Reaktion #600388

ord-6944b3299ea24086a180d73923f76289

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe mixture was concentrated in vacuo
  2. 2
    Sonstigethe crude material was purified on silica (gradient elution, 0-30% EtOAc/hexanes)

Vorschrift

To a solution of tert-butyl 7-chloro-3-(2-hydroxyethyl)-1H-pyrrolo[2,3-c]pyridine-1-carboxylate (233 mg, 0.79 mmol) in PhMe (15 mL) was added 4-trifluoromethoxyphenol (0.15 mL, 1.2 mmol), triphenylphosphine (309 mg, 1.2 mmol), and diisopropylazodicarboxylate (0.23 mL, 1.2 mmol) at r.t. After 20 min, the mixture was concentrated in vacuo, and the crude material was purified on silica (gradient elution, 0-30% EtOAc/hexanes) to yield the title product (349 mg). HRMS (ESI) calc (M+H)+=457.1136. found 457.1133.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09102673B2uspto-grants-2015_08