Reaktion #66651

ord-c20be94e95f4401a9559a6587a8630f8

Reaktionsgleichung

O=C([O-])O.[Na+]
NaHCO3
COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1C(C)O
1-[5-(2,4-Diamino-pyrimidin-5-yloxy)-4-isopropyl-2-methoxy-phenyl]-ethanol
CCN(CC)S(F)(F)F
DAST
C=Cc1cc(Oc2cnc(N)nc2N)c(C(C)C)cc1OC
5-(2-Isopropyl-4-methoxy-5-vinyl-phenoxy)-pyrimidine-2,4-diamine
Ausbeute 3.0%
COc1cc(C(C)C)c(Oc2cnc(N)nc2N)cc1C(C)OC
5-[2-Isopropyl-4-methoxy-5-(1-methoxy-ethyl)-phenoxy]-pyrimidine-2,4-diamine
Ausbeute 4.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe mixture was extracted by CH2Cl2
  2. 2
    WaschenThe combined organics were washed with brine and dried Na2SO4
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated in vacuo
  5. 5
    SonstigePurification via silica gel chromatography (95:5 CH2Cl2/MeOH)

Vorschrift

To a solution of 1-[5-(2,4-Diamino-pyrimidin-5-yloxy)-4-isopropyl-2-methoxy-phenyl]-ethanol (1.613 g, 5.3 mmol) in 30 ml CH2Cl2 at −78° C. was added DAST (0.935 g, 5.8 mmol). After stirring 1.5 h, saturated NaHCO3 was added and the mixture was extracted by CH2Cl2. The combined organics were washed with brine and dried Na2SO4, filtered and concentrated in vacuo. Purification via silica gel chromatography (95:5 CH2Cl2/MeOH) gave 5-(2-Isopropyl-4-methoxy-5-vinyl-phenoxy)-pyrimidine-2,4-diamine (0.044 g, 3%) as a foam ([MH]+=301) and 5-[2-Isopropyl-4-methoxy-5-(1-methoxy-ethyl)-phenoxy]-pyrimidine-2,4-diamine (0.075 g, 4%) as foam. [MH]+=303.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08524725B2uspto-grants-2013_09