Reaktion #426862

ord-23c2aa3a353b42d9b12e66f18f67609f

Reaktionsgleichung

COCCOc1ccn2c(-c3ccc4cccc(OS(=O)(=O)C(F)(F)F)c4n3)nnc2c1
2-(7-(2-methoxyethoxy)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-yl trifluoromethane sulfonate
CC(C)(C)OC(=O)NCC1CCNCC1
tert-butyl piperidin-4-ylmethylcarbamate
CC(C)(C)OC(=O)N1CCNCC1
tert-butyl piperazine-1-carboxylate
CC(C)(C)OC(=O)NCC1CCN(c2cccc3ccc(C=O)nc23)CC1
tert-butyl(1-(2-formylquinolin-8-yl)piperidin-4-yl)methylcarbamate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigePrepared

Vorschrift

Prepared as described in Example 1, Step H, substituting 8-bromoquinoline-2-carbaldehyde for 2-(7-(2-methoxyethoxy)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-yl trifluoromethane sulfonate, and tert-butyl piperidin-4-ylmethylcarbamate for tert-butyl piperazine-1-carboxylate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08895550B2uspto-grants-2014_11