VOIE D'ACCES ORIGINALE A DES ACETAMIDO-3 AMINO-4 (1H) PYRIDONES-2 PAR HYDROGENATION-REARRANGEMENT DES NITRO-3 AMINO-4 PYRIDINES

DOI: 10.1016/S0040-4020(01)83497-9

Source and publish data:

Tetrahedron p. 2457 - 2459 (1984)

Update date:2022-08-04

Topics:

Authors:

Rivalle, C.

Bisagni, E.

Rousseau, C.

Chardon, A. L.

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Article abstract of DOI:10.1016/S0040-4020(01)83497-9

3-Nitro 4-alkyl (or aryl) amino pyridines were converted to 3-acetamido 4-alkyl (or aryl) amino (1H) pyridine-2-ones by a catalytic hydrogenation-rearrangement in acetic acid medium.

Full text of DOI:10.1016/S0040-4020(01)83497-9

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Product name:Acetamide, N-[1,2-dihydro-4-[(4-methoxyphenyl)amino]-2-oxo-3-pyridinyl]-

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