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Cyclization reactions of l-pyrimidinyi-3-arylthiourea derivatives with oxalyl dichloride

DOI: 10.1515/HC.2010.16.2-3.79

Source and publish data:

Heterocyclic Communications p. 79 - 83 (2010)

Update date:2022-08-05

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Authors:

Oenal, ZuelbiyeOenal, Zuelbiye

Korkusuz, ElifKorkusuz, Elif

Ilhan, Ilhan OezerIlhan, Ilhan Oezer

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Article abstract of DOI:10.1515/HC.2010.16.2-3.79

N.N′-Disubstituted thioureas (la-g) can be cyclized by use of oxalyl dichloride to the 4,5-dioxo-2-thioxo-perhydroimidazolyl-pyrimidine-2(H)-thiones (2a-g) in good yields (50-68%). The structures of these compounds were determined by elemental analysis, I

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Full text of DOI:10.1515/HC.2010.16.2-3.79

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Brought to you by | University of California  
Authenticated  
Download Date | 6/1/15 9:21 PM  
Brought to you by | University of California  
Authenticated  
Download Date | 6/1/15 9:21 PM  
Brought to you by | University of California  
Authenticated  
Download Date | 6/1/15 9:21 PM  
Brought to you by | University of California  
Authenticated  
Download Date | 6/1/15 9:21 PM  
Brought to you by | University of California  
Authenticated  
Download Date | 6/1/15 9:21 PM  

Products guided by the article

Product name:5-(4-methylbenzoyl)-(4-methylpheny)-1-(4,5-dioxo-3-p-nitrophenyl-2-thioxoperhydroimidazol-1-yl)pyrimidine-2(H)-thione

Cas No:1285705-83-0

1285705-83-0

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