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Synthesis of 1,2-dihydro-2-oxo-4-quinolinyl phosphates from 2-acyl-benzoic acids.


ABSTRACT: We report a facile synthesis of 1,2-dihydro-2-oxo-4-quinolinyl phosphates (1a-l) starting from 2-acyl-benzoic acids (2a-l) in the presence of phosphoryl azides via a one-pot cascade reaction involving a Curtius rearrangement, an intramolecular nucleophilic addition of the enol carbon to the isocyanate intermediate, and an addition-elimination of the enol oxygen to the phosphoryl azide. During the reaction three new bonds are formed under mild conditions to yield 1,2-dihydro-2-oxo-4-quinolinyl phosphates in modest yields.

SUBMITTER: He X 

PROVIDER: S-EPMC4415384 | biostudies-literature | 2015 Mar

REPOSITORIES: biostudies-literature

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Synthesis of 1,2-dihydro-2-oxo-4-quinolinyl phosphates from 2-acyl-benzoic acids.

He Xinhua X   Aglio Tharcilla T   Deschamps Jeffrey R JR   Rai Rachita R   Xue Fengtian F  

Tetrahedron letters 20150301 11


We report a facile synthesis of 1,2-dihydro-2-oxo-4-quinolinyl phosphates (<b>1a</b>-<b>l</b>) starting from 2-acyl-benzoic acids (<b>2a</b>-<b>l</b>) in the presence of phosphoryl azides via a one-pot cascade reaction involving a Curtius rearrangement, an intramolecular nucleophilic addition of the enol carbon to the isocyanate intermediate, and an addition-elimination of the enol oxygen to the phosphoryl azide. During the reaction three new bonds are formed under mild conditions to yield 1,2-d  ...[more]

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