Pyridine, 3-bromo amination

Basu et al. have reported palladium-catalyzed selective cross coupling of bromo-pyridines and amines on the surface of potassium fluoride supported basic aluminium oxide [5]. For example, amination of 2,6-dibromopyridine by this method afforded the monoaminated products predominantly, even after prolonged the reaction time and using excess amine, whereas previous method [6] gave only bis-aminated products (Scheme 5.3). 

Den Hertog and his co-workers have found that amination of 2-chloro-, 2-bromo-, and 2-iodo-pyridine with H2N yields only... 

The inferior activation in the 3- or 6eto-position is illustrated by the very large difference in reactivity in the following aminations and alkoxylations. In the reaction of 2-chloro-5-iodopyridine or 2,3-dibromopyridine (cf. 295) with boiling methanolic methoxide, only the 2-halogen is displaced as is also the case in the amination of 2-chloro-3,5-diiodopyridine and of 2,3,6-tribromopyridine. 4-Amination of 3,4-dibromo-, 2,3,4,5-tetrabromo-, and 3-bromo-4-chloro-pyridine occurred. Only 2-amination (aqueous NH3, 190°, 36 hr) occurred with 2,3-dichloropyridine (295) and only 4-ethoxyla-tion (alcoholic ethoxide, 160°, 4 hr) with 3,4-dichloropyridine. ... 

The dinitro derivative of compound 2 reacts with anhydro bases of pyridine and quinoline to give zwitterions such as 215 (99RCB1391). Compound 216 has been made from the 3-bromo derivative of compound 3 by reaction with an amine, as an intermediate in the production of stomach secretion inhibitors (80EUP48555),... 

Palladium-catalyzed aminations of aryl halides is now a well-documented process [86-88], Heo et al. showed that amino-substituted 2-pyridones 54 and 55 can be prepared in a two-step procedure via a microwave-assisted Buchwald-Hartwig amination reaction of 5- or 6-bromo-2-benzyloxypyri-dines 50 and 51 followed by a hydrogenolysis of the benzyl ether 52 and 53, as outlined in Fig. 9 [89]. The actual microwave-assisted Buchwald-Hartwig coupling was not performed directly at the 2-pyridone scaffold, but instead at the intermediate pyridine. Initially, the reaction was performed at 150 °C for 10 min with Pd2(dba)3 as the palladium source, which provided both the desired amino-pyridines (65% yield) as well as the debrominated pyridine. After improving the conditions, the best temperature and time to use proved... 

Fig. 9 Examples of Buchwald-Hartwig amination of bromo-pyridines and subsequent hydrogenolysis leading to amino-substituted 2-pyridones...

The reaction can be applied to simple epoxides if polyhydrogen fluoride-pyridine is the reagent. The epoxide-to-fluorohydrin conversion has also been carried out with Sip4 and a tertiary amine.Chloro-, bromo-, and iodohydrins can also be... 

DL-Valiolamine (205) was synthesized from the exo-alkene (247) derived from 51 with silver fluoride in pyridine. Compound 247 was treated with a peroxy acid, to give a single spiro epoxide (248, 89%) which was cleaved by way of anchimeric reaction in the presence of acetate ion to give, after acetylation, the tetraacetate 249. The bromo group was directly displaced with azide ion, the product was hydrogenated, and the amine acety-lated, to give the penta-A, 0-acetyl derivative (250,50%). On the other hand. 

Unsymmetric compartmental ligands that allow for the controlled synthesis of unsymmetric Ni2 or heterobimetallic NiM complexes have received particular attention.1876,1892 A wide range of such ligands derived particularly from 2-hydroxy-3-hydroxymethyl-5-methylbenzaldehyde and 2-hydroxy-3-hydroxymethyl-bromo-benzaldehyde has now been prepared and used for Ni com-plexation. These ligands have monopodal iminic pendent arms and either mono- or dipodal aminic pendent arms and the terminal donors of the pendent arms can be provided by pyridine, imidazole, and tertiary amino groups.1893-1897 Complexes are usually prepared by reaction of the requisite Ni11 salts with the preformed ligand. 

With the aim of developing new analogues of the cyclic AMP phosphodiesterase inhibitor lixazinone (554), the synthesis of agents 553 and 555-557 was undertaken (Scheme 167) (88JMC2136). Thus, all possible 1,2-related N-r-Boc aldehydes 551 were prepared by directed metalation on isomers 549, with the exception of that which required the use of a metal-halogen exchange reaction on the bromo precursor 550 (attempts to metalate 4-TMS-3-N-f-Boc pyridine proved inefficient). As exemplified for one particular isomer, conversion of 551 into 552 by reductive amination... 

Dialkylaminopyridines, which are active acylation catalysts, have been prepared by Patell and Sparrow,226 using secondary amines and 4-bromo-pyridine hydrochloride under liquid-liquid PT conditions. 

Another approach in the study of the mechanism and synthetic applications of bromination of alkenes and alkynes involves the use of crystalline bromine-amine complexes such as pyridine hydrobromide perbromide (PyHBts), pyridine dibromide (PyBn), and tetrabutylammonium tribromide (BiMNBn) which show stereochemical differences and improved selectivities for addition to alkenes and alkynes compared to Bn itself.81 The improved selectivity of bromination by PyHBn forms the basis for a synthetically useful procedure for selective monoprotection of the higher alkylated double bond in dienes by bromination (Scheme 42).80 The less-alkylated double bonds in dienes can be selectively monoprotected by tetrabromination followed by monodeprotection at the higher alkylated double bond by controlled-potential electrolysis (the reduction potential of vicinal dibromides is shifted to more anodic values with increasing alkylation Scheme 42).80 The question of which diastereotopic face in chiral allylic alcohols reacts with bromine has been probed by Midland and Halterman as part of a stereoselective synthesis of bromo epoxides (Scheme 43).82... 

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