50656-04-7

Upstream product

• 88405-47-4 p-cyano-N'-phenylbenzohydrazine 
• 105-07-7 4-cyanobenzaldehyde 
• 100-63-0 phenylhydrazine 
• 100726-23-6 4-((2-phenylhydrazono)methyl)benzonitrile 
• 6068-72-0 4-cyanobenzoyl chlorIde 

Downstream Products

• 67223-81-8 4-(1,5-diphenyl-4,5-dihydro-1H-pyrazol-3-yl)benzonitrile 
• 67223-85-2 4-(1,5,5-triphenyl-4,5-dihydro-1H-pyrazol-3-yl)-benzonitrile 
• 1251005-02-3 (3aR,6aR,3a'S,6a'S)-4,4'-[oxybis[(4,1-phenylene)(3a,4,6,6a-tetrahydro-4,6-dioxo-1-phenylpyrrolo[3,4-c]pyrazole-5,3(1H)-diyl)]]bis[benzonitrile] 
• 1251005-19-2 (3aR,6aR,3a'S,6a'S)-4,4'-[(4,1-phenylene)bis(3a,4,6,6a-tetrahydro-4,6-dioxo-1-phenylpyrrolo[3,4-c]pyrazole-5,3(1H)-diyl)]bis[benzonitrile] 
• 1251004-76-8 (3aR,6aR,3a'S,6a'S)-4,4'-[methylenebis[(4,1-phenylene)(3a,4,6,6a-tetrahydro-4,6-dioxo-1-phenylpyrrolo[3,4-c]pyrazole-5,3(1H)-diyl)]]bis[benzonitrile] 
• 1354908-63-6 4-[(3aS,6aS)-1,3a,4,5,6,6a-hexahydro-4,6-dioxo-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazol-3-yl]benzonitrile 

Relevant academic research and scientific papers

Sequential [3+2] annulation reaction of prop-2-ynylsulfonium salts and hydrazonyl chlorides: Synthesis of pyrazoles containing functional motifs

A novel sequential [3+2] annulation reaction has been developed using prop-2-ynylsulfonium salts and hydrazonyl chlorides, affording a series of pyrazoles with functional motifs that can be post modified in the preparation of various drugs or drug candidates. Further transformation and gram-scale operations could also be achieved efficiently. This journal is

Synthesis and stereochemistry of some novel dihydropyrrolo[3,4-c]pyrazoles

Eleven novel dihydropyrrolo[3,4-c]pyrazole derivatives were obtained by the reaction of chiral (1R)-N-(1-phenylethyl)maleimide and C,N-aryl-substituted nitril-imines. The reaction afforded the cycloadducts as a regioisomeric mixture which can be separable in some cases. The structure and stereochemistry of cycloadducts were assigned on the basis of infrared (IR), 1H and 13C nuclear magnetic resonance (NMR), mass and X-ray spectra, optical rotation measurements, and CHN analyses.

Synthesis, UV-Vis spectra, and Hammett correlation of some novel bis(dihydropyrrolo[3,4-c]pyrazoles)

Twenty-nine novel bis(dihydropyrrolo[3,4-c]pyrazole) derivatives were obtained by reacting C, N-phenyl-substituted nitrilimines generated in situ from corresponding hydrazonyl chlorides with bismaleimides. The structures were elucidated by physical and spectroscopic methods [m.p., Rf, infrared (IR),1H nuclear magnetic resonance (NMR), 13C NMR, correlation spectroscopy (COSY), heteronuclear correlation (HETCOR), nuclear Overhauser effect (NOE), and high-resolution mass spectrometry (HRMS)]. Also, Hammett correlation graphs were obtained between Hammett constants σp and λmax values of bis(pyrrolopyrazoles) carrying p-substituted phenyl-ring-bearing electron-withdrawing and electrondonating groups and discussed in terms of substituent effects. Springer-Verlag 2010.

The Preparation and Spectroscopic Properties of Some Di- and Tri-substituted 1,3,5-Triphenyl-2-pyrazolines and Related 2-Pyrazolines

The effect of substituents on the absorption and fluorescence properties of a number of di- and tri-para-substituted 1,3,5-triphenyl-2-pyrazolines, several substituted 1,3,5,5-tetraphenyl-and trans-1,3,4,5-tetraphenyl-2-pyranolines, and some 1,3-diphenyl-