| Identification | More | [Name]
4-N-Boc-4-N-Methyl-aminopiperidine | [CAS]
108612-54-0 | [Synonyms]
4-AMINOPIPERIDINE-N-METHYL, N-BOC PROTECTED
4-N-BOC-4-N-METHYL-AMINOPIPERIDINE
BUTTPARK 90\06-17
METHYL-PIPERIDIN-4-YL-CARBAMIC ACID TERT-BUTYL ESTER
tert-butyl n-methyl-n-(4-piperidyl)carbamate
4-(Methylamino)piperidine, N4-BOC protected
4-Boc-4-methylaminopiperidine
4-Boc-methylaminopiperidine
4-N-Boc-amino-piperidinecitrate
tert-butyl methyl(piperidin-4-yl)carbamate
methyl-piperidine-4-yl-carbamic acid tert-butyl ester | [EINECS(EC#)]
672-392-7 | [Molecular Formula]
C11H22N2O2 | [MDL Number]
MFCD02683051 | [Molecular Weight]
214.3 | [MOL File]
108612-54-0.mol |
| Chemical Properties | Back Directory | [Melting point ]
50°C(lit.) | [Boiling point ]
287.9±29.0 °C(Predicted) | [density ]
1.01±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [form ]
crystalline powder | [pka]
10.05±0.10(Predicted) | [color ]
White | [InChI]
InChI=1S/C11H22N2O2/c1-11(2,3)15-10(14)13(4)9-5-7-12-8-6-9/h9,12H,5-8H2,1-4H3 | [InChIKey]
DJJOYDXRUBOZON-UHFFFAOYSA-N | [SMILES]
C(OC(C)(C)C)(=O)N(C)C1CCNCC1 | [CAS DataBase Reference]
108612-54-0(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Uses]
4-N-Boc-4-N-methyl-aminopiperidine, or Tert-butyl methyl(piperidin-4-yl)carbamate (TBMPC) is a derivative of piperidine and is structurally similar to other carbamates. It inhibits the enzyme cyclooxygenase and modulates the activity of the neurotransmitter GABA. This compound has demonstrated anticonvulsant and anti-inflammatory activity. TBMPC has been studied for its potential use in various in vivo and in vitro applications. It has been reported to reduce the frequency and duration of seizures in animal models and reduce the production of pro-inflammatory cytokines in cell culture.
| [Synthesis]
General procedure for the synthesis of 4-N-tert-butoxycarbonyl-4-N-methylaminopiperidine from tert-butyl (1-benzylpiperidin-4-yl)(methyl)carbamate: 10% (w/w) humidity Pd/C catalyst (1.1 g) was added to a 250 mL three-necked flask. After sealing the flask, three evacuations and backfilling with nitrogen were performed. Subsequently, a methanol solution of 1-benzyl-4-(N-Boc-N-methyl)aminopiperidine (10.7 g, 35.2 mmol) was added to the flask. The operation was again carried out with three evacuations and backfilled with hydrogen. The reaction mixture was stirred at room temperature for three days, during which the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, three evacuations and backfilling with nitrogen were performed. The reaction mixture was filtered and the filtrate was concentrated under vacuum to give 6.8 g of the target product 4-N-tert-butoxycarbonyl-4-N-methylaminopiperidine as a white solid in 90% yield. | [References]
[1] Journal of Medicinal Chemistry, 1999, vol. 42, # 24, p. 4981 - 5001
[2] Tetrahedron Letters, 2017, vol. 58, # 20, p. 1976 - 1979
[3] Patent: US2012/71461, 2012, A1. Location in patent: Page/Page column 144 |
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