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Cesium fluoride → 6-Chloro-3'-fluoro-4-(pyridazin-4-yl)biphenyl-3-ol

HRID 1619699
ノート
印刷プレビュー

反応式

HRID 1619699 の反応式
[F-].[Cs+].[Cl:3][C:4]1[C:9]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=2)=[CH:8][C:7]([OH:17])=[C:6](I)[CH:5]=1.C([Sn](CCCC)(CCCC)[C:24]1[CH:29]=[CH:28][N:27]=[N:26][CH:25]=1)CCC>C(#N)C.C(OCC)(=O)C.[Cu](I)I.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[Cl:3][C:4]1[C:9]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([F:16])[CH:11]=2)=[CH:8][C:7]([OH:17])=[C:6]([C:24]2[CH:29]=[CH:28][N:27]=[N:26][CH:25]=2)[CH:5]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 3

HCID 25953Cesium fluorideHCID 64097334-(Tributylstannyl)pyridazineHCID 580423086-Chloro-3'-fluoro-4-iodobiphenyl-3-ol

生成物 1

HCID 1362008776-Chloro-3'-fluoro-4-(pyridazin-4-yl)biphenyl-3-ol収率 85.4%

試薬・触媒・溶媒 4

HCID 83717Copper iodide触媒
HCID 9811564
Bis(dibenzylideneacetone)palladium
触媒
HCID 6342Acetonitrile溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

Caesium fluoride (219 mg, 1.44 mmol) was added to a solution of 6-chloro-3′-fluoro-4-iodobiphenyl-3-ol (Preparation 99, 251 mg, 0.72 mmol) and 4-(tributylstannyl)pyridazine (345 mg, 0.93 mmol) in acetonitrile (5 mL). The reaction mixture was degassed and copper iodide (28 mg, 0.15 mmol) and tetrakistriphenylphosphinepalladium (0) (83 mg, 0.07 mmol) were added. The reaction mixture was stirred at 80° C. for 3 hours. The cooled reaction mixture was diluted with ethyl acetate (20 mL) and quenched with a solution of ammonia (10%, 10 mL) and stirred for a further 10 minutes. The organic layer was separated and washed with brine (1×10 mL), dried over MgSO4, filtered and concentrated in vacuo. The residue was purified using silica gel chromatography (Biotage) eluting with heptane:ethyl acetate (93:7 to 0:100) to give the title compound (185 mg, 62%) as a yellow solid.

後処理

  1. customThe reaction mixture was degassed
  2. customThe cooled reaction mixture
  3. customquenched with a solution of ammonia (10%, 10 mL)
  4. stirringstirred for a further 10 minutes
  5. customThe organic layer was separated
  6. washwashed with brine (1×10 mL)
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified
  11. washeluting with heptane:ethyl acetate (93:7 to 0:100)

出典と根拠

ORDレコード
ord-b9c241deedde462cbf745ecbe0469d05
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08772293B2

反応ノート

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