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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189263Generated: October 29, 2026

3-Aminobenzoic Acid → 3-((4-Methyl-1-piperazinyl)carbonyl)aniline

https://huagongshe.com/reaction/2189263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Aminobenzoic AcidHCID 7419—
ReactantTriethylamineHCID 8471—
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDichloromethaneHCID 6344—
Product3-((4-Methyl-1-piperazinyl)carbonyl)anilineHCID 1677321879.8%

Reaction Steps

A solution of 3-aminobenzoic acid (1.51 g, 11 mmol), 1-methylpiperazine (1.1 mL, 10 mmol), EDCI.HCl (2.87 g, 15 mmol) and Et3N (2.8 mL, 20 mmol) in CH2Cl2 (10 mL) is stirred at room temperature for 20 hours. Then saturated NaHCO3 aqueous solution is added. The aqueous layer was extracted with CH2Cl2, and the organic extracts were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product is purified by column chromatography (SiO2, MeOH:CH2Cl2=0.7:99.3 to 6:93) to give 1.75 g of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324225B2
Source datasetuspto-grants-2012_12
ORD IDord-ae8829c787794d65813b74d708d683af
Source noteuspto-grants-2012_12