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Hydrogen Peroxide → HCID 22863078、化合物

HRID 1939054
ノート
印刷プレビュー

反応式

HRID 1939054 の反応式
C([O:5][C:6](=[O:43])[CH2:7][C@@H:8]([CH2:28][C:29]1[N:30]=[C:31]([NH:34][C:35]([O:37][CH2:38][C:39]([Cl:42])([Cl:41])[Cl:40])=[O:36])[S:32][CH:33]=1)[C:9](N[C@@H](CC1CCCCC1)[C@@H](O)[C@@H](O)CC(C)C)=[O:10])(C)(C)C.[OH2:44].OO.O.[OH-].[Li+]>C1COCC1>[Cl:40][C:39]([Cl:42])([Cl:41])[CH2:38][O:37][C:35]([NH:34][C:31]1[S:32][CH:33]=[C:29]([CH2:28][C@H:8]([CH2:7][C:6]([OH:5])=[O:43])[C:9]([OH:10])=[O:44])[N:30]=1)=[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 784Hydrogen PeroxideHCID 962WaterHCID 168937Lithium hydroxide, monohydrateHCID 86749666HCID 86749666、化合物

生成物 1

HCID 22863078HCID 22863078、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

The protected amido acid, 4-{[1(S)-(cyclohexylmethyl)-2(R),3(S)-dihydroxy-5 -methylhexyl]amino}-4-oxo-3-(R)-{{2-[(2,2,2-trichloroethoxy) carbonylamino]-4-thiazolyl}methyl}butanoic acid tert-butyl ester: A solution of the product of section (f) of this example (57.5 mg, 0.10 mmol) in THF (1.5 mL) and H2O (0.5 mL) was cooled to 0°. A 30% aqueous solution of H2O2 (91.3 μL, 0.80 mmol of H2 O2) and lithium hydroxide monohydrate (8.5 mg, 0.20 mmol) were added serially to the cooled solution. The mixture was stirred at 0° for 5 min and then at room temperature for 2.5 h. Excess H2O2 was quenched by the addition of a 1.5M aqueous solution of Na2SO3 (as judged by a KI stick indicator). The resulting mixture was diluted with H2O and washed with CH2Cl2 (3X). The aqueous layer was rendered acidic with 1N aqueous HCl and extracted with EtOAc (3X). The combined EtOAc extracts were washed with brine, dried (MgSO4) and concentrated to dryness to yield the desired monoprotected dicarboxylic acid, i.e. the 4-tert-butyl ester of 2(R)-{{2-[(2,2,2-trichloroethoxy) carbonylamino]-4-thiazolyl}-methyl}-butanedioic acid. The monoprotected dicarboxylic acid was used for the following coupling step without purification.

後処理

  1. customwas cooled to 0°
  2. waitat room temperature for 2.5 h
  3. customExcess H2O2 was quenched by the addition of a 1.5M aqueous solution of Na2SO3 (
  4. additionThe resulting mixture was diluted with H2O
  5. washwashed with CH2Cl2 (3X)
  6. extractionextracted with EtOAc (3X)
  7. washThe combined EtOAc extracts were washed with brine
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-fb057025c83b4cfdb58eeae4c017b6cf
出典データセット
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05693619

反応ノート

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