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Hydrogen Peroxide → HCID 22863078、化合物

HRID 1737111
ノート
印刷プレビュー

反応式

HRID 1737111 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 H2O2) 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 (3×). The aqueous layer was rendered acidic with 1N aqueous HCl and extracted with EtOAc (3×). 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 (3×)
  6. extractionextracted with EtOAc (3×)
  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-dfbaca5defc7467797e0b5dfd555b237
出典データセット
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05541163

反応ノート

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