Literature DB >> 17165896

Judicious application of allyl protecting groups for the synthesis of 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl triflate, a key precursor of DNA-dependent protein kinase inhibitors.

Sonsoles Rodriguez Aristegui1, Marine Desage El-Murr, Bernard T Golding, Roger J Griffin, Ian R Hardcastle.   

Abstract

[Structure: see text] 2-morpholin-4-yl-4-oxo-4H-chromen-8-yl 2,2,2-trifluoromethanesulfonate is a key intermediate for the synthesis of the DNA-dependent protein kinase (DNA-PK) inhibitor 8-dibenzothiophen-4-yl-2-morpholin-4-yl-chromen-4-one (NU7441). Two improved methods for the synthesis of this triflate have been developed: (A) in 35% overall yield, through modification of the published route, and (B) in 15% overall yield, by a new route employing a Baker-Venkataraman rearrangement to enable generation of the chromenone scaffold. Both syntheses depend on the judicious use of allyl protecting groups.

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Year:  2006        PMID: 17165896     DOI: 10.1021/ol062297x

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Ultrasound-promoted two-step synthesis of 3-arylselenylindoles and 3-arylthioindoles as novel combretastatin A-4 analogues.

Authors:  Zhiyong Wen; Xiaona Li; Daiying Zuo; Binyue Lang; Yang Wu; Mingyang Jiang; Huizhuo Ma; Kai Bao; Yingliang Wu; Weige Zhang
Journal:  Sci Rep       Date:  2016-04-05       Impact factor: 4.379

  1 in total

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