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Triphenylphosphine → (3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)-N-(3-methoxyphenyl)-N-methyltetrahydrofuran-2-carboxamide

HRID 1045346
ノート
印刷プレビュー

反応式

HRID 1045346 の反応式
C([O:9][C@@H:10]1[C@H:14]([O:15]C(=O)C2C=CC=CC=2)[C@@H:13]([CH2:24][O:25]C(=O)C2C=CC=CC=2)[O:12][CH:11]1[C:34]([OH:36])=O)(=O)C1C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1C=C(SSC2N=CC=CC=2)N=CC=1.[CH3:70][O:71][C:72]1[CH:73]=[C:74]([CH:77]=[CH:78][CH:79]=1)[NH:75][CH3:76]>C1COCC1>[OH:9][C@@H:10]1[C@H:14]([OH:15])[C@@H:13]([CH2:24][OH:25])[O:12][CH:11]1[C:34]([N:75]([C:74]1[CH:77]=[CH:78][CH:79]=[C:72]([O:71][CH3:70])[CH:73]=1)[CH3:76])=[O:36]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 11776TriphenylphosphineHCID 650932,2'-Dipyridyl disulfideHCID 84349N-Methyl-m-anisidineHCID 69165848(3R,4R,5R)-3,4-Bis(benzoyloxy)-5-(benzoyloxymethyl)tetrahydrofuran-2-carboxylic acid

生成物 1

HCID 58446426(3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)-N-(3-methoxyphenyl)-N-methyltetrahydrofuran-2-carboxamide収率 42.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

(3R,4R,5R)-3,4-Bis(benzoyloxy)-5-(benzoyloxymethyl)tetrahydrofuran-2-carboxylic acid (3,4,6-Tri-O-benzoyl-2,5-anhydro-D-allonic acid, 2 g, 4 mmol) was dissolved in anhydrous THF (40 mL) under argon. Triphenylphosphine (2.1 g, 8 mmol) was then added, and the resulting mixture was stirred until it was completely dissolved. Subsequently 2,2′-dipyridyldisulfide (1.8 g, 8 mmol) was added to the reaction mixture. The mixture was stirred at room temperature for 2 hours, after which 3-methoxy-N-methylaniline (0.7 g, 5.6 mmol) was added and stirring was continued at room temperature for 16 hours. The solvent was evaporated to dryness, the residue was dissolved in chloroform (150 mL), the solution was washed twice with 0.1M NaOH solution (100 mL), twice with 0.2 M HCl solution (100 mL), once with saturated NaHCO3 solution (100 mL), and dried (Na2SO4). The solution was evaporated to dryness and the residue dissolved in 7M solution of ammonia in methanol (250 mL). The solution was stirred for 16 hours at room temperature and evaporated to dryness. The residue was dissolved in chloroform and applied to a column of silica gel. Elution with a mixture of chloroform-methanol (3:1) and evaporation of the appropriate fractions yielded the title compound as a colorless oil (0.51 g, 1.7 mmol, 42%): MS (ES) m/z 399 [M+H+C6H15N]+, 296 [M−H]−.

後処理

  1. dissolutionwas completely dissolved
  2. stirringThe mixture was stirred at room temperature for 2 hours
  3. stirringstirring
  4. customThe solvent was evaporated to dryness
  5. dissolutionthe residue was dissolved in chloroform (150 mL)
  6. washthe solution was washed twice with 0.1M NaOH solution (100 mL), twice with 0.2 M HCl solution (100 mL), once with saturated NaHCO3 solution (100 mL)
  7. dry with materialdried (Na2SO4)
  8. customThe solution was evaporated to dryness
  9. dissolutionthe residue dissolved in 7M solution of ammonia in methanol (250 mL)
  10. stirringThe solution was stirred for 16 hours at room temperature
  11. customevaporated to dryness
  12. dissolutionThe residue was dissolved in chloroform
  13. washElution
  14. additionwith a mixture of chloroform-methanol (3:1) and evaporation of the appropriate fractions

出典と根拠

ORDレコード
ord-15c7f121f32943a0a4f6c3d3a75e8afa
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569259B2

反応ノート

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