Reaktion #155913

ord-c9034252dcdb4bc1bbd92a1cf36d3ebd

Reaktionsgleichung

CCc1nn(-c2ccccc2)c2nc(C3CCNCC3)nc(O)c12.Cl
3-ethyl-1-phenyl-6-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidin-4-ol hydrochloride
CC(C)(C)OC(=O)N1CCC(=O)C1
3-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester
Cl
HCl
CCc1nn(-c2ccccc2)c2nc(C3CCN(C4CCNC4)CC3)nc(O)c12.Cl
title compound
CCc1nn(-c2ccccc2)c2nc(C3CCN(C4CCNC4)CC3)nc(O)c12.Cl
3-Ethyl-1-phenyl-6-(1-pyrrolidin-3-yl-piperidin-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-ol hydrochloride

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound was prepared according to the procedure as described in Example 88 reacting via reductive amination 3-ethyl-1-phenyl-6-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidin-4-ol hydrochloride and 3-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester followed by de-protection of the adduct with HCl.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08822447B2uspto-grants-2014_09