Isopropanol → 6-Isopropoxy-5-piperidin-1-yl-pyrazine-2-carboxylic acid

HRID 639325

Reaktionsgleichung

C[O:2][C:3]([C:5]1[CH:10]=[N:9][C:8]([N:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)=[C:7](Br)[N:6]=1)=[O:4].[CH:18]([OH:21])([CH3:20])[CH3:19].[H-].[Na+].[OH-].[K+]>O1CCOCC1.CN(C=O)C.C(O)=O.O>[CH:18]([O:21][C:7]1[N:6]=[C:5]([C:3]([OH:2])=[O:4])[CH:10]=[N:9][C:8]=1[N:11]1[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1)([CH3:20])[CH3:19]

Komponenten

Reaktionsbedingungen

Temperatur: 60 °C

Versuchsvorschrift

A mixture of 0.212 g (0.707 mmol) 6-bromo-5-piperidin-1-yl-pyrazine-2-carboxylic acid methyl ester, 0.006 g (0.778 mmol) isopropanol and 0.034 g (0.778 mmol) NaH (55% dispersion in oil) in 1.7 mL dioxane was heated to 60° C. for 16 h. Water and 5N KOH was added and the mixture was heated to 50° C. for 4 h. Formic acid and DMF was added and the mixture was subjected to purification by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile, water and formic acid. The product fractions were combined and evaporated to yield 0.04 g (21%) of the title compound. m/z (ES+): 266.4 (M+H).

Aufarbeitung

temperaturethe mixture was heated to 50° C. for 4 h
customthe mixture was subjected to purification by preparative HPLC on reversed phase
washeluting with a gradient
customformed from acetonitrile, water and formic acid
customevaporated

Quellen und Nachweise

ORD-Eintrag: ord-3fb8e08a922a48e4bc637cbb983a6acc
Quelldatensatz: uspto-grants-2010_04
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07691863B2

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