3,3,4,4-Tetracyanoalkanones as expedient reagents for utilization of N,N-dimethylhydrazine

被引：0

作者：

Nasakin, Oleg E. ^{[1
]}

Ivanova, Elizaveta S. ^{[1
]}

Maryasov, Maxim A. ^{[1
]}

Andreeva, Vera V. ^{[1
]}

Karpov, Sergey V. ^{[1
]}

Lodochnikova, Olga A. ^{[2
]}

Grishaev, Denis Yu. ^{[3
]}

机构：

[1] IN Ulyanov Chuvash State Univ, Cheboksary 428015, Russia

[2] A E Arbuzov Inst Organ & Phys Chem, AE Arbuzov Inst Organ & Phys Chem, FRC Kazan Sci Ctr, Kazan 420088, Russia

[3] Kazan Fed Univ, Pharm Res & Educ Ctr, Kazan 420021, Russia

来源：

MENDELEEV COMMUNICATIONS | 2023年 / 33卷 / 06期

基金：

俄罗斯科学基金会;

关键词：

N; N-dimethylhydrazine; formaldehyde dimethylhydrazone; tetracyanoethylene; 3; 4; 4-tetracyanoalkanones; Thorpe-Ziegler type cyclization; 1; 2-dihydro-3H-pyrrole-3; 4-tricarbonitriles; 5-dihydro-1H-pyrrolo[3; 4-c]pyridine-3a; 7a-dicarbonitriles; SUBSTITUTION;

D O I：

10.1016/j.mencom.2023.10.039

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

To utilize N,N-dimethylhydrazine, the corresponding formaldehyde hydrazone was reacted with 1,1,2,2-tetra-cyanoethane or 3,3,4,4-tetracyanoalkanones. The first process yielded 5-amino-1-dimethylamino-1,2-dihydro-3H- pyrrole-3,3,4-tricarbonitrile while the second afforded pyrrolo[3,4-c]quinolone multifunctional derivatives. These resultant products hold promise in molecular design and pharmaceutical chemistry.

引用

页码：856 / 857

页数：2

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