34160-40-2Relevant articles and documents
Non-symmetrical, potentially redox non-innocent imino NHC pyridine 'pincers': Via a zinc ion template-assisted synthesis
Simler, Thomas,Danopoulos, Andreas A.,Braunstein, Pierre
, p. 5955 - 5964 (2017)
New non-symmetrical, redox-active imino NHC pyridine pincer ligands, 2-(R1-imidazol-2-ylidene)-6-(R2NCH)-pyridine (R1 = 2,6-diisopropylphenyl (DiPP), R2 = 2,4,6-trimethylphenyl (Mes), 4B; R1 = R2 = DiPP, 4C), have been accessed by a ZnII-promoted modular synthesis involving the quaternization of R1-imidazole by [Zn(κNimineκNpyridine)(2-(R2NCH)-6-bromo-pyridine)Cl2], followed by ZnII removal and deprotonation of imidazolium pro-ligands. Redox active forms of 4B were implicated in the two complexes obtained by its reaction with FeBr2/KC8; metrical data analysis pointed to the occurrence of radical anionic and dianionic redox states of 4B.
Synthesis, Structures, and Norbornene Polymerization Behavior of Imidazo[1,5- a]pyridine-sulfonate-Ligated Palladacycles
Dong, Jie,Li, Minliang,Wang, Baiquan
, p. 3786 - 3795 (2019)
Two imidazo[1,5-a]pyridine-sulfonate proligands, L1 and L2, were synthesized in five-step reactions. Treatment of the proligands with palladacycles {[Pd(OAc)(8-Me-quin-H)]2, [Pd(dmba)(μ-Cl)]2, and [Pd(o-acetanilido)(μ-trifluoroacetato)]2} yielded the desired five-membered C(sp3),N-chelated (Pd1, Pd2), C(sp2),N-chelated (Pd3, Pd4), and six-membered C(sp2),O-chelated (Pd5, Pd6) palladacycles, respectively. All these complexes were fully characterized by 1H and 13C NMR, IR, high-resolution mass spectrometry, and elemental analysis. The molecular structures of complexes Pd1, Pd2, Pd4, and Pd5 were determined by single-crystal X-ray diffraction analysis. In the presence of MAO or Et2AlCl, Pd1-Pd6 exhibited activities toward the addition polymerization of norbornene which decreased in the order Pd6 > Pd5 > Pd4 > Pd2 > Pd3 > Pd1. The Pd1-Pd6/MAO catalytic system showed high thermal stability and reached the highest activity at 100 °C (6.0 × 107 g of PNB (mol of Pd)-1 h-1 with 99.9% conversion). In the presence of Et2AlCl with low loading (100 equiv), Pd5 and Pd6 exhibited high activities (up to 2.9 × 107 g of PNB (mol of Pd)-1 h-1 with 96.5% conversion). It was demonstrated that the structures of palladacycles and the substituents on the ligands significantly affected the activities of these complexes.
Adenosine receptor antagonists
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Paragraph 0234-0236, (2020/12/15)
The invention provides a compound shown as a formula (I) and a pharmaceutical composition thereof. The compounds of formula (I) of the present invention are useful as adenosine receptor inhibitors, especially A2A and/or A2B inhibitors, for example, the product can be used for prevention or treatment of diseases associated with A2A and/or A2B activity or expression.
2 - Bromo -6 - aldehyde pyridine and its preparation method
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Paragraph 0058-0086, (2019/07/01)
The present invention provides a 2 - bromo - 6 - aldehyde pyridine and its preparation, wherein the preparation method comprises the following steps: step S1, in the 2 - bromo - 6 - methyl pyridine in an organic solution to react [...], generating 2 - bromo - 6 - bromo pyridine and 2 - bromo - 6 - ([...]) pyridine mixture; step S2, adding ethanol in the mixture, and wherein add hexamine, allowing the mixture to react, to obtain 2 - bromo - 6 - formyl pyridine; step S3, after the addition of an acid in the reaction system, make it undergo hydrolytic reaction, generating the 2 - bromo - 6 - aldehyde pyridine. According to the embodiment of the invention of 2 - bromo - 6 - aldehyde pyridine of the preparation method, can obtain a high purity of the product, and the method is safe, easy to process, the process is simple, and is suitable for industrial production.