Reaktion #8350

ord-12f27f75f99d47e4a40c92fcb9b23588

Reaktionsgleichung

[Cl][Mg][CH2]c1ccccc1
benzyl magnesium chloride
Brc1cccc(-c2nn3c(c2-c2ccnc4ccccc24)CCC3)n1
4-[2-(6-bromo-pyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl]-quinoline
c1ccc(Cc2cccc(-c3nn4c(c3-c3ccnc5ccccc35)CCC4)n2)cc1
title compound
c1ccc(Cc2cccc(-c3nn4c(c3-c3ccnc5ccccc35)CCC4)n2)cc1
4-[2-(6-Benzyl-pyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl]-quinoline

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigequenched with saturated aqueous ammonium chloride (1 mL)
  2. 2
    EinengenThe reaction mixture is concentrated in vacuo
  3. 3
    Filtrationfiltered
  4. 4
    Sonstigethe residue chromatographed on SiO2 (20-50% acetone/hexanes)

Vorschrift

Zinc(II) chloride (0.34 mL, 1.0 M solution, 0.34 mmol) is added, at room temperature with stirring, to a solution of benzyl magnesium chloride (0.15 mL, 2.0 M solution, 0.31 mmol) in tetrahydrofuran (1 mL). After 15 min, Pd(PPh3)2Cl2 (5.4 mg, 0.0076 mmol) is added followed by a solution of 4-[2-(6-bromo-pyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl]-quinoline (60 mg 0.153 mmol) in tetrahydrofuran (1 mL). The reaction mixture is stirred for 18 h at room temperature and quenched with saturated aqueous ammonium chloride (1 mL). The reaction mixture is concentrated in vacuo, filtered, and the residue chromatographed on SiO2 (20-50% acetone/hexanes) to yield the title compound, 33.4 mg (54%), as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087626B2uspto-grants-2006_08