10330-56-0

Upstream product

• 1722-10-7 3-chloro-6-methoxypyridazine 
• 5720-05-8 4-methylphenylboronic acid 
• 124-41-4 sodium methylate 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 106-38-7 para-bromotoluene 
• 195062-57-8 p-tolylboronic pinacol ester 
• 624-31-7 4-tolyl iodide 

Relevant academic research and scientific papers

Suzuki-miyaura cross-coupling under solvent-free conditions

A solvent-free reaction protocol for Suzuki-Miyaura cross-couplings was developed. (Hetero)aryl bromides and chlorides are coupled with pinacol arylboronates in high yields. The reaction is catalyzed by conventional bis(triphenylphosphine)palladium(II) chloride [(PPh3) 2PdCl2] and/or palladium(II) acetate/SPhos [Pd(OAc) 2/SPhos] under air. Copyright

Substituent-dependent structures and catalysis of benzimidazole-tethered N-heterocyclic carbene complexes of Ag(i), Ni(ii) and Pd(ii)

Homoleptic cationic benzimidazole-imidazolin-2-ylidene N-heterocyclic carbene (NHC = L) complexes of NiII and PdII have been prepared directly from the ligand precursor in salt form [H.L]Cl and from the transmetallation route via AgI. The N-tether of the imidazolinylidene ring imposes a significant influence on the nuclearity of the intermediate Ag(i)-NHC complexes and the geometric isomer outcome of the d8 products. Use of a benzyl-substituted NHC gives [Ag4(L Bn)2Cl4], 2a (from [HLBn]Cl, 1a, and Ag2O) (Bn = benzyl), which shows an alignment of four silver atoms bridged by the difunctional C-N ligands and chlorides. Its transmetallation with NiCl2(PPh3)4 and PdCl2(MeCN) 2 results in double-metal salts 2[M(LBn)2] 2+[Ag4Cl8]4- (M = Ni (3a) and Pd (4a)). The nuclearity of the Ag4 aggregate is maintained in the transmetallation process. Their Ag-free forms [M(LBn) 2]Cl2 (M = Ni (5) and Pd (6)) were prepared by direct deprotonation of 1a with M(OAc)2. The two carbenic carbon donor are cis- to each other in both 3a and 4a, thus imposing the weaker σ-benzimidazole nitrogen donor to be trans to them. A sterically demanding mesityl pendant however gives the dinuclear dissymmetic [Ag2(L Mes)2Cl2], 2b (Mes = mesityl) that shows a 12-membered metallomacrocyclic ring with a 2-coordinated [AgI(NHC) 2] and 4-coordinated [AgI(Imd)2Cl2] (Imd = imidazole). Transmetallation of the latter, or direct metallation from [HLMes]Cl, 1b, gives [M(LMes)2]Cl2 (M = Ni (3b) and Pd (4b)) with the two carbonic carbon trans to each other. The catalytic potential of 3b and 4b, which are more effective than 5 and 6, has been demonstrated by their high activities in Ni-catalyzed Kumada at room temperature and Pd-catalyzed Heck couplings of aryl and/or heteroaryl halides, respectively.

Preparation of functionalized aryl- and heteroarylpyridazines by nickel-catalyzed electrochemical cross-coupling reactions

(Chemical Equation Presented) A general efficient electrochemical method for the preparation of aryl- and heteroarylpyridazines in a nickel-catalyzed cross-coupling reaction of 3-chloro-6-methoxypyridazine and 3-chloro-6- methylpyridazine with a range of functionalized aryl or heteroaryl halides is reported.

Synthesis of substituted 3-amino-6-arylpyridazines via Suzuki reaction

Starting from the commercially available 3,6-dichloropyridazine, N3- substituted 3-amino-6-arylpyridazines were prepared in good yields and under mild conditions by means of two simple steps: a nucleophilic substitution and a palladium-catalyzed Suzuki coupling.