Reaktion #68970

Reaktionsgleichung

(R)-5-(8-Chloroisoquinolin-3-ylamino)-3-(1-(dimethylamino)propan-2-yloxy)pyrazine-2-carbonitrile

3-Chloroperoxybenzoic acid

→

title compound

Ausbeute 73.1%

(R)-2-(6-(8-Chloroisoquinolin-3-ylamino)-3-cyanopyrazin-2-yloxy)-N,N-dimethylpropan-1-amine oxide

Ausbeute 73.1%

Lösungsmittel

DCM

DCM

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas added dropwise to the solution
2. 2
   Temperaturwas then warmed to room temperature
3. 3
   Sonstigethe layers partitioned
4. 4
   Extraktionthe aqueous phase extracted with DCM
5. 5
   WaschenThe combined organic phases were washed with brine
6. 6
   Trocknendried (Na2SO4)
7. 7
   Einengenconcentrated to dryness
8. 8
   workup.DISSOLUTIONThe residue was dissolved in methanol
9. 9
   Sonstigeabsorbed on to an SPE (TsOH) cartridge
10. 10
    WaschenThe cartridge was washed with methanol
11. 11
    Waschenthe compound eluted with 2 M and 7 M ammonia in methanol

Vorschrift

(R)-5-(8-Chloroisoquinolin-3-ylamino)-3-(1-(dimethylamino)propan-2-yloxy)pyrazine-2-carbonitrile (30 mg, 0.078 mmol) was dissolved in DCM (1 mL) and cooled to −10° C. 3-Chloroperoxybenzoic acid (77% wt., 12 mg, 0.086 mmol) dissolved in DCM (1 mL) was added dropwise to the solution. The reaction mixture was stirred at −10° C. for 15 minutes, and was then warmed to room temperature. The reaction mixture was diluted with water, the layers partitioned and the aqueous phase extracted with DCM. The combined organic phases were washed with brine, dried (Na2SO4) and concentrated to dryness. The residue was dissolved in methanol and absorbed on to an SPE (TsOH) cartridge. The cartridge was washed with methanol and the compound eluted with 2 M and 7 M ammonia in methanol. Preparative HPLC afforded the title compound (23 mg, 0.057 mmol, 73%). 1H NMR (d6-DMSO, 400 MHz) δ 9.25 (s, 1H), 8.39 (s, 1H), 8.30 (s, 1H), 8.12 (s, 1H), 7.73-7.71 (m, 1H), 7.57-7.56 (m, 1H), 6.10-6.07 (m, 1H), 4.16-4.10 (m, 1H), 3.77 (br d, 1H, J=14 Hz), 3.43 (s, 3H), 3.28 (s, 3H), 1.44 (d, 3H, J=6.6 Hz). LC-MS (2) Rt=2.20 min; m/z (ESI+) 399 & 401 (M+H).

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