhoi, Manoj N.; Bhavsar, Zeel A.; Rathwa, Sanjay K.; Rajani, Dhanji P.; Patel, Hitesh D.; Journal of Molecular Structure; vol. 1184; (2019); p. 168 – 192;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, belongs to pyrazines compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows. Computed Properties of C6H8ClF3N4

Example 2: Preparation of benzyl (R)-4-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-alpha]pyrazin-7(8H)-yl)-1-(2,4,5-trifluorophenyl)-4-oxobutan-2-ylcarbamate (Compound of formula 2 wherein R is Cbz) [39] (R)-3-Cbz-amino-4-(2,4,5-trifluorophenyl)-butanoic acid (3.0g, 8.2mmol) and tetrahydrofuran (THF, 30ml) were charged and dissolved in a dry flask, and N-methylmorpholine (2.7ml, 24.5mmol) was added thereto. Then, the mixture was cooled to a temperature of 0 to 5C, and 2-chloro-4,6-dimethoxy-1,3,5-triazine (1.86g, 10.6mmol) was added thereto. After being stirred at a temperature of 0 to 5C for one hour, 3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-alpha]pyrzine hydrochloride (2.05g, 9.0mmol) was added and the reaction mixture was stirred while warming to room temperature (20 to 25C). After the completion of the reaction was confirmed by TLC, the reaction liquid was cooled to 10C, and dichloromethane (30.0ml) and water (30.0ml) were added thereto, followed by separation of layers. The organic layer was washed with saturated sodium bicarbonate (30.0ml) and saline (30.0ml), dried over anhydrous sodium sulfate, concentrated under reduced pressure, and then crystallized from ethyl acetate (12.0ml) and isopropyl alcohol (6.0ml) to afford 3.98g (yield: 90%) of benzyl-(R)-4-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]-triazolo[4,3-alpha]pyrazin-7(8H)-yl)-1-(2,4,5-trifluorophenyl)-4-oxobutan-2-ylcarbamate.[40] 1H NMR delta7.10-7.34(m, 5H), 7.04(dd, 1H, J=0.012), 6.84(dd, 1H, J=0.013), 5.01(s, 2H), 4.90(NH), 4.20(s, 2H), 4.10(t, 2H), 4.04(t, 2H), 3.97(m, 1H), 2.97(t, 2H), 2.70(t, 2H)

The synthetic route of 762240-92-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; ST PHARM CO., LTD.; LIM, Geun Gho; CHANG, Sun Ki; BYEON, Chang Ho; WO2012/99381; (2012); A2;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, belongs to pyrazines compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows. Safety of 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride

Example-8: Preparation of 7-[(3R)-3-amino-l-oxo-4-(2,4,5-trifluorophenyl) butyl] – 5,6,7,8-tetrahydro-3-(trifluoromethyl)-l,2,4-triazoIo [4.3-a] pyrazine compound of formula- 1.; To 24 ml of dimethylformamide added 4 gms of (R)-3-(tert-butoxycarbonylamino)-4- (2,4,5-trifluorophenyl)butanoic acid and cooled the reaction mixture to 0-5C. 3.3 gms of NjN’-dicyclohexylcarbodiimide (DCC) was dissolved in 10 ml of dimethylformamide and make upto 20 ml. Added 7 ml of above prepared NjN’-dicyclohexylcarbodiimide (DCC) solution to the above 0-5 C cooled reaction mixture. Added 3.15 gms of 3-(trifluoromethyl)-5,6,7,8-tetra hydro-[l,2,4]triazolo[4,3-a]pyrazine hydrochloride and 3.3 ml of triethylamine to the reaction mixture and stirred for 15 minutes. Added 0.9 gms of dimethylaminopyridine (DMAP) and stirred the reaction mixture for 3 hrs at 0-50C. Added 6.5 ml of N,N’-dicyclohexylcarbodiimide solution and stirred for 3 hrs. Again added 6.5 ml of N,N’-dicyclohexylcarbodiimide solution and stirred for 3 hrs at 0-50C. Raised the temperature to 25C and stirred the reaction mixture for 12 hrs at same temperature. The unwanted precipitated solids were separated by filtration and to the filtrate added water and ethyl acetate. Separated the both aqueous and organic layers. Washed the organic layer with 5% hydrochloric acid solution followed by washed with 5% sodium bicarbonate solution. Distilled off the solvent completely under reduced pressure. Added 30 ml of isopropyl alcohol to the obtained compound and stirred for 45 minutes at 25-300C temperature. Filtered the precipitated solid and dried the material. To the obtained compound added 10 ml of isopropyl alcohol and 3.8 ml of cone, hydrochloric acid. Stirred the reaction mixture for 3 hrs at 500C. Cooled the reaction mixture to 25C and added water. Extracted the compound from reaction mixture with methylene chloride. Distilled off the solvent completely to get the title compound. Yield: 2.5 gms.

The synthetic route of 762240-92-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; MSN LABORATORIES LIMITED; SATYANARAYANA REDDY, Manne; ESWARAIAH, Sajja; SATYANARAYANA, Revu; KONDAL REDDY, Bairy; SRINIVAS, Aluru; WO2010/122578; (2010); A2;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem

Application of 762240-92-6, A common heterocyclic compound, 762240-92-6, name is 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride, molecular formula is C6H8ClF3N4, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route.

To a solution of the acid (VII?) (1.00 g, 2.62 mmol) in THF (5 mL) at 0 C is added carbonyldiimidazole (510 mg, 3.15 mmol) and 10 minutes later triethylamine (0.4 mL, 2.62 mmol), previously solubilised in THF (5 mL), and triazolopiperazine hydrochloride (VIII) (599 mg, 2.62 mmol). The mixture, under an inert atmosphere of N2, is magnetically stirred under reflux for 16 hours until completion, then the mixture is cooled to room temperature, water added and the mixture extracted with toluene. The combined organic phases are dried and evaporated under reduced pressure. 1H NMR (300 MHz, d6-dmso, 100 C.) delta 7.4-7.2 (m, 7H), 6.90 (bs, 1H) 4.97 & 4.90 (AB system, J=12.9 Hz, 2×1H), 4.92 (s, 2H), 4.26-4.14 (m, 3H), 3.97 (t, J=5.5 Hz, 2H), 2.92 & 2.67 (2×dd, J=14.1, 4.9 Hz, 2×1H), 2.83-2.72 (m, 2H).

The synthetic route of 762240-92-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; CHEMO IBERICA S.A.; Rasparini, Marcello; Tufaro, Roberto Rocco; Minelli, Cosima; US2014/81026; (2014); A1;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem