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Picolinic acid → 1-(2,6-diisopropylphenyl)-2-(3-(3-(1-(2,6-diisopropylphenyl)-1H-imidazol-2-yl)-5-methylphenoxy)phenyl)-1H-imidazole

HRID 539455
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HRID 539455 반응식
[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[N:13]1[CH:17]=[CH:16][N:15]=[C:14]1[C:18]1[CH:19]=[C:20]([OH:25])[CH:21]=[C:22]([CH3:24])[CH:23]=1)([CH3:3])[CH3:2].Br[C:27]1[CH:28]=[C:29]([C:33]2[N:34]([C:38]3[C:43]([CH:44]([CH3:46])[CH3:45])=[CH:42][CH:41]=[CH:40][C:39]=3[CH:47]([CH3:49])[CH3:48])[CH:35]=[CH:36][N:37]=2)[CH:30]=[CH:31][CH:32]=1.N1C=CC=CC=1C(O)=O.O.[O-]P([O-])([O-])=O.[K+].[K+].[K+]>[Cu]I.CS(C)=O>[CH:44]([C:43]1[CH:42]=[CH:41][CH:40]=[C:39]([CH:47]([CH3:49])[CH3:48])[C:38]=1[N:34]1[CH:35]=[CH:36][N:37]=[C:33]1[C:29]1[CH:28]=[CH:27][CH:32]=[C:31]([O:25][C:20]2[CH:21]=[C:22]([CH3:24])[CH:23]=[C:18]([C:14]3[N:13]([C:5]4[C:6]([CH:10]([CH3:12])[CH3:11])=[CH:7][CH:8]=[CH:9][C:4]=4[CH:1]([CH3:2])[CH3:3])[CH:17]=[CH:16][N:15]=3)[CH:19]=2)[CH:30]=1)([CH3:45])[CH3:46]
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참가 물질

7

반응물 4

HCID 1018Picolinic acidHCID 22031701Potassium phosphate, tribasic, monohydrateHCID 706542932-(3-bromophenyl)-1-(2,6-diisopropylphenyl)-1H-imidazoleHCID 706544253-(1-(2,6-diisopropylphenyl)-1H-imidazol-2-yl)-5-methylphenol

생성물 1

HCID 706543461-(2,6-diisopropylphenyl)-2-(3-(3-(1-(2,6-diisopropylphenyl)-1H-imidazol-2-yl)-5-methylphenoxy)phenyl)-1H-imidazole

시약·촉매·용매 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 679Dimethyl Sulfoxide용매

반응 조건

온도
200 °C

실험 절차

To a 300 mL 3-neck round bottom flask was added 3-(1-(2,6-diisopropylphenyl)-1H-imidazol-2-yl)-5-methylphenol (2.5 g, 7.47 mmol), 2-(3-bromophenyl)-1-(2,6-diisopropylphenyl)-1H-imidazole (3.15 g, 8.22 mmol), picolinic acid (1.380 g, 11.21 mmol), copper(I) iodide (0.427 g, 2.242 mmol), potassium phosphate tribasic monohydrate (6.02 g, 26.2 mmol), 100 mL DMSO. Nitrogen was bubbled directly into the mixture and then was heated to 200° C. overnight under nitrogen. The reaction mixture was diluted with ethyl acetate and water and was filtered through Celite. The layers were separated and the aqueous layer was extracted with ethyl acetate. The organic layers were washed with 10% LiCl, brine, dried over magnesium sulfate, filtered, and evaporated leaving a residue. The residue was purified by column chromatography eluting with 40 and 50% ethyl acetate/hexane (1.95 g, 41%).

후처리

  1. customNitrogen was bubbled directly into the mixture
  2. additionThe reaction mixture was diluted with ethyl acetate and water
  3. filtrationwas filtered through Celite
  4. customThe layers were separated
  5. extractionthe aqueous layer was extracted with ethyl acetate
  6. washThe organic layers were washed with 10% LiCl, brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. customevaporated
  10. customleaving a residue
  11. customThe residue was purified by column chromatography
  12. washeluting with 40 and 50% ethyl acetate/hexane (1.95 g, 41%)

출처 및 근거

ORD 기록
ord-d47b5d3470494e4d8cdd487ce2c233f3
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871361B2

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