2015
DOI: 10.1016/j.tet.2014.11.034
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Synthesis of 1,5-disubstituted-4-oxo-4,5-dihydro-1 H -pyrazolo[4,3- c ]pyridine-7-carboxamides

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Cited by 12 publications
(3 citation statements)
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“…Following our previous successful applications of BPC as an activating agent for acids, i.e. for the formation of activated pentafluorophenyl esters for the peptide bond formation [18][19][20], 1 was treated with BPC in the presence of Et 3 N in anhydrous MeCN. The in situ formed reactive ester 11 was coupled with a variety of aliphatic amines 12a-k, thus furnishing the corresponding amides 13a-k in 59-91 % isolated yields.…”
Section: Resultsmentioning
confidence: 99%
“…Following our previous successful applications of BPC as an activating agent for acids, i.e. for the formation of activated pentafluorophenyl esters for the peptide bond formation [18][19][20], 1 was treated with BPC in the presence of Et 3 N in anhydrous MeCN. The in situ formed reactive ester 11 was coupled with a variety of aliphatic amines 12a-k, thus furnishing the corresponding amides 13a-k in 59-91 % isolated yields.…”
Section: Resultsmentioning
confidence: 99%
“…Synthesis of this was achieved starting from the commercially available diethyl beta-ketoglutarate ( 29 ) and reacting with N,N -dimethylformamide dimethyl acetal ( Scheme 1 ). 20 Addition of tert -butyl 4-hydrazinopiperidine-1-carboxylate led to the pyrazole ( 31 ), which was further functionalised by refluxing with Bredereck’s reagent followed by the addition of dichlorobenzylamine. Partial cyclisation was observed at this stage, however, the crude product was fully cyclised with sodium ethoxide.…”
Section: Introductionmentioning
confidence: 99%
“…There are several methods reported for the preparation of dihydropyridine [21][22][23][24][25] and spirooxindole derivatives [26][27][28][29][30][31].…”
Section: Introductionmentioning
confidence: 99%