Lysergic acid
| Lysergic acid | |
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7-Methyl- 4,6,6a,7,8,9- hexahydro- indolo [4,3-fg] quinoline- 9-carboxylic acid |
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Other names
6-Methyl- 9,10- didehydroergoline- 8-carboxylic acid |
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| Identifiers | |
| CAS number | 82-58-6  , [478-95-5], [6915-32-8], [23953-76-6], [68985-97-7], [68985-98-8] |
| ChemSpider | 6461 |
| ChEBI | CHEBI:6604 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C16H16N2O2 |
| Molar mass | 268.31 g mol−1 |
| Melting point |
238 - 240 °C |
 (verify) (what is:  / ?)Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Lysergic acid, also known as D-lysergic acid and (+)-lysergic acid, is a precursor for a wide range of ergoline alkaloids that are produced by the ergot fungus and found in the Hawaiian Baby Woodrose and the seeds of Morning glory. Amides of lysergic acid, lysergamides, are widely used as pharmaceuticals and as psychedelic drugs (LSD). Lysergic acid received its name as it was a product of the lysis of various ergot alkaloids.[1]
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Synthesis [edit]
Lysergic acid is generally produced by hydrolysis[2] of natural lysergamides, but can also be synthesized in the laboratory by a complex total synthesis for example by Woodward's team in 1956.[3] An enantioselective total synthesis based on a palladium catalyzed domino cyclization reaction has been described in 2011 by Fujii and Ohno.[4] Lysergic acid monohydrate crystallizes in very thin hexagonal leaflets when recrystallized from water. Lysergic acid monohydrate, when dried (140 °C at 2 mmHg or 270 Pa) forms anhydrous lysergic acid. The biosynthetic route is based on the alkylation of the amino acid tryptophan with dimethylallyl diphosphate (isoprene derived from 3R-mevalonic acid) giving 4-dimethylallyl-L-tryptophan which is N-methylated with S-adenosyl-L-methionine. Oxidative ring closure followed by decarboxylation, reduction, cyclization, oxidation, and allylic isomerization yields D-(+)-lysergic acid.[1]
Isomers [edit]
Lysergic acid is a chiral compound with two stereocenters. The isomer with inverted configuration at carbon atom 8 close to the carboxy group is called isolysergic acid. Inversion at carbon 5 close to the nitrogen atom leads to L-lysergic acid and L-isolysergic acid, respectively. Lysergic acid is listed as a Table I precursor under the United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances.[5]
See also [edit]
References [edit]
- ^ a b Schiff PL (2006 Oct 15). "Ergot and its alkaloids". Am J Pharm Educ. 70 (5): 98. PMID 17149427.
- ^ Martínková L, Kren V, Cvak L, Ovesná M, Prepechalová I (2001 Nov 17). "Hydrolysis of lysergamide to lysergic acid by Rhodococcus equi A4". J Biotechnol. 84 (1): 63–6.
- ^ Edmund C. Kornfeld, E.J. Fornefeld, G. Bruce Kline, Marjorie J. Mann, Dwight E. Morrison, Reuben G. Jones and R.B. Woodward (1956). "The Total Synthesis of Lysergic Acid". Journal of the American Chemical Society 78: 3087–3114.
- ^ S. Inuki, A. Iwata, S. Oishi, N. Fujii and H. Ohno, J. Org. Chem. 2011, 76 (7), pp 2072–2083, doi:10.1021/jo102388e.
- ^ List of Precursors and Chemicals Frequently Used in the Illicit Manufacture of Narcotic Drugs and Psychotropic Substances Under International Control, International Narcotics Control Board
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