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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266965Generated: October 30, 2026

Triethylamine → (2S)-N-[(1S)-1-Formyl-3-methylbutyl]-3-methyl-2-[(2-naphthalenylsulfonyl)amino]butanamide

https://huagongshe.com/reaction/1266965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 10916536HCID 10916536—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Product(2S)-N-[(1S)-1-Formyl-3-methylbutyl]-3-methyl-2-[(2-naphthalenylsulfonyl)amino]butanamideHCID 1088398175.8%

Reaction Steps

N-(2-Naphthalenesulfonyl)-L-valyl-L-leucinol (1.3 g) was dissolved in dimethyl sulfoxide (20 ml) and dichloromethane (10 ml), and triethylamine (1.9 g) was added. The solution was stirred at room temperature while adding a solution (20 ml) of sulfur trioxide-pyridine complex (2.0 g) in dimethyl sulfoxide, which was followed by stirring for 2 hr. After the completion of the reaction, ethyl acetate was added. The mixture was washed with dilute hydrochloric acid, saturated aqueous solution of sodium hydrogencarbonate and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was washed with a mixed solution of hexane-ethyl acetate to give 0.98 g of N-(2-naphthalenesulfonyl)-L-valyl-L-leucinal (Compound 34) as white crystals. [Step 1]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06551999B1
Source datasetuspto-grants-2003_04
ORD IDord-6eef8e0702454ef1bb9801ed5e35fa5a
Source noteuspto-grants-2003_04