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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436656Generated: October 30, 2026

Triethylamine → 5-Amino-N-methyl-N-propyl-isophthalamic acid methyl ester

https://huagongshe.com/reaction/1436656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-MethylpropylamineHCID 12315—
Reactant1,3-Benzenedicarboxylic acid, 5-nitro-, 1-methyl esterHCID 74776—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-Amino-N-methyl-N-propyl-isophthalamic acid methyl esterHCID 68814759—

Reaction Steps

Mix 5-nitro-isophthalic acid monomethylester (3.0 g, 13.32 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (3.20 g, 16.65 mmol), and 1-hydroxybenzotriazole (2.25 g, 16.65 mmol) in dichloromethane (100 mL) at room temperature for 20 min. Add propylmethylamine (1.46 g, 16.65 mmol) and triethylamine (3.36 g, 33.3 mmol). Stir at room temperature for 1 h, dilute with ethyl acetate, wash with 10% aqueous potassium carbonate, 1 N citric acid, saturated aqueous sodium chloride and concentrate. Dissolve in ethanol (100 mL), add a slurry of 10% Pd/C (300 mg) in ethanol (10 mL) and place under a hydrogen atmosphere using a balloon and stir overnight. Flush with nitrogen, filter and concentrate to give the title-compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618978B2
Source datasetuspto-grants-2009_11
ORD IDord-a9ad8e3f68ac4a618b9c9b099b8139f5
Source noteuspto-grants-2009_11