반응 #1446543

반응 방정식

2-benzyl-3-iodo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine

N-chlorosuccinimide

sodium thiosulfate

→

2-benzyl-3-iodo-5-chloro-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine

수율 59.2%

용매

N,N-dimethylformamide

반응 조건

후처리

1. 1
   온도under heating for 5 hours in an oil bath
2. 2
   기타kept at 60° C
3. 3
   workup.ADDITIONwas added to the reaction solution
4. 4
   기타the mixture was partitioned between ethyl acetate and water
5. 5
   세척The organic phase was washed with water and brine
6. 6
   건조dried over anhydrous magnesium sulfate
7. 7
   농축concentrated

실험 절차

A mixture of 500 mg of 2-benzyl-3-iodo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine obtained in Example 118c, 174 mg of N-chlorosuccinimide and 5 ml of N,N-dimethylformamide was stirred under heating for 5 hours in an oil bath kept at 60° C. 1 ml of aqueous solution containing 1 mol of sodium thiosulfate was added to the reaction solution, the mixture was partitioned between ethyl acetate and water. The organic phase was washed with water and brine, dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography using 5-10% ethyl acetate/hexane, to give 320 mg of 2-benzyl-3-iodo-5-chloro-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine, and then the title compound was obtained in the same procedures as in Example 118d.

출처