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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527872Generated: October 29, 2026

3-Iodo-p-toluidine → N-(3-Iodo-4-methylphenyl)-4-((4methylpiperazin-1-yl) methyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1527872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Iodo-p-toluidineHCID 118889—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant4-((4-Methylpiperazin-1-yl)methyl)-3-(trifluoromethyl)benzoic acidHCID 23145880—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductN-(3-Iodo-4-methylphenyl)-4-((4methylpiperazin-1-yl) methyl)-3-(trifluoromethyl)benzamideHCID 4683891150%

Reaction Steps

To a flask containing 1.0 g (2.67 mmol) of 4-[(4-methyl-1-piperazinyl)methyl]-3-(trifluoromethyl)-benzoic acid (CAS#859027-02-4; prepared according to Asaki, T. et al. Bioorg. Med. Chem. Lett. (2006), 16, 1421-1425), 0.62 g (2.67 mmol) of 3-Iodo-4-methylaniline, 0.77 g (4.0 mmol) of N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDAC), and 0.43 g (3.2 mmol) of N-hydroxybenzotriazole monohydrate (HOBt.H2O) was added 5 mL of DCM and 5 mL of triethylamine. The solution was stirred at ambient temperature under an atmosphere of N2 for 3 days, concentrated, and the crude product purified by silica gel chromatography (eluted with 100% EtOAc then 10% MeOH/EtOAc), to provide 0.69 g of product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090561B2
Source datasetuspto-grants-2015_07
ORD IDord-893c0a1d5fc14ebbacbc24971a3262c9
Source noteuspto-grants-2015_07