Reaktion #2349665

Reaktionsgleichung

4-Nitrophenyl chloroformate

1-(4-fluoro-phenyl)-piperazine

DIPEA

1,4-dimethyl-(S)-2-hydroxymethyl piperazine

Intermediate 3

1,4-dimethyl-(S)-2-hydroxymethyl piperazine

→

[(2S)-1,4-dimethylpiperazin-2-yl]methyl 4-(4-fluorophenyl)piperazine-1-carboxylate

Ausbeute 60.0%

Lösungsmittel

DCM

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigesplit into three equal volumes
2. 2
   workup.STIRRINGthe mixture was stirred for 48 h
3. 3
   SonstigeThe solvent was removed in vacuo
4. 4
   Sonstigethe residue partitioned between EtOAc (500 mL) and 1.0M NaOH solution (200 mL)
5. 5
   WaschenThe organic layer was washed with 10M aq NaOH solution (5×125 mL), brine (100 mL)
6. 6
   Trocknendried (MgSO4)
7. 7
   Sonstigethe solvent removed in vacuo
8. 8
   workup.DISSOLUTIONThe residue was dissolved in DCM (100 mL)
9. 9
   workup.ADDITIONisocyanate resin (3 g) was added
10. 10
    workup.STIRRINGthe reaction mixture was shaken for 14 h
11. 11
    Filtrationfiltered
12. 12
    Sonstigethe solvent was removed in vacuo
13. 13
    SonstigeThe residue was purified by reverse phase column chromatography (LiChroprep RP-18, 40-63 μm, 460×26 mm (100 g), 30 mL/min, gradient 0% to 30% (over 75 min) to 100% (over 13 min) MeOH in water with 1% formic acid)

Vorschrift

4-Nitrophenyl chloroformate (5.17 g, 25.7 mmol) was dissolved in DCM (200 mL) at room temperature and the reaction mixture was cooled to 0° C. and DIPEA (6.94 g, 9.38 mL, 53.9 mmol) and 1,4-dimethyl-(S)-2-hydroxymethyl piperazine (Intermediate 3; 3.70 g, 25.7 mmol) were added. The reaction mixture was stirred at room temperature for 2 h, and then split into three equal volumes. To one portion was added 1-(4-fluoro-phenyl)-piperazine (1.53 g, 8.5 mmol) and the mixture was stirred for 48 h. The solvent was removed in vacuo and the residue partitioned between EtOAc (500 mL) and 1.0M NaOH solution (200 mL). The organic layer was washed with 10M aq NaOH solution (5×125 mL), brine (100 mL), dried (MgSO4) and the solvent removed in vacuo. The residue was dissolved in DCM (100 mL) and isocyanate resin (3 g) was added, the reaction mixture was shaken for 14 h, filtered and the solvent was removed in vacuo. The residue was purified by reverse phase column chromatography (LiChroprep RP-18, 40-63 μm, 460×26 mm (100 g), 30 mL/min, gradient 0% to 30% (over 75 min) to 100% (over 13 min) MeOH in water with 1% formic acid). The residue was de-salted using K2CO3 in DCM to give [(2S)-1,4-dimethylpiperazin-2-yl]methyl 4-(4-fluorophenyl)piperazine-1-carboxylate (1.78 g, 60.0%) as a light yellow gum.

Quelle