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23600-44-4

CHEMBRDG-BB 4022614 synthesis

7synthesis methods
33667-88-8 Synthesis
4-Methyl-N-(4-nitrophenyl)benzaMide

33667-88-8
5 suppliers
$28.60/50MG

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Yield:23600-44-4 62%

Reaction Conditions:

with iron(III) chloride;pyrographite;hydrazine hydrate in ethanol at 85; for 2 h;

Steps:

1.2. General procedure for the preparation of the N-(4-aminophenyl)-2-methylbenzamide derivatives 13a-u

General procedure: A mixture of 12a-u (3.8 mmol) in ethanol (40 mL) was heated to 60 oC. FeCl3 (0.1 g) and activated charcoal (0.5 g) were added, and the mixture was heated to 85 oC. Hydrazine hydrate (8 mmol, 4 mL) was added dropwise, and the reaction was stirred for 2 h. Upon completion, the mixture was filtered, washed with ethanol, and concentrated in vacuo to afford compounds 13a-u.

References:

Wang, Ru;Liu, Hu;You, Yuan-Yuan;Wang, Xin-Yu;Lv, Bing-Bing;Cao, Li-Qin;Xue, Jia-Yu;Xu, Yun-Gen;Shi, Lei [Bioorganic and Medicinal Chemistry Letters,2021,vol. 36,art. no. 127788] Location in patent:supporting information