Synthesis of 9H-Indeno [1, 2-b] Pyrazine and 11H-Indeno [1, 2-b] Quinoxaline Derivatives in One-step Reaction from 2-Bromo-4-chloro-1-indanone

S Jasouri; Jabbar Khalafy; Mohammad Badali; Rolf Prager

Synthesis of 9H-Indeno [1, 2-b] Pyrazine and 11H-Indeno [1, 2-b] Quinoxaline Derivatives in One-step Reaction from 2-Bromo-4-chloro-1-indanone

S Jasouri, Jabbar Khalafy, Mohammad Badali, Rolf Prager

Research output: Contribution to journal › Article › peer-review

5 Citations (Scopus)

Abstract

The reaction of 2-bromo-4-chloro-1-indanone with 2, 3-diaminomaleonitrile, benzene-1, 2-diamine and 4-methylbenzene-1, 2-diamine in glacial acetic acid gave 8-chloro-9H-indeno[1, 2-b]pyrazine-2, 3-dicarbonitrile, 1-chloro-11H-indeno[1, 2-b]quinoxaline and 1-chloro-7-methyl-11H-indeno[1, 2-b]quinoxaline, respectively, in good yield.

Original language	English
Pages (from-to)	105-107
Number of pages	3
Journal	South African Journal of Chemistry. Suid-Afrikaanse Tydskrif Vir Chemie
Volume	64
Publication status	Published - 2011

Cite this

@article{4db39ecec8a44cf5bf0e0b050866c2e1,

title = "Synthesis of 9H-Indeno [1, 2-b] Pyrazine and 11H-Indeno [1, 2-b] Quinoxaline Derivatives in One-step Reaction from 2-Bromo-4-chloro-1-indanone",

abstract = "The reaction of 2-bromo-4-chloro-1-indanone with 2, 3-diaminomaleonitrile, benzene-1, 2-diamine and 4-methylbenzene-1, 2-diamine in glacial acetic acid gave 8-chloro-9H-indeno[1, 2-b]pyrazine-2, 3-dicarbonitrile, 1-chloro-11H-indeno[1, 2-b]quinoxaline and 1-chloro-7-methyl-11H-indeno[1, 2-b]quinoxaline, respectively, in good yield.",

author = "S Jasouri and Jabbar Khalafy and Mohammad Badali and Rolf Prager",

year = "2011",

language = "English",

volume = "64",

pages = "105--107",

journal = "South African Journal of Chemistry. Suid-Afrikaanse Tydskrif Vir Chemie",

issn = "0379-4350",

}

Synthesis of 9H-Indeno [1, 2-b] Pyrazine and 11H-Indeno [1, 2-b] Quinoxaline Derivatives in One-step Reaction from 2-Bromo-4-chloro-1-indanone. / Jasouri, S; Khalafy, Jabbar; Badali, Mohammad et al.

In: South African Journal of Chemistry. Suid-Afrikaanse Tydskrif Vir Chemie, Vol. 64, 2011, p. 105-107.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Synthesis of 9H-Indeno [1, 2-b] Pyrazine and 11H-Indeno [1, 2-b] Quinoxaline Derivatives in One-step Reaction from 2-Bromo-4-chloro-1-indanone

AU - Jasouri, S

AU - Khalafy, Jabbar

AU - Badali, Mohammad

AU - Prager, Rolf

PY - 2011

Y1 - 2011

N2 - The reaction of 2-bromo-4-chloro-1-indanone with 2, 3-diaminomaleonitrile, benzene-1, 2-diamine and 4-methylbenzene-1, 2-diamine in glacial acetic acid gave 8-chloro-9H-indeno[1, 2-b]pyrazine-2, 3-dicarbonitrile, 1-chloro-11H-indeno[1, 2-b]quinoxaline and 1-chloro-7-methyl-11H-indeno[1, 2-b]quinoxaline, respectively, in good yield.

AB - The reaction of 2-bromo-4-chloro-1-indanone with 2, 3-diaminomaleonitrile, benzene-1, 2-diamine and 4-methylbenzene-1, 2-diamine in glacial acetic acid gave 8-chloro-9H-indeno[1, 2-b]pyrazine-2, 3-dicarbonitrile, 1-chloro-11H-indeno[1, 2-b]quinoxaline and 1-chloro-7-methyl-11H-indeno[1, 2-b]quinoxaline, respectively, in good yield.

UR - http://journals.sabinet.co.za/sajchem/

M3 - Article

VL - 64

SP - 105

EP - 107

JO - South African Journal of Chemistry. Suid-Afrikaanse Tydskrif Vir Chemie

JF - South African Journal of Chemistry. Suid-Afrikaanse Tydskrif Vir Chemie

SN - 0379-4350

ER -

Synthesis of 9H-Indeno [1, 2-b] Pyrazine and 11H-Indeno [1, 2-b] Quinoxaline Derivatives in One-step Reaction from 2-Bromo-4-chloro-1-indanone

Abstract

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