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2-Bromopyridine → Methyl 1-cyclopentyl-3-methyl-2-(2-pyridyl)indole-5-carboxylate

HRID 11418
ノート
印刷プレビュー

反応式

HRID 11418 の反応式
Br[C:2]1[NH:3][C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2.COB([O:16][CH3:17])OC.[C:18]1([CH3:25])[CH:23]=[CH:22][C:21](P)=CC=1.Br[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][N:28]=1.[C:33](=[O:36])([O-])[O-].[K+].[K+].[CH2:39]1COCC1>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.O.CC(OC)(C)C.CO>[CH:21]1([N:3]2[C:4]3[C:9](=[CH:8][C:7]([C:33]([O:16][CH3:17])=[O:36])=[CH:6][CH:5]=3)[C:10]([CH3:39])=[C:2]2[C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][N:28]=2)[CH2:22][CH2:23][CH2:18][CH2:25]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

11

反応物 6

HCID 79732-BromopyridineHCID 8028Tetrahydrofuran2 回HCID 8470Trimethyl borateHCID 11430Potassium CarbonateHCID 43799374-TolylphosphineHCID 118056312-bromo-1H-indole

生成物 1

HCID 21974266
Methyl 1-cyclopentyl-3-methyl-2-(2-pyridyl)indole-5-carboxylate

試薬・触媒・溶媒 4

HCID 167845palladium(II) acetate触媒HCID 887Methanol溶媒HCID 962Water溶媒HCID 15413tert-Butyl methyl ether溶媒

反応条件

温度
-78 °C

実験手順

The 2-bromoindole from above (1.53 g, 4.55 mmol, 1.0 equiv.) was dissolved in anhydrous THF (20 mL) and the solution was cooled to −78° C. under an argon atmosphere. N-BuLi (solution in hexane, 4.78 mmol, 1.05 equiv.) was added dropwise and the mixture was stirred 30 min in the cold. Trimethylborate (0.62 mL, 5.46 mmol, 1.2 equiv.) was added dropwise and the solution stirred at −78° C. for 40 min and then at 0° C. for 1 h. Finally the reaction mixture was allowed to warm up to room temperature and additional THF (20 mL) was added. para-Tolylphosphine (0.083 g, 0.27 mmol, 0.06 equiv.) and 2-bromopyridine (0.86 g, 5.46 mmol, 1.2 equiv.) were then added and the solution was degassed by bubbling argon through for 30 min. Palladium acetate (10 mg, 0.046 mmol, 0.01 equiv.), anhydrous potassium carbonate (1.26 g, 9.1 mmol, 2 equiv.) and MeOH (20 mL) were added and the mixture was refluxed overnight under an argon atmosphere. After cooling to RT, TBME (12 mL) and water (12 mL) were added, the organic phase was separated and the aqueous phase extracted with additional TBME (2×25 mL). The combined organic layers were washed with brine, dried (Na2SO4) and concentrated to give a residue that was purified by flash chromatography on silica gel using 5–10% EtOAc in hexane as eluent: 1.21 g (79%).

後処理

  1. stirringthe solution stirred at −78° C. for 40 min
  2. waitat 0° C. for 1 h
  3. temperatureto warm up to room temperature
  4. customthe solution was degassed
  5. customby bubbling argon through for 30 min
  6. temperaturethe mixture was refluxed overnight under an argon atmosphere
  7. temperatureAfter cooling to RT
  8. customthe organic phase was separated
  9. extractionthe aqueous phase extracted with additional TBME (2×25 mL)
  10. washThe combined organic layers were washed with brine
  11. dry with materialdried (Na2SO4)
  12. concentrationconcentrated
  13. customto give a residue that
  14. customwas purified by flash chromatography on silica gel using 5–10% EtOAc in hexane as eluent

出典と根拠

ORDレコード
ord-94e6a89524ad4bca9996f48f9741aa00
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07098231B2

反応ノート

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