The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 61-19-8, Name is Adenosine 5′-monophosphate, SMILES is O[C@@H]([C@H]([C@H](N1C=NC2=C1N=CN=C2N)O3)O)[C@H]3COP(O)(O)=O, in an article , author is Sporar, Joze, once mentioned of 61-19-8, Application In Synthesis of Adenosine 5′-monophosphate.
ENAMINO ESTERS IN THE SYNTHESIS OF HETEROCYCLIC SYSTEMS. TRANSFORMATION OF DIMETHYL ACETONE-1,3-DICARBOXYLATE INTO POLYSUBSTITUTED 1,6-NAPHTHYRIDINE-8-CARBOXYLATES
A simple two-step synthesis of 1,6-naphthyridine derivatives is described. Methyl 2-(2-methoxy-2-oxoethyl)-6-oxo-1,6-dihydropyridine-3-carboxylate (3), prepared from dimethyl acetone-1,3-dicarboxylate (1) and propyolic acid amide (2) according to the known procedure, was transformed with N,N-dimethylformamide dimethyl acetal (DMFDMA) first into 2-[1-(dimethylamino)-3-methoxy-3-oxoprop-1-en-2-yl]-6-oxo-1,6-dihydropyridin e-3-dicarboxylate (4). This was followed by reaction with monosubstituted hydrazines 5a-h to afford substituted 1,6-naphthyridine-8-carboxylates 7a-h.
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Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem