Isonipecotic acid
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| Names | |||
|---|---|---|---|
| IUPAC name
4-Piperidinecarboxylic acid | |||
| Identifiers | |||
| 498-94-2 | |||
| 3D model (Jmol) | Interactive image | ||
| ChEMBL | ChEMBL279998 | ||
| ChemSpider | 3641 | ||
| ECHA InfoCard | 100.007.158 | ||
| EC Number | 207-872-3 | ||
| 4227 | |||
| PubChem | 3773 | ||
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| Properties | |||
| C6H11NO2 | |||
| Molar mass | 129.16 g/mol | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
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| Infobox references | |||
Isonipecotic acid is a heterocyclic compound which acts as a GABAA receptor partial agonist.[1]
It consists of a piperidine ring with a carboxylic acid moiety in the iso position (and as such is also known as "4-piperidinecarboxylic acid").
Uses
- A known use of isonipecotic acid is to prepare 4-(4-Chlorobenzoyl)-piperidine,[2] which in-turn finds an application in the synthesis of Cloroperone (Cloperone).
- An alternative use in in the preparation of (4-bromophenyl)(4-piperidyl)methanone-(Z)—O-ethyloxime.[3]
- The 4-(p-fluorobenzoyl)piperidine moiety[4][5] is known to have application in the synthesis of Ketanserin, Setoperone, Lidanserin, Pirenperone, altanserin & Duoperone.
References
- ↑ Mortensen M, Kristiansen U, Ebert B, Frølund B, Krogsgaard-Larsen P, Smart TG (June 2004). "Activation of single heteromeric GABA(A) receptor ion channels by full and partial agonists". The Journal of Physiology. 557 (Pt 2): 389–413. doi:10.1113/jphysiol.2003.054734. PMC 1665090
. PMID 14990676. - ↑ Cavallini et al. Farmaco, Edizione Scientifica, 1957 , vol. 12, p. 853,862.
- ↑ George S. K. Wong, Jeonghan Park, Weidong Tong, Ramani Raghavan, U.S. Patent 6,914,142 (2005 to Schering Corporation).
- ↑ Chumpradit, S.; Choi, S. R.; Hou, C.; Acton, P. D.; Kung, H. F. (2001). "Novel TC-99M N2S2 derivatives for imaging 5HT2A receptors". Journal of Labelled Compounds and Radiopharmaceuticals. 44 (S1): S524–S526. doi:10.1002/jlcr.25804401186. ISSN 0362-4803.
- ↑ Journal of Medicinal Chemistry, vol. 46, # 25 p. 5512 - 5532. doi:10.1021/jm0309349
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