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1263320-07-5

3-Amino-N-(4-butoxyphenyl)-5-nitro-1H-indazole-1-carboxamide synthesis

1synthesis methods
41339-17-7 Synthesis
3-Amino-5-nitroindazole

41339-17-7
138 suppliers
$15.00/250mg

3-Amino-N-(4-butoxyphenyl)-5-nitro-1H-indazole-1-carboxamide

1263320-07-5
5 suppliers
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Yield:1263320-07-5 72%

Reaction Conditions:

in tetrahydrofuran at 20; for 24 h;

Steps:

5.1.2. General procedure for the preparation of compounds 1c-h,l,m

General procedure: A solution of equimolar amounts of indazole derivative 2c,e [16], g [17] or indazole 2l [18] and phenyl isocyanate derivative 3a,b [18] (7 mmol) in THF (20 mL) was stirred at room temperature for 24 h. Then, the solvent was removed under reduced pressure and the solid residue was crystallized from a suitable solvent or purified as described below.

References:

Maggio, Benedetta;Raimondi, Maria Valeria;Raffa, Demetrio;Plescia, Fabiana;Cascioferro, Stella;Plescia, Salvatore;Tolomeo, Manlio;Di Cristina, Antonietta;Pipitone, Rosaria Maria;Grimaudo, Stefania;Daidone, Giuseppe [European Journal of Medicinal Chemistry,2011,vol. 46,# 1,p. 168 - 174] Location in patent:experimental part