1609102-47-7

Basic information

• Product Name: 3-nitro-6-p-fluorobenzylaminopyridin-2-ylaminoformic acid tert-butyl ester
• Synonyms: 3-nitro-6-p-fluorobenzylaminopyridin-2-ylaminoformic acid tert-butyl ester
• CAS NO: 1609102-47-7
• Molecular Weight: 362.361
• Mol File: 1609102-47-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-nitro-6-p-fluorobenzylaminopyridin-2-ylaminoformic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-nitro-6-p-fluorobenzylaminopyridin-2-ylaminoformic acid tert-butyl ester(1609102-47-7)
• EPA Substance Registry System: 3-nitro-6-p-fluorobenzylaminopyridin-2-ylaminoformic acid tert-butyl ester(1609102-47-7)

Safety Data

• Hazardous Substances Data: 1609102-47-7(Hazardous Substances Data)

Upstream product

• 140-75-0 para-fluorobenzylamine 
• 27048-04-0 2-amino-6-chloro-3-nitropyridine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 33400-49-6 2-amino-3-nitro-6-(p-fluoro-benzylamino)-pyridine 

Downstream Products

• 1482053-40-6 C₃₂H₄₁FN₄O 
• 1609102-48-8 C₁₇H₂₁FN₄O₂ 
• 1609102-49-9 C₃₇H₄₉FN₄O₃ 
• 33400-45-2 flupirtine hydrochloride 

Relevant articles and documents

Synthesis method for flupirtine maleate compound

The invention discloses a synthesis method for a flupirtine maleate compound. The method comprises the steps that 2-amino-3-nitro-6-chloropyridine (a first compound) is used as a starting material to react with fluorobenzylamine (a second compound) to generate 2-amino-3-nitro-6-p-fluorobenzylamine pyridine (a third compound), the third compound is processed through di-tert-butyl dicarbonate ester protection to obtain 2-amino-3-nitro-6-p-fluorobenzylamine pyridine-3-based-tert-butyl acetate (a fourth compound), the fourth compound is processed through hydrogenation reduction and then react with ethyl chloroformate, after reacting is finished, deprotection is performed to obtain flupirtine hydrochloride (a fifth compound), and the fifth compound is salified with maleic acid to obtain flupirtine maleate (the sixth compound). According to the synthesis method, the starting material is cheap and easy to obtain, byproduct generation is avoided through amino protection, therefore, the impurity content is decreased, and the product quality is improved; catalytic reduction is performed by adopting palladium chloride, the reaction condition is mild, the reaction process is easy to operate, and the method is suitable for industrial production.