Reaktion #1902901

Reaktionsgleichung

4-Chloro-7-methoxy-2-pyridin-2-yl-quinoline

N—Boc-4-hydroxyproline

t-BuOK

→

product

Ausbeute 51.3%

4-(7-Methoxy-2-pyridin-2-yl-quinolin-4-yloxy)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester

Ausbeute 51.3%

Lösungsmittel

DMSO

water

DMSO

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGThe reaction mixture was stirred for 38 h
2. 2
   Extraktionextracted with EtOAc/ether (1/4, 2×)
3. 3
   Extraktionextracted with EtOAc/THF (5×)
4. 4
   Extraktionthe combined extract
5. 5
   Trocknenwas dried (Na2SO4/MgSO4)
6. 6
   Sonstigeremoved the solvent in vacuo
7. 7
   Sonstigethe residue was purified by preparative HPLC (0-80% solvent B)

Vorschrift

To a solution of N—Boc-4-hydroxyproline (1.6 g, 6.7 mmol) in DMSO (20 mL) was added t-BuOK (1.9 g, 16.8 mmol). The generated mixture was stirred for 1.5 h and 4-Chloro-7-methoxy-2-pyridin-2-yl-quinoline (2.0 g, 7.4 mmol) and DMSO (10 mL) were added. The reaction mixture was stirred for 38 h, diluted with cold water and extracted with EtOAc/ether (1/4, 2×). the aqueous layer was acidified to pH 4 and extracted with EtOAc/THF (5×). the combined extract was dried (Na2SO4/MgSO4), removed the solvent in vacuo and the residue was purified by preparative HPLC (0-80% solvent B) to provide the product (1.6 g, 50%): LC-MS (retention time: 1.23, Method I), MS m/z 466 (M++1).

Quelle