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| | 5-Acetyl-1H-Pyrazole-3-carboxylic acid Basic information |
| Product Name: | 5-Acetyl-1H-Pyrazole-3-carboxylic acid | | Synonyms: | 5-ACETYL-1H-PYRAZOLE-3-CARBOXYLIC ACID;ODM-201 int1;ODM-201 intermediate 1;1H-Pyrazole-3-carboxylic acid, 5-acetyl-;5-ACETYL-1H-PYRAZOLE-3-CARBOXYLIC ACID(For export only);5-Acetylpyrazole-3-carboxylic Acid;3-Acetyl-1H-pyrazole-5-carboxylic acidQ: What is
3-Acetyl-1H-pyrazole-5-carboxylic acid Q: What is the CAS Number of
3-Acetyl-1H-pyrazole-5-carboxylic acid;5-Acetyl-1H-pyrazole-3-carboxylic acic | | CAS: | 1297537-45-1 | | MF: | C6H6N2O3 | | MW: | 154.12 | | EINECS: | 218-362-5 | | Product Categories: | | | Mol File: | Mol File |  |
| | 5-Acetyl-1H-Pyrazole-3-carboxylic acid Chemical Properties |
| Melting point | 257-269 °C (decomp)(Solv: ethanol (64-17-5); benzene (71-43-2)) | | Boiling point | 479.2±30.0 °C(Predicted) | | density | 1.467±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 3.60±0.10(Predicted) | | InChI | InChI=1S/C6H6N2O3/c1-3(9)4-2-5(6(10)11)8-7-4/h2H,1H3,(H,7,8)(H,10,11) | | InChIKey | HFBWRCZRDIVAMQ-UHFFFAOYSA-N | | SMILES | N1C(C(C)=O)=CC(C(O)=O)=N1 |
| | 5-Acetyl-1H-Pyrazole-3-carboxylic acid Usage And Synthesis |
| Uses | 5-acetyl-1H-pyrazole-3-carboxylic acid can be used in the industrialization of substances such as polyurethanes. Impurities in this chemical are removed through filtration before it is used for synthesis. | | Definition | 5-Acetyl-1H-pyrazole-3-carboxylic acid can be considered a valuable building block for other types of organic and medicinal chemistry transformations and is the essential starting material for the preparation of Darolutamide, which is chemically known as N-{(2S)-1-[3-(3-chloro-4- cyanophenyl)-1H-pyrazol-1-yl]propan-2-yl}-5-(1-hydroxyethyl)-1H-pyrazole-3- 10 carboxamide. Orion Corporation and Bayer Health Care developed Darolutamide. It is an anti-androgen medication that is used for the treatment of prostate cancer in men. Recently, a safe and metal-free process using ethyl glycinate hydrochloride as the starting material has been developed to prepare 5-Acetyl-1H-Pyrazole-3-carboxylic acid[1-2]. | | Synthesis | 5-Acetyl-1H-pyrazole-3-carboxylic acid is a chemical compound that is synthesized from hydrazine and acetyl chloride.
Potassium tert-butoxide (102 g) was added lot-wise to the pre-cooled mixture of 3,3-dimethoxybutane-2-one (100 g) in toluene (1000 ml) at 5-10°C and stirred for 45 minutes. Diethyl oxalate (132 g) was added to the mixture at 10-15°C and stirred for 4 hours. Filtered the solid. To the filtered solid water (3000 ml) was added and cooled to 5-10°C. Solution of Hydrazine monohydrochloride (51.8 g) was slowly added to the mixture at 5-10°C and stirred for 4 hrs. Dichloromethane (1000 ml) was added to the mixture at 5-10°C and stirred for 15 minutes. Allowed to heat the mixture to 25-30°C and stirred for 15 minutes. Filtered the mixture through hyflow. Organic layer was separated from the filtrate. Distilled-off the organic layer and co-distilled in n-heptane (50 ml). n-heptane (300 ml) was added to the mixture at 25-30°C. Heated the mixture at 45-50°C and stirred for 1 hrs. Allowed to cool the mixture to 25-30°C and stirred for 3 hours. Filtered the solid. THF (150 ml) was added to the obtained solid. aq. Sodium hydroxide solution was added to the mixture at 10-15°C. Heated the mixture to 55-60°C and stirred for 2 hrs. Allowed to cool the mixture to 25-30°C and stirred for 15 minutes. Separated the aqueous layer from organic layer. Water was added to the aqueous layer at 25-30°C. Cooled the mixture to 20-25°C. Treated the mixture with hydrochloric acid at 20-25°C. Allowed to heat the mixture to 25-30°C and stirred for 4 hours. Filtered the solid and dried. Tetrahydrofuran (300 ml) was added to the obtained solid at 25-30°C. Heated the mixture to 50-55°C and stirred for 60 minutes. Allowed to cool the mixture to 25-30°C and stirred for 3 hours. Filtered the solid and dried to get 5-Acetyl-1H-pyrazole-3-carboxylic acid, Yield: 63 gm Purity by HPLC: 99.93%.
| | References | [1] László Poszávácz. "New, Scalable Process for the Preparation of 5-Acetyl-1 H -pyrazole-3-carboxylic Acid, a Key Intermediate of Darolutamide." Synthesis-Stuttgart 33 2 (2023): 2061–2069.
[2] Bence Szilágyi. "Safe and Efficient Continuous-Flow Synthesis and Batchwise Hydrolysis of Ethyl 5-Acetyl-1 H -pyrazole-3-carboxylate: A Key Synthon of Darolutamide." Synthesis-Stuttgart 212 1 (2022): 959–966. |
| | 5-Acetyl-1H-Pyrazole-3-carboxylic acid Preparation Products And Raw materials |
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