반응 #74263

ord-e4e8285435754c6d807f16ded550280b

반응 방정식

Brc1cc[nH]n1
3-bromo-1H-pyrazole
Clc1cccnc1Cl
2,3-dichloropyridine
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CN(C)C=O
N,N-dimethylformamide
Clc1cccnc1-n1ccc(Br)n1
2-(3-bromo-1H-pyrazol-1-yl)-3-chloropyridine
수율 68.5%

용매

반응 조건

온도
100°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도to cool to room temperature
  2. 2
    추출the reaction mixture was extracted with methyl tert-butyl ether two times
  3. 3
    세척washed with sequentially with water
  4. 4
    건조a saturated solution of sodium chloride, dried over magnesium sulfate
  5. 5
    농축concentrated under reduced pressure

실험 절차

A mixture of 10.7 g of 3-bromo-1H-pyrazole, 11.8 g of 2,3-dichloropyridine, 57.3 g of cesium carbonate and 80 ml of N,N-dimethylformamide was stirred at 100° C. for 8 hours. The reaction mixture was allowed to cool to room temperature. After water was added, and the reaction mixture was extracted with methyl tert-butyl ether two times. The organic layers were combined, washed with sequentially with water and a saturated solution of sodium chloride, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 12.9 g of 2-(3-bromo-1H-pyrazol-1-yl)-3-chloropyridine.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08541613B2uspto-grants-2013_09