Synthesis of 2-cyanamino-4,6-diphenyl-pyridine-3-carbonitrile

Pedro Victory; JoséI I. Borrell; Joan Cirujeda; Anton Vidal-Ferran

doi:10.3987/com-92-6237

Synthesis of 2-cyanamino-4,6-diphenyl-pyridine-3-carbonitrile

Pedro Victory^*, JoséI I. Borrell, Joan Cirujeda, Anton Vidal-Ferran

^*Autor corresponent d’aquest treball

Producció científica: Article en revista indexada › Article › Avaluat per experts

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Resum

The nucleophilic displacement of bromo, alkylthio and alkylsulphonyl groups from pyridine systems by cyanamide is studied in order to obtain a previously unreported 2-cyanaminopyridine-3-carbonitrile. A one-step synthesis of the same compound by cyclization in basic medium of the non-isolated Michael adduct of (E)-1,3-diphenylpropenone and propanedinitrile is also described.

Idioma original	Anglès
Pàgines (de-a)	777-783
Nombre de pàgines	7
Revista	Heterocycles
Volum	36
Número	4
DOIs	https://doi.org/10.3987/com-92-6237
Estat de la publicació	Publicada - 1 d’abr. 1993

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title = "Synthesis of 2-cyanamino-4,6-diphenyl-pyridine-3-carbonitrile",

abstract = "The nucleophilic displacement of bromo, alkylthio and alkylsulphonyl groups from pyridine systems by cyanamide is studied in order to obtain a previously unreported 2-cyanaminopyridine-3-carbonitrile. A one-step synthesis of the same compound by cyclization in basic medium of the non-isolated Michael adduct of (E)-1,3-diphenylpropenone and propanedinitrile is also described.",

author = "Pedro Victory and Borrell, \{Jos{\'e}I I.\} and Joan Cirujeda and Anton Vidal-Ferran",

year = "1993",

month = apr,

day = "1",

doi = "10.3987/com-92-6237",

language = "English",

volume = "36",

pages = "777--783",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

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TY - JOUR

T1 - Synthesis of 2-cyanamino-4,6-diphenyl-pyridine-3-carbonitrile

AU - Victory, Pedro

AU - Borrell, JoséI I.

AU - Cirujeda, Joan

AU - Vidal-Ferran, Anton

PY - 1993/4/1

Y1 - 1993/4/1

N2 - The nucleophilic displacement of bromo, alkylthio and alkylsulphonyl groups from pyridine systems by cyanamide is studied in order to obtain a previously unreported 2-cyanaminopyridine-3-carbonitrile. A one-step synthesis of the same compound by cyclization in basic medium of the non-isolated Michael adduct of (E)-1,3-diphenylpropenone and propanedinitrile is also described.

AB - The nucleophilic displacement of bromo, alkylthio and alkylsulphonyl groups from pyridine systems by cyanamide is studied in order to obtain a previously unreported 2-cyanaminopyridine-3-carbonitrile. A one-step synthesis of the same compound by cyclization in basic medium of the non-isolated Michael adduct of (E)-1,3-diphenylpropenone and propanedinitrile is also described.

UR - https://www.scopus.com/pages/publications/43949170325

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:A1993KU81700017&DestLinkType=FullRecord&DestApp=WOS_CPL

U2 - 10.3987/com-92-6237

DO - 10.3987/com-92-6237

M3 - Article

AN - SCOPUS:43949170325

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VL - 36

SP - 777

EP - 783

JO - Heterocycles

JF - Heterocycles

IS - 4

ER -

Synthesis of 2-cyanamino-4,6-diphenyl-pyridine-3-carbonitrile

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