Triethylamine → Ethyl 5-hydroxypyridine-2-carboxylate

HRID 230774

反応式

HRID 230774 の反応式
C(N(CC)CC)C.Cl[C:9]1[N:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=1.[C]=O.[CH2:18]([OH:20])[CH3:19].CN([CH:24]=[O:25])C>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(P(C2C=CC=CC=2)[C-]2C=CC=C2)C=CC=CC=1.[C-]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=C1.[Fe+2]>[OH:15][C:12]1[CH:11]=[CH:10][C:9]([C:24]([O:20][CH2:18][CH3:19])=[O:25])=[N:14][CH:13]=1

参加物

7

反応物 4

HCID 8471TriethylamineHCID 8198212-Chloro-5-hydroxypyridineHCID 19794673N,N-dimethylformamide ethanolHCID 178418416HCID 178418416、化合物

生成物 1

HCID 23145820Ethyl 5-hydroxypyridine-2-carboxylate

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 635956Ferrocene-1,1'-bis-(diphenylphosphine)触媒

実験手順

Palladium acetate (267 mg), 1,1′-bis(diphenylphosphino)ferrocene (1.3 g) and triethylamine (3.2 mL) were added to an ethanol-DMF mixed solvent (1/1, 20 mL) of 6-chloropyridin-3-ol (1.5 g), and stirred overnight in a carbon monoxide atmosphere (1 atmospheric pressure) at 50° C. Ethanol was evaporated off under reduced pressure from the reaction solution, water was added to the resulting residue, and extracted with chloroform/methanol (10/1). The organic layer was dried with anhydrous magnesium sulfate, and the solvent was evaporated off under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=2/3) to obtain the entitled compound (500 mg).

後処理

  1. customEthanol was evaporated off under reduced pressure from the reaction solution, water
  2. additionwas added to the resulting residue
  3. extractionextracted with chloroform/methanol (10/1)
  4. dry with materialThe organic layer was dried with anhydrous magnesium sulfate
  5. customthe solvent was evaporated off under reduced pressure
  6. customThe resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=2/3)

出典と根拠

ORDレコード
ord-54ca4460d27647448c9b4774d48e1acd
出典データセット
uspto-grants-2009_07
特許番号
US07566781B2

関連ノート

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