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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888715Generated: November 3, 2026

N-Acetyl-DL-alanine → Nalpha-acetyl-N-(2-hydroxy-4-methoxyphenyl) alaninamide

https://huagongshe.com/reaction/1888715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-DL-alanineHCID 7345—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Amino-5-methoxyphenol HydrochlorideHCID 12210184—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductNalpha-acetyl-N-(2-hydroxy-4-methoxyphenyl) alaninamideHCID 866609059.8%

Reaction Steps

To a solution of 2-amino-5-methoxyphenol hydrochloride (5.24 g, 29.8 mmol), N-acetyl-D,L-alanine (3.91 g, 29.8 mmol) and 1-hydroxybenzotriazole (4.03 g, 29.8 mmol) in DMF (5 mL) were added triethylamine (4.15 mL, 29.8 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (5.72 g, 29.8 mmol), and the mixture was stirred at room temperature for 3 days. The reaction mixture was diluted with ethyl acetate, and the mixture was washed with 1N hydrochloric acid, 10% aqueous potassium carbonate solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by basic silica gel column chromatography (ethyl acetate to methanol:ethyl acetate=1:4), and triturated with ethyl acetate to give the title compound (740 mg, yield 9.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501804B2
Source datasetuspto-grants-2013_08
ORD IDord-95c503edeeea4957b7bdf76588e45991
Source noteuspto-grants-2013_08