Reaktion #1705906

ord-90f84912eab949ea8736de86e90fcbf1

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigePrepared
  2. 2
    Sonstigeat 100° C.
  3. 3
    Sonstigefor 14 h
  4. 4
    SonstigePurification by column chromatography (hexanes:EtOAc, 1:0 to 1:1)

Vorschrift

Prepared according to procedure N by using tert-butyl 7-chloro-2,3-dihydro-1H-pyrido[2,3-b][1,4]thiazine-1-carboxylate (340 mg, 1.19 mmol), Pd2dba3 (109 mg, 0.119 mmol), XPhos (113 mg, 0.237 mmol), sodium ter-butoxide (228 mg, 2.371 mmol), morpholine (0.13 mL, 1.54 mmol) in toluene (8 mL) at 100° C. for 14 h. Purification by column chromatography (hexanes:EtOAc, 1:0 to 1:1) gave tert-butyl 7-morpholino-2,3-dihydro-1H-pyrido[2,3-b][1,4]thiazine-1-carboxylate. Mass Spectrum (ESI) m/e=338.2 (M+1).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08765940B2uspto-grants-2014_07