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3-Substituted 2-amino-imidazo pyridine

Reaction of 2 equiv of 2-aminopyridines with 2-hydropolyfluoroalk-2-anoates 351 in MeCN in the presence of NEts at 90 °C for 50 h afforded a mixture of the isomeric 2-oxo-2H- and 4-oxo-4//-pyrido[l,2-n]pyrimidines 110 and 111. Reaction of 3 equiv of 2-amino-pyridines and 2-hydropoly-fluoroalk-2-enoates 351 in MeCN in the presence K2CO3 could be accelerated by ultrasonic irradiation (125W). 2-Amino-6-methylpyridine yielded only 2-substituted 6-methyl-4//-pyrido[l,2-n]pyrimidin-4-ones 111 (R = 6-Me), whereas 2-amino-5-bromopyridine gave a mixture of 7-bromo-4//-pyrido[l,2-n]pyrimidin-4-one (111, R = 7-Br, R = CF2C1) and 2-(chlor-o,difluoromethyl)-6-bromoimidazo[l, 2-n]pyrimidine-3-carboxylate in 44 and 8% yields, respectively (97JCS(P 1)981). Reactions in the presence of K2CO3 in MeCN at 90°C for 60h afforded only imidazo[l,2-n]pyrimidine-3-carboxylates. [Pg.243]

Reactions with methylphenylcyclopropenone (154) provided an opportunity to compare the reactivities of the two different C—CO bonds. The reaction of 2-aminopyridines with methylphenylcyclopropenone (154) proceeded more slowly than with the diphenyl analog (153). In ether, formation of the ds-2-oxopyrido[l,2-a]pyrimidines (158 R1 = Me) and/or the imidazo[l,2-c<]pyridines (162) was observed, indicating that the cycloaddition proceeds via cleavage of the PhC—CO bond. The methyl-substituted trans-2-oxopyrido[l,2-a]pyrimidine (160 R1 = Me) was only detected in the reaction mixture of 2-amino-3-methylpyridine, where the H NMR spectrum exhibited signals assigned to 160 (R1 = Me, R = 9-Me). The compound was not isolated. The imidazo[l,2-a]pyridines (162) readily hydrolyzed to the acids (163), work-up therefore leading mainly to isolation of the acids. [Pg.283]

Imidazopyridodiazepines 56 are formed by />m-annulation of imidazo[l,2- ]pyridines 55 (route a Scheme 8 Table 7) <2002TL9119>. These compounds can alternatively be synthesized directly from the 2-substituted-3-amino imidazopyridines 54 and simple aldehydes or a,/3-unsaturated aldehydes in good yields. Products are formed as cis//rans-m xtutes. [Pg.172]

Rearrangement of alkoxycarbonyl imidazole acryl azides in diphenyl ether at high temperatures afforded imidazo[l,5-c]pyrimidinone or imidazo[4,5-c]pyridinone derivatives <02TL5879>. Efficient synthesis of imidazopyridodiazepines from peri annulation in imidazo[l,2-a]pyridine has been described <02TL9119>. A convenient synthesis of 3,6-disubstituted-2-aminoimidazo[l, 2-a]pyridines has been published <02TL9051>. Novel 2,3-dihydroimidazo[2,l-h][l,3]oxazoles were prepared from intramolecular nucleophilic i/wo-substitution of 2-alkylsulfonylimidazoles <02S2691>. 4,4 -Bi-l//-imidazol-2-ones were efficiently synthesized from 5-amino-ot-imino-1 //-imidazole-4-acetonitriles and isocyanates <02JOC5546>. [Pg.216]


See other pages where 3-Substituted 2-amino-imidazo pyridine is mentioned: [Pg.341]    [Pg.156]    [Pg.782]    [Pg.225]    [Pg.154]    [Pg.237]    [Pg.164]    [Pg.167]    [Pg.168]    [Pg.170]    [Pg.170]    [Pg.551]    [Pg.636]    [Pg.128]    [Pg.48]    [Pg.317]    [Pg.215]    [Pg.202]    [Pg.202]    [Pg.298]    [Pg.342]    [Pg.218]    [Pg.395]    [Pg.615]    [Pg.631]    [Pg.635]    [Pg.637]    [Pg.225]    [Pg.615]    [Pg.635]    [Pg.637]    [Pg.3]    [Pg.232]    [Pg.177]    [Pg.184]    [Pg.265]    [Pg.260]    [Pg.463]    [Pg.268]    [Pg.463]    [Pg.660]   


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2- [ amino pyridin

3- imidazo pyridin

7- Amino-2- imidazo

7-Substituted pyridines

Amino substitution

Imidazo- pyridines, substituted

Pyridine, 3-amino

Pyridines substitution

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