Reaktion #835904

Reaktionsgleichung

1,5-diiodopentane

2-chloro-3-(4-chlorophenylsulfonylmethyl)pyridine

2-Chloro-3-(4-chlorophenylsulfonylmethyl)pyridine

butyl lithium

hexane

→

title compound

Ausbeute 38.0%

2-Chloro-3-[1-(4-chlorophenylsulfonyl) cyclohexyl]pyridine

Ausbeute 38.0%

Lösungsmittel

dimethoxyethane

Water

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAt −78° C.
2. 2
   Sonstigewas gradually elevated to room temperature, at which
3. 3
   workup.STIRRINGstirring
4. 4
   workup.WAITwas performed for 15 hours
5. 5
   Extraktionfollowed by extraction with ethyl acetate
6. 6
   WaschenThe organic layer was washed with brine
7. 7
   Trocknendried over anhydrous sodium sulfate
8. 8
   FiltrationAfter filtration
9. 9
   Einengenthe filtrate was concentrated under reduced pressure
10. 10
    Sonstigethe fraction obtained from the 15% ethyl acetate/hexane eluate
11. 11
    Einengenwas concentrated under reduced pressure
12. 12
    SonstigeThe residue thus obtained
13. 13
    Sonstigewas purified by high performance liquid chromatography (

Vorschrift

At −78° C., butyl lithium (a 1.57M hexane solution; 0.66 ml, 1.03 mmol) was added dropwise to a dimethoxyethane (5 ml) solution of the 2-chloro-3-(4-chlorophenylsulfonylmethyl)pyridine (156 mg, 0.516 mmol) obtained in Example 98. At −78° C., the resulting mixture was stirred for 20 minutes, followed by the addition of 1,5-diiodopentane (0.092 ml, 0.619 mmol). The temperature of the reaction mixture was gradually elevated to room temperature, at which stirring was performed for 15 hours. Water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with brine and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was subjected to flash chromatography on a silica gel column, and the fraction obtained from the 15% ethyl acetate/hexane eluate was concentrated under reduced pressure. The residue thus obtained was purified by high performance liquid chromatography (using a mixed solvent of water/acetonitrile/formic acid) to give the title compound (72 mg, 38%) as a white solid. The resulting solid was washed with hexane-ether and then collected by filtration, whereby the title compound was obtained as a white powder.

Quelle