Synthesis of Ketamine Derivatives by Mannich Reactions
Pharmaceutical Science-Microbiology
DOI:
https://doi.org/10.22376/ijlpr.2023.13.1.P27-38Keywords:
Ketamine, Arylcyclohexamine, Mannich Reaction, Ketal, Hemiaminal, NMRAbstract
Arylcyclohexylamine Ketamine (HCL) has played an important role in Veterinary and Human Medicine as safe and reliable anesthetic agent but asit produces dysphoria several new derivatives of Ketamine have been synthesized till date. In this Research we have Utilized Mannich reaction to Synthesize The ammonia, primary amine and secondary amine are treated with hydrochloric acid and then added to the formaldehyde. Three novel derivatives were synthesized namely2-(2-chlorophenyl)- 6-[(diethyl amino) methyl]-2-(methylamino) cyclohexanone by RXN:102 Mannich Reaction of Ketamine with Di-ethylamine , rxn 113 2-(2chlorophenyl-6-dinitrophenyl hydrazine-methyl2(methylamino) cyclohexanone by Reaction of Ketamine with Di-nitro Phenyl Hydrazine & Rxn: 601. Mannich Reaction of Ketamine with Piperazine to form (2-chlorophenyl)-2-(methylamino)-6-(piperazine -1-yl) methyl cyclohexanone. Other reactions were also undergone to prepare oxazolidine derivatives of ketamine namely Synthesis of ketamine dioxolane derivative:Ketal and Hemiaminal Formation , Rxn: 103 Reaction of Ketamine with Glycerin [6-(2-chlorophenyl)-6-(methylamino)-1, 4-dioxaspiro [4.5] dec-2-yl] methanol and Rxn: 801 Reaction of Ketamine with Ephedrine N ,3,4-trimethyl-2,6 diphenyl-1oxa-4azaspiro [4.5] decan-6-amine derivative was formed. Thin layer chromatography of the synthesized derivatives was performed by using a solvent system of ethyl acetate and chloroform (50:50) and the RF values were calculated. The solubility test proves that compounds obtained from ketamine are polar in nature. All derivatives show similarity in solubility of ketamine. Although the melting points were not exactly comparable to that of ketamine, the range was not more than 5-10°C. This relatively narrow range of melting points proved that these were pure compounds. NMR spectroscopy was performed on all newly synthesized derivatives of ketamine. The notable ones obtained from reactions i.e. Rxn 102, 113, 103, 601and 801. The results of spectroscopy demonstrate that the compounds obtained were completely new species however they were structurally related to ketamine. These derivatives synthesized and confirmed by NMR technology. The derivatives can potentially be formulated for therapeutical purpose. Despite some limitations which are being considered in current drug design, the derivatives have the potential to develop into chemically modified entities that can play a major role in clinical therapeutics. Additional research studies will potentially help to determine the advanced method for high and sophisticated yield of these derivatives. Moreover, synthesis of ketamine metabolites namely N-demethyl compound and N-demethyl-5,6-dehydro analogues is established. However, further studies and modifications of these compounds will open new ventures of drug design and development of clinical implications in health care system.
References
Quevedo R, Moreno-Murillo B. One-step synthesis of a new heterocyclophane family. Tetrahedron Lett. 2009;50(8):936-8. doi: 10.1016/j.tetlet.2008.12.023.
Rivera A, Quevedo R. Solvent-free Mannich-type reaction as a strategy for synthesizing novel heterocalixarenes. Tetrahedron Lett. 2004;45(45):8335-8. doi: 10.1016/j.tetlet.2004.09.066.
Dunn MI, Dunlap JL. Guanadrel. A new antihypertensive drug. JAMA. 1981;245(16):1639-42. doi: 10.1001/jama.245.16.1639, PMID 7206175.
Carbazol-9-yl-methanol Milata Viktora, Kada Rudolfa, Lokaj J¨¢nb Molbank. Vol. M354; 2004.
Fleming JJ, McReynolds MD, Du Bois J. (+)-saxitoxin: a first and second generation stereoselective synthesis. J Am Chem Soc. 2007 Aug 15;129(32):9964-75. doi: 10.1021/ja071501o, PMID 17658800.
Chaterjee D, Mitra A, Dey GS. Ruthenium PolyaminocarboxylateComplexes: prospects for their use as metallopharmaceuticals. Platinum Met Rev. 2006;50(1):2-12.
Kronenberg RH. Pharmacist†, thunderbird Samaritan Medical Center, Glendale, AZ, USA. J Pain Palliat Care Pharmacother. 2002;16(3):27-35. doi: 10.1080/J354v16n03_03, PMID 14640353.
Anis NA, Berry SC, Burton NR, Lodge D. The dissociative anaesthetics, ketamine and phencyclidine, selectively reduce excitation of central mammalian neurones by N-methyl-aspartate. Br J Pharmacol. 1983;79(2):565-75. doi: 10.1111/j.1476-5381.1983.tb11031.x, PMID 6317114. Merck. Index. 11th ed. Vol. 5174.
Hocking G, Cousins MJ. Ketamine in chronic pain management: an evidence-based review. Anesth Analg. 2003;97(6):1730-9. doi: 10.1213/01.ANE.0000086618.28845.9B, PMID 14633551.
Sulake RS, Chen C, Lin HR, Lua AC. Synthesis of deuterium labeled ketamine metabolite dehydronorketamine-d₄. Bioorg Med Chem Lett. 2011 Oct 1;21(19):5719-21. doi: 10.1016/j.bmcl.2011.08.021. PMID 21865041.
Jansen KLR. A review of the nonmedical use of ketamine: use, users and consequences. J Psychoactive Drugs. 2000;32(4):419-33. doi: 10.1080/02791072.2000.10400244, PMID 11210204.
Meller ST. Ketamine: relief from chronic pain through actions at the NMDA receptor? Pain. 1996 Dec;68(2-3):435-6. doi: 10.1016/s0304-3959(96)03167-3, PMID 9121834.
Chen L, Gong Y, Salter R. Synthesis of carbon-14 labeled ketamine and norketamine. J Labelled Comp Radiopharm. 2018 Sep;61(11):864-8. doi: 10.1002/jlcr.3669. PMID 29992626.
White P F. M.D. Way, Walter L. M.D.; Trevor, anthony. J Phys D. “Ketamine-Its Pharmacology and Therapeutic Uses.” Research 21, monograph series by National Institute of Drug Abuse, SE Lerner, RS Burns - PCP, 1978 - 209.237.226.93.
Okon T. Ketamine: an introduction for the pain and palliative medicine physician. Pain Phys. May 2007;10(3):493-500. PMID 17525784.
Mannich C, Krösche W. Ueber ein Kondensationsprodukt aus Formaldehyd, Ammoniak und Antipyrin. Arch Pharm Pharm Med Chem. 1912;250(1):647-67. doi: 10.1002/ardp.19122500151.
Alltounian HS, Moore M. Journeys into the bright world. Rockport, MA: Para Research. ISBN 0-914918-12-5; 1978.
Joe-Laidler K, Hunt G. Sit down to float: the cultural meaning of ketamine use in Hong Kong. Addict Res Theory. Jan 1 2008;16(3):259-71. doi: 10.1080/16066350801983673, PMID 19759834.
Hocking G, Cousins MJ. Ketamine in chronic pain management: an evidence-based review. Anesth Analg. 2003;97(6):1730-9. doi: 10.1213/01.ANE.0000086618.28845.9B, PMID 14633551.
Wayne RB. Iron transport and storage in microorganisms, plants and animals. J Am Coll Nutr. 1999;18(1):368-9.
Ramabadran K, Bansinath M, Turndorf H, Puig MM. Tail immersion test for the evaluation of a nociceptive reaction in mice. Methodological considerations. J Pharmacol Methods. 1989;21(1):21-31. doi: 10.1016/0160-5402(89)90019-3, PMID 2704245.
Correction to “Ketamine and Ketamine Metabolite Pharmacology: Insights into Therapeutic Mechanisms”. Pharmacol RevPharmacol Rev. 2018;70(4):879. doi: 10.1124/pr.116.015198err. PMID 30282701.
Sinner B, Graf BM. Ketamine. Handb Exp Pharmacol. 2008;182(182):313-33. doi: 10.1007/978-3-540-74806-9_15, PMID 18175098.
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Copyright (c) 2022 Syed Muzzammil Masaud, Ghulam Abbas Miana, Taha Nazir, Saeed Ur Rasheed Nazir, Humayun Riaz, Misbah Sultana, Safia Sultana Munir, Pervaiz Akhtar Shah, Humaira Nadeem, Ishtiaq Rabi

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