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Phosphate → {3-[(1R,2S,3R)-3-Hydroxy-2-((S)-(E)-3-hydroxyoct-1-enyl)-5-oxocyclopentylsulfanyl]propylsulfanyl}acetic acid

HRID 253520
ノート
印刷プレビュー

反応式

HRID 253520 の反応式
C[O:2][C:3](=[O:26])[CH2:4][S:5][CH2:6][CH2:7][CH2:8][S:9][C@H:10]1[C:14](=[O:15])[CH2:13][C@@H:12]([OH:16])[C@@H:11]1/[CH:17]=[CH:18]/[C@@H:19]([OH:25])[CH2:20][CH2:21][CH2:22][CH2:23][CH3:24].P([O-])([O-])([O-])=O>CC#N>[OH:16][C@@H:12]1[CH2:13][C:14](=[O:15])[C@H:10]([S:9][CH2:8][CH2:7][CH2:6][S:5][CH2:4][C:3]([OH:26])=[O:2])[C@H:11]1/[CH:17]=[CH:18]/[C@@H:19]([OH:25])[CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]
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

4

反応物 2

HCID 1061PhosphateHCID 10111873{3-[(1R,2S,3R)-3-Hydroxy-2-((S)-(E)-3-hydroxyoct-1-enyl)-5-oxocyclopentyl-sulfanyl]propylsulfanyl}acetic Acid Methyl Ester

生成物 1

HCID 9886718{3-[(1R,2S,3R)-3-Hydroxy-2-((S)-(E)-3-hydroxyoct-1-enyl)-5-oxocyclopentylsulfanyl]propylsulfanyl}acetic acid収率 11%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
23 °C

実験手順

Methyl ester 8 (50 mg, 0.124 mmol) was dissolved in CH3CN (10 mL) and pH 7.2 phosphate buffer (3.0 mL) was added. The mixture was treated with PLE (400 μL, 1.34 mol/L) and stirred for 16 h at 23° C. The reaction mixture was extracted with EtOAc (3×). The combined organics were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography (silica gel, 100% EtOAc) gave 5.3 mg (11%) of the above titled compound.

後処理

  1. additionThe mixture was treated with PLE (400 μL, 1.34 mol/L)
  2. extractionThe reaction mixture was extracted with EtOAc (3×)
  3. washThe combined organics were washed with brine
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customPurification of the residue by flash column chromatography (silica gel, 100% EtOAc)

出典と根拠

ORDレコード
ord-cb238f0e737a4689a158fffa5f6237e3
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07872045B2

反応ノート

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