4833-42-5

Upstream product

• 62-53-3 aniline 
• 538-75-0 dicyclohexyl-carbodiimide 
• 122-66-7 diphenyl hydrazine 
• 3878-67-9 N-phenyl-N'-cyclohexyl carbodiimide 
• 108-91-8 cyclohexylamine 
• 722-03-2 N-cyclohexyl-N'-phenylthiourea 
• 103-72-0 phenyl isothiocyanate 
• 29882-02-8 N',N''-dicyclohexyl-N,N-dimethylguanidine 

Downstream Products

• 1392502-74-7 C₂₁H₂₇N₃O₂ 

Relevant academic research and scientific papers

Two unprecedented aromatic guanidines supramolecular chains self-assembled by hydrogen bonding interaction

Two aromatic guanidine derivatives, C6H5N = C(NHCy)2 (1), (n-TBA)C6H5NHC(NHCy)2Mo2O7 (2) (Cy = cyclohexyl), were synthetized with high yields. Both of them self-assemb

L-Cysteine capped Zn nanoparticles catalyzed synthesis of guanidines

A highly chemoselective method for the coupling of carbodiimides with primary amines to synthesize guanidines is achieved using L-cysteine capped zinc nanoparticles (NPs) as a catalyst. The efficiency of the catalyst is proved by recyclability and reusability studies. Surface characterization of the catalyst before and after its repetitive usage proved the stability of the catalyst.

Nanoparticulate copper(II) oxide catalyzed synthesis of guanidine derivatives and their conversion into functionalized iminoguanidines

Abstract A simple synthesis of functionalized iminoguanidines from N-sulfoketenimines and N,N′,N′′-trisubstituted guanidines, generated by nanoparticulate copper(II) oxide-catalyzed hydroamination of di(cyclo)alkylcarbodiimides, is described.

Five-coordination aluminum complexes: Synthesis, crystal structures and utilization for the construction of substituted guanidines

Insertion of 2,6-iPr2C6H3N(Li)SiMe3 or PhN(Li)SiMe3 to the CN bond of Me2NCN or PhCN afforded the lithium complexes [Li(2,6-iPr2C6H3)NC(NMe2)NC(NMe2)N(SiMe3)]2 (1a) and [Li(PhNC(Ph)NSiMe3)]2 (1b). Complexes 1a and 1b were used as precursors to react with AlCl3 affording [(2,6-iPr2C6H3)NC(NMe2)NC(NMe2)N(SiMe3)]2AlCl (2) and [(PhNC(Ph)NSiMe3)]2AlCl (3), respectively. The structures of 2 and 3 were presented. Both 2 and 3 exhibit good activity to catalyze the addition reaction of arylamines to N,N'-diisopropylcarbodiimide.

Combination of air/moisture/ambient temperature compatible organolithium chemistry with sustainable solvents: Selective and efficient synthesis of guanidines and amidines

Highly-efficient and selective fast addition of in situ generated lithium amides [LiN(H)R] (obtained via an acid-base reaction between n-BuLi and the desired primary amine) into carbodiimides (R-NCN-R) or nitriles (R-CN) has been studied, for the first ti

Synthesis, structure and catalytic activity of rare-earth metal amino complexes incorporating imino-functionalized indolyl ligand

The reactions of the imino-functionalized indolyl ligand (HL, L = 3-(4-Me2N-C6H4CH=N-CH2CH2)C8H5N) with the rare-earth metal amides [(Me3Si)2N]3RE(μ-Cl)Li(THF)3 producing different types of rare-earth metal amido complexes were investigated. The reactions of HL with 1 equiv. of [(Me3Si)2N]3RE(μ-Cl)Li(THF)3 generated a series of hetero-nuclear bimetallic rare-earth metal amino complexes {[η1:μ-η2-3-(4-Me2N-C6H4CH=N-CH2CH2)C8H5]RE[N(SiMe3)2]2(μ-Cl)Li(THF)} (RE = Y(1), Sm(2), Gd(3), Er(4), Yb(5)). By extending the reaction time, only the reaction of HL with [(Me3Si)2N]3Gd(μ-Cl)Li(THF)3 gave an unexpected binuclear rare-earth metal complex {[(μ-η5:η1):η1:η1-3-[(Me2N)2-C14H9]-(NCH2CH2-C8H5N)2]Gd2[N(SiMe3)2]3} (6) incorporating a novel polycyclic ligand through C-C and C-N coupling. Treatment of HL with [(Me3Si)2N]3Sm(μ-Cl)Li(THF)3 in a 2:1 ratio generated the bis(indolyl) heteronuclear bimetallic rare-earth metal amino complex {(η1:η1-[μ-η2:η1-3-(4-Me2N-C6H4CH=N-CH2CH2)C8H5]Li[μ-η2:η1-3-(4-Me2N-C6H4CH=N-CH2CH2)C8H5])Sm[N(SiMe3)2]2} (7) in low yield probably due to accompanying with the formation of the complex 2. The above results indicated that reaction conditions play important roles in the formation of different coordination modes of the imino-functionalized indolyl rare-earth metal amido complexes. All new complexes 1?7 are fully characterized including X-ray structural determination. The catalytic activity of complexes 1-7 for the addition of amines to carbodiimides was explored. The results showed that all complexes displayed an excellent activity towards the addition of amines to carbodiimides producing guanidine under solvent-free condition.

Synthesis and Reactivity of NNNNN-Pincer Multidentate Pyrrolyl Rare-Earth-Metal Amido-Chloride or Dialkyl Complexes

The NNNNN-pincer multidentate pyrrolyl rare-earth-metal amido-chloride complexes {η1:κ3-2,5-[CH3N(CH2CH2)2NCH2]2C4H2N}RECl[N(SiMe3)2] (RE = Y (2a), Sm (2b), Dy (2c), Er (2d), Yb (2e)) were synthesized by one step from reactions of [(Me3Si)2N]3RE(μ-Cl)Li(T

A silica-supported titanium catalyst for heterogeneous hydroamination and multicomponent coupling reactions

Highly dehydrated silica gel, SiO2700, gave a material with a total surface hydroxyl density of 0.31 ± 0.05 mmol g-1, 0.9 ± 0.1 Si-OH sites per nm2. Treatment of this material with Ti(NMe2)4/sub

Micelle-Enabled One-Pot Guanidine Synthesis in Water Directly from Isothiocyanate using Hypervalent Iodine(III) Reagents under Mild Conditions

In this work, we developed a one-pot synthesis of guanidine directly from isothiocyanate using DIB (diacetoxyiodobenzene) as a desulfurizing agent under micellar conditions in water. Our optimization study revealed that the use of 1 % TPGS-750-M as a surfactant with NaOH as an additive base at room temperature can convert a variety of isothiocyanates and amines into corresponding guanidines in excellent yields (69–95 %). This synthetic process in water can be applied to prepare guanidine at gram-scale quantity. Our aqueous micellar medium also demonstrated high reusability as the reaction can be performed for several cycles without losing its efficiency. The reaction is metal-free, utilizes water as solvent and practical (room temperature and open flask).

2-Picolylamino(diphenylphosphinoselenoic)amide supported zinc complexes: Efficient catalyst for insertion of N–H bond into carbodiimides, isocyanates, and isothiocyanate

We report here the hydroamination of heterocumulenes such as carbodiimides, isocyanates, and isothiocyanates by zinc complexes supported by the ligand 2-picolylamino-(diphenylphosphinoselenoic)amide [{(Ph2P-(?Se)}2NCH2(C5H4N)] (1). A series of zinc complexes [κ2-{(Ph2P-(?Se)}2NCH2(C5H4N)ZnX2] [(X?Cl (2), Br (3a), I (4)] were prepared from ligand 1 and the corresponding zinc dihalide in a 1:1 molar ratio at 60°C in a chloroform solvent. The reaction of ligand 1 and ZnBr2 in methanol yielded another zinc complex [κ2-{(Ph2P-(?Se)}2NCH2(C5H4N)ZnBr2(CH3OH)] (3b). The molecular structures of compounds 3a, 3b, and 4 were established through single-crystal X-ray diffraction analyses. The solid-state structures of all the complexes revealed a κ2- chelation through pyridine nitrogen and selenium atoms of ligand 1 to the zinc ion. Complex 2 proved to be a competent pre-catalyst for the addition of the amine N–H bond to carbodiimides, isocyanates, and isothiocyanates. The reaction scope was expanded to reactions of aliphatic and aromatic amines with phenylisocyanate and phenylisothiocyanate in toluene solvents, which proceeded rapidly at room temperature with 5 mol% catalyst loading to yield (up to 99%) the corresponding derivatives of urea and thio-urea. However, a temperature of 90°C was needed for the hydroamination of N,N′ dicyclohexylcarbodiimide. We also report the most plausible mechanism of the hydroamination reaction.