Hydrochloric Acid → Ethyl 3-(2-[(4-methylpyridin-3-yl)amino]ethyl}piperidine-3-carboxylate trihydrochloride

HRID 1639986Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1639986
[ClH:1].[CH3:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][C:4]=1[NH:9][CH2:10][CH2:11][C:12]1([C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH2:17][CH2:16][CH2:15][N:14](C(OC(C)(C)C)=O)[CH2:13]1>O1CCOCC1.C(OCC)(=O)C>[ClH:1].[ClH:1].[ClH:1].[CH3:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][C:4]=1[NH:9][CH2:10][CH2:11][C:12]1([C:25]([O:27][CH2:28][CH3:29])=[O:26])[CH2:17][CH2:16][CH2:15][NH:14][CH2:13]1

Komponenten

5

Edukt 2

HCID 313Hydrochloric AcidHCID 667226241-Tert-butyl 3-ethyl 3-{2-[(4-methylpyridin-3-yl)amino]ethyl}piperidine-1,3-dicarboxylate

Produkt 1

HCID 66722530Ethyl 3-(2-[(4-methylpyridin-3-yl)amino]ethyl}piperidine-3-carboxylate trihydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8857Ethyl AcetateLösungsmittelHCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

Hydrogen chloride in 1,4-dioxane (4.0 M, 2.0 mL) was added to a solution of 1-tert-butyl 3-ethyl 3-{2-[(4-methylpyridin-3-yl)amino]ethyl}piperidine-1,3-dicarboxylate (0.036 g, 0.000092 mol) in ethyl acetate (0.5 mL) and the mixture was stirred for 2 h. Then the solvent was removed in-vacuo to afford the product. LC-MS: 292.3 (M+H)+.

Aufarbeitung

  1. customThen the solvent was removed in-vacuo
  2. customto afford the product

Quellen und Nachweise

ORD-Eintrag
ord-8ff4a140cb7a4ef3b39ab188205b76af
Quelldatensatz
uspto-grants-2012_02
Patentnummer
US08110581B2

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