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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 10916536 | HCID 10916536 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S)-N-[(1S)-1-Formyl-3-methylbutyl]-3-methyl-2-[(2-naphthalenylsulfonyl)amino]butanamide | HCID 10883981 | 75.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06551999B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-6eef8e0702454ef1bb9801ed5e35fa5a |
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| Source note | uspto-grants-2003_04 |
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