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ChemicalBook CAS DataBase List Mepanipyrim
110235-47-7

Mepanipyrim synthesis

6synthesis methods
The industrial production of mepanipyrim begins with the synthesis of a substituted pyrimidine core, typically derived from 2-amino-4,6-dimethylpyrimidine. This intermediate undergoes acylation with 4-methylbenzoyl chloride to form a key amide linkage. The reaction is carried out under controlled conditions using organic solvents like dichloromethane and a base such as triethylamine to neutralize by-products and drive the reaction to completion. The resulting compound, mepanipyrim, is then purified through crystallisation or solvent extraction to ensure high chemical purity.
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Yield:110235-47-7 90%

Reaction Conditions:

with bis-triphenylphosphine-palladium(II) chloride;copper(l) iodide;triethylamine in 1,4-dioxane at 100; for 12 h;Inert atmosphere;

Steps:

1.4 (4) Synthesis of Mepanipyrim
Ar atmosphere, at room temperature into PdCl2 (PPh3)2 (0·01mmol, 10 mg, 0.1mol %), CuI (0.5mmol, 5mol %) and 2-chloropyrimidinamine (10·0mmol) Anhydrous anaerobic dioxide (30mL) solution added the 10mL of Et3N, pass through the propyne gas, warm up at 100 ° C, stir the reaction for 12 h, cool at the greenhouse, the reaction is quenched by the addition of saturated NH4C1 (10mL), extracted with ethyl acetate three times, the organic phase is washed with a saturated NaCl solution, NaS04 drying, the solvent is distilled off under reduced pressure, the crude product was re-crystallized from n-hexane/isopropyl ether (ν/ν = 1/1), obtained product (2.0 g, yield 90%). The total yield of Mepanipyrim is 45%.

References:

Northwest Normal University;Quan Zhengjun;Yan Zhongfei;Wang Xicun CN104003944, 2016, B Location in patent:Paragraph 0014; 0018

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