Potassium Carbonate → Methyl 5-(benzyloxy)-2-(4-fluorophenyl)furo[2,3-c]pyridine-3-carboxylate

HRID 2068377

反応式

HRID 2068377 の反応式
[C:1]([O-])(=O)C.[Na+].[C:6]([O-:9])([O-])=[O:7].[K+].[K+].[CH2:12]([O:19][C:20]1[N:25]=[CH:24][C:23]([OH:26])=[C:22]([C:27]#[C:28][C:29]2[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=2)[CH:21]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>CO.O.O.[Cu](Cl)Cl.[Pd](Cl)Cl>[CH2:12]([O:19][C:20]1[CH:21]=[C:22]2[C:27]([C:6]([O:9][CH3:1])=[O:7])=[C:28]([C:29]3[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=3)[O:26][C:23]2=[CH:24][N:25]=1)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1

参加物

7

反応物 3

HCID 11430Potassium CarbonateHCID 517045Sodium AcetateHCID 672172956-(Benzyloxy)-4-((4-fluorophenyl)ethynyl)pyridin-3-ol

生成物 1

HCID 67217578Methyl 5-(benzyloxy)-2-(4-fluorophenyl)furo[2,3-c]pyridine-3-carboxylate収率 100%

試薬・触媒・溶媒 3

HCID 24290Palladium Chloride触媒HCID 61482Cupric chloride dihydrate触媒HCID 887Methanol溶媒

実験手順

Sodium acetate (1.14 g, 13.9 mmol), K2CO3 (1.92 g, 13.9 mmol), copper (II) chloride dihydrate (3.56 g, 20.9 mmol), palladium (II) chloride (0.205 g, 1.15 mmol) was added to a stirring solution of 6-(benzyloxy)-4-((4-fluorophenyl)ethynyl)pyridin-3-ol (2.22 g, 6.95 mmol) in MeOH (150 mL) at room temperature in a Parr Bomb. The vessel was charged with 300 PSI of CO (g) and allowed to stir at room temperature overnight. The mixture was concentrated then diluted with EtOAc and washed with H2O, and sat NaCl. The organic phase was dried over Na2SO4, filtered and concentrated to give the expected product methyl 5-(benzyloxy)-2-(4-fluorophenyl)furo[2,3-c]pyridine-3-carboxylate (2.62 g, 6.95 mmol, 100% yield) by LCMS. LC-MS retention time: 2.66 min; m/z (MH+): 378. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Waters SunFire 5 u C18 4.6×50 mm column using a SPD-10AV UV-Vis detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 5 ml/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 3 min, a hold time of 1 min, and an analysis time of 4 min where solvent A was 10% acetonitrile/90% H2O/0.1% trifluoroacetic acid and solvent B was 10% H2O/90% acetonitrile/0.1% trifluoroacetic acid. MS data was determined using a Micromass Platform for LC in electrospray mode.

後処理

  1. additionThe vessel was charged with 300 PSI of CO (g)
  2. concentrationThe mixture was concentrated
  3. additionthen diluted with EtOAc
  4. washwashed with H2O
  5. dry with materialThe organic phase was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-2775f57f364f4cd79040034c652f06c6
出典データセット
uspto-grants-2012_10
特許番号
US08293909B2

関連ノート

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