A Novel Approach for the Synthesis of ( R ) and ( S )-Nicotine

Nicotine is an alkaloid mainly found in leaves of tobacco and is used thera-peutically for patients seeking relief from tobacco dependence in the form of products such as gums, patches, lozenges etc. In these products, majorly nicotine derived from tobacco is used which is inherently contaminated with undesirable nicotine related substances as impurities at low levels and is difficult to remove. Hence, use of synthetic nicotine is considered as an option which will be devoid of such impurities. In this work, a short and efficient synthesis of (R) and (S) nicotine was achieved by leveraging a key esterification between racemic homoallylic alcohol intermediate (2) and (S)-Ibuprofen (3) to produce diastereomers (5a) and (5b) which were easily separable under standard column chromatography conditions. Use of (S)-Ibuprofen (3) as a chiral re-solving agent constitutes a novel approach which was not reported earlier. A subsequent hydrolysis of the diastereomers furnished the homoallylic alcohol intermediates (S)-6a and (R)-6a with high enantiopurity, which was effectively translated to the corresponding (R)-nicotine and (S)-nicotine respectively


Introduction
Nicotine {(S)-3-(1-Methyl-2-pyrrolidinyl)pyridine} is a weakly basic bicyclic tertiary amine mostly found in tobacco plants (up to 2% -8%) as well as in few vegetables such as potatoes and tomatoes in minor quantities. There has been tremendous interest in nicotine chemistry, related pharmacology and metabolism primarily due to widespread exposure of nicotine among people through recreational use of tobacco products [1]. Being a molecule with one chiral centre, nicotine can exist in two sterioisomeric forms viz. (R) & (S) respectively ( Figure  1), with latter being the predominant enantiomer found in tobacco plants (>99%) [2] and is known to exhibit significant pharmacologic activity.
Though nicotine is traditionally known for its dependence potential, lately nicotine has attracted much attention because of its pharmacological effects on central nervous system (CNS) diseases. In particular, (S)-nicotine may have beneficial effects in the treatment of Parkinson's disease (PD), Alzheimer's disease (AD), Tourette's syndrome, schizophrenia, attention-deficit hyperactivity disorder (ADHD), smoking cessation, epilepsy, and depression [1]. Nicotine is administered in low dose levels to patients seeking relief from withdrawal symptoms associated with cessation of tobacco consumption. Products in this category, known as nicotine replacement therapy, include nicotine gums, nicotine lozenges, nicotine pouches, nicotine patches, nicotine nasal spray, mouth spray etc. In all these products, nicotine derived from tobacco is used as active pharmaceutical ingredient (API) either in its free form or as salt/resinate. However, nicotine derived from tobacco extraction is typically contaminated with a few inseparable alkaloids known as nicotine related substances. These alkaloids include nornicotine, anabasine, anatabine, myosmine, nicotyrine and cotinine. United States Pharmacopeia regulates certain levels for these impurities to ascertain nicotine purity. Additionally products utilizing nicotine sourced from tobacco falls under the regulatory arms of government bodies (For e.g. US FDAs Tobacco Control Act definition of "tobacco product" includes any product made or derived from tobacco and intended for human consumption, including any component, part or accessory of a tobacco product). Until recently, synthetic nicotine wasn't considered with-in US FDAs purview for regulation. These factors combined have prompted researchers to develop an efficient route to enantiomerically pure nicotine as it will be devoid of related impurities. Unlike tobacco derived nicotine, synthetic nicotine is colorless, odorless and does not impart harsh taste.
A thorough literature survey of earlier nicotine synthetic methods was conducted. The first synthesis of optically active nicotine was achieved by Chavdarian and co-workers in 1982 [3]. Other reported methods include strategies that utilize β-allyldiisopinocampheylborane to form chiral alcohol [4] [5] [6]. Another literature example revealed synthesis of nornicotine enantiomers by treating racemic nornicotine with optically pure (-) menthyl chloroformate, separating the N'-(menthoxycarbonyl) nor nicotine diastereomers and subsequent hydrolysis of the separated diastereomers to yield optically pure nornicotine [7]. Carolin Welter and co-workers reported enantioselective synthesis of (R) and (S)-nicotine based on Ir-catalysed allylic amination [8]. Other approaches to synthesis of nicotine were also reported in [9]- [14].
Synthesis of nicotine has been patented by few companies. Examples can be seen in synthesis and resolution of nicotine patented by NJOY, LLC (US) [15]. London based Zanoprima Life Sciences Ltd, have a patented method to produce (S) nicotine utilizing enzymatic reduction of myosmine as a key step [16]. United States based Next Generation Labs, LLC have patented their technology for the preparation of (R, S) nicotine [17]. Synthesis of nicotine was also patented by few other organizations such as CSIR India [18], Siegfried and Contraf-Nicotex-Tobacco GmbH [19] [20].
The strategy employed in this work is novel and differntiative from earlier reported synthesis in that we have successfully demonstrated use of (S)-Ibuprofen as a chiral resolving agent leading to the synthesis of (R) and (S) nicotine, circumventing any late stage separation of isomers. Also (S)-Ibuprofen can be recovered during the process (Step 4, Scheme A) and can be reused, which will make the process cost effective.

Synthesis of (R) and (S) Nicotine
Synthesis of (R) and (S) nicotine outlined in scheme A (separation and isolation of racemic alcohol in to enantiomerically pure forms) and Scheme B (conversion of separated enantiomerically pure alcohols in to (R) and (S) nicotine respectively). Data on specific rotation was recorded for the alcohols (S)-6a and (R)-6a and was compared against that reported in literature [21]. Same is captured in Table   1 below.

Separation and Quantification of (R) and (S) Nicotine through Chiral HPLC
Many methods are available for the separation and quantification of (R) and (S) nicotine in racemic mixture [22]- [27]. Based on these available literature me-thods, a simple one-step chiral high performance liquid chromatography (HPLC) method was developed to separate (R) and (S) enantiomers of nicotine using chiral amylose column.
(S)-nicotine and (R)-nicotine standards were procured from Sigma Aldrich for the quantification of synthesized (R) and (S) nicotine. The purity of these standards was determined using HPLC. Purity of (S)-nicotine standard was 100%, whereas purity of (R)-nicotine was observed as 97.5%.
(R) and (S)-nicotine in corresponding samples were determined by extracting the sample with n-hexane. The extracted solution was analyzed using HPLC equipped with Diode Array Detector (DAD) at 254 nm by using amylose column (5 µm × 4.6 mm × 250 mm), Flow was maintained at 0.5 mL/min, oven temperature was at 30˚C, injection volume was 10 µl and mobile phase was n-hexane and isopropanol in 98:2 ratio in isocratic condition. Total runtime was 30 min.
The peak resolution of (S)-nicotine and (R)-nicotine is found to be good ( Figure 2). The developed method has good precision and recovery rates for (S)-nicotine and (R)-nicotine (i.e., 97.2% & 98.9%, respectively.) Table 2 summarizes chiral purity obtained for synthesized (R) and (S) Nicotine using developed method.

Conclusion
Synthesis of (R) and (S) nicotine was achieved via a novel approach, which effectively separated racemic homoallylic alcohol intermediate (2) to its optically pure forms (S)-6a & (R)-6a. In this work, we reported the use of (S)-Ibuprofen as a chiral resolving agent, which facilitated the separation of racemic alcohol (2) through formation of separable Ibuprofen ester diastereomers and subsequent hydrolysis. Separation of racemic alcohol as reported here was found to be simple and straightforward method without requiring the need of expensive catalysts or enzymes.