A Straightforward and Efficient Method for the Synthesis of Diversely Substituted β-Aminoketones and γ-Aminoalcohols from 3-( N , N-Dimethylamino ) propiophenones as Starting Materials

Bibliotecas de novos β-aminocetonas e γ-aminoálcoois que mostram uma grande diversidade estrutural foram facilmente obtidas a partir de uma abordagem simple, utilizando os derivados da 3-(N,N-dimetilamino)propiofenona como material de partida chave. O procedimento envolveu inicialmente a N-alquilação de benzilaminas secundárias com derivados de propiofenona produzindo as desejadas β-aminocetonas. A redução química ou catalítica dos grupos carbonilo atinge a obtenção dos γ-aminoálcoois em bons rendimentos. Este protocolo mostrou ser uma via alternativa conveniente para a síntese do anestésico local Falicain e para a droga tópica antifúngica Naftifina.


Introduction
Amino-ketones and aminoalcohols are compounds with superior importance not only for their practical applications displayed by themselves but also because they have been found forming part of the structure of synthetic and naturally occurring compounds of diverse practical interest. 1Thus, Falicain ® (a local anesthetic and bronchomotor), 2 compound BE-2254 (antihypertensive and very selective α 1 -adrenoceptor antagonist, precursor of the 3-125 I-derivative), 3 Moban (a neuroleptic) 4 and the benzylamine derivative 1 (a potent Jak3 kinase inhibitor), 5 are representative examples of this large family of amino-compounds (Figure 1), as well as the naturally occurring aminoalcohols Anisomycin (a potent activator of stress-activated protein kinases (JNK/SAPK) and p38 MAP kinase) 6 and Castanospermine (a potent inhibitor of αand β-glucosidases inhibits HIV syncytium formation and replication), 7 the synthetic aminoalcohols Salbutamol (a non-selective β-adrenergic agonist, more potent for β 2 than β 1 receptors) 8 and the phenyl/thienylγ-aminoalcohols 2 (direct precursors for the synthesis of Fluoxetine (Ar = Ph) and Duloxetine (Ar = 2-thyenyl), selective serotonin reuptake inhibitors). 9articularly, Guarna et al. 10 reported the synthesis of new γ-aminoalcohols 7 as potential 125 I-radioligands for dopamine and serotonin receptors.The synthesis of these compounds was achieved in a four-step sequence as described in Scheme 1. Continuing with our studies toward the synthesis and functionalization of benzylamine derivatives, [11][12][13] herein, we report our results on alternative and simple approaches for the synthesis of new β-aminoketones 10 and their subsequent reduction to the corresponding γ-aminoalcohols 11, structurally Vol. 24, No. 9, 2013 related to the active compounds 1, 2 and 7, from secondary benzylamines and 3-(N,N-dimethylamino)propiophenone derivatives, as easily accessible starting materials (Scheme 2).

Experimental
Melting points were determined on a Büchi B-450 melting point apparatus and are uncorrected.Infrared (IR) spectra were recorded on a Shimadzu FTIR 8400 spectrophotometer in KBr disks and films. 1 H and 13 C nuclear magnetic resonance (NMR) spectra were recorded on a Bruker Avance 400 spectrometer operating at 400 and 100 MHz, respectively, using CDCl 3 as solvent and tetramethylsilane as internal standard for 1 H NMR. Mass spectra were run on a Shimadzu 2010-DI-2010 GC-MS apparatus (equipped with a direct inlet probe) operating at 70 eV.Microanalyses were performed on an Agilent elemental analyzer and the results are within ± 0.4% of the theoretical values.Silica gel plates (Merck 60 F 254 ) were used for analytical TLC.The starting amines 8a-d and 8f-h (Figure 2) were purchased from Aldrich, Fluka and Acros and were used without further purification.Owing that benzylamine 8e is commercially unavailable, it was synthesized by a reductive amination from benzylamine and 3,4,5-trimethoxybenzaldehyde, following a similar procedure as described previously. 11,12The 3-(N,N-dimethylamino) propiophenone hydrochlorides 9a-d were synthesized from their respective acetophenones by following a procedure similar to that described in the literature. 14neral procedure for the synthesis of the β-aminoketones (10)   A mixture of amine 8 (500 mg) and the corresponding 3-(N,N-dimethylamino)propiophenone hydrochloride 9 (1 mmol) was dissolved in a mixture of 1,4-dioxane (5 mL) and triethylamine (TEA, 1 mL).The solution was stirred at reflux for 0.5-2 h until the starting materials were not further detected by TLC.After cooling, the solvent was removed under reduced pressure and the crude was purified by column chromatography on silica gel, using a mixture of CH 2 Cl 2 :AcOEt (5:1) as eluent.General procedure for the synthesis of γ-aminoalcohols (11)   Approach A: Raney-nickel was added (100 mg) to a sample of aminoketone 10 (300 mg) dissolved in ethanol (15 mL), and then was stirred for 3-4 h at room temperature under hydrogen pressure (50 psi) in a Parr apparatus.When the starting material was not detected by TLC and by the IR spectrum, the catalyst was filtered off, the solvent was removed under reduced pressure and the residue was purified by column chromatography on silica gel, using a mixture of CH 2 Cl 2 :MeOH (20:1) as eluent.
Approach B: Solid NaBH 4 (2 mmol) was added portionwise to a sample of aminoketone 10 (300 mg, 1 mmol) dissolved in methanol (5 mL), and then was stirred for 0.5-1 h at room temperature.When the starting material 10 was not further detected by TLC, the volume of the reaction mixture was reduced to 1 mL under reduced pressure, and water (5 mL) was added.The aqueous solution was extracted with ethyl acetate (2 × 5 mL), and the combined organic extracts were dried with Na 2 SO 4 .After removal of the solvent, the residue was purified by column chromatography on silica gel, using a mixture of CH 2 Cl 2 :MeOH (20:1) as eluent.

Results and Discussion
Initially, a mixture of benzylmethylamine 8a (R = Me, 1 mmol) and N,N-dimethylaminopropiophenone hydrochloride 9a (Ar = Ph, 1 mmol) 14 was subjected to reflux for 4 h in ethanol (step i, Scheme 2).This (approach 1) provided the corresponding β-aminoketone 10a (R = Me, Ar = Ph) as a pale yellow oily material in only 30% isolated yield.Repeating the same reaction but using a 4:1 ethanol:TEA mixture (approach 2), afforded 10a in 68% isolated yield, after 2 h of heating.Pursuing to improve the efficiency of the formation of ketone 10a, the reaction was repeated but using a 5:1 v/v mixture of 1,4-dioxane:TEA (approach 3).After heating for 1 h and verifying complete consumption of the starting materials (TLC control), product 10a was obtained in 88% isolated yield.
Once established the better reaction conditions and in order to determine its scope and general character, the approach 3 was extended to the benzylamine chemset 8a-e and propiophenone chemset 9a-d (Figure 2).To our satisfaction, the corresponding β-aminoketones 10a-k were fairly obtained in 0.5-2 h reaction times and 62-90% isolated yields, as shown in Table 1.The IR spectra of compounds 10 showed absorption bands corresponding to the C=O moiety in the range of 1671-1696 cm -1 .In the case of 10f, an additional hydroxyl broad band was observed at 3426 cm -1 corresponding to the OH group.The main signals in the 1 H NMR spectra corresponded to a triplet integrating for 2H in the range of 2.70-3.01ppm, assigned to the H-2 protons, a triplet for 2H in the range of 3.08-3.22ppm, assigned to the H-3 protons, and a singlet for 2H (or 4H) in the range of 3.56-3.98ppm, assigned to the benzylic protons.The more relevant features in the 13 C NMR spectra of compounds 10 corresponded to signals in the ranges 36.4-36.9,48.5-52.4,58.2-62.5 and 197.9-199.6 ppm, which were assigned to the C-2 carbon atoms, the C-3 carbons, the methylene carbon atom of the benzyl functionality and the C=O carbon atoms, respectively.
Most of the mass spectra of compounds 10 are characterized by low-intensity peaks for their molecular ions and base peaks at m/z 91, corresponding to the tropylium ion resulting from the benzyl functionality.In the case of structures 10j and 10k, which possess two possible tropylium ions, the base peak appears at m/z 181 due to the higher stability of its trimethoxy analogue than the proper tropylium ion.
Once the β-aminoketones 10 were efficiently obtained, reduction of their carbonyl groups was undertaken (step ii, Scheme 2).Recently, Cho and Kang 15 reported an efficient chemical reduction of carbonyl derivatives by grinding a mixture of the respective carbonyl compound and NaBH 4 in the presence of benzoic acid in a mortar.Unfortunately, the extension of this procedure to β-aminoketone 10a was unsuccessful and no product 11a was formed.Moreover, this reaction was difficult to handle.In a second approach, compound 10a was dissolved in methanol and subjected to a catalytic hydrogenation at room temperature in a Parr   16 affording the corresponding γ-aminoalcohol 11a as a light oily material in 84% isolated yield.Trying to simplify the reduction procedure, aminoketone 10a was treated with NaBH 4 in methanol at room temperature, affording the γ-aminoalcohol 11a in 82% isolated yield.At this point, it is worth mentioning that catalytic hydrogenation provided a slightly better yield and an easier work-up than the borohydride-mediated reduction.According to these results, the reduction of the remaining aminoketones 10 either by catalytic hydrogenation or chemical reduction afforded the corresponding γ-aminoalcohols 11 in 72-93 or 57-96% isolated yields, respectively (Table 1).The absence of the C=O absorption bands and the observation of new O-H absorption broad bands in the range of 3218-3409 cm -1 were the main features of the IR spectra of compounds 11.The main signals in the 1 H NMR spectra corresponded to a multiplet integrating for 2H in the range of 1.73-2.04ppm, assigned to the H-2 protons, a double-double-doublet for 1H in the range of 2.56-2.68ppm, assigned to a diastereotopic H-3 proton, a double-double-doublet for 1H in the range of 2.69-3.64ppm, assigned to the other H-3 proton, a pair of doublet (1H each) in the ranges 3.29-3.64and 3.61-3.88ppm, assigned to both diastereotopic benzylic methylene protons (PhCH 2 ), and a double-doublet for 1H in the range of 4.71-5.00ppm assigned to the H-1 proton.Some hydroxyl protons appeared as broad singlets in the range of 5.42-6.46ppm.Likewise, the more relevant feature in the 13 C NMR spectra of compounds 11 was the appearance of a new aliphatic signal in the range of 73.7-75.6 ppm, assigned to the C-1 carbon atom.The disappearance of the C=O signals are also in agreement with the assigned structures.The mass spectra also showed the tropylium ions as base peaks and as the main signals.
According to the results, the formation of the β-aminoketones 10 should proceed via two possible processes, either a S N 2 type reaction or alternatively through a Michael type addition, as shown in Scheme 3.
A S N 2 process is more likely to proceed under neutral or acidic conditions, in which the dimethyl ammonium moiety of the aminoketone salt (9) should behave as a good leaving group. 25,26In this sense, the formation of the product 10a under approach 1 should be governed mainly by this mechanistic pathway.Meanwhile, when the reaction was carried out in basic media (approaches 2 and 3), a Michael type addition should be the more likely mechanistic pathway, mediated by an arylvinyl ketone (12). 27Formation of this intermediate should be facilitated by the action of TEA via a Hofmann type β-elimination. 26The detection of this intermediate in the reaction media and some reports of the literature  24 Vol.24, No. 9, 2013 support this proposal, 27 which is also reinforced by the relative acidity of the α-hydrogen atoms in 9, which should be relatively easy to be removed by TEA as the initial step for the elimination process (Scheme 3).
To evaluate the scope of this two-step protocol, the heterocyclic derivatives 11l and 11m were efficiently obtained by treatment of propiophenones 9a and 9b, respectively, with morpholine 8f and the subsequent reduction of their carbonyl groups.Likewise, the β-aminoketone 10n was fairly obtained from the reaction of propiophenone 9c with piperidine 8g.Interestingly, the piperidine derivative 10n is structurally close to the anesthetic Falicain ® (Scheme 1); Therefore, this approach could become an alternative synthetic route for Falicain ® and derivatives (Scheme 4).
To further confirm the practical scope of our two-step protocol, we envisioned the possibility of developing an alternative synthetic route towards Naftifine, ® a recognized and highly active antifungal agent. 31Initially, the commercially available naphthylamine 8h was treated with propiophenone 9a to afford the aminoketone 10o in 89% isolated yield.Then, reduction of 10o with NaBH 4 /MeOH at room temperature afforded the aminoalcohol 11o in 98% isolated yield, which was dehydrated by treatment with refluxing 5 eq-g L -1 HCl to afford the expected product in 86% isolated yield (Scheme 5).

Conclusion
In summary, we developed a straightforward, versatile and simple approach for the synthesis of new β-aminoketones (10) and their corresponding γ-aminoalcohols (11), structurally related to relevant active compounds, by reaction of secondary benzylamines with 3-(N,N-dimethylamino)propiophenone salts.Several of the obtained compounds and 11 have previously been reported elsewhere; however, under our modified conditions they have been obtained in better or at least comparable yields.Finally, the usefulness of the procedure as an alternative synthesis of biologically active products like Falicain ® and Naftifine ® was explored.
a c