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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887774Generated: November 1, 2026

Oxygen → (2R)-2-(2-amino-2-methylpropanamido)-N-(8-(2-hydroxy-5-oxopyrrolidin-1-yl)-2-oxo-1-(thiophen-3-ylmethyl)-1,2,3,4-tetrahydroquinolin-3-yl)-4-methylpentanamide

https://huagongshe.com/reaction/1887774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantL-Ascorbic AcidHCID 54670067—
Reactant(2R)-2-(2-amino-2-methylpropanamido)-4-methyl-N-[2-oxo-8-(2-oxopyrrolidin-1-yl)-1-(thiophen-3-ylmethyl)-1,2,3,4-tetrahydroquinolin-3-yl]pentanamideHCID 59620332—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product(2R)-2-(2-amino-2-methylpropanamido)-N-(8-(2-hydroxy-5-oxopyrrolidin-1-yl)-2-oxo-1-(thiophen-3-ylmethyl)-1,2,3,4-tetrahydroquinolin-3-yl)-4-methylpentanamideHCID 59620396—

Reaction Steps

(2R)-2-(2-Amino-2-methylpropanamido)-4-methyl-N-[2-oxo-8-(2-oxopyrrolidin-1-yl)-1-(thiophen-3-ylmethyl)-1,2,3,4-tetrahydroquinolin-3-yl]pentanamide (1.08 g) was dissolved in acetic acid (30 mL), and a solution of L-(+)-ascorbic acid (3.52 g) and Cu(ClO4)2.6H2O (741 mg) in water (40 mL) was added thereto, followed by stirring at room temperature for 15 minutes while oxygen gas was bubbled into the mixture. Saturated aqueous sodium chloride solution was added to the reaction mixture, and the mixture was washed with ethyl acetate twice. Sodium bicarbonate (88.2 g) was added to the aqueous layer, and the mixture was extracted with chloroform twice. The organic layer was concentrated under reduced pressure, and the thus-recovered residue was purified through chromatography, whereby the title compound (0.5 mg) was yielded.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501772B2
Source datasetuspto-grants-2013_08
ORD IDord-150c346f94c54103b0add4a22cdce0f3
Source noteuspto-grants-2013_08