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Tetrahydroisoquinoline

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This article is about the simple heterocyclic amine. For the selective MC4 agonist, see THIQ.
Tetrahydroisoquinoline
Names
Other names
1,2,3,4-Tetrahydroisoquinoline
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.001.864 Edit this at Wikidata
RTECS number
  • NX4900000
  • InChI=1S/C9H11N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-4,10H,5-7H2 checkY
    Key: UWYZHKAOTLEWKK-UHFFFAOYSA-N checkY
  • InChI=1/C9H11N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-4,10H,5-7H2
    Key: UWYZHKAOTLEWKK-UHFFFAOYAB
  • c1ccc2c(c1)CCNC2
Properties
C9H11N
Molar mass 133.19 g/mol
Appearance Deep yellow liquid
Density 1.05 g/mL
Melting point −30 °C (−22 °F; 243 K)
Boiling point 235 to 239 °C (455 to 462 °F; 508 to 512 K)
Hazards
Flash point 99 °C (210 °F; 372 K) (closed cup)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Tetrahydroisoquinoline (TIQ)[1] is an organic compound with the chemical formula C9H11N. Classified as a secondary amine, it is derived from isoquinoline by hydrogenation. It is a colorless viscous liquid that is miscible with most organic solvents. The tetrahydroisoquinoline skeleton is encountered in a number of bioactive compounds and drugs.[2]

Reactions

As a secondary amine, tetrahydroisoquinoline has weakly basic properties and forms salts with strong acids. It can be dehydrogenated to give isoquinoline and hydrogenated to decahydroisoquinoline. Like other secondary amines, tetrahydroisoquinoline can be oxidized to the corresponding nitrone using hydrogen peroxide, catalyzed by selenium dioxide.[3]

Toxicology

Tetrahydroisoquinoline derivatives may be formed in the body as metabolites of some drugs, and this was once thought to be involved in the development of alcoholism.[4] This theory has now been discredited and is no longer generally accepted by the scientific community,[5] but endogenous production of neurotoxic tetrahydroisoquinoline derivatives such as norsalsolinol continue to be investigated as possible causes for some conditions such as Parkinson's disease.[6][7][8][9][10][11]

Tetrahydroisoquinolines

The tetrahydroisoquinoline skeleton is encountered in a number of drugs,[12] tubocurarine, one of the quaternary ammonium muscle relaxants. Drugs based on 4-substituted tetrahydroisoquinolines include nomifensine[13] and diclofensine. They can be prepared by N-alkylation of benzyl amines with haloacetophenones.[14] Naturally occurring tetrahydroisoquinolines includes cherylline.[15] and latifine.

Esproquin,[16] which shows hypotensive activity by virtue of its α-adrenergic blocking properties, is made from THIQ.

References

  1. ^ Antkiewicz-Michaluk, Lucyna; Wąsik, Agnieszka; Michaluk, Jerzy (2013). "1-Methyl-1,2,3,4-Tetrahydroisoquinoline, an Endogenous Amine with Unexpected Mechanism of Action: New Vistas of Therapeutic Application". Neurotoxicity Research. 25 (1): 1–12. doi:10.1007/s12640-013-9402-7. ISSN 1029-8428.
  2. ^ Mitchinson, Andrew; Nadin, Alan "Saturated nitrogen heterocycles" Perkin 1 2000, pp. 2862-2892. doi:10.1039/A908537H
  3. ^ Murahashi, S. (1987). "Selenium dioxide catalyzed oxidation of secondary amines with hydrogen peroxide. Simple synthesis of nitrones from secondary amines". Tetrahedron Letters. 28 (21): 2383–2386. doi:10.1016/S0040-4039(00)96130-6.
  4. ^ Blum, K.; Hamilton, M. G.; Hirst, M.; Wallace, J. E. (1978). "Putative role of isoquinoline alkaloids in alcoholism: a link to opiates". Alcoholism: Clinical and Experimental Research. 2 (2): 113–120. doi:10.1111/j.1530-0277.1978.tb04710.x. PMID 350073.,Altshuler, H. L.; Shippenberg (1982). "Tetrahydroisoquinoline and opioid substrates of alcohol actions". Progress in clinical and biological research. 90: 329–344. PMID 7202207., Myers, R. D. (1989). "Isoquinolines, beta-carbolines and alcohol drinking: involvement of opioid and dopaminergic mechanisms". Experientia. 45 (5): 436–443. doi:10.1007/BF01952025. PMID 2656285.
  5. ^ Myers, R. D. (1996). "Tetrahydroisoquinolines and alcoholism: where are we today?". Alcoholism: Clinical and Experimental Research. 20 (3): 498–500. doi:10.1111/j.1530-0277.1996.tb01081.x. PMID 8727243., Musshoff, F.; Daldrup, T.; Bonte, W.; Leitner, A.; Lesch, O. M. (1996). "Formaldehyde-derived tetrahydroisoquinolines and tetrahydro-beta-carbolines in human urine". Journal of Chromatography B. 683 (2): 163–176. doi:10.1016/0378-4347(96)00106-5. PMID 8891913., Sällström Baum, S.; Hill, R.; Kiianmaa, K.; Rommelspacher, H. (1999). "Effect of ethanol on (R)- and (S)-salsolinol, salsoline, and THP in the nucleus accumbens of AA and ANA rats". Alcohol (Fayetteville, N.Y.). 18 (2–3): 165–169. doi:10.1016/S0741-8329(98)00080-9. PMID 10456568., Musshoff, F.; Lachenmeier, D. W.; Schmidt, P.; Dettmeyer, R.; Madea, B. (2005). "Systematic regional study of dopamine, norsalsolinol, and (R/S)-salsolinol levels in human brain areas of alcoholics". Alcoholism: Clinical and Experimental Research. 29 (1): 46–52. doi:10.1097/01.ALC.0000150011.81102.C2. PMID 15654290.
  6. ^ Kotake Y, Tasaki Y, Makino Y, Ohta S, Hirobe M (December 1995). "1-Benzyl-1,2,3,4-tetrahydroisoquinoline as a parkinsonism-inducing agent: a novel endogenous amine in mouse brain and parkinsonian CSF". Journal of Neurochemistry. 65 (6): 2633–8. doi:10.1046/j.1471-4159.1995.65062633.x. PMID 7595560.
  7. ^ McNaught KS, Carrupt PA, Altomare C, Cellamare S, Carotti A, Testa B, Jenner P, Marsden CD (October 1998). "Isoquinoline derivatives as endogenous neurotoxins in the aetiology of Parkinson's disease". Biochemical Pharmacology. 56 (8): 921–33. doi:10.1016/S0006-2952(98)00142-7. PMID 9776302.
  8. ^ Lorenc-Koci E, Smiałowska M, Antkiewicz-Michaluk L, Gołembiowska K, Bajkowska M, Wolfarth S (2000). "Effect of acute and chronic administration of 1,2,3,4-tetrahydroisoquinoline on muscle tone, metabolism of dopamine in the striatum and tyrosine hydroxylase immunocytochemistry in the substantia nigra, in rats". Neuroscience. 95 (4): 1049–59. doi:10.1016/S0306-4522(99)00511-4. PMID 10682712.
  9. ^ Storch A, Ott S, Hwang YI, Ortmann R, Hein A, Frenzel S, Matsubara K, Ohta S, Wolf HU, Schwarz J (March 2002). "Selective dopaminergic neurotoxicity of isoquinoline derivatives related to Parkinson's disease: studies using heterologous expression systems of the dopamine transporter". Biochemical Pharmacology. 63 (5): 909–20. doi:10.1016/S0006-2952(01)00922-4. PMID 11911843.
  10. ^ Lorenc-Koci E, Antkiewicz-Michaluk L, Kamińska A, Lenda T, Zieba B, Wierońska J, Smiałowska M, Schulze G, Rommelspacher H (October 2008). "The influence of acute and chronic administration of 1,2-dimethyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline on the function of the nigrostriatal dopaminergic system in rats". Neuroscience. 156 (4): 973–86. doi:10.1016/j.neuroscience.2008.08.050. PMID 18809471.
  11. ^ Kobayashi H, Fukuhara K, Tada-Oikawa S, Yada Y, Hiraku Y, Murata M, Oikawa S (January 2009). "The mechanisms of oxidative DNA damage and apoptosis induced by norsalsolinol, an endogenous tetrahydroisoquinoline derivative associated with Parkinson's disease". Journal of Neurochemistry. 108 (2): 397–407. doi:10.1111/j.1471-4159.2008.05774.x. PMID 19012744.
  12. ^ Scott, Jack D.; Williams, Robert M. (2002). "Chemistry and Biology of the Tetrahydroisoquinoline Antitumor Antibiotics". Chemical Reviews. 102: 1669–1730. doi:10.1021/cr010212u.
  13. ^ Schneider, C. S.; Weber, K. H.; Daniel, H.; Bechtel, W. D.; Boeke-Kuhn, K. (1984). "Synthesis and antidepressant activity of 4-aryltetrahydrothieno[2,3-c]pyridine derivatives". Journal of Medicinal Chemistry. 27 (9): 1150–1155. doi:10.1021/jm00375a011.
  14. ^ BG 49761 
  15. ^ cherylline
  16. ^ Gray, Allan P.; Shiley, Richard H. (1973). "Preparation and cardiovascular actions of a group of tetrahydroisoquinoline derivatives". Journal of Medicinal Chemistry. 16 (7): 859–861. doi:10.1021/jm00265a028. ISSN 0022-2623.
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