50324-46-4Relevant academic research and scientific papers
Decarboxylative cross-couplings of 2-aminopyrimidine-5-carboxylic acids
Le Pham, Ngoc Son,Lee, Jihong,Shin, Hyunik,Sohn, Jeong-Hun
, p. 3843 - 3851 (2018)
Decarboxylative C–C cross-couplings of 2-aminopyrimidine-5-carboxylic acids under a Pd/Ag-based catalytic system opens a new platform for the introduction of diverse C5 substituents. The reaction methods proceeded efficiently with a wide range of the acids and the coupling partners of aryl iodides, alkenes, bromoalkynes, and azoles. Considering ready availability of 2-aminopyrimidine-5-carboxylic acid from the oxidative dehydrosulfurative C–N cross-coupling of the 3,4-dihydropyrimidin-1H-2-thiones, this reaction method unambiguously pave a shortcut to densely substituted 2-aminopyrimidine derivatives with unprecedented diversity.
Dihydropyrimidines and Related Structures. I. N2-Substituted 2-Pyrimidinamines and Dihydro-2-pyrimidinamines by Reaction of Phenylbutenones and Monosubstituted Guanidines
Wendelin, Winfried,Schermanz, Karl
, p. 65 - 69 (2007/10/02)
The reactions of monosubstituted guanidines 2 with phenylbutenones 7 and 10 exclusively yield N2-substituted 2-pyrimidinamines 8 and 9.The structure of the reaction products is proved and their differing stability is discussed.Action of methyl- and benzylguanidine respectively (2b,c) on 4-phenyl-3-buten-2-one (7) and of 2c on 1-phenyl-2-buten-1-one (10) under atmospheric oxygen affords aromatic N2-substituted 2-pyrimidinamines 9b and c.The dihydropyrimidines 8b and c, probable intermediates of the reactions, could not be isolated.In contrast, heating of arylguanidines 2d,e with 7 leads to stable dihydropyrimidinamines 8d and e, which can be isolated as bases.Addition of methanol to 8d yields 6-methoxy-2-pyrimidinamine 11d, boiling of 8d in DMF affords 9d.Under nitrogen, guanidine adds to 7 to yield aminopyrimidinol 13a, which is transformed by heating in benzene into pyrimidine 9a.The low stability of 8a-c is attributed to their strong basicity, the greater stability of 8d and e to their lower basicity.The structural formulae of 8d, e and 9b-d and their salts respectively were established partly (8e) by nmr and partly (9b-d) by comparison of the corresponding picrates with authentic samples .
Reactions of Monosubstituted Guanidines with 1-Phenyl-1-butane-1,3-dione
Wendelin, Winfried,Schermanz,Karl,Schweiger, Klaus,Fuchsgruber, Alfred
, p. 1371 - 1380 (2007/10/02)
Methyl-, benzyl- and phenylguanidine (2b-d) react with 1-phenyl-1,3-butanedione to yield exclusively N2-substituted 4-methyl-6-phenyl-2-pyrimidinamines 10b-d.The formation of isomeric N1-substituted 2(1H)-pyrimidinimines 11 or 12 cannot be observed.The structural formulae of 10b and c were proved by spectroscopical methods.The structure of the phenylguanidine-phenylbutanedione-condensate was determined by comparison and establishment of the identity of its picrate with an authentical sample of 10d-picrate, which had been synthetized from pyrimidinthione 13 (via methylthiopyrimidine 16*HCl).Boiling 13 with aniline in butanol yields thiodipyrimidine 15 (and not 10d). - (Keywords: 1,3-Butanedione, 1-phenyl, reactions with monosubstituted guanidines; β-Diketones, reactions with monosubstituted guanidines; Guanidines, monosubstituted, reactions with 1-phenyl-1,3-butanedione; Pyridmidine, 4-methyl-2-methylthio-6-phenyl, hydroiodide; 2-Pyrimidine-amines, 4-methyl-6-phenyl-N2-substituted, and salts; 2,2'-Thiodipyrimidine, 4,4'-dimethyl-6,6'-diphenyl)
Dimroth-Type Ring Transformation of 1,4,6-Trisubstituted-2(1H)-Pyrimidinethiones with Ammonia and Primary Alkyl Amines
Kashima, Choji,Katoh, Akira,Yokota, Yuko,Omote, Yoshimori
, p. 1942 - 1946 (2007/10/02)
1,4,6-Trisubstituted-2(1H)-pyrimidinethiones (Ia-k) underwent Dimroth-type ring transformation with ammonia and prymary alkyl amines in the presence of silver perchlorate to afford 2-(N-substituted)aminopyrimidines (IIa, c, d, f, j, k) and pyrimidinium perchlorates (IIIa-c, e-j), respectively.Furthermore, pyrimidinium perchlorates (III) were converted into 2(1H)-pyrimidinones (IV) in high yields by hydrolysis with concentrated hydrochloric acid.Keywords --- Dimroth-type ring transformation reaction; ammonia; primary alkyl amines; 2-(N-substituted)aminopyrimidines; silver perchlorate; 2-(N-substituted)aminopyrimidinium perchlorates; hydrolysis; concentrated hydrochloric acid
