380253
2-哌啶甲酸乙酯 盐酸盐
97%
别名:
2-哌啶羧酸乙酯 盐酸盐
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关于此项目
经验公式（希尔记法）:
C8H15NO2 · HCl
化学文摘社编号:
分子量:
193.67
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
2-哌啶甲酸乙酯 盐酸盐, 97%
InChI
1S/C8H15NO2.ClH/c1-2-11-8(10)7-5-3-4-6-9-7;/h7,9H,2-6H2,1H3;1H
SMILES string
Cl[H].CCOC(=O)C1CCCCN1
InChI key
KGAWPIXNSIYQPC-UHFFFAOYSA-N
assay
97%
mp
211-213 °C (lit.)
Application
Ethyl pipecolinate hydrochloride (Ethyl 2-piperidinecarboxylate hydrochloride) may be used in the preparation of:
- 1,4-diazabicyclo[4.4.0]decane
- small molecule inhibitors of Legionella MIP protein
- antiinflammatory and analgesic molecules
- anti-amnesic agents
General description
Ethyl pipecolinate hydrochloride is a heterocyclic building block. It is reported to participate in the total synthesis of the (+)-epiquinamide, a quinolizidine alkaloid.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
A concise synthesis of (?) and a total synthesis of (+)-epiquinamide.
Tong STA and Barker D.
Tetrahedron Letters, 47(29), 5017-5020 (2006)
Christina Juli et al.
Journal of medicinal chemistry, 54(1), 277-283 (2010-12-15)
The macrophage infectivity potentiator (MIP) protein is a major virulence factor of Legionella pneumophila, the causative agent of Legionnaires' disease. MIP belongs to the FK506-binding proteins (FKBP) and is necessary for optimal intracellular survival and lung tissue dissemination of L.
S Zhao et al.
Bioorganic & medicinal chemistry, 7(8), 1637-1646 (1999-09-11)
Tacrine, one of the drugs available for Alzheimer's disease based on the cholinergic approach, suffers from considerable toxicity. Many analogues of tacrine have been prepared which retain the pharmacologically rich aminopyridine or aminoquinoline motifs. The current research was undertaken to
Syntheses of 1, 4-Diazabicyclo [4.4. 0] decanes, 1, 4-Diazabicyclo [4.3. 0] nonanes and 1, 8-Diazabicyclo [4.3. 0] nonanes.
Freed ME and Day AR.
J. Org. React., 25(12), 2108-2113 (1960)
G. A. Gevorgyan, et al.,
Khim.-Farm. Zh., 37, 152-154 (2003)
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