Patent Application
20240076274
The present invention relates to a triazine based self-assembling system. More particularly, the present invention relates to a Janus G-C base as building block for a triazine based self-assembly of formula (I), a process for the preparation, and its application in developing supramolecular polymers, peptide nucleic acids (PNAs) and smart polymers thereof.
Molecular self-assembling systems has ushered as a promising approach to construct complex nanostructures with wide range of attractive mechanical characteristics that find diverse applications such as in chemical synthesis, polymer science, nanotechnology, tissue engineering, in medical applications and for fabricating advanced materials.
By virtue of their structural similarity with nucleobases, synthetic molecular self-assembling systems have also found application in developing novel peptide nucleic acids (PNA)—a class of nucleic acid mimics made of pseudopeptide backbone with excellent recognition-specificity. Inspired by the nucleic acid base-pairing, researchers and chemists have pursued in developing such self-assembling molecules with diverse H-bonding characteristics as a building block for supramolecular polymer networks.
One of the extensively studied self-assembling motifs that instantaneously forms supramolecular polymers is the melamine-cyanuric/barbituric acid complementary dual motif (MA-CA/BA) is shown below:
Depending upon the substitution pattern on melamine, MA-CA/BA assembly can give rise to three different types of aggregates: the cyclic rosettes (finite), linear tapes (infinite), and crinkled tapes (infinite), however, the multiple possibilities of self-assembly pathways are detrimental to applications particularly when formation of a mixture of polymeric aggregates is not desired. Further, the need to maintain equimolar proportion of the complementary self-assembling components for effecting self-assembly adds to the practical difficulties.
A need exists in the art for self-assembling motifs capable of instant supramolecular polymerization, but devoid of multiple assembly pathways that could be of considerable advantage for practical applications.
The main object of the present invention is to provide a triazine based self-assembling Janus G-C-base nucleic acid motif of formula (I) that could possess advantageous applications. Another object of the present invention is to provide a process for the synthesis of a triazine based self-assembling Janus G-C-base nucleic acid motif of formula (I).
Yet another object of the present invention is to provide an application of a triazine based self-assembling Janus G-C-base nucleic acid motif of formula (I) in developing supramolecular polymers, peptide nucleic acids (PNAs) and smart polymers.
The primary objective of the present invention is to provide a triazine based self-assembling Janus G-C-base motif of formula (I) capable of efficient self-assembly, leading exclusively to a single set of linear supramolecular polymer thereby avoiding formation of mixture of supramolecular polymers.
In an aspect of an embodiment, the present invention provides a triazine based self-assembling Janus G-C-base motif of formula (I):
wherein, ‘R’ is selected from the group comprising of linear or branched unsubstituted and substituted C1-C7 alkyl, unsubstituted and substituted aryl, unsubstituted and substituted natural amino acids which may be protected, linear or branched unsubstituted and substituted C1-C7 alcohols, or linear or branched unsubstituted and substituted C1-C7 amines. In another embodiment, the present invention provides a process for the synthesis of a triazine based self-assembling Janus G-C-base motif of formula (I); wherein the process comprises the steps of:
In an aspect of an embodiment, the present invention provides an intermediate (3) possessing below structural formula:
Yet another aspect of an embodiment, the present invention provides a process for the preparation of an intermediate (3), wherein said process comprises the steps of:
Yet another embodiment of the present invention provides an application of a triazine based self-assembling Janus G-C-base motif of formula (I) in developing a supramolecular polymer, peptide nucleic acids (PNAs) and smart polymers.
The invention will now be described in detail in connection with certain preferred and optional embodiments, so that various aspects thereof may be more fully understood and appreciated.
The present invention has developed a novel class of bifacial triple hydrogen-bonding a triazine based self-assembling Janus G-C-base motif of formula (I), inspired by DNA base-pairing. These nucleobases could serve as potential building blocks for multiple application purposes vis-a-vis: molecular self-assembly, nucleic acid interactions and smart polymers. The Janus G-C base, endowed with self-complementary H-bonding codes reminiscent of guanine (G) and cytosine (C) nucleic acid bases, is capable of undergoing efficient self-assembly leading to supramolecular polymers, peptide nucleic acids (PNAs) and smart polymers.
In an embodiment, the present invention provides a triazine based self-assembling Janus G-C-base motif of formula (I):
wherein, ‘R’ is selected from the group comprising of linear or branched unsubstituted and substituted C1-C7 alkyl, unsubstituted and substituted aryl, unsubstituted and substituted natural amino acids which may be protected, linear or branched unsubstituted and substituted C1-C7 alcohols, or linear or branched unsubstituted and substituted C1-C7 amines.
In a preferred embodiment, a triazine based self-assembling Janus G-C-base motif of formula (I) comprises of:
In another embodiment, the present invention provides a process for the synthesis of a triazine based self-assembling Janus G-C-base motif of formula (I); wherein the process comprises the steps of:
In the present process, the solvent for the reaction is selected from polar or non-polar, protic or aprotic solvent such as lower alcohols, nitriles, ketones, halogenated hydrocarbons, TFA or combinations thereof. In a particularly useful embodiment, solvent is acetonitrile.
The base for the reaction is selected from organic bases such as ethylamine, triethylamine, DIPEA, pyridine or from inorganic base such as sodium hydroxide, alkali or alkaline earth metal carbonates and bicarbonates or combination thereof. In a particularly useful embodiment, base is DIPEA.
The deprotecting agent in step (v) of the present invention depends upon the protecting agent of the nucleobase (5). Accordingly, the debenzylation is carried out using H2/Pd-C, the Boc protecting group and the Pbf protecting groups are deprotected using 95% TFA in DCM.
The process is depicted in Scheme-1 below:
Another aspect of an embodiment provides an intermediate, N-tert-Butoxycarbonylguanidin-1H-imidazole-1-carbonyl, of formula (3);
Yet another aspect of an embodiment provides a process for preparation of the intermediate (3), wherein said process comprises the steps of:
PNA monomer building blocks carrying unnatural nucleobases have found application in developing PNAs for site-specific interaction with DNAs and RNAs. PNA oligomers have been shown to inhibit transcription (antigene) and translation (antisense) of genes by tight binding to DNA or mRNA.
In another embodiment, the present invention provides a process for the synthesis of a triazine-based Janus G-C nucleobase containing PNA building blocks of formula 13 and 14, wherein said process comprises the steps of:
V. coupling the intermediate (8) or (11) of step (I) and (III) at a temperature in the range of 30-35° C. for a period in the range of 12-16 hours with the compound (12a, b) to obtain the Fmoc analog (13a, b) and Cbz analog (14a, b), respectively.
The reaction is depicted in Scheme 2 below:
According to the process, ethylenediamine (7) is reacted with Cbz-OSu in a solvent-water mixture in 1:1 ratio to obtain Cbz protected ethylene diamine which is further reacted with ethyl bromoacetate in presence of base and solvent to yield Cbz-protected ethyl (2-aminoethyl) glycinate (Cbz-AEG-OEt) (8).
In another pot, N-Boc ethylene diamine (9) is reacted with benzyl bromoacetate in presence of solvent and base to yield the Boc-protected ester (10) which is Boc deprotection in TFA-DCM (1:1) and further reacted with Fmoc-OSu in presence of base and solvent to obtain Fmoc-protected benzyl 2 glycinate (Fmoc-AEG-OBn) (11).
The glycine derived (5e) and/or arginine derived (5g) Boc-protected triazine benzyl esters obtained in Scheme 1 are debenzylated by hydrogenation with H2/Pd-C to yield the carboxylic acid (12a, b).
One part of the compound (12a, b) is dissolved in dry solvent and added HBTU, HOBt in presence of base and stirred, followed by addition of compound (11) to afford the Fmoc analog (13a, b).
The remaining part of the compound (12a, b) is dissolved in dry solvent and added HBTU, HOBt in presence of base and stirred, followed by addition of compound (8) to afford the Cbz analog (14a, b).
The solvent for the process is selected from polar or non-polar, protic or aprotic solvent such as lower alcohols, nitriles, ketones, halogenated hydrocarbons, TFA or combinations thereof. The base for the reaction is selected from organic base such as ethylamine, triethylamine, DIPEA, pyridine or from inorganic base such as sodium hydroxide, alkali or alkaline earth metal carbonates and bicarbonates or combination thereof.
In an embodiment, the synthesis of a triazine-based Janus G-C nucleobase-containing PNA building blocks (13a, b) or (14a, b) are useful for Fmoc-based solid-phase synthesis or Cbz-based solution-phase synthesis of PNAs.
Hydrogen-bonding plays a vital role in the designing of smart polymers and functional materials featuring controlled self-assembly.
In another embodiment, the present invention relates to a process for the synthesis of polymer building blocks 16 containing the Janus G-C nucleobase unit in a protected form, wherein said process comprises the steps of:
The process is depicted below in Scheme 3:
The solvent for the process is selected from polar or non-polar, protic or aprotic solvent such as lower alcohols, nitriles, ketones, halogenated hydrocarbons, TFA or combinations thereof. The base for the reaction is selected from organic base such as ethylamine, triethylamine, DIPEA, pyridine or from inorganic base such as sodium hydroxide, alkali or alkaline earth metal carbonates and bicarbonates or combination thereof.
In a preferred embodiment, the free amino triazine compound (17) comprises of:
In another embodiment, the building block (16) is subjected to covalent polymerization. On deprotection after copolymerization, the Janus G-C nucleobase being self-complementary triggers 3+3 type H-bonded supramolecular polymerization, which substantially influences the overall property of the polymers.
In yet another embodiment, the compound (Id) shown in Scheme 1 and polymer monomer building block (17b) of Scheme 3 are crystallized from hot aqueous methanol containing traces of HCl and hot DMSO respectively. Analysis of their single-crystal X-ray structure (
Following examples are given by way of illustration and therefore should not be construed to limit the scope of the invention.
Experimental
All reagents were purchased of highest commercial quality and used without further purification unless otherwise stated. All reactions were carried out with laboratory-grade solvent and purity of intermediates and final compounds were checked on pre-coated silica gel G254 TLC plates (Merck). Visualization of spot on TLC was achieved by the use of UV light (254 nm) and ninhydrin test. All synthesized compounds were purified on silica gel column chromatographic by using of 100-200, 230-400 Mesh Silica gel.
[A]: Synthesis of the Compounds of General Formula (I)
The synthesis of compound 2 was as per the earlier reported procedure. (Tetrahedron 2010, 66, 6224-6237). Accordingly, Guanidinium chloride monohydrate (23 g, 1 equiv., 240 mmol) was dissolved in water (48 mL), added NaOH (19.2 g, 2 equiv. 481 mmol) and stirred at 0° C. for 15 min., followed by addition of a solution of di-tert-butyl dicarbonate (13.1 g, 0.25 equiv., 60 mmol) in acetone (200 mL) and stirred at 30° C. for an additional 10 hour. The solvent was removed under vacuum and the resultant residue was dissolved in water (30 mL) and extracted with ethyl acetate (3×100 mL). The organic layer was washed with brine solution, dried (Na2SO4), filtered and concentrated in vacuo to dryness. The resultant residue was suspended in cold diethyl ether and solid was filtered under vacuum to afford compound 2 as a white powder.
Yield: 80%; Rf=0.2 (silica gel TLC, 10% methanol in DCM); 1H NMR (400 MHz, DMSO-d6) δ 6.80 (bs, 4 H), 1.34 (s,9 H); 13C NMR (101 MHz, DMSO-d6) δ 162.97, 162.27, 75.07, 27.83, 27.83, 27.83; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C6H14N3O2 160.1081; Found 160.1079; [M+Na]+ Calcd for C6H13N3O2 Na 182.0900; Found 182.0898.
N-Boc-guanidine 2 (14 g, 87.1 equiv., 95 mmol, 1 equiv) was suspended in dichloromethane (50 mL), added 1,1-carbonyldiimidazole (CDI) (15.69 gm, 1.1 equiv., 96.94 mmol) and solution was stirred at 30° C. for 5 hour. The resultant solution washed with water (3×30 mL), dried (Na2SO4) and concentrated under vacuum to afford 3 as crystalline white solid, which was carried forward for the next step.
Yield: 20 g, 90%, Rf=0.3 tailing (silica gel TLC, 60% ethyl acetate in pet ether); mp. 155-160° C.; 1H NMR (400 MHZ, CDCl3) δ 11.10 (bs., 1H), 9.29 (bs., 1H), 8.91 (bs., 1H), 8.56 (s, 1H), 7.56 (s, 1H), 7.00 (s, 1H), 1.56 (s, 9H); 13C NMR (101 MHz, CDCl3) δ 160.85, 157.91, 153.77, 137.83, 128.82, 117.01, 83.60, 28.06, 28.06, 28.06; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C10H16N5O3 254.1248; Found 254.1243.
The compound 3 (1 equiv., 2.00 gm, 7.9 mmol) was dissolved in acetonitrile (50 mL), added benzylamine (1.2 equiv., 1.01 g, 9.52 mmol) and stirred at 50° C.for 4 hour. The reaction mixture was cooled at 37° C. and concentrated under vacuo. The resultant residue was dissolved in ethyl acetate (100 mL) and subsequently washed with diluted KHSO4 solution, brine solution and dried (Na2SO4). The organic layer was concentrated under vacuum to afford 4a as white solid.
Yield: 87%; mp. 90-100° C.; Rf=0.5 (silica gel TLC, 70% ethyl acetate in pet ether); 1H NMR (400 MHz, CDCl3) δ 8.89 (bs, 3 H) 7.77 (bs, 1 H) 7.33-7.29 (m, 5 H) 4.41-4.39 (d, J=5.34 Hz, 2 H) 1.53 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 155.21, 154.22, 137.28, 128.79, 128.69, 128.57, 127.73, 127.59, 127.35, 86.09, 43.99, 27.94, 27.94, 27.94; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C14H21N4O3 293.1608; Found 293.1601; [M +Na]+ Calcd for C14H20N4O3 Na 315.1428; Found 315.1419.
The synthetic method of 4a was adopted to synthesize 4b; white solid.
Yield: 84%; mp.100-110° C.; Rf=0.5 tailing (silica gel TLC, 80% ethyl acetate in pet ether); 1H NMR (400 MHZ, CDCl3) δ 10.12 (bs., 2 H), 7.55 (bs., 1H), 6.98 (bs., 1H), 3.05-3.03 (s, 2H), 1.53 (s, 9H), 0.94 (s, 9H); 13C NMR (101 MHz, CDCl3); δ159.42, 154.81, 154.01, 86.27, 51.36, 32.09, 27.84, 27.84, 27.84, 27.15, 27.15, 27.15; HRMS (ESI-TOF) m/z: [M+H]+Calcd for C12H25N4O3 273.1921; Found 273.1914; [M+Na]+Calcd for C12H24N4O3 Na 295.1741; Found 295.1733.
Tert-butyl (2-(benzyloxy) ethyl) carbamate (5 g, 1 equiv, 19.89 mmol, which was synthesized as per earlier reported procedure (J. Pept. Sci. 2009, 15, 366-368.) was dissolved in 50% solution of TFA in DCM (50 mL) and stirred at 0° C., for 45 min. The solvent was evaporated under vacuum and co-evaporated with toluene (2×20 mL) to take off the residual TFA from reaction mixture to afford TFA salt as a semisolid. The resultant TFA salt (1 equiv., 5.2 g, 1 equiv., 19.60 mmol) was dissolved in acetonitrile (40 mL), added compound 3 (1.1 equiv., 5.43 g, 21.56 mmol) and DIPEA (3 equiv., 10.22 mL, 58.81 mmol) and stirred at 50° C. for 4 h.
The resultant reaction mixture was cooled at 37° C. and concentrated under vacuum. The residue was dissolved in ethyl acetate (100 mL) and subsequently washed with dilute KHSO4 solution, brine solution, dried (Na2SO4) and concentrated under vacuum for dryness to obtain crude 4c as white solid, which was purified by column chromatography using 10 to 90% ethyl acetate in pet ether. The resultant white solid was triturated using cold 50% diethyl ether in pet-ether (10 mL) to afford 4c as pale semisolid.
Yield: 88%; Rf=0.5 (silica gel TLC, 70% ethyl acetate in pet ether); 1H NMR (400 MHZ, CDCl3) δ 9.31 (bs., 1 H), 8.17 (bs., 1 H), 7.33-7.28 (m, 5 H), 6.38 (bs., 1 H), 4.51 (s, 2 H), 3.54-3.52 (m, 2 H), 3.40-3.38 (m, 2 H), 1.47 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 158.08, 157.47, 152.96, 137.88, 128.41, 128.41, 128.41, 127.77, 127.73, 81.97, 73.15, 69.21, 39.84, 28.09. 28.09, 28.09; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C16H25N4O4 337.1870; Found 337.1867.
The synthetic method of 4a was adopted to synthesize 4d. The benzyl (2-aminoethyl) carbamate was synthesized as per earlier reported procedure (J. Pept. Sci. 2009, 15, 366-368). The resulting residue was directly purified by column chromatography using 100-200 mesh size and mobile 0-10% MeOH in dichloromethane. The solvent was removed under vacuum and residue was triturated with diethyl ether to afford 4d as off-white solid.
Yield: 85%; mp. 80-90° C.; Rf=0.3 (silica gel, TLC, 10% methanol in DCM); 1H NMR (400 MHz, CDCl3) δ 8.23 (bs., 1 H), 7.30 (m, 5 H), 6.55 (m, 1 H), 6.36 (bs, 1 H), 5.80 (bs., 1 H), 5.10 (bs, 1H), 5.06 (m., 2 H), 3.27 (m., 4 H), 1.48 (m, 9 H); 13C NMR (101 MHz, CDCl3) δ 162.45, 158.21, 157.13, 157.13, 136.68, 128.65, 128.65, 128.23, 128.23, 128.23, 82.40, 66.85, 41.55, 39.95, 28.27, 28.27, 28.27; HRMS (ESI-TOF) m/z: [M+H]+Calcd for C17H26N5O5 380.1928; Found 380.1924; [M+Na]+ Calcd for C17H25N5O5Na 402.1748; Found 402.1737.
Compound 3 (2.00 gm, 1 equiv., 7.9 mmol) was dissolved in acetonitrile (30 mL) were added Gly-OBn. PTSA (1.2 equiv., 1.07 gm, 9.48 mmol, which was synthesized by previously reported procedure (J. Org. Chem. 2009, 74, 8988-8996.) and DIPEA (2.74 mL, 2 equiv. 15.81 mmol) and stirred at 50° C.for 4 hours. The reaction mixture was cool at 37° C. and diluted with ethyl acetate (70 mL) and subsequently washed with dilute KHSO4 solution, brine solution, dried (Na2SO4). The resultant organic layer was concentrated under vacuum to dryness and solid residue triturated with diethyl ether to afford 4e as white solid.
Yield: 80%; mp. 110-115° C.; Rf=0.4 (silica gel TLC, 80% ethyl acetate in pet ether); 1H NMR (400 MHz, DMSO-d6) δ 10.87 (bs., 1 H), 9.29 (bs., 1 H), 8.69 (bs., 1 H), 7.39-7.38 (m, 5 H), 5.17 (s, 2 H), 4.00-3.99 (d, J=6.1 Hz, 2 H), 1.49 (s, 9 H); 13C NMR (101 MHZ, DMSO-d6) δ 169.08, 154.07, 153.80, 151.92, 135.53, 128.26, 128.26, 127.97, 127.81, 125.30, 83.60, 65.53, 41.17, 28.35, 28.35, 28.35; HRMS (ESI-TOF) m/z: [M+H]+Calcd for C16H23N4O5 351.1663; Found 351.1653; [M+Na]+ Calcd for C16H22N4O5Na 373.1482; Found 373.1470.
Benzyl N6-((benzyloxy) carbonyl)-L-lysinate TFA salt (2.1 g, 1 equiv., 4.33 mmol, which was synthesized as per previously reported method (J. Bioorg. Med. Chem. Lett. 2020, 30, 127039.) was dissolved in acetonitrile, added compound 3 (1.20 g, 1.1 equiv., 4.76 mmol) and DIPEA (2.26 mL, 3 equiv., 13.00 mmol), and stirred at 50° C. for 4-5 h. The resultant solution was cooled at 37° C.and concentrated under vacuum. The residue was diluted with ethyl acetate (100 mL) and subsequently washed with dilute KHSO4 solution, brine solution, dried (Na2SO4). The solvent was evaporated under reduced pressure to afford 4f as white solid.
Yield: 87%; mp. 80-90° C.; Rf=0.4 (silica gel TLC, 80% ethyl acetate in pet ether); 1H NMR (500 MHz, DMSO-d6) δ 9.82 (bs., 1H), 8.23 (bs, 1H), 7.76 (bs, 1 H), 7.37-7.30 (m, 10 H), 7.25 (t, J=5.5 Hz, 1 H), 5.17-5.11 (m, 2 H), 5.01 (s, 2 H), 4.20-4.16 (d, J=5.3 Hz, 1 H), 3.36 (s, 1 H), 2.96 (q, J=6.6 Hz, 2 H), 1.74-1.65, (d, J=8.0 Hz, 2 H), 1.46-1.36 (m, 11 H), 1.31-1.29 (m, 2 H); 13C NMR (125 MHz, DMSO-d6) δ 172.37, 157.79, 156.25, 137.44, 136.13, 128.58, 128.58, 128.50, 128.50, 128.50, 128.21, 128.21, 127.89, 127.89, 127.64, 127.89, 78.76, 65.10, 64.29, 59.92, 52.82, 30.74, 29.13, 28.07, 28.07, 28.07, 22.66, 14.25; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C28H38N5O7 556.2771; Found 556.2766. Note: δ 4.10, 2.07,1.27 are residual peak of ethyl acetate.
Benzyl N2-(tert-butoxycarbonyl)-N{dot over (ω)}) ((2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran-5-yl) sulfonyl)-L-argininate (5.00 gm, 1 equiv., 8.11 mmol, which was synthesized as per previously reported method (J. Bioorg. Med. Chem. Lett. 2020, 30, 127039.) was dissolved 50% TFA in DCM (30 mL) and stirred at ice-bath temperature for 45 min. The solvent was removed under vacuum and remaining TFA was stripped off by co-evaporating with toluene (2×20 mL) to afford TFA salt as a semisolid that was carried forward for next step. The resultant TFA salt (5 gm, 1 equiv., 7.92 mmol, was dissolved in acetonitrile (40 mL), added compound 3 (2.69 g, 1.1 equiv., 8.72 mmol) and DIPEA (4.13 mL, 3 equiv., 23.78 mmol), and stirred at 50° C. for 4-5 h. The resultant solution was cooled at 37° C. and concentrated under vacuum. The residue was diluted with ethyl acetate (150 mL) and subsequently washed with dilute KHSO4 solution, brine solution, dried (Na2SO4). The solvent was evaporated under reduced pressure to afford 4g as a white solid:
Yield: 80%; mp. 90-100° C.; Rf=0.3 (silica gel TLC, 80% ethyl acetate in pet ether); 1H NMR (400 MHz, DMSO-d6) δ 9.22 (bs., 1 H), 8.61 (bs., 1 H), 8.25-8.16 (bs., 1 H), 7.43-7.42 (m, J=5.4 Hz, 5 H), 6.86 (bs., 1 H), 6.49 (bs., 2 H), 5.14 (bs., 2 H), 4.22 (d, J=5.3 Hz, 1 H), 3.44 (bs, 1 H), 3.03-305 (dd, J=6.1, 10.2 Hz, 2 H), 2.93 (s, 2 H), 2.48 (s, 3 H), 2.42 (s, 3 H), 1.99 (s, 4 H), 1.68 (bs., 1 H), 1.47 (s, 9 H), 1.44-1.35 (m, 8 H); 13C NMR (101 MHZ, DMSO-d6) δ 172.68, 171.86, 170.81, 157.91, 156.66, 155.59, 137.72, 136.13, 134.64, 131.87, 128.93, 128.93, 128.60, 128.60, 128.37, 124.80, 116.74, 86.74, 82.92, 66.7, 60.23, 53.11, 42.92, 28.75, 28.75, 28.12, 28.12, 28.12, 21.00, 19.43, 18.08, 14.55, 12.72; HRMS (ESI-TOF) m/z: [M+H]+Calcd for C33H48N7O8S 702.3280; Found 702.3274; [M+Na]+Calcd for C33H47N7O8SNa 724.3099; Found 724.3082.
Compound 4a (2 g, 5.27 mmol, 1 equiv.), was dissolved in acetonitrile (25 mL), added NaHCO3 (0.886 g, 10.5 mmol, 1.5 equiv) and CDI (1.28 g, 7.91 mmol, 1.2 equiv.) and stirred at 35° C. for 48 hours. The resultant precipitate was filtered under vacuum and precipitate was suspended in ethyl acetate (100 mL) and acidified with dilute KHSO4 solution organic layer was washed with brine solution, dried (Na2SO4) and concentrated under vacuum to dryness. The resulting white solid was washed with diethyl ether to afford 5a as a white solid.
Yield: 70%; mp. >400° C.; Rf=0.5 (silica gel TLC, 10% methanol in DCM); 1H NMR (400 MHz, CDCl3) δ 11.24 (bs, 1 H), 10.29 (bs, 1 H), 7.48 (d, J=6.10 Hz, 2 H), 7.28 (s, 3 H), 5.05 (s, 2 H), 1.49 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 154.45, 154.09, 152.82, 148.99, 136.13, 129.06, 129.06, 128.41, 128.41, 127.85, 85.50, 44.74, 27.80, 27.80, 27.80; HRMS (ESI-TOF) m/z: [M+H]+Calcd for C15H19N4O4 319.1401; Found 319.1393; [M+Na]+Calcd for C15H18N4O4 Na 341.1220; Found 341.1212. Note: Feebly UV active but ninhydrin active with green color on long heating.
The synthetic method of 5a was adopted to synthesize 5b as white solid. Yield: 66%; mp. >400° C.; Rf=0.5 (silica gel TLC, 10% methanol in DCM); 1H NMR (400 MHz, CDCl3) δ 11.17 (bs., 1 H), 9.82 (bs., 1 H), 3.80 (s, 2 H), 1.53 (s, 9 H), 0.96 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 154.37, 153.52, 152.71, 149.71, 85.38, 51.24, 33.97, 28.34, 28.34, 28.34, 27.88, 27.88, 27.88; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C13H23N4O4 299.1714; Found 299.1712; [M+Na]+ Calcd for C13H22N4O4Na 321.1533; Found 321.1531. Note: Feebly UV active but ninhydrin active with green color on long heating.
The synthetic method of 5a was adopted to synthesize 5c; white solid.
Yield: 75%; mp.>250 ° C.; Rf=0.6 (silica gel TLC, 10% methanol in DCM); 1H NMR (400 MHz, CDCl3) δ 11.13 (bs., 1 H), 9.91 (bs., 1 H), 7.32-7.31 (m, 5 H), 4.53 (s, 2 H), 4.14 (m, 2 H), 3.72 (t, J=5.7 Hz, 2 H), 1.51 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 154.16, 152.88, 152.88, 149.06, 137.99, 128.36, 128.36, 127.75, 127.75, 127.62, 85.39, 72.73, 66.43, 40.61, 27.81, 27.81, 27.81; HRMS (ESI-TOF) m/z: [M+H]+ C17H23N4O5 363.1663; Found 363.1656; Calcd m/z: [M+Na]+ C17H22N4O5Na 385.1482; Found 385.1475. Note: Feebly UV active but ninhydrin active with green color on long heating.
The synthetic method of 5a was adopted to synthesize 5d; white solid.
Yield: 76%, mp.>350° C.; Rf=0.4 (silica gel TLC, 80% ethyl acetate in pet ether); 1H NMR (400 MHz, CDCl3) δ 11.05 (bs., 1H), 9.16 (bs., 1 H), 7.35-7.34 (m, 5 H), 5.33 (bs, 1 H), 5.08 (s, 2 H), 4.09-4.06 (m, 2 H), 3.54-3.50 (m, 2 H), 1.54 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 156.58, 155.16, 153.69, 152.55, 149.10, 136.54, 128.45, 128.45, 128.05, 128.05, 128.05, 85.89, 66.67, 41.09, 39.80, 27.85, 27.85, 27.85; HRMS (ESI-TOF) m/z: [M+H]+Calcd for C18H24N5O6 406.1721; Found 406.1716Note: 1H NMR δ 1.53 residual CH2Cl2, δ 1.56 residual water. Note: Feebly UV active but ninhydrin active with green color on long heating.
The synthetic method of 5a was adopted to synthesize 5e; white solid.
Yield: 60%; mp. 280-290° C.; Rf=0.4 (silica gel TLC, 70% ethyl acetate in pet ether); 1H NMR (400 MHZ, CDCl3) δ 11.09 (bs., 2 H), 7.36-735 (d, J=3.0 Hz, 5 H), 5.19 (s, 2 H), 4.68 (s, 2 H), 1.51 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 167.22, 158.72, 154.48, 152.87, 135.11, 128.64, 128.64, 128.47, 128.47, 128.26, 85.87, 67.40, 60.41, 42.24, 27.81, 27.81, 28.81; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C17H21N4O6 377.1456; Found 377.1452; [M+Na]+ Calcd for C17H20N4O6Na 399.1275; Found 399.1271. Note: residual peak of ethyl acetate at δ 1.27, 2.07, 4.26 Note: Feebly UV active but ninhydrin active with green color on long heating.
The synthetic method of 5a was adopted to synthesize 5f; white solid.
Yield: 45%; mp. 80-90° C.; Rf=0.5 (silica gel TLC, 45% ethyl acetate in pet ether); 1H NMR (400 MHz, DMSO-d6) δ 11.22 (bs., 1 H), 7.37-7.30 (m, 10 H), 5.23 (t, J=5.5 Hz, 1 H), 5.21-5.10 (m, 3 H), 5.07-4.99 (m, 2 H), 3.00-2.92 (m, 2 H), 2.08 (dd, J=5.9, 8.9 Hz, 1 H), 2.03-1.94 (m, 1 H), 1.47 (s, 9 H), 1.44-1.33 (m, 3 H), 1.26 (d, J=6.9 Hz, 2 H); 13C NMR (101 MHz, DMSO-d6) δ 172.51, 172.34, 169.48, 156.56, 154.56, 153.72, 137.73, 136.34, 128.85, 128.85, 128.79, 128.79, 128.56, 128.56, 128.43, 128.31, 128.20, 128.03, 83.99, 66.67, 65.57, 54.01, 29.53, 28.98, 28.05, 28.05, 28.05, 23.16, 14.87; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C29H36N5O8 582.2558; Found 582.2547; Note: Feebly UV active but ninhydrin active with green color on long heating.
The synthetic method of 5a was adopted to synthesize 5g; white solid.
Yield: 49%; mp. 220-230° C.; Rf=0.4 (silica gel TLC, 10% methanol in DCM); 1H NMR (400 MHz, CDCl3) δ 11.23 (bs, 1 H), 7.89 (bs, 1 H), 7.29-7.28 (m, 5 H), 6.29-6.20 (bs., 3 H), 5.30-5.16 (m, 1 H), 5.13-5.10 (m, 3 H), 5.07 (d, J=2.3 Hz, 1 H), 3.58-3.50 (m, 2 H), 2.92 (s, 3 H), 2.54 (s, 3 H), 2.47 (s, 3 H), 2.17 (bs., 1 H), 2.06 (s, 3 H), 1.46-1.45 (d, J=5.3 Hz, 15 H); 13C NMR (101 MHz, CDCl3) δ 169.01, 158.59, 156.19, 153.19, 153.16, 148.63, 138.26, 135.25, 132.18, 132.18, 128.52, 128.31, 128.31, 128.31, 128.13, 124.52, 117.37, 86.33, 67.34, 65.86, 54.22, 43.18, 40.62, 28.58, 28.58, 27.76, 27.76, 27.76, 25.69, 25.47, 19.27, 17.92, 15.27, 12.47; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C34H46N7O9S 728.3072; Found 728.3071; Note: Feebly UV active but ninhydrin active with green color on long heating.
A mixture of 5a (101 mg, 1 equiv. 0.331 mmol) in 50% TFA in DCM (5 mL) was stirred at 0-4° C. for 45 min. The reaction mixture was concentrated in vacuo and co-evaporated with dichloromethane (2×10 mL). The resulting residue was diluted with the diethyl ether (5 mL) and solid was filtered under vacuum to afford Ia as a white solid.
Yield: 90%; mp.>400° C.; 1H NMR (400 MHZ, DMSO-d6) δ 12.52 (bs, 2H), 9.22 (bs, 1H), 7.32-7.22 (m, 5 H), 4.85 (s, 2 H); 13C NMR (101 MHz, DMSO-d6) δ 159.67, 153.24, 149.05, 136.66, 129.08, 128.51, 128.51, 128.25, 128.25, 44.84; HRMS (ESI-TOF) m/z: [M+H]+ Calcd for C10H11N4O2+ 219.0877; Found 219.0876; Note: poor solubility even in hot DMSO-d6.
The synthetic method of Ia was adopted to synthesize Ib as a white solid.
Yield: 92%; mp.>400° C.; The product was poorly soluble in any solvent; HRMS ESI-TOF: Calcd m/z: [M+H]+ calculated for C8H15N4O2+ 199.1190; Found; 199.1189; M+Na]+ Calcd for C8H14N4O2 221.1009; Found 221.1007 Note: no solubility in DMSO-d6.
The compound 5c (1 g, 1 equiv. 2.47 mmol) was dissolved in methanol (5 mL) followed by addition of Pd/C (20 mol %) and stirred at 35° C. for 4 h under hydrogen (H2) atmosphere. The reaction mixture was passed through a celite pad (thin pad) and pad was washed repetitively by MeOH (4×20 mL). The resultant filtrate was concentrated under vacuum to afford benzyl free intermediate (0.6 g) as a white solid. Further, the resultant solid (0.1 g, 1 equiv.) was dissolved in 50% solution of TFA in DCM and stirred at 0-4° C. for 45 min. The solvent was removed under vacuum and co-evaporated with DCM (2×5 mL) and the resultant residue was diluted with diethyl ether (10 mL) and resultant solid was washed by filtration under vacuum to afford Id as a white solid; overall yield: 80%; mp.>250° C.; 1H NMR (400 MHZ, DMSO-d6) δ 7.53 (bs. 1 H), 5.01 (bs., 3 H), 3.75-3.72 (m, 2 H), 3.49-3.45 (t, J=6.5 Hz, 2 H), 3.17 (s, 1H); 13C NMR (400 MHz, DMSO-d6) δ 159.51, 155.20, 151.98, 58.14, 42.96; HRMS ESI-TOF: Calcd m/z: [M+H]+ Calcd for CsHON403 173.0669; Found 173.0669. Note: poor solubility in hot DMSO-d6.
The synthetic method of Ia was adopted to synthesize Ic white solid; over all Yield: 70%; mp.>250° C.; 1H NMR (400 MHZ, DMSO-d6) δ 11.54 (bs, 1H), 7.80 (bs. 2 H), 7.46 (bs., 2H), 3.93 (d, 2 H), 2.99 (d, J=6.5 Hz, 2 H); HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C5H10N5O2+ 172.0829; Found 172.0829. [M+H]+ Note: poor solubility in DMSO-d6, δ 3.39 (bs, residual water).
The synthetic method of Ia was adopted to synthesize Ie.
Yield: 80%; mp. >250° C.; 1H NMR (400 MHz, DMSO-d6) δ 7.39-7.34 (m, 5 H), 7.23 (bs., 2 H), 5.16 (s, 2 H), 4.48 (s, 2 H), 13C NMR (100 MHz, DMSO-d6) δ 168.76, 156.82, 156.82, 153.17, 136.23, 129.98, 128.67, 128.39, 128.39, 128.39, 66.72, 42.02; HRMS ESI-TOF: Calcd m/z: [M+H]+ C12H13N4O4+ 277.0931; Found 277.0931; [M+Na]+ Calcd for C12H12N4O4Na; 299.0756; Found 299.0751.
The synthetic method of Ia was adopted to synthesize If as a white solid.
Yield: 78%; mp.270-280° C.; 1H NMR (400 MHz, DMSO-d6) δ 7.37-7.29 (m, 10 H), 7.22 (bs., 2H), 5.19-5.15 (dd, J=5.0, 9.5 Hz, 1 H), 5.13-5.05 (m, 2 H), 4.99 (s, 2 H), 2.97 (q, J=6.6 Hz, 2 H), 2.06-1.96 (m, 2 H), 1.49-1.31 (m, 2 H), 1.20 (dd, J=6.5, 14.9 Hz, 2 H); 13C NMR (101 MHz, DMSO-d6) δ 170.14, 159.62, 156.75, 156.59, 153.30, 137.81, 136.55, 128.88, 128.88, 128.45, 128.45, 128.25, 128.25, 128.01, 128.01, 128.01, 28.01, 66.48, 65.61, 53.41, 29.60, 28.48, 23.38, 18.38; HRMS (ESI-TOF): Calcd m/z: [M+H]+ C24H28N5O6+ 482.2034; Found 482.2034 [M+H]+.
Deprotection of 5g using 95% TFA-DCM afforded Ig as an insoluble material. Owing to poor solubility, it could not be satisfactorily characterized. Yield: 62%; mp. 175-185° C.; HRMS ESI-TOF: Calcd m/z: [M +H]+ C16H22N7O4+ 376.1728; Found 376.1724.
[B] Synthesis of Triazine-Based Janus G-C Nucleobase Containing PNA Building Blocks
Compound 5e was dissolved in methanol (5 mL) added Pd/C (20 mol %) and stirred at 35° C. under H2 atmosphere for 5 h. The resultant reaction mixture was passed through thin celite pad and the filtrate was concentrated under vacuo to afford 12a as a white solid.
Yield: 90%; mp. >250° C.; 1H NMR (400 MHz, DMSO-d6) δ 11.79 (m, 3 H), 4.37 (s, 2 H), 1.48 (s, 9 H); 13C NMR (101 MHz, DMSO-d6) δ168.82, 168.82, 153.76, 153.76, 153.12, 83.29, 41.65, 27.44, 27.44, 27.44; HRMS (ESI-TOF): Calcd m/z: [M+H]+ C10H15N4O6 287.0986; Found 287.0981. Note: Residual ethyl acetate peak at δ 1.07.
The synthetic method of 12a was adopted to synthesize 12b.
Yield: 86%; mp.220-230° C.; 1H NMR (400 MHz, DMSO-d6) δ 11.35 (bs., 2 H), 6.59 (bs., 1 H), 6.38 (bs., 1 H), 5.02 (bs., 1 H), 3.37 (m, 3 H), 3.02 (d, J=5.3 Hz, 2 H), 2.96 (s, 2 H), 2.47 (s, 3 H), 2.42 (s, 3 H), 2.03-1.98 (m, 4 H), 1.48 (s, 9H), 1.41 (s, 6 H), 1.35 (d, J=10.7 Hz, 2 H); 13C NMR (101 MHz, DMSO-d6) δ 166.04, 161.29, 157.44, 156.06, 137.27, 134.11, 131.42, 124.34, 116.27, 112.15, 110.0, 86.31, 64.94, 61.18, 59.77, 42.47, 28.33, 28.33, 27.64, 27.64, 27.64, 25.31, 18.95, 17.58, 15.19, 14.10, 12.28; HRMS (ESI-TOF): Calcd m/z: [M+H]+Calcd for C27H40N7O9S 638.2603; Found 638.2604 [M+H]+.
Compound 12a (0.3 g, 1.05 mmol, 1 equiv.) was dissolved in dry DMF (5 mL) and added HBTU (0.597 g, 1.57 mmol, 1.5 equiv), HOBt (212 mg, 1.57 mmol, 1.5 equiv), DIPEA (0.364 mL, 2.09 mmol, 2 equiv) and stirred at 0° C. After stirring for 10 min. at 0° C., compound (11) (541 mg, 1.2 equiv., 1.26 mmol, which was synthesized as per earlier reported procedure4 was added and the reaction mixture was stirred at 35° C. for an additional 12 hour. The resultant solution was diluted with ice cold water and the solid precipitate was filtered under vacuum. The solid residue was dissolved in ethyl acetate and subsequently washed with KHSO4 solution, NaHCO3 solution and brine solution, dried (Na2SO4) and concentrated under vacuo to get white solid product which was purified by chromatography on silica and mobile phase was 50-100% EtOAc in pet-ether to afford 13a as a white solid:
Yield: 95%; mp. 180-190° C.; 1H NMR (400 MHz, DMSO-d6) δ 11.41 (bs, 1H), 7.89-7.87 (d, J=7.4 Hz, 2 H), 7.69-7.67 (d, J=7.4 Hz, 2 H), 7.40-7.32 (m, 10 H), 5.12 (s, 1 H), 4.69 (s, 1 H), 4.55 (s, 1 H), 4.43 (bs., 1 H), 4.34-4.32 (d, J=6.9 Hz, 1 H), 4.29-4.23 (dd, J=6.8, 18.8 Hz, 2 H), 4.13 (s, 1 H), 3.50-4.47 (t, J=6.3 Hz, 2 H), 3.35-3.33 (m, 2 H), 3.25-3.24 (d, J=5.9 Hz, 2 H), 1.48 (s, 9 H); 13C NMR (100 MHz, DMSO-d6) δ 169.29, 168.87, 166.77, 166.62, 156.28, 153.72, 143.81, 140.65, 135.68, 128.35, 128.35, 128.09, 128.09, 127.95, 127.95, 127.78, 127.78, 127.49, 126.97, 125.07, 120.01, 83.33, 66.44, 65.85, 65.43, 59.66, 46.80, 46.78, 46.64, 40.07, 27.54, 27.54, 27.54, 20.96, 20.67, 14.00; HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C36H39N6O9 699.2779; Found 699.2776; [M+Na]+ Calcd for C36H38N6O9Na 721.2598; Found 721.2592.
The synthetic method of 13a was adopted to synthesize 13b as a white solid:
Yield: 78%; mp. 210-220° C.; 1H NMR (400 MHz, DMSO-d6) δ 11.24 (bs., 1 H), 7.86 (d, J=7.1 Hz, 2 H), 7.67 (d, J=6.6 Hz, 2 H), 7.38-7.30 (m, 10 H), 7.16 (bs., 1 H), 6.68 (bs., 1 H), 6.39 (bs., 1 H), 5.20-5.14 (m, 1 H), 5.87-4.84 (m, 2 H), 4.28 (d, J=6.8 Hz, 2 H), 4.22-4.19 (m, 2 H), 4.11 (d, J=5.8 Hz, 1 H), 4.05-3.89 (m, 2 H), 3.34 (bs., 4 H), 3.20-3.19 (m, 1 H), 3.14 (bs., 2 H), 3.08-2.98 (m, 2 H), 2.94 (s, 2 H), 2.69 (s, 1 H), 2.47 (s, 2 H), 2.41 (s, 3 H), 2.01-1.97 (m, 3 H), 1.44 (s, 6 H), 1.41-1.37 (m, 9 H); 13C NMR (101 MHz, DMSO-d6) δ 169.98, 157.89, 156.54, 144.35, 141.18, 137.74, 135.61, 131.90, 128.88, 128.88, 128.73, 128.73, 128.67, 128.52, 128.52, 128.32, 128.32, 128.05, 128.05, 127.52, 127.52, 125.63, 124.80, 120.55, 116.73, 86.74, 67.06, 66.31, 65.83, 60.23, 52.49, 48.94, 47.18, 42.91, 38.16, 30.57, 29.46, 28.76, 28.05, 28.05, 28.05, 28.00, 28.00, 26.42, 21.55, 21.24, 19.42, 18.06, 17.69, 14.79, 14.55, 14.44, 12.73; HRMS (ESI-TOF): Calcd m/z: [M+H]+Calcd for C53H64N9O12S 1050.4390; Found 1050.4382.
Compound 12a (0.3 g, 1.05 mmol, 1 equiv.) was dissolved in DMF (5 mL) and added HBTU (0.597 g, 1.57 mmol, 1.5 equiv), HOBt (212 mg, 1.57 mmol, 1.5 equiv), DIPEA (0.364 mL, 2.09 mmol, 2 equiv) and stirred for 5 min, at 0° C. Ethyl (2-(((benzyloxy) carbonyl) amino) ethyl) glycinate (8) (Cbz-AEG-OEt) (0.352 g, 1.26 mmol, 1.2 equiv, synthesized as per earlier procedure 4 was added and the reaction mixture was stirred at 35° C. for an additional 16 hour. The resultant solution was diluted with ice-cold water and solid precipitate was filtered under vacuum. The solid residue was dissolved in ethyl acetate and subsequently washed with dilute KHSO4 solution, NaHCO3 solution and brine solution, dried (Na2SO4) and concentrated under vacuo to get white solid crude product which was purified by column chromatography silica gel (230-400) and the mobile phase was EtOAc (50-90%) in pet-ether to afford 14a as a white solid:
Yield: 79%; mp, 150-160° C.; 1H NMR (400 MHz, CDCl3) δ 11.07 (bs, 1H), 7.39-7.30 (m, 5 H), 6.00 (bs., 1 H), 5.13 (m, 2 H), 5.09 (m, 2H), 4.71 (m., 1 H), 4.58 (s, 1 H), 4.25-4.23 (m, 2 H), 4.00 (bs., 1 H), 3.55 (bs., 2 H), 3.48-3.34 (m, 2 H), 1.51 (s, 9 H), 1.29-1.23 (m, 3 H); 13C NMR (101 MHz, CDCl3) δ 169.61, 168.86, 166.78, 156.85, 153.97, 152.71, 136.62, 128.43, 128.21, 127.99, 127.99, 85.78, 66.87, 66.62, 62.20, 61.57, 49.13, 48.74, 42.00, 39.29, 27.85, 27.85, 27.85, 14.08; HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C24H33N6O9 549.2304; Found 549.2294.
The synthetic method of 14a was adopted to synthesize 14b as a white solid.
Yield: 72%; mp 150-160° C.. 1H NMR (400 MHZ, DMSO-d6) δ 11.47 (bs, 1H), 11.04 (bs, 1H), 7.37-7.32 (m, 5 H), 7.19-7.01 (m, 1 H), 6.67 (bs, 1H), 6.37 (bs., 1 H), 5.17-5.14 (m, 1 H), 5.00-4.98 (m, 2 H), 4.08-4.08 (m, 4 H), 3.43-3.40 (dd, J=5.7, 12.7 Hz, 2 H), 3.15-3.08 (m, 3 H), 3.02-2.96 (m, 5 H), 2.47 (s, 3 H), 2.41 (s, 3 H), 2.04-1.96 (m, 4 H), 1.53-1.43 (m, 10 H), 1.41 (s, 7 H), 1.20-1.10 (m, 3 H); 13C NMR (101 MHz, DMSO-d6) δ 169.93, 168.89, 157.90, 156.57, 156.50, 137.73, 137.67, 134.65, 131.90, 128.80, 128.80, 128.21, 128.14, 128.14, 124.80, 116.72, 86.76, 84.07, 65.84, 65.68, 65.41, 61.43, 60.90, 60.23, 52.51, 47.78, 42.93, 38.83, 32.39, 31.46, 28.77, 28.77, 28.03, 28.03, 28.03, 25.94, 19.04, 18.0, 14.47, 14.21, 12.7; HRMS (ESI-TOF): Calcd m/z: [M+H]+Calcd for C41H58N9O12 900.3920; Found 900.3925.
[C] Synthesis of Polymer Building Blocks
Tert-butyl (2-(allyloxy) ethyl) carbamate (5 g, 1 equiv. 24.87 mmol, synthesized as per earlier reported procedure (J. Pept. Sci. 2009, 15, 366-368.) was dissolved in 50% TFA in DCM and allowed to stir at 0° C. for 45 min. The resultant solution was stripped off and co-evaporated using toluene (2×20 mL) to obtain the TFA salt. The resultant TFA salt (5 g, 1 equiv. 23.25 mmol) was dissolved in acetonitrile (50 mL), added compound 3 (6.44 g, 1.1 equiv. 25.58 mmol) followed by the addition of DIPEA (8 mL, 2 equiv. 46.511 mmol) and stirred at 50° C. for 5 h. The resulting reaction mixture was cooled at 37° C. and concentrated under vacuum and the acquired residue was dissolved in ethyl acetate (150 mL) and subsequently washed with KHSO4 solution, brine solution, dried (Na2SO4). The organic layer was concentrated under vacuum to afford 15a as pale semisolid.
Yield: 76%; Rf=0.4 (silica gel TLC, 60% ethyl acetate in pet-ether); 1H NMR (400 MHZ, CDCl3) δ 9.32 (bs., 1 H), 8.09 (m, 1 H), 6.39 (m, 1 H), 5.89-5.82 (m, 1 H), 5.25-5.14 (m, 2 H), 3.97-3.96 (d, J=5.3 Hz, 2 H), 3.51-3.48 (m, 3 H), 3.37-3.35 (d, J=5.3 Hz, 2 H), 1.45 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 158.06, 134.46, 117.39, 82.03, 73.37, 72.11, 70.57, 69.25, 39.85, 28.12, 28.12, 28.12; HRMS (ESI-TOF): Calcd m/z: [M+H]+Calcd for C12H23N4O4 287.1714; Found 287.1710; [M+Na]+Calcd for C12H22N4O4Na; 309.1533 Found 309.1526.
2-((tert-butoxycarbonyl) amino) ethyl acrylate (10 g, 1 equiv. 46.46 mmol, synthesized as per earlier reported procedure (Tetrahedron, 2013, 69, 6810-6820) was dissolved in 50% TFA in DCM (40 mL) and stirred at 0° C. for 60 min, monitored by TLC. The resultant solution was stripped off and co-evaporated using toluene (2×20 mL) at 30° C. (to avoid undesired polymerization) to obtain TFA salt which was carried forward for the next step without purification. The resultant TFA salt (10 g, 1 equiv. 43.66 mmol), was dissolved in acetonitrile (80 mL) and added compound 3 (12.15 g, 1.1 equiv. 4.80 mmol) followed by addition of DIPEA (14.96 mL, 2 equiv. 8.73 mmol) and stirred at 50° C.for 5 h. The solution was cooled at 37° C. and concentrated under vacuum. The resultant residue was diluted with ethyl acetate (200 mL) and subsequently washed with dilute KHSO4 solution, brine solution, dried (Na2SO4). The solvent was removed under vacuum to afford 15b as a pale semi-solid.
Yield: 75%; Rf=0.5 (silica gel TLC, 60% ethyl acetate in pet-ether); 1H NMR (500 MHZ, CDCl3) δ 9.12, (bs, 1H), 8.32 (bs., 1 H), 6.32 (d, J=17.5 Hz, 1 H), 6.09 (bs, 1H), 6.06 (m, 1 H), 5.80-5.78 (d, J=10.7 Hz, 1 H), 4.19 (bs., 2 H), 3.45 (bs., 2 H), 1.99 (bs, 1H), 1.42 (d, J=1.5 Hz, 9 H); 13C NMR (101 MHz,CDCl3) δ 166.02, 158.34, 131.22, 128.02, 81.95, 63.46, 60.34, 49.41, 38.84, 28.08, 28.08, 28.08; HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C12H21N4O5 301.1506; Found 301.1510; [M+Na]+ Calcd for: C12H20N4O5Na 323.1326; Found 323.1330.
Tert-butyl (2-acrylamidoethyl) carbamate (4.28 gm, 1 equiv., 20.00 mmol which was synthesized as per earlier reported procedure (ACS Macro Lett. 2018, 75, 592-597.) was deprotected by using 50% solution of TFA in DCM (40 mL) at ice temperature for 45 min. The resultant solution was stripped off and co-evaporated at 30° C.(to avoid undesired polymerization) using toluene (2×20 mL) to obtain the TFA salt (4.52 gm, 1 equiv., 19.84 mmol) as a semisolid, which was dissolved in acetonitrile, added compound 3 (5 gm, 1 equiv., 19.84 mmol) and DIPEA (3 equiv., 10.34 mL, 59.52, mmol), and the solution was stirred at 50° C. for 5 hours. The resultant solution was cooled at 37° C., filtered through cotton pad and filtrate was diluted with ethyl acetate (100 mL) and subsequently washed with dilute KHSO4 solution, brine solution, dried (Na2SO4). The solvent was removed under vacuum to afford 15c as a white solid.
Yield: 80%; mp. 95-105° C.; Rf=0.3 (silica gel TLC, 80% ethyl acetate in pet-ether); 1H NMR (400 MHZ, CDCl3), δ 8.23 (bs, 3H), 7.06 (bs., 2H), 6.59 (bs, 3H), 6.27-6.09 (m, 2H), 5.61 (d, J=10.7 Hz, 1H), 3.46-3.38 (m, 4H), 1.48 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 171.24, 166.44, 157.74, 130.92, 126.30, 82.21, 60.43, 40.63, 39.44, 28.10, 28.10, 28.10; HRMS (ESI-TOF): Calcd m/z: [M+H]+Calcd for C12H22N5O4 300.1666; Found 300.1662.[Note δ 1.26, δ 2.05, δ 4.12 are residual peak of ethyl acetate]
The synthetic method of 4a was adopted to synthesize 15d. The mono-endo-amine was synthesized via earlier reported procedure. (J. Org. Chem. 2004, 69, 8340-8344.)
Yield: 79%; Rf=0.4 (silica gel TLC, 60% ethyl acetate in pet-ether); 1H NMR (400 MHZ, CDCl3) δ 9.29 (m, 1 H), 8.31 (m, 1 H), 6.08 (s, 2 H), 5.89 (bs, 1 H), 3.51-3.48 (m, 2 H), 3.34 (bs., 2 H), 3.27 (q, J=6.1 Hz, 2 H), 3.23 (bs., 2 H), 1.71-1.68 (m, 1 H), 1.51 (d, J=9.2 Hz, 1 H), 1.45 (s, 9 H), 13C NMR (101 MHz, CDCl3) δ 177.93, 177.93, 161.88, 158.24, 157.79, 134.53, 134.53, 82.42, 60.45, 53.53, 52.25, 45.87, 44.92, 37.98, 37.98, 28.19, 28.19, 28.19; HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C18H26N5O5 392.1928; Found 392.1919.
The synthetic method of 5a was adopted to synthesize 16a.
Yield: 65%; mp. 130-135° C.; Rf=0.45 (silica gel TLC, 60% ethyl acetate in pet-ether); 1H NMR (400 MHz, CDCl3) δ 9.98 (bs., 1 H), 5.86 (tdd, J=5.6, 11.0, 16.7 Hz, 1 H), 5.26-5.13 (m, 2 H), 4.10 (t, J=5.7 Hz, 2 H), 3.98 (d, J=6.1 Hz, 2 H), 3.65 (t, J=5.7 Hz, 2 H), 1.51 (s, 9 H); 13C NMR (101 MHz, CDCl3) δ 154.29, 152.95, 151.62, 149.38, 134.54, 117.27, 85.51, 71.74, 66.28, 40.70, 27.89, 27.89, 27.89; HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C13H21N4O5 313.1506; Found 313.1496; [M+Na]+Calcd for C13H20N4O5Na 335.1326; Found 335.1315.
A mixture of 15b (2.5 g, 8.33 mmol, 1 equiv), NaHCO3 (1.0 g, 12.5 mmol, 1.5 equiv) and CDI (1.62 g, 10 mmol, 1.2 equiv.) in 30 ml acetonitrile was stirred at 35° C. for 48 h. The resultant reaction mixture was filtered under vacuum and solid residue was suspended in ethyl acetate (100 mL) and acidified with dilute KHSO4 solution, organic layer washed with brine solution, dried (Na2SO4), filtered and concentrated under vacuum at 30° C. (to avoid undesired polymerization) and resulting semisolid was purified by column chromatography using ethyl acetate 0-80% in petroleum ether. The solvent was removed under vacuum at 30° C. to get viscous oil which was kept in refrigerator overnight to afford 16b as a white solid. Yield: 30%; mp. 95-105° C.; Rf=0.6 (silica gel TLC, 60% ethyl acetate in pet-ether); 1H NMR (400 MHz, CDCl3) δ 11.16 (bs, 1 H), 9.85 (bs, 1 H), 6.41-6.37 (m, 1 H), 6.12-6.09 (m, 1 H), 5.85-5.82 (m, 1 H), 4.40-4.39 (m, 2 H), 4.23-4.20 (m, 2 H), 1.52 (s, 9 H) 13C NMR (101 MHz, CDCl3) δ 166.23, 154.67, 154.40, 153.01, 149.19, 131.63, 128.26, 86.02, 61.50, 40.74, 28.11, 28.11, 28.11; HRMS (ESI-TOF): Calcd m/z: [M+H]+Calcd for C13H19N4O6 327.1299; Found 327.1295; [M+Na]+Calcd for C13H18N4O6Na 349.1119; Found 349.1115.
The synthetic method of 16b was adopted to synthesize 16c.
Yield: 82%; mp. >250° C.; Rf=0.3 (silica gel TLC, 10% Methanol in DCM); 1H NMR (400 MHz, DMSO-d6) δ 8.17 (s, 1 H), 6.10-6.05 (m, 2 H), 5.58-5.55 (dd, J=3.1, 9.9 Hz, 1 H), 3.82-3.79 (bs, 3H), 3.35 (d, J=6.1 Hz, 2 H), 1.48 (s, 9 H); 13C NMR (101 MHz, DMSO-d6) δ 165.27, 165.27, 160.00, 159.0, 153.92, 132.10, 125.46, 83.68, 40.49, 36.40, 28.01,28.01, 28.01; HRMS (ESI-TOF): Calcd m/z:[M+H]+ Calcd for C13H20N5O5 326.1459; Found 326.1452; [M+Na]+ Calcd for C13H19N5O5Na 348.1284; Found 348.1271.
The synthetic method of 16b was adopted to synthesize 16d.
Yield: 78%; mp.>250° C.; Rf=0.45 (silica gel TLC, 10% MeOH in DCM); 1H NMR (400 MHz, CDCl3) δ 11.04 (bs., 1 H), 9.27 (bs., 1 H), 6.07-6.06 (m, 2 H), 4.02-4.03 (m, 2 H), 3.69 (td, J=2.3, 4.6 Hz, 2 H), 3.34-3.27 (d, J=19.1 Hz, 4 H), 1.72-1.70 (m, 2H), 1.54 (m, 9 H); 13C NMR (100 MHz, CDCl3) δ 177.74, 177.74, 154.50, 153.35, 152.19, 148.71, 134.08, 134.08, 85.42, 51.98, 45.60, 45.60, 45.60, 44.27, 39.87, 35.68, 27.53, 27.53, 27.53; HRMS (ESI-TOF): Calcd m/z: [M+H]+Calcd for C19H24N5O6 418.1721; Found 418.1716; [M+Na]+ Calcd for C19H23N5O6Na; 440.1541; Found 440.1536.
A solution of 16a in 50% TFA in DCM was stirred for 45 min at 0-4° C. The reaction mixture was concentrated in vacuo; the resulting residue was dissolved in diethyl ether and the solid was filtered in vacuum to afford 17a as a white solid.
Yield: 80%; mp. >250; The 1H NMR (500 MHz, CDCl3) δ 11.08 (bs., 1 H), 7.69 (bs., 1 H), 6.47 (bs., 1 H), 5.84 (tdd, J=5.3, 10.4, 17.2 Hz, 1 H), 5.23-5.22 (m, 2 H), 5.10 (m, 2 H), 3.92 (td, J=1.5, 5.3 Hz, 2 H), 3.83 (t, J=6.5 Hz, 2 H), 3.48 (t, J=6.3 Hz, 2 H) 13C NMR (125 MHz, CDCl3) δ 156.16, 156.16, 135.13, 116.32, 70.63, 69.32, 66.20, 41.01; HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C8H13N4O3+ 213.0982; Found 213.0982.
The synthetic method of 17a was adopted to synthesize 17b.
Yield: 78%; mp.>300° C.; 1H NMR (400 MHz, DMSO-d6) δ 7.14 (bs., 1 H), 6.30-6.26 (dd, J=1.6, 17.3 Hz, 1 H), 6.13-6.06 (dd, J=10.4, 17.3 Hz, 1 H), 5.90-5.93 (dd, J=1.5, 10.4 Hz, 1 H), 4.27-4.24 (t, J=5.4 Hz, 2 H), 3.97-3.94 (t, J=5.5 Hz, 2 H); 13C NMR (100 MHZ, DMSO-d6) δ 165.55, 156.20, 153.06, 150.26, 131.79, 128.40, 61.46, 40.35. HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C8H11N4O4+ 227.0775; Found 227.0775.
The synthetic method of 16a was adopted to synthesize 17c.
Yield: 78%; mp.>300° C.; Note: no solubility in DMSO-d6, HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C8H12N5O3+ 226.0935; Found 227.0935.
The synthetic method of 16a was adopted to synthesize 17d.
Yield: 84%; mp.>250° C.; 1H NMR (400 MHz, DMSO-d6) δ 7.11 (bs., 3 H), 6.01 (s, 2 H), 3.76-3.73 (m, 2 H), 3.46-3.44 (d, J=10.7 Hz, 2 H), 3.24-320 (d, J=13.0 Hz, 4 H), 1.54 (s, 2 H); 13C NMR (101 MHz, DMSO-d6) δ 177.87, 177.55, 168.43, 156.48, 156.48, 153.47, 134.86, 134.86, 52.31, 45.82, 44.60, 39.41, 39.41, 36.19; HRMS (ESI-TOF): Calcd m/z: [M+H]+ Calcd for C14H16N5O4+ 318.1197; Found 318.1197.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202111003499 | Jan 2021 | IN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IN2022/050057 | 1/25/2022 | WO |
