Patent Application
20250188028
Provided herein is a method for the chemical synthesis of an ionizable lipid.
Nucleic acid-based therapeutics have enormous potential in medicine. To realize this potential, however, the nucleic acid must be delivered to a target site in a patient. This presents challenges since nucleic acid is rapidly degraded by enzymes in the plasma upon administration. Even if the nucleic acid is delivered to a disease site, there still remains the challenge of intracellular delivery. To address these problems, lipid nanoparticles have been developed that protect nucleic acid from such degradation and facilitate delivery across cellular membranes to gain access to the intracellular compartment, where the relevant translation machinery resides.
A key component of lipid nanoparticles is an ionizable lipid. The ionizable lipid is typically positively charged at low pH, which facilitates association with the negatively charged nucleic acid. However, the ionizable lipid is neutral at physiological pH, making it more biocompatible in biological systems. Further, it has been suggested that after the lipid nanoparticles are taken up by a cell by endocytosis, the ionizability of these lipids at low pH enables endosomal escape. This in turn enables the nucleic acid to be released into the intracellular compartment.
An earlier example of a lipid nanoparticle product approved for clinical use and reliant on ionizable lipid is Onpattro®, developed by Alnylam. Onpattro® is a lipid nanoparticle-based short interfering RNA (siRNA) drug for the treatment of polyneuropathies induced by hereditary transthyretin amyloidosis. Onpattro® is reliant on an ionizable lipid referred to as “DLin-MC3-DMA” or more commonly “MC3”, 1 (
While the foregoing ionizable lipids are especially efficacious for the delivery of siRNA-containing LNPs to hepatic cells, they are much less effective for the hepatic delivery of mRNA-containing LNPs. To illustrate, mRNA vaccines, including the COVID-19 Pfizer/BioNTech and Moderna vaccines, rely on lipid nanoparticles to deliver mRNA to the cytoplasm of liver cells. After entry into the host cell, the mRNA is transcribed to produce antigenic proteins. In the case of the COVID-19 vaccines, the mRNA encodes the highly immunogenic Sars-Cov-2 spike protein. Such vaccines, however, incorporate no MC3 or KC2, but other types of ionizable lipids. In particular, the Pfizer/BioNTech vaccine comprises an ionizable lipid referred to as “ALC-0315”, 3 (Scheme 1).
The synthesis of 3 has been described in U.S. Pat. No. 10,166,298. However, the disclosed synthesis is low-yielding and it generates large quantities of byproducts, thereby making the synthesis wasteful. Moreover, the synthesis employs problematic reagents, such as pyridinium chlorochromate (PCC). The PCC compound is a chemical oxidant based on hexavalent chromium [“Cr(VI)”], which is a known carcinogen.
There is a pressing need in the art for a better synthesis of lipids including, but not limited to, ALC-0315, that affords higher yields, is less wasteful, and/or avoids the use of problematic Cr(VI)-based reagents. Such a need remains unmet in the industry. The present disclosure addresses the shortcomings in the art and/or provides an alternative synthetic process that circumvents one or more of the above difficulties.
The present disclosure provides methods for the preparation of amino lipids. Examples include ALC-0315 [systematic name: ((4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate)] and other lipids, including but not limited to those that are structurally similar to ALC-0315.
According to one aspect of the disclosure, there is provided a method for producing an ionizable amino lipid, or a pharmaceutically acceptable salt thereof, the method comprising a nucleophilic displacement of a leaving group L in a compound of Formula II,
According to one embodiment, the n of (CH2)n in G1 is 2 to 8.
According to another embodiment, the R of Formula II is a branched chain that comprises two hydrophobic carbon chains, R1 and R2, each of the chains being independently linear, unsubstituted C2 to C12 alkyl with 0 double bonds and wherein a carbon branch point is at an alpha, beta or gamma position relative to the carbonyl group of Formula II.
According to a further embodiment, the nucleophilic displacement comprises reacting a compound of Formula II with an amino alcohol in the single alkylation reaction and wherein Formula II has the structure of Formula I below:
According to a further embodiment, the nucleophilic displacement comprises reacting the first and second compounds of Formula II in the sequential displacement reactions and wherein the first or second compound of Formula II has a structure of Formula IV below:
According to a further embodiment, the amino alcohol is 4-amino-1-butanol.
In yet a further embodiment, the nucleophilic displacement is carried out in a polar solvent with a base and optionally with a source of iodide ion.
According to a further embodiment, the base is a metal carbonate.
According to another embodiment, the optional source of iodide ion is lithium iodide, sodium iodide, potassium iodide, or a tetraalkylammonium iodide.
According to another embodiment, the method further comprises producing the compound of Formula II via an esterification reaction between a carboxylic acid having the structure of Formula V, wherein R1 and R2 are independently substituted, unsubstituted, branched or unbranched C1-C20 alkyl having 0 to 3 double bonds, and an alcohol with a terminal leaving group L as defined by the structure of Formula VI, wherein G1 is (CH2)n, and wherein n is 2 to 10 and L is the leaving group
In yet another embodiment, the method further comprises producing the compound of Formula II via an esterification reaction between a carboxylic acid having a structure of Formula V, wherein R1 and R2 are independently substituted, unsubstituted, branched or unbranched C1-C20 alkyl having 0 to 3 double bonds, and a hydroxyl group of a diol having the structure of Formula VII, wherein G1 is (CH2)n, and wherein n is 2 to 10; and wherein
According to a further embodiment, the esterification reaction is a Fischer esterification that is carried out in an inert solvent capable of forming an azeotrope with water.
According to another embodiment, the inert solvent is toluene, cyclohexane, 1,2-dichloroethane.
According to a further embodiment, the water produced during the esterification is removed such that the carboxylic acid serves as an acid catalyst for the esterification reaction.
According to a further embodiment, an acid catalyst is used in the esterification, the acid catalyst selected from sulfuric acid, phosphoric acid, para-toluenesulfonic acid, sodium hydrogen sulfate, or a sulfonated polystyrene resin.
In a further embodiment, the nucleophilic displacement comprises the single alkylation and wherein the ionizable lipid produced is ALC-0315.
According to another aspect, there is provided an intermediate for preparing an amino ionizable lipid, the intermediate having a structure of Formula I:
According to another aspect, there is provided an intermediate for preparing an amino ionizable lipid, the intermediate having a structure of Formula IX,
According to another aspect, there is provided an intermediate for preparing an amino ionizable lipid, the intermediate having a structure of Formula X below:
According to another embodiment, the L of either of the foregoing intermediates is bromine, chlorine, a tosylate or a mesylate.
According to another aspect, there is provided a method for preparing the intermediate of any one of the aspects or embodiments described above, comprising:
or
According to a further embodiment, the esterification reaction is a Fischer esterification that is carried out in an inert solvent capable of forming an azeotrope with water.
According to a further embodiment, the inert solvent is toluene, cyclohexane, 1,2-dichloroethane.
According to another embodiment, the water produced during the esterification is removed such that the carboxylic acid serves as an acid catalyst for the esterification reaction.
In a further embodiment, an acid catalyst is used in the esterification, the acid catalyst selected from sulfuric acid, para-toluenesulfonic acid, sodium hydrogen sulfate, or a sulfonated polystyrene resin.
In some non-limiting embodiments, the foregoing methods comprise the nucleophilic displacement of a leaving group L in a compound of Formula I with 4-amino-1-butanol, resulting in formation of an amino lipid, such as ALC-0315 or structurally related ionizable lipids.
Group L can be a halogen, such as bromide, or a sulfonate, such as mesylate or tosylate. Furthermore, the nucleophilic displacement is carried out in an appropriate solvent, at an appropriate temperature, and in the presence of a base such as a metal carbonate.
Provided herein are also methods for the preparation of compounds of Formula I wherein L=Br or L=O—SO2-4-tolyl (tosylate) or L=O—SO2—CH3 (mesylate).
Compounds of Formula I wherein L=halogen (bromide, chloride) can be prepared by Fischer esterification of a 6-halohexanol, for example, 6-bromohexanol, with 2-hexyldecanoic acid, leading to 6-bromohexyl-2-hexyldecanoate. This reaction can be carried out in an inert solvent having an appropriate boiling point and capable of forming an azeotrope with water, such as toluene, cyclohexane, 1,2-dichloroethane, and the like, whereupon the use of an apparatus for continuous removal of the water produced in the course of the esterification process, for example, a Dean-Stark trap, allows 2-hexyldecanoic acid itself to serve as the acid catalyst for the esterification reaction, thereby suppressing the need for an additional acid catalyst. However, an acid catalyst such as sulfuric acid, para-toluenesulfonic acid, sodium hydrogen sulfate, or sulfonated polystyrene resins, may be optionally employed as catalysts in the esterification step.
Compounds of Formula I wherein L=O—SO2-4-tolyl (tosylate) or L=O—SO2—CH3 (mesylate) can be prepared by Fischer esterification of 1,6-hexanediol with 2-hexyldecanoic acid, leading to 6-hydroxyhexyl-2-hexyldecanoate. This reaction can be carried out in an inert solvent of appropriate boiling point and capable of forming an azeotrope with water, such as toluene, cyclohexane, 1,2-dichloroethane, and the like, whereupon the use of an apparatus for continuous removal of the water produced in the course of the esterification process, for example, a Dean-Stark trap, allows 2-hexyldecanoic acid itself to serve as the acid catalyst for the esterification reaction, thereby suppressing the need for an additional acid catalyst. However, an acid catalyst such as sulfuric acid, para-toluenesulfonic acid, sodium hydrogen sulfate, or sulfonated polystyrene resins, may be optionally employed as catalysts in the esterification step. The OH group in the 6-hydroxyhexyl-2-hexyldecanoate thus produced is subsequently converted into a sulfonate ester, such as a tosylate or a mesylate, by reaction with tosyl chloride or mesyl chloride in an appropriate solvent, such as CH2Cl2, and in the presence of a base such as triethylamine and optionally of a catalyst such as 4-dimethylaminopyridine (DMAP).
Advantages of the synthesis schemes of the present disclosure include in some embodiments higher overall yields (60-70% instead of 15-20% achieved with a known process described herein) and/or method steps that: (a) avoid use of coupling agents; (b) eschew hazardous reagents such as PCC, which contains carcinogenic Cr(VI); (c) bypass the need for redox operations, (d) are easier to implement, (e) reduce the amount of waste generated, and/or (f) proceed more cleanly, greatly facilitating the purification of the final product, thus realizing significant economies in terms of solvents, chromatographic supports, and plant and operator time.
The above summary is intended to illustrate non-limiting embodiments of the disclosure but is in no way intended to limit the scope of the invention.
The detailed description and examples below are intended to illustrate non-limiting embodiments of the disclosure but are in no way intended to limit the scope of the invention.
Provided herein is a method for the chemical synthesis of ionizable amino lipids, including a lipid known as ALC-0315, which is a component of the Pfizer-BioNTech COVID-19 vaccine. As described above, previous methods of ALC-0315 synthesis are problematic and have low yields. The present disclosure provides a solution to such difficulties and outlines an improved chemical route to produce the ionizable lipid as well as other related compounds.
As those of ordinary skill in the art will appreciate, the reactions employed herein may be carried out in any appropriate solvent, or mixtures of solvents, and at appropriate temperatures.
The known synthesis of ALC-0315 (
Furthermore, steps 2 and 3 of the synthesis of
Step 3 of
The inventors recognize that a more desirable pharmaceutical process avoids or reduces the use of reduction or oxidation (“redox”) reactions. In this regard, the present disclosure provides, in some non-limiting embodiments, a method comprising a two-or three-step synthesis that avoids (i) the use of a coupling agent in a first step of the method; (ii) the oxidation of an alcohol to an aldehyde; and (iii) the reductive amination reaction. Furthermore, the method may only necessitate chromatographic operations for the purification of the final product.
The synthesis method in some embodiments comprises an initial Fischer esterification of 2-hexyldecanoic acid, 4, with 6-bromohexanol, 5, leading to 6-bromohexyl-2-ethyldecanoate, 7. While Fischer esterification reactions are often carried out in the presence of a strong Brønsted acid catalyst such as HCl, H2SO4, H3PO4, TsOH, sodium hydrogen sulfate, sulfonated polystyrene (Dowex® IR resin), and the like, the inventors have determined that such catalysts are unnecessary in embodiments of the present method. Thus, refluxing a solution of 2-hexyldecanoic acid and 6-bromohexanol in a solvent that forms an azeotrope with water, for example, toluene, cyclohexane, or 1,2-dichloroethane, with continuous removal of water, for example by the use of a Dean-Stark trap, results in quantitative formation of 6-bromohexyl 2-hexyldecanoate, in that the 2-hexyldecanoic acid itself functions as the acid catalyst for the reaction. However, the esterification reaction can be optionally carried out in the presence of a small quantity of a non-volatile acid, such as H2SO4, H3PO4, TsOH, sodium hydrogen sulfate, or a sulfonated polystyrene resin. In either case, the yield of 6-bromohexyl-2-ethyldecanoate is 95-97% (Scheme 2).
In alternative embodiments, the synthesis may start with the Fischer esterification of 2-hexyldecanoic acid with 1,6-hexanediol, leading to 6-hydroxyhexyl-2-ethyldecanoate. While Fischer esterification reactions are often carried out in the presence of a strong Brønsted acid catalyst such as HCl, H2SO4, H3PO4, TsOH, sodium hydrogen sulfate, sulfonated polystyrene (Dowex® IR resin), and the like, the inventors have determined that such catalysts are unnecessary in certain embodiments. Thus, refluxing a solution of 2-hexyldecanoic acid and 1,6-hexanedol in a solvent that forms an azeotrope with water, for example, toluene, cyclohexane, or 1,2-dichloroethane, with continuous removal of water, for example by the use of a Dean-Stark trap, results in quantitative formation of 6-bromohexyl 2-hexyldecanoate, in that the 2-hexyldecanoic acid itself functions as the acid catalyst for the reaction. However, the esterification reaction can be optionally carried out in the presence of a small quantity of a non-volatile acid, such as H2SO4, H3PO4, TsOH, sodium hydrogen sulfate, or a sulfonated polystyrene resin. In either case, the yield of 6-hydroxyhexyl-2-ethyldecanoate is 95-97%.
The free OH group in the 6-hydroxyhexyl 2-hexyldecanoate thus obtained is activated toward nucleophilic displacement by conversion into a good leaving group. Such a leaving group may be a sulfonate ester such as a tosylate, a mesylate, a triflate, a 4-nitrobenzenesulfonate, and the like. The sulfonate esters above may be prepared by reaction of the alcohol with an appropriate sulfonyl chloride or sulfonic anhydride. For example, and without intending to be limiting, the reaction of 6-hydroxyhexyl 2-hexyldecanoate with methanesulfonyl chloride (mesyl chloride) produces 6-(mesyloxy)hexyl 2-hexyldecanoate (Scheme 3).
The double N-alkylation of 4-amino-1-butanol with halide 10 or sulfonate 11 is carried out in a polar solvent, at an appropriately elevated temperature typically between 50 and 100° C. and optionally with microwave irradiation, in the presence of a metal carbonate, and optionally in the presence of a source of iodide ion, such as lithium iodide, sodium iodide, potassium iodide, a tetraalkylammonium iodide, and the like. Such a reaction is most advantageously carried out in a solvent in which compounds 8, 10 or 11, and optionally the source of iodide ion are soluble, but in which the product 3 is poorly soluble or insoluble. Accordingly, as the reaction progresses the reaction mixture separates into two layers: one comprising a solution of starting compounds 8, 10 or 11, and optionally the source of iodide ion in the reaction solvent, and one comprised largely of product 3. This greatly facilitates the recovery of the product and its subsequent purification.
Without intending to be limiting, the process is exemplified in Scheme 4 with the reaction of 10 or 11 with 8 in acetonitrile (MeCN) at 75° C. and in the presence of Na2CO3, resulting in formation of 3 in 70-80% yield after chromatography.
It is apparent from Scheme 4 that the formation of product 3 involves a double N-alkylation of the amine, whereby a pair of identical alkyl groups become bound to the N atom of the starting amine. their will be appreciated by those of skill in the art that the first N-alkylation step, namely, the mono-alkylation of the amine, is faster that the second step, i.e., the dialkylation of the amine. The inventors have discovered a noteworthy solvent-and temperature effect in the relative rates of the two steps. Accordingly, conduct of the reaction in an appropriate solvent at a suitably lower temperature results in selective mono-alkylation of a starting amine such as 8. The product of such a mono-N-alkylation reaction may then be subjected to a second N-alkylation reaction, in another appropriate solvent and at a higher temperature, resulting in formation of a product in which two different alkyl groups have become bound to the N atom of the starting amine.
Without intending to be limiting, this is exemplified in Scheme 5 with the synthesis of ionizable lipid 15, which is also described in co-pending and co-owned U.S. provisional patent application No. 63/410,273 filed on Sep. 27, 2022. Thus, the reaction of amine 8 with alkyl bromide 12, in N,N-dimethylformamide (DMF), at room temperature and in the presence of K2CO3 produces largely mono-alkylated product 13. Further reaction of 13 with alkyl chloride 14 in MeCN at 80° C. and in the presence of Na2CO3, optionally with microwave irradiation, results in formation of lipid 15.
The ionizable amino lipids produced by the method of the disclosure can be in the form of a pharmaceutical salt, such as but not limited to an acid addition salt. Such salts are known to those of skill in the art and include any suitable inorganic acid used in pharmaceutical formulations. Non-limiting examples include acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, and the like.
Experimental section. Unless otherwise specified, all reagents and solvents were commercial products and were used without further purification, except CH2Cl2 (freshly distilled from CaH2 under Ar) and CH3CN (freshy obtained from a solvent purification system). All reactions were performed under an argon atmosphere. Reaction mixture from aqueous workups were dried by passing over a plug of anhydrous Na2SO4 held in a filter tube and concentrated under reduced pressure on a rotary evaporator. Thin-layer chromatography was performed on silica gel plates coated with silica gel (Merck 60 F254 plates) and column chromatography was performed on 230-400 mesh silica gel. Visualization of the developed chromatogram was performed by staining with I2 or potassium permanganate solution. 1H and 13C nuclear magnetic resonance (NMR) spectra were recorded at room temperature in CDCl3 solutions. 1H NMR spectra (300 MHz for 1H and 75 MHz for 13C) were obtained at room temperature from CDCl3 solutions. Chemical shifts are reported in parts per million (ppm) on the 8 scale. Multiplicities are reported as “s” (singlet), “d” (doublet), “t” (triplet), “q” (quartet), “m” (multiplet), and further qualified as “app” (apparent) and “br” (broad). Proton NMR spectra were referenced to residual CHCl3 (7.26 ppm) and 13C NMR spectra were referenced to the central line of the CDCl3 triplet (77.00 ppm). Mass spectra (m/z) were obtained in the electrospray (ESI) mode.
6-Bromohexyl 2-hexyldecanoate, 10. Two drops of 98% sulfuric acid were added to solution of 2-hexvldecanoic acid (15.6 g. 60.8 mmol, 1.1 equiv) and 6-bromohexanol (10 g, 55.2 mmol, 1 equiv) in cyclohexane (30 mL), and the mixture was brought to reflux with continuous removal of water (Dean-Stark trap). After 24 h, some starting alcohol (ca. 10% by 1H NMR) was still present. One drop of 98% H2SO4 was added and the mixture was refluxed for another 24 h, whereupon the reaction was complete (1H NMR). The reaction mixture was cooled to room temperature, diluted with hexanes (20 mL), washed with 5% aqueous Na2CO3 solution (2×10 mL), dried (Na2SO4) and evaporated. The crude product thus obtained (22 g, 97%) was used directly in the next step. 1H NMR δ 4.10 (t, 2H, J=6.5), 3.40 (t, 2H, J=6.8), 2.31 (m, 1H), 1.87 (m, 2H), 1.8-1.4 (m, 30H), 0.88 (t, 6H, J=6.2 Hx). 13C NMR δ 176.8, 63.8, 45.9 33.6, 32.7, 32.5 (2 peaks), 31.9, 31.7, 29.6, 29.5, 29.2 (2 peaks), 28.5, 27.8, 27.5, 27.4, 25.2, 22.6 (2 peaks), 14.1 (2 peaks). LRMS: m/z 419 [M+H]+.
6-Hydroxyhexyl 2-hexyldecanoate, 6. A solution of 2-hexyldecanoic acid (10 g, 39.0 mmol, 1 equiv) and 1,6-hexanediol (7.0 g, 58.5 mmol, 1.5 equiv) in toluene (70 mL) was refluxed with continuous removal of water (Dean-Stark trap) for 12 h, whereupon almost all the starting 2-hexyldecanoic acid disappeared. The mixture was cooled to room temperature and washed with deionized water to remove excess 1,6-hexanediol, which was subsequently recovered upon evaporation of the water and recycled. The toluene solution was further washed with 1 N aq. NaOH solution (3×20 mL), then it was percolated through a plug of anhydrous Na2SO4 and evaporated. The oily residue was purified by column chromatography on silica gel (5→15% AcOEt in hexanes) to afford 11 g (80%) of pure product. 1H NMR δ 4.07 (t, 2H, J=6.7 Hz), 3.65 (t, 2H, J=6.3 Hz), 2.30 (m, 1H), 1.70-1.50 (m, 6H), 1.45-36 (br m, 7H), 1.32-1.19 (m, 20H), 0.87 (br t, 6H, J=6.2 Hz). 13C NMR δ 176.7, 63.9, 62.8, 45.8, 32.6, 32.5 (2 peaks), 31.8, 31.7, 29.5, 29.4, 29.2 (2 peaks), 28.7, 27.5 (2 peaks), 25.8, 25.4, 22.7 (2 peaks), 14.1 (2 peaks). LRMS: m/z 379 [M+Na]+.
6-(Tosyloxy)hexyl 2-hexyldecanoate. Solid para-toluenesulfonyl chloride (402 mg, 2.1 mmol, 1.5 equiv) was added to a solution of 6-hydroxyhexyl 2-hexyldecanoate (500 mg, 1.4 mmol, 1 equiv) and triethylamine (285 mg, 392 uL, 2.8 mmol, 2 equiv) in CH2Cl2 (1.8 mL) and the resulting mixture was stirred at room temperature overnight. A white precipitate appeared. The solution was sequentially washed with aqueous saturated NaHCO3 solution, water, and brine, dried (Na2SO4), and evaporated to give 570 mg of crude tosylate (80%), which was used without purification. 1H NMR δ 7.78 (app d, 2H J=8.2 Hz), 7.34 (app d, 2H, J=8.2 Hz), 4.01 (4H, 2 overlapping t, J=6.1 Hz), 2.45 (s, 3H), 2.29 (m, 1H), 1.69-1.51 (m, 8H), 1.47-1.13 (m, 24H) 0.86 (br t, 6H, J=6.3 Hz). 13C NMR δ 176.6, 145.0, 133.0, 130.0, 128.2, 70.3, 63.7, 45.8, 32.5, 31.8, 31.7, 29.5 (2 peaks), 29.2 (2 peaks), 28.7, 28.5, 27.4 (2 peaks), 25.4, 25.0, 22.6 (2 peaks), 21.6, 14.1 (2 peaks).
6-(Mesyloxy)hexyl 2-hexyldecanoate, 11. Methanesulfonyl chloride (2.0 g, 1.3 mL, 17 mmol, 1.2 equiv) was added to a solution of 6-hydroxyhexyl 2-hexyldecanoate (5 g, 14 mmol, 1 equiv) and triethylamine (2.2 g, 21 mmol, 2.9 mL, 1.5 equiv) in CH2Cl2 (15 mL) and the resulting mixture was stirred at room temperature overnight. A white precipitate appeared. The solution was evaporated and the residue was taken up with hexane. The resulting solution was sequentially washed with aqueous saturated NaHCO3 solution (3×10 mL), water (2×10 mL), and brine (2×10 mL), dried (Na2SO4), filtered through Celite and evaporated to afford 5.3 g (87%) of crude mesylate, which was used without further purification. 1H NMR δ 4.18 (br t, 2H, J=6.0 Hz), 4.03 (br t, 2H, J=6.0Hz), 2.96 (s, 3H), 2.27 (m, 1H), 1.78-1.2 (m, 32H), 0.83 (br t, 6H, J=6.5 Hz). 13C NMR δ 176.5, 69.7, 63.6, 45.7, 37.2, 32.4 (2 peaks), 31.7, 31.6, 29.4, 29.3, 21.1 (2 peaks), 28.9, 28.4, 27.3 (2 peaks), 25.4, 25.0, 22.5 (2 peaks), 13.9 (2 peaks).
((4-Hydroxybutyl)azanediyl)bis(hexane-6,1-diyl) bis(2-hexyldecanoate) (ALC-0315) from bromide 10. A solution of 4-amino-1-butanol (465 mg, 5.2 mmol, 1 equiv) and 6-bromohexyl 2-hexyldecanoate (5.0 g, 11.9 mmol, 2.3 equiv) in dry acetonitrile (25 mL) containing suspended anhydrous Na2CO3 (1.2 g, 10.4 mmol, 2.0 equiv) and NaI (560 mg, 2.83 mmol, 0.5 equiv) was heated to 75° C. in a sealed reactor, under argon atmosphere. The reaction was monitored by TLC, MS and 1H NMR. A lower layer immiscible with MeCN and containing the desired product separated. After 20 hours, the mixture was cooled and diluted with water (10 mL) and hexanes (20 mL). The organic phase was separated and sequentially washed with water (2×10 mL) and brine (10 mL), then dried (Na2SO4) and evaporated. The residue was purified by column chromatography (0→3% MeOH in CH2Cl2) to afford 2.5 g (63%) of pure product. The same procedure was employed for the reaction of sulfonate derivatives of alcohol 6, such as mesylate 11 or the corresponding tosylate (yield of 3:55-60%). 1H NMR δ 4.05 (t, 4H, J=6.6 Hz), 3.58 (br m, 2H), 2.53 (br m, 6H), 2.30 (m, 2H), 1.76-1.50 (m, 14H), 1.47-1.12 (m, 54H), 0.87 (br t, 12H, J=6.9 Hz). The OH proton is not visible. 13C NMR δ 176.7, 63.9, 62.1, 53.4, 45.8, 32.5 (2 peaks), 31.8, 31.7, 29.5, 29.4, 29.2 (2 peaks), 28.6, 27.4 (2 peaks), 27.1, 25.8, 22.6 (2 peaks), 14.0 (2 peaks). Overlapping resonances reduce the number of unique signals from 26 to 22). LRMS: 766 [M+H]+.
6-bromohexyl-N-(2-hexyldecanoyl)prolinate (12). A solution of N-(2-mmol), 6-bromo-1-hexanol (543 mg, 3.00 mmol), EDCI-HCl (665 mg, 3.47 mmol) and DMAP (424 mg, 3.47 mmol) in DCM (10.0 mL) was stirred under inert atmosphere for 18 hours then concentrated. The residue was purified by silica chromatography (0-20% EtOAc in Hexanes) to yield 12 (995 mg, 78%) as an oil. 1H NMR (400 MHZ, CDCl3, rotamers) δ 4.51-4.45 (m, 1H), 4.21-4.03 (m, 2H), 3.71-3.63 (m, 1H), 3.61-3.51 (m, 1H), 3.43-3.39 (m, 2H), 2.49-2.43 (m, 1H), 2.23-1.75 (m, 6H), 1.68-1.59 (m, 4H), 1.49-1.34 (m, 6H), 1.26-1.24 (br m, 20H), 0.89-0.85 (m, 6H). LRMS: 516 & 518 [M+H]+.
5-chloropentyl 2-hexyldecanoate (14). Obtained from 2-hexyldecanoic acid and 5-chloro-1-pentanol by the method described above for 10. 1NMR (400 MHZ, CDCl3) δ 4.12-4.08 (t, 2H), 5.67-3.543 (t, 2H), 2.36-2.29 (m, 1H), 1.79-1.86 (m, 2H), 1.71-1.42 (m, 8H), 1.27 (br s, 22H), 0.91-0.87 (m, 6H).
6-((4-hydroxybutyl)amino)hexyl (2-hexyldecanoyl)prolinate (15). A solution of bromide 12 (229 mg, 0.468 mmol), 4-amino-1-butanol (44 mg, 0.491 mmol) and K2CO3 (68 mg, 0.491 mmol) in DMF (5 mL) was stirred at room temperature for 18 hours under nitrogen atmosphere. The mixture was then diluted with water (10 mL) and extracted with Et2O (3×10 mL). The combined extracts were washed with brine (10 mL), dried (Na2SO4) and concentrated. The residue was purified by silica chromatography (0-45% MeOH in DCM) to yield the secondary amine 13 (136 mg, 58%). 1H NMR (400 MHZ, CDCl3, rotamers) δ 4.13-4.10 (m, 4H), 3.61 (br t, 1H), 3.12 & 3.01 (s, 3H, rotamers 3:1), 2.65-2.72 (m, 4H), 1.68-1.61 (m, 8H), 1.45-1.26 (m, 30H), 0.89-0.86 (m, 6H).
6-((5-((2-hexyldecanoyl)oxy)pentyl)(4-hydroxybutyl)amino)hexyl (2-hexyl-decanoyl) prolinate (15). A mixture of 13 (126 mg, 0.252 mmol), chloride 14 (116 mg, 0.278 mmol) and K2CO3 (42 mg, 0.302 mmol) in MeCN (2.5 mL) was stirred at 80° C. in a sealed reaction vessel for 18 hours. The mixture was cooled, diluted with water (5 mL) and extracted with DCM (3×5 mL). The combined extracts were dried (Na2SO4) and concentrated. The residue was purified by silica chromatography (0-5% MeOH in DCM) to yield lipid 15 (135 mg, 64%) as an oil. 1H NMR (400 MHZ, CDCl3, rotamers) δ 4.51-4.45 (m, 1H), 4.21-4.03 (m, 4H), 3.71-3.63 (m, 1H), 3.61-3.51 (m, 1H), 3.48 (br m, 2H), 2.85-2.30 (m, 8H), 2.23-1.78 (m, 14H), 1.75-1.20 (m, 56H), 0.89-0.85 (m, 12H).
This application claims priority from U.S. Ser. No. 63/269,297 filed on Mar. 14, 2022, which is incorporated herein by reference in its entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CA2023/050287 | 3/6/2023 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 63269297 | Mar 2022 | US |
