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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966450Generated: October 30, 2026

Water → HCID 46199062, compound

https://huagongshe.com/reaction/1966450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 44814403HCID 44814403—
SolventDimethylformamideHCID 6228—
ProductHCID 46199062HCID 4619906290%

Reaction Steps

A solution of 5-(4-benzoylpiperazin-1-yl)-2-nitro-N-phenylbenzenamine (2.0 g, 5.00 mmol), methyl iodide (0.31 ml, 5.00 mmol) and sodium hydroxide (0.26 g, 6.5 mmol) in 25 ml DMF was stirred at 0° C. for 2 hours. 100 ml water was added to the mixture to quench the run, and the mixture was extracted with ethyl acetate (2×20 ml). The extraction was washed with water (3×30 ml) and dried over anhydrous sodium sulfate. N-methyl-5-(4-benzoylpiperazin-1-yl)-2-nitro-N-phenylbenzenamine (1.8 g, 90%) was obtained after remove of solvents. 1H NMR (500 MHz, CDCl3) δ (ppm) 3.38 (s, 3H), 3.37-3.87 (m, 8H), 6.72 (m, 4H), 6.84 (m, 1H), 7.21 (m, 2H), 7.45 (m, 5H), 8.07 (d, J=9.9 Hz, 1H). 13C NMR (125 MHz, CDCl3): δ (ppm) 40.5, 47.7, 47.9, 111.1, 114.6, 115.3, 119.8, 127.6, 129.1, 129.2, 129.6, 130.7, 135.6, 137.3, 145.4, 148.4, 155.1, 171.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420640B2
Source datasetuspto-grants-2013_04
ORD IDord-335dbb87c251412ea1838c46060930a5
Source noteuspto-grants-2013_04