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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456869Generated: October 30, 2026

Triethylamine → 2-Chloro-5-(6-methyl-pyridin-3-yl)-N-(1-p-tolyl-cyclohexylmethyl)-benzamide

https://huagongshe.com/reaction/456869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Chloro-5-(6-methylpyridin-3-yl)benzoic acidHCID 18438661—
Reactant1-[1-(4-Methylphenyl)cyclohexyl]methanamineHCID 18438708—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Chloro-5-(6-methyl-pyridin-3-yl)-N-(1-p-tolyl-cyclohexylmethyl)-benzamideHCID 5881817327.9%

Reaction Steps

To a solution of 2-chloro-5-(6-methyl-pyridin-3-yl)-benzoic acid (73 mg, 0.29 mmol) in N,N-dimethylformamide (4 mL) was added sequentially, stirring at room temperature for 10 minutes after each addition, 1-hydroxybenzotriazole (48 mg, 0.35 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (62 mg, 0.32 mmol), C-(1-p-tolyl-cyclohexyl)-methylamine (60 mg, 0.29 mmol) and triethylamine (31 mg, 0.31 mmol). The mixture was stirred at room temperature for 3 h. The reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by reverse phase chromatography to afford the title compound (35 mg). LCMS (m/z) 433.2 M+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186742B2
Source datasetuspto-grants-2007_03
ORD IDord-8d53060b1671446182038bb3fa056a9a
Source noteuspto-grants-2007_03