Tag: M.W:100-200

These common heterocyclic compound, 92933-47-6, name is 5-Isopropyl-1H-pyrazole-3-carboxylic acid, 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. Formula: C7H10N2O2

Example 1. Synthesis of 5-(propan-2-yl)-N-{4-[(pyrimidin-2- yl)sulfamoyl]phenyl}-lH-pyrazole-3-carboxamide, 1-17 1-17 [00265] HATU (460mg, 1.2 mmol) and DIPEA (0.42 ml, 2.4 mmol) were added at Rt to a stirred solution of 3-(propan-2-yl)-lH-pyrazole-5-carboxylic acid (120mg, 0.8 mmol) in DMF (HPLC grade, 7 ml) followed by 4-amino-N-(pyrimidin-2-yl)benzenesulfonamide (200mg, 0.8 mmol). The resulting mixture was stirred at Rt for 20h. The solvent was removed in vacuo and the remaining material was purified by prep HPLC (MeCN/Water, 0.1% formic acid) to afford lOmg (3%) of 5-(propan-2-yl)-N-{4-[(pyrimidin-2-yl)sulfamoyl]phenyl}-lH-pyrazole-3- carboxamide 1-17 as a colourless solid. 1H NMR (500 MHz, DMSO-d6) delta 13.15 (s, 1H), 10.29 (s, 1H), 8.48 (d, J = 4.8 Hz, 2H), 7.98 (d, J = 8.6 Hz, 2H), 7.91 (d, J = 8.6 Hz, 2H), 7.01 (s, 1H), 6.54 (s, 1H), 3.11 – 2.77 (m, 1H), 1.25 (d, J = 6.9 Hz, 6H).

The synthetic route of 5-Isopropyl-1H-pyrazole-3-carboxylic acid has been constantly updated, and we look forward to future research findings.

Synthetic Route of 948570-75-0, 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. 948570-75-0, name is 1-(2-Methoxyethyl)-4-nitro-1H-pyrazole, This compound has unique chemical properties. The synthetic route is as follows.

Intermediate 33.2 (90 mg, 0.53 mmol, 1.00 equiv) in methanol (5 mL) was added 10% palladium on carbon (18 mg) under nitrogen. The flask was degassed three times with hydrogen (2 atm) and the mixture was stirred 1 h at room temperature. The solids were filtered out and the filtrate was concentrated under vacuum to give 74 mg (crude) of intermediate 33.2 as a yellow solid. LCMS (ES, mlz): 142 [M+H].

The chemical industry reduces the impact on the environment during synthesis 1-(2-Methoxyethyl)-4-nitro-1H-pyrazole. I believe this compound will play a more active role in future production and life.

Electric Literature of 175137-46-9,Some common heterocyclic compound, 175137-46-9, name is 5-Cyclopropyl-1H-pyrazol-3-amine, molecular formula is C6H9N3, 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 solution of S-cyclopropyl-lH-pyrazol-S -amine (1.9g, 16.0 mmol) in CH3CN (20 ml) was added dropwise to a solution of 2,6-dichloro-5-fluoronicotinonitrile (3.0g, 16.0 mmol) and triethylamine (2.1g, 20.0 mmol) in CH3CN (80 ml) at 25 C. The resulting solution was then heated to 82 C for 18 hrs, and then cooled to 25 C, at which point the product precipitated from solution. The resulting solid was filtered, and washed with CH3CN (100 ml) to give the title compound (3.2g, 73%). MS: Calcd.: 277; Found: [M+H]+ 278.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route 5-Cyclopropyl-1H-pyrazol-3-amine, its application will become more common.

89202-89-1, name is 1,4-Dimethyl-1H-pyrazole-3-carboxylic acid, belongs to pyrazoles-derivatives compound, is considered to be a conventional heterocyclic compound, which is widely used in drug synthesis. The chemical synthesis route is as follows. COA of Formula: C6H8N2O2

Intermediate 971 ,4-Dimethyl-1 H-pyrazole-3-carbonyl chloride Thionyl chloride (4 ml) was added to 1 ,4-dimethyl-1 H-pyrazole-3-carboxylic acid (0.5g) and the reaction was heated at 800C for 2h. Further thionyl chloride (2ml) was added and the reaction was heated at 800C for 1 h. The reaction was evaporated, then azeotroped with toluene to give title compound, 511 mg. 1H NMR (CDCI3) delta 7.3 (s, 1 H), delta 4 (s, 3H), delta 2.2 (s, 3H).

The synthetic route of 89202-89-1 has been constantly updated, and we look forward to future research findings.

Related Products of 57999-06-1, A common heterocyclic compound, 57999-06-1, name is 4-Phenyl-1H-pyrazol-5-amine, molecular formula is C9H9N3, 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 mixture of ethyl-2-benzyl-3-oxo-butanoate ( 100 rng, 454.01 muetaiotaomicron, 96.15 mu^, 1.00 eq) and 4-phenyl-lH-pyrazol-5-amine (80 mg, 499.41 wmol, 1.10 eq) in EtOH (5 mL) was added H3PQ4 (98 mg, 454.01 iotaetaomicron, 50.00 ,uL, 85% v/v, 1 .00 eq). Then the reaction mixture was stirred at 100 C for 16 h. LC-MS indicated the desired product was detected. Water ( 10 mL) was added and the mixture was stirred at 5 C for 1 h. Then the mixture was filtered and the filter cake was dried in vacuo to give 6-benzyl-5-methyl-3-phenyl- pyrazolo[l,5-a]pyrimidin-7-ol (65.3 mg, 195.92 mutaueta, 43% yield) as a white solid. NMR (400 MHz, DMSO-ifc) delta 1 1.79 (brs, I I I ). 8.12 (s, 1H), 7.57 (d, J = 7.6, 2H), 7.46 (t, 2H), 7.34-7.26 (m, 6H), 3.89 (s, 2H), 2.39 (s, 3H); I3C NMR (100 MHz, DMSQ-tfc) delta 157.4, 148.7, 142,6, 140.8, 137.3, 131.3, 129,3, 128.8, 128.4, 127.9, 126,9, 126.3, 106.0, 104 ,4, 30.5, 1 7.6, LC-MS (ESI): m/z 316.0 ( i } .

The synthetic route of 57999-06-1 has been constantly updated, and we look forward to future research findings.

Synthetic Route of 4522-35-4,Some common heterocyclic compound, 4522-35-4, name is 3-Iodo-1H-pyrazole, molecular formula is C3H3IN2, 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.

INTERMEDIATE 15 5-(3-Iodo-lH-pyrazol-l -yl)-2-(trifluorometyl)pyridine To a solution of 3-iodopyrazole (0.588 g, 3.03 mmol) in DMSO (15.0 mL) was added sodium hydride (60% in oil, 0.145 g, 3.64 mmol) and stirred for 0.5 h before 5-fluoro- 2-(trifluoromethyl)pyridines added. The reaction mixture was stirred at 90 C overnight. The reaction was quenched by the addition of water and extracted with EtOAc. The combined organic extracts were washed with water and brine, dried over MgS04 and concentrated in vacuo. The crude mixture was purified by passing through the silica gel funnel with CH2C12 to give 5-(3-iodo-lH-pyrazol-l -yl)-2- (trifiuorometyl)pyridine, as a yellow solid. LCMS calc. = 339.95; found = 339.89 (M+H)+. 1H NMR (500 MHz, CDC13): delta 9.03 (d, J= 2.3 Hz, 1 H); 8.24 (dd, J= 8.4, 2.1 Hz, 1 H); 7.86 (d, J= 2.5 Hz, 1 H); 7.80 (d, J= 8.5 Hz, 1 H); 6.73 (d, J = 2.6 Hz, 1 H).

The synthetic route of 4522-35-4 has been constantly updated, and we look forward to future research findings.

Reference of 56984-32-8, A common heterocyclic compound, 56984-32-8, name is Ethyl 5-chloro-1-methyl-1H-pyrazole-4-carboxylate, molecular formula is C7H9ClN2O2, 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 11; [Show Image] Compound 6 was reacted with various benzylalcohols to give Compounds A-21, A-22, A-23 and A-24 via Mitsunobu reaction.

The synthetic route of 56984-32-8 has been constantly updated, and we look forward to future research findings.

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. 304903-10-4, name is 1-Ethyl-1H-pyrazole-4-carbaldehyde, This compound has unique chemical properties. The synthetic route is as follows., Computed Properties of C6H8N2O

General procedure: Corresponding aryl-carbaldehyde (1.0 eq.) and l-(triphenyl-phosphanylidene)propan-2-one (1.2 eq.) were dissolved in DCM. The mixture was stirred at r.t for 1-168 hours. The solvent was evaporated. The residue was purified by flash chromatography (hexane:EEO) to give the appropriate (¡ê)-4-(aryl)but-3-en-2-one.

According to the analysis of related databases, 304903-10-4, the application of this compound in the production field has become more and more popular.

Application of 175137-46-9, As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 175137-46-9 name is 5-Cyclopropyl-1H-pyrazol-3-amine, This compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below.

Intermediate 172-Chloro-N-(5-cvclopropyl-lH-pyrazol-3-yl)-5-nitropyrimidin-4-amine; A mixture of 2,4-dichloro-5-nitropyrimidine (2 g) and S-cyclopropyl-lH-pyrazol-S-amine (2 g) in acetonitrile (20 mL) with diisopropylethylamine (2 mL) was stirred at room temperature for 24 hours, The resulting mixture was concentrated, and the resulting residue was separated by silica gel column (etaexane/Ethyl acetate) to afford 2.1 g desired product. MS (electrospray): 281 (M+l) for Ci0H9ClN6O2.

At the same time, in my other blogs, there are other synthetic methods of this type of compound, 5-Cyclopropyl-1H-pyrazol-3-amine, and friends who are interested can also refer to it.

Synthetic Route of 16461-94-2, 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. 16461-94-2, name is 4-Bromo-1H-pyrazol-3-amine belongs to pyrazoles-derivatives compound, it is a common compound, a new synthetic route is introduced below.

3-Amino-4-bromopyrazole (5 g, 30.9 mmol) and 4-methoxybenzyl chloride (21 g, 134 mmol, 4.3 equiv.) werecombined in anhydrous DMF (25 mL) and added dropwise to a stirred suspension of sodium hydride (60% dispersionin mineral oil, 6.25 g, 156 mmol, 5 equiv.) in anhydrous DMF (50 mL). The presuming suspension was stirred 2 days atroom temperature. Water (300 mL) was added slowly and the resulting mixture was extracted with ether (4 x 350 mL).The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate and concentrated underreduced pressure. The crude product was dissolved in dichloromethane and purified by silica gel chromatography using a gradient from 10% to 20% ethyl acetate-hexanes. The product, a white solid, is obtained as a 60:40 mixture of the 1-benzylated-1 H product and the 2-benzylated-2H product (14.96 g total, 93% yield).

The synthetic route of 4-Bromo-1H-pyrazol-3-amine has been constantly updated, and we look forward to future research findings.