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ChemicalBook CAS DataBase List 5-(3-METHOXY-PHENYL)-2H-PYRAZOL-3-YLAMINE
96799-04-1

5-(3-METHOXY-PHENYL)-2H-PYRAZOL-3-YLAMINE synthesis

5synthesis methods
3-Methoxybenzoylacetonitrile

21667-60-7

5-(3-METHOXY-PHENYL)-2H-PYRAZOL-3-YLAMINE

96799-04-1

b) Synthesis of 5-(3-methoxyphenyl)-2H-pyrazol-3-amine To a solution of 3-(3-methoxyphenyl)-3-oxopropanenitrile (8.96 mmol) in anhydrous ethanol (20 mL) was added hydrazine monohydrate (0.52 mL, 15 mmol), and the reaction mixture was heated and refluxed for 18 hours. After completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to remove the solvent. The crude product was washed with ether and filtered to give 1.4 g of the title compound in 83% yield. Product Characterization: Molecular formula: C10H11N3O Theoretical mass-to-charge ratio (m/z): 189 Measured mass-to-charge ratio (m/z): [M + H+] = 190 Liquid chromatography retention time (LC Rt): 1.13 min (5 min method) 1H-NMR (400 MHz, MeOH-d4) δ: 3.82 (3H, s, OCH3); 5.93 (1H, s, CH); 6.86-6.88 (1H, m, ArH); 7.19-7.31 (3H, m, ArH).

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Yield:96799-04-1 95%

Reaction Conditions:

with toluene-4-sulfonic acid;hydrazine hydrate in ethanol at 78; for 2 h;

Steps:

4.1.2. Synthesis of key intermediates 10a-c

General procedure: To a solution of 9 (5 mmol) and p-toluenesulfonic acid (TsOH,0.1 mmol) in ethanolwas added 80% hydrazine hydrate dropwise at78 °C. On completion of the reaction (TLC check), the solvent wasremoved under reduced pressure and the crude product was purifiedby silica gel column chromatography to afford intermediates10a-c as white solid in excellent yields.

References:

Zhai, Min'an;Liu, Shiyuan;Gao, Meiqi;Wang, Long;Sun, Jun;Du, Jianan;Guan, Qi;Bao, Kai;Zuo, Daiying;Wu, Yingliang;Zhang, Weige [European Journal of Medicinal Chemistry,2019,vol. 168,p. 426 - 435]

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