反応 #955930

ord-5efe91b4a1324fc7b1c3c9f4be2e82c3

反応方程式

Clc1ccc(Cl)nn1
3,6-dichloropyridazine
[H-].[Na+]
NaH
OCc1ccccn1
pyridin-2-ylmethanol
Clc1ccc(OCc2ccccn2)nn1
3-chloro-6-(pyridin-2-ylmethoxy)pyridazine
収率 62.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe mixture was stirred at 55° C. for 4 hours
  2. 2
    その他The reaction was quenched with water and sat. NaHCO3
  3. 3
    workup.ADDITIONwas added
  4. 4
    抽出The product was then extracted with EtOAc
  5. 5
    乾燥dried over MgSO4
  6. 6
    ろ過filtered
  7. 7
    その他evaporated
  8. 8
    その他The residue was purified on silica gel(Eluent: 80% EtOAc in hexanes)

実験手順

To a solution of NaH (1.44 g, 36 mmol, 60% in mineral oil) in THF (15 mL) was added pyridin-2-ylmethanol (1.16 ml, 12 mmol) and the mixture was stirred for 30 min at rt. Then 3,6-dichloropyridazine (1.79 g, 14 mmol) was added and the mixture was stirred at 55° C. for 4 hours. The reaction was quenched with water and sat. NaHCO3 was added. The product was then extracted with EtOAc, dried over MgSO4 filtered and evaporated. The residue was purified on silica gel(Eluent: 80% EtOAc in hexanes) to give 3-chloro-6-(pyridin-2-ylmethoxy)pyridazine as a white solid (1.64 g, 62%). 1H NMR (300 MHz, dMSO): δ 5.57 (s, 2H), 7.35-7.38 (m, 1H), 7.48-7.54 (m, 2H), 7.82-7.88 (m, 2H), 8.57-8.59 (dd, 1H); MS (M+H, 222).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08968708B2uspto-grants-2015_03