Electrochemical synthesis and studies of substituted 2-thiopyridines Full article
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Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285 |
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| Output data | Year: 1994, Volume: 43, Number: 12, Pages: 2095-2099 Pages count : 5 DOI: 10.1007/bf00700178 | ||||
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Abstract:
A series of substituted 2-alkyl(aryl-, hetaryl-)thiopyridines was prepared by cathodic electrolysis of thiols in the presence of 2-chloro-3-cyano-4-methoxymethyl-6-methylpyridine or 4-chloro-6-methyl-3-oxo-1H-furo[3,4-c]pyridine. The reaction of 3-cyano-4-methoxymethyl-6-methyl-2(1H)-thiopyridone with alkyl halides in the presence of KOH is regioselective and leads toS-alkyl derivatives. The advantages of electrosynthesis for the preparation of 2-alkylthiopyridines fused with 2(5H)-furanone and of 3-aminothieno [2,3-b]pyridines is demonstrated.
Cite:
Kaigorodova E.A.
, Konyushkin L.D.
, Niyazymbetov M.E.
, Kvak S.N.
, Zaplishny V.N.
, Litvinov V.P.
Electrochemical synthesis and studies of substituted 2-thiopyridines
Russian Chemical Bulletin. 1994. V.43. N12. P.2095-2099. DOI: 10.1007/bf00700178 WOS Scopus OpenAlex
Electrochemical synthesis and studies of substituted 2-thiopyridines
Russian Chemical Bulletin. 1994. V.43. N12. P.2095-2099. DOI: 10.1007/bf00700178 WOS Scopus OpenAlex
Identifiers:
| ≡ Web of science: | WOS:A1994QX86900028 |
| ≡ Scopus: | 2-s2.0-4344664471 |
| ≡ OpenAlex: | W2076515414 |