反応 #2286281

ord-4530955f6b084e0b889cb0c25c9d896e

反応方程式

Cl
hydrochloric acid
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COC(=O)Cc1cc(C)c(O)c(C)c1
(3,5-dimethyl-4-hydroxy-phenyl)-acetic acid methyl ester
CC(C)c1cc(Cl)nnc1Cl
3,6-dichloro-4-isopropyl pyridazine
COC(=O)Cc1cc(C)c(Oc2cc(C(C)C)c(Cl)nn2)c(C)c1
[4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester
収率 67.2%
COC(=O)Cc1cc(C)c(Oc2cc(C(C)C)c(Cl)nn2)c(C)c1
[4-(6-Chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester
収率 67.2%

反応条件

温度
90°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度At this time, the reaction was cooled to room temperature
  2. 2
    抽出extracted with ethyl acetate (2×500 mL)
  3. 3
    workup.ADDITIONby the addition of a 1N aqueous sodium hydroxide solution
  4. 4
    抽出The water layer was extracted again with ethyl acetate (1×500 mL)
  5. 5
    洗浄The combined organics were washed with a saturated aqueous sodium chloride solution
  6. 6
    乾燥dried with magnesium sulfate
  7. 7
    ろ過filtered
  8. 8
    濃縮concentrated under vacuum
  9. 9
    その他The resulting residue was purified by column chromatography
  10. 10
    洗浄eluted with 5-15% ethyl acetate in petroleum ether

実験手順

A solution of (3,5-dimethyl-4-hydroxy-phenyl)-acetic acid methyl ester (6a) (12.5 g, 0.064 mol) in anhydrous dimethyl sulfoxide (256 mL) under argon at room temperature was treated with 3,6-dichloro-4-isopropyl pyridazine (7) (18.43 g, 0.096 mol) followed by anhydrous potassium carbonate (17.69 g, 0.12 mol) and copper (I) iodide (6.09 g, 0.032 mol). The reaction mixture was heated to 90° C. for 24 h. At this time, the reaction was cooled to room temperature and was poured onto a 1N aqueous hydrochloric acid solution (200 mL) and ice. The aqueous layer was diluted with water (100 mL) and extracted with ethyl acetate (2×500 mL). The aqueous layer was made basic (pH=8) by the addition of a 1N aqueous sodium hydroxide solution. The water layer was extracted again with ethyl acetate (1×500 mL). The combined organics were washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum. The resulting residue was purified by column chromatography using silica gel eluted with 5-15% ethyl acetate in petroleum ether to afford [4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-3,5-dimethyl-phenyl]-acetic acid methyl ester (8a) (15 g, 67%) and a minor amount of isomer as a white solid; EI(+)-HRMS m/z calcd for C18H21ClN2O3 (M+) 348.1241, found 348.1237. Molecular Weight=348.8327; Exact Mass=348.1241

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE046024E1uspto-grants-2016_06