Synthesis and reactivity of thieno[2,3-b]pyridine-2,3-diamines Full article
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Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122 |
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| Output data | Year: 2007, Volume: 43, Number: 9, Pages: 1189-1196 Pages count : 8 DOI: 10.1007/s10593-007-0182-y | ||||||
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Abstract:
It has been established that the interaction of N1-(2-hydroxyphenylmethylthieno[2,3-b]pyrid-3-yl)arylamides with hydrazine hydrate leads to thieno[2,3-b]pyridine-2,3-diamines. It was shown that the reaction of the latter with acetylacetone and acetoacetic ester occurs regioselectively at the amino group in position 3 of the thiophene ring.
Cite:
Lipunov M.M.
, Kaigorodova E.A.
, Konyushkin L.D.
, Firgang S.I.
, Krapivin G.D.
Synthesis and reactivity of thieno[2,3-b]pyridine-2,3-diamines
Chemistry of Heterocyclic Compounds. 2007. V.43. N9. P.1189-1196. DOI: 10.1007/s10593-007-0182-y Scopus OpenAlex
Synthesis and reactivity of thieno[2,3-b]pyridine-2,3-diamines
Chemistry of Heterocyclic Compounds. 2007. V.43. N9. P.1189-1196. DOI: 10.1007/s10593-007-0182-y Scopus OpenAlex
Identifiers:
| ≡ Scopus: | 2-s2.0-36949027523 |
| ≡ OpenAlex: | W2950435541 |