2013
DOI: 10.1080/10426507.2012.745075
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and Biological Activity of Novel Diphenyl N- Substituted Carbamimidoylphosphoramidate Derivatives

Abstract: An efficient synthesis of a series of novel diphenyl N-substituted carbamimidoyl phosphoramidate derivatives was accomplished in two steps. Diphenyl phosphorochloridate (1) was reacted with cyanamide (2) in the presence of 1,4-dimethylpiperazine as a base in THF at 50-55 • C to form an intermediate, diphenyl cyanophosphoramidate (3). Subsequently 3 was reacted with various aromatic/heterocyclic amines (4) in the presence of 1,4-dimethyl piperazine as a base at 55-60 • C to form the corresponding title compound… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
5
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 11 publications
(5 citation statements)
references
References 17 publications
0
5
0
Order By: Relevance
“…The chemical structures of all the title compounds 7a-e and 8a-e were characterized by IR, 1 H, 13 C, 31 P NMR, mass spectral data and elemental analyses and their data were presented in the experimental section. IR absorptions in the regions 3345-3308, 1236-1210 and 1018-1012 cm -1 were assigned to NH, P=O and P-O-C stretching vibrations respectively for the title compounds (Subramanyam et al, 2013). The 1 H NMR spectra gave signals due to Ar-H in the range of δ 8.13-6.82 ppm.…”
Section: Chemistrymentioning
confidence: 96%
“…The chemical structures of all the title compounds 7a-e and 8a-e were characterized by IR, 1 H, 13 C, 31 P NMR, mass spectral data and elemental analyses and their data were presented in the experimental section. IR absorptions in the regions 3345-3308, 1236-1210 and 1018-1012 cm -1 were assigned to NH, P=O and P-O-C stretching vibrations respectively for the title compounds (Subramanyam et al, 2013). The 1 H NMR spectra gave signals due to Ar-H in the range of δ 8.13-6.82 ppm.…”
Section: Chemistrymentioning
confidence: 96%
“…G‐Type (German‐agents) CWAs were developed starting from 1930s to 1940s, and include Cyanophosphoramidate, [20] Tabun (GA), [21] Sarin (GB), [22] Soman (GD) [23] and Cyclosarin (GF) [24] …”
Section: Classification Of Op Cwasmentioning
confidence: 99%
“…Today, OP CWAs can be classified into three main groups: G-type, V-type and, the most recent, Atype (also called Novichok) (Figure 1). [17][18][19] G-Type (German-agents) CWAs were developed starting from 1930s to 1940s, and include Cyanophosphoramidate, [20] Tabun (GA), [21] Sarin (GB), [22] Soman (GD) [23] and Cyclosarin (GF). [24] V-Type (venomousagents) CWAs, discovered after World War 2, are methylphosphothioates and collect two compounds: VX [25] and RVX.…”
Section: Classification Of Op Cwasmentioning
confidence: 99%
“…The first generation of NA, also called "G-Type" (German-agents), was discovered in the late 1930s and early 1940s. They include the Cyanophosphoramidate [19], Tabun (GA) [20] and methylfluorophosphonates compounds, such as Sarin (GB) [21], Soman (GD) [22] and Cyclosarin (GF) [23] (Figure 1).…”
Section: Definition Of Nasmentioning
confidence: 99%