Category: 37622-90-5

Adding a certain compound to certain chemical reactions, such as: 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, belongs to pyrazoles-derivatives compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 37622-90-5, Computed Properties of C6H8N2O2

To a solution of NaH (1.08 g, 25.70 mmol) in THF (30 mL) at ambient temperature under nitrogen atmosphere was added a solution of ethyl 1H-pyrazole-4-carboxylate (3.00 g, 21.41 mmol) in THF (10 mL) and stirring was continued for I h. Then benzyl bromide (3.06 mL, 25.7 mmol) was added over the period of 15 mm and the reaction was stirred for 22 h. Thereaction mixture was cooled to 10 C diluted with aqueous NH4CI (100 mL) and extracted with ethyl acetate (2 x 80 mL). The combined organic layers were washed with brine (30 mL), dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography (Redisep-120 g, 0-30% EtOAc/n-Hexane) to obtain Intermediate 45A (450 g, 88%) as a white solid. 1H NMR. (400 MHz, 1)MSO-d6) 6 ppm 1.23 – 1 .28 (m, 3 H),4.21 (q. J:::: 719 Hz, 2 H), 537 (s, 2 H), 7.25 – 738 (in, 5 H), 787 (s, 1 H), 8.46 (s, 1 H). LCMS Method-H): retention time 1.8 mm, [M±H] 2310.

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, Ethyl 4-pyrazolecarboxylate, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; BRISTOL-MYERS SQUIBB COMPANY; GUNAGA, Prashantha; BHIDE, Rajeev S.; BORA, Rajesh Onkardas; PANDA, Manoranjan; YADAV, Navnath Dnyanoba; PRIESTLEY, Eldon Scott; RICHTER, Jeremy; (321 pag.)WO2018/93569; (2018); A1;,
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

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. 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, This compound has unique chemical properties. The synthetic route is as follows., Application In Synthesis of Ethyl 4-pyrazolecarboxylate

To a suspension of LAH (45.2 mL, 45.2 mmol, 1M in THF) in a flame-driedRBF was added a solution of ethyl 1H-pyrazole-4-carboxylate (3.17 g, 22.6 mmol) inTHF (20 mL) dropwise at 0 °C. The reaction was gradually warmed up to rt and stirred atrt overnight. The reaction mixture was cooled in an ice bath and carefully quenched bysequential dropwise addition of 1.36 mL H20, and 10 mL of 1MNaOH, then stirred 20 mm. Solid Mg504 was added, the ice bath was removed, and stirring was continued for 30 mm at room temp. Solids were removed by filtration through CELITE® and washed with THF, then MeOH. The combined filtrate was evaporated to give (1H-pyrazol-4-yl)methanol (1.75 g, 78.9percent), as a white solid. ?HNMR(500MF-Tz, DMSO-d6)oe 12.58(br. s., 1H), 7.58 (s, 1H), 7.40 (s, 1H), 4.74 (t, J=5.5 Hz, 1H), 4.37 (d, J=5.2 Hz, 2H).

According to the analysis of related databases, 37622-90-5, the application of this compound in the production field has become more and more popular.

Synthetic Route of 37622-90-5, These common heterocyclic compound, 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, 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 suspension of LiAlH4 (5.3 g) in dry THF (100 mL) in a round-bottomed flask, under inert atmosphere (N2), was added portionwise ethyl pyrazole-4-carboxylate (10.0 g) at rt. The reaction mixture was stirred at rt overnight and then poured into a sat. aq. Rochelle salt solution. The mixture was stirred at rt for 3 h and diluted with EA. The layers were separated and the aq. layer was extracted with EA (3x). The combined org. layers were dried over MgS04, filtered and concentrated under reduced pressure. The title compound was obtained, after drying, as a white solid (5.2 g; 76percent yield).1H NMR (d6-DMSO) delta: 12.60 (s, 1H); 7.50 (s, 2H); 4.77 (br. s, 1H); 4.38 (br. s, 2H).

The synthetic route of 37622-90-5 has been constantly updated, and we look forward to future research findings.

Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps, and cheap raw materials. 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, A new synthetic method of this compound is introduced below., category: pyrazoles-derivatives

General procedure: Under the nitrogen atmosphere, a mixture of compounds 3a-d (0.24g, 1.0mmol), 1H-pyrazole-3-carboxylate (0.11g, 0.8mmol), K2CO3 (0.23g, 1.7mmol), (E)-N, N?-Dimethyl-1, 2-cyclohexanediamine (82mg, 0.96mmol), CuI (15mg, 0.08mmol) in DMF (5mL) were added in 25mL reaction vial, which was heated to 110C and stirred for 24h. Then the reaction mixture was cooled to room temperature and diluted with H2O (20mL), the resulting mixture was added EtOAc (20mL). The organic layer was separated, and the aqueous phase was extracted with EtOAc (15mL×3). The combined organic extracts were washed with brine (50mL), dried over anhydrous Na2SO4. After that, the organic phase was concentrated in a vacuum and was purified by flash column chromatography (6-12% EtOAc/petroleum ether) to afford the desired products 4a-d. Ethyl 1-(3-cyano-4-(isopropylthio)phenyl)-1H-pyrazole-4-carboxylate (4a). White solid (yield: 98.0%); 1H NMR (CDCl3) delta 8.44 (s, 1H, CH), 8.13 (s, 1H, CH), 8.05 (d, 1H, J=2.5Hz, Ar-H), 7.89 (dd, 1H, J=2.5, 8.6Hz, Ar-H), 7.64 (d, 1H, J=8.7Hz, Ar-H), 4.37 (q, 2H, J=7.1Hz, CH2CH3), 3.62 (m, 1H, CH(CH3)2), 1.44-1.40 (overlap, 3H, CH2CH3), 1.41-1.35 (d, 6H, J=1.4Hz, CH(CH3)2).

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Reference of 37622-90-5,Some common heterocyclic compound, 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, molecular formula is C6H8N2O2, 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.

Step 1: l-(4-Methoxy-benzyl)-lH-pyrazole-4-carboxylic acid ethyl ester [00202] A solution of lH-pyrazole-4-carboxylic acid ethyl ester (0.55 g, 3.95 mmol), 4- methoxybenzyl bromide (0.74 g, 4.74 mmol) and potassium carbonate (1.64 g, 11.9 mmol) in acetone (20 ml) was left to stir at ambient temperature for 16 h then heated at 500C for 1 h. The reaction mixture was allowed to cool to ambient temperature, concentrated under reduced pressure then diluted with water and extracted with dichloromethane (4 x 20 ml). The combined organic phase was washed with saturated ammonium chloride solution (20 ml) and brine (20 ml), dried over anhydrous sodium sulfate, filtered and evaporated. The resultant residue was purified by flash column chromatography on silica (ISCO, 4Og) eluting with pentane on a gradient of ethyl acetate (0-30%). Collecting appropriate fractions afforded the title compound as a colourless oil (1.0 g, 97%). 1H NMR (CDCl3, 300 MHz) 7.92 (s, IH), 7.81 (s, IH), 7.33-7.15 (m, 2H), 6.92-6.86 (m, 2H), 5.23 (s, 2H), 4.26 (q, J = 7.1Hz, 2H), 3.81 (s, 3H), 1.29 (t, J = 7.1Hz, 3H). LCMS (method B): Rtau = 3.27 min, M+H+ = 261.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Ethyl 4-pyrazolecarboxylate, its application will become more common.

Synthetic Route of 37622-90-5,Some common heterocyclic compound, 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, molecular formula is C6H8N2O2, 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 suspension of LAH (45.2 mL, 45.2 mmol, 1M in THF) in a flame-dried flask was added a solution of ethyl 1H-pyrazole-4-carboxylate (3.17 g, 22.6 mmol) in THF (20 mL) dropwise at 0 C. The reaction mixture was gradually warmed to rt and stirred overnight. The reaction mixture was cooled in an ice bath, and carefully quenched by sequential dropwise addition of 1.36 mL H2O, and 10 mL of 1M NaOH, followed by 20 min of stirring. Solid MgSO4 was added, the ice bath was removed, and stirring was continued for 30 min at rt. Solids were removed by filtration through Celite® and washed with THF, then MeOH. The combined filtrate was evaporated to give (1H- pyrazol-4-yl)methanol (1.75 g, 78.9percent), as a white solid.1H NMR (500MHz, DMSO-d6) delta 12.58 (br. s., 1H), 7.58 (s, 1H), 7.40 (s, 1H), 4.74 (t, J=5.5 Hz, 1H), 4.37 (d, J=5.2 Hz, 2H).

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route Ethyl 4-pyrazolecarboxylate, its application will become more common.

Electric Literature of 37622-90-5, These common heterocyclic compound, 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, 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.

a) 1-(4-Hydroxymethyl-benzyl)-1H-pyrazole-4-carboxylic acid ethyl ester A mixture of (4-Chloromethyl-phenyl)-methanol (600 mg, 3.8 mmol), ethyl 1H-pyrazole-4-carboxylate (537 mg, 3.8 mmol) and potassium carbonate (2.6 g, 19 mmol) in 30 mL acetone was stirred at 50 C. for 3 h. The mixture was filtrated and concentrated in vacuo. The crude was purified by preparative HPLC (Waters Sunfire Prep C18 PBD 5 um, 30*100 mm, 5 to 100% ACN and 0.1% TFA, flow 40 ml/min) to yield the title compound. LCMS (method A) RtA=1.403 min; [M+H]+=261.0.

The synthetic route of 37622-90-5 has been constantly updated, and we look forward to future research findings.

Electric Literature of 37622-90-5, The chemical industry reduces the impact on the environment during synthesis 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, I believe this compound will play a more active role in future production and life.

Polymer-supported triphenylphospine (3.0mmol/g, 3 equiv, 1.0g) was swollen inTH F /dichloromethane (1: 1, 1 OOmls) under a nitrogen atmosphere. Ethyl 1 H-pyrazole-4-carboxylate (500mg, 3.57mmol) and 4-(chloromethyl)benzyl alcohol (671mg, 4.28mmol) were30 added followed by a solution of diisopropyl azodicarboxylate (1.08g, 5.35mmol) inTHF/dichloromethane (1: 1, 1 Omls) over a period of 30m ins. The reaction mixture was stirred at room temperature for 18 hours, the mixture was filtered through celite and the resin waswashed with 3 cycles of dichloromethane/methanol (1Smls). The combined filtrates wereevaporated in vacuo and triturated with ethanol to give a white solid identified as 1-(4-chloromethyl-benzyl)-1 H-pyrazole-4-carboxylic acid ethyl ester (7 41 mg, 2 .66m mol, 7S%).S [M+Hr = 279.0S

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, Ethyl 4-pyrazolecarboxylate, other downstream synthetic routes, hurry up and to see.

Electric Literature of 37622-90-5, A common heterocyclic compound, 37622-90-5, name is Ethyl 4-pyrazolecarboxylate, molecular formula is C6H8N2O2, 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 1H-pyrazole-4-carboxylic acid ethyl ester (35.0 g, 0.25 mole) in THF (100 mL) was added suspension of sodium hydride (17.38 g, 0.43 mole) in THF (100 mL) solution under N2 at 25 C and stirred for one hour. Methyl iodide (24 mL, 0.38 mole) was added at RT and the reaction mixture was heated to 60-65 C for6 hours. Reaction mixture was quenched in to ice water (200 mL) and extracted with ethyl acetate (100 mL x 3). The combined organic phase was washed with water (50 mL), brine solution (50 mL), dried over Na2504 and concentrated under vacuum to obtain ethyl 1-methyl- 1H-pyrazole-4-carboxylate.Yield: 32.36 g (83 %); ?H – NMR (CDC13, 400 MHz) oe ppm: 1.30 – 1.33 (s, 3H), 3.91(s, 3H), 4.25 – 4.30 (q, 2H), 7.83 (s, 1H), 7.88 (s, 1H); Mass (mlz): 155.0 (M+H).

The basis of chemical reaction formula synthesis, the synthesis route is composed of some specific reactions and combined according to certain logical thinking. We look forward to the emergence of more reaction modes in the future.

Chemistry, like all the natural sciences, begins with the direct observation of nature¡ª in this case, of matter.37622-90-5, Name is Ethyl 4-pyrazolecarboxylate, SMILES is C1=N[NH]C=C1C(OCC)=O, belongs to pyrazoles-derivatives compound. In a document, author is Lopera, Alberto, introduce the new discover, Recommanded Product: Ethyl 4-pyrazolecarboxylate.

Hybrid GMP-polyamine hydrogels as new biocompatible materials for drug encapsulation

Here we present the preparation and characterization of new biocompatible materials for drug encapsulation. These new gels are based on positively charged [1+1] 1H-pyrazole-based azamacrocycles which minimise the electrostatic repulsions between the negatively charged GMP molecules. Rheological measurements confirm the electroneutral hydrogel structure as the most stable for all the GMP-polyamine systems. Nuclear magnetic resonance (NMR) was employed to investigate the kinetics of the hydrogel formation and cryo-scanning electron microscopy (cryo-SEM) was used to obtain information about the hydrogel morphology, which exhibited a non-homogeneous structure with a high degree of cross-linking. It is possible to introduce isoniazid, which is the most employed antibiotic for tuberculosis treatment, into the hydrogels without disrupting the hydrogel structure at appropriate concentrations for oral administration.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 37622-90-5 is helpful to your research. Recommanded Product: Ethyl 4-pyrazolecarboxylate.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics