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Cornforth reagent → [(S)-4-Benzyloxycarbonyl-1-tert-butoxycarbonyl-piperazin-2-yl]-acetic acid

HRID 1963067
ノート
印刷プレビュー

反応式

HRID 1963067 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]([O:16][CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[O:15])[CH2:10][C@@H:9]1[CH2:24][CH2:25][OH:26])=[O:7])([CH3:4])([CH3:3])[CH3:2].[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=[O:28].[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1>C(Cl)Cl.[Cl-].[Na+].O>[CH2:17]([O:16][C:14]([N:11]1[CH2:12][CH2:13][N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C@@H:9]([CH2:24][C:25]([OH:28])=[O:26])[CH2:10]1)=[O:15])[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 2724130Cornforth reagentHCID 68205819(S)-2-(2-Hydroxy-ethyl)-piperazine-1,4-dicarboxylic acid 4-benzyl ester 1-tert-butyl ester

生成物 1

HCID 68205818[(S)-4-Benzyloxycarbonyl-1-tert-butoxycarbonyl-piperazin-2-yl]-acetic acid収率 74.9%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 57417360
Sodium chloride; water
溶媒

実験手順

(S)-2-(2-Hydroxy-ethyl)-piperazine-1,4-dicarboxylic acid 4-benzyl ester 1-tert-butyl ester (cf. WO 96/31501; S. Fustero et al., Org. Lett. 9 (2007), 5283; 2.862 g, 7.85 mmol) was dissolved in 78.5 ml of DCM and pyridinium dichromate (14.772 g, 39.27 mmol) was added. The mixture was stirred at room temperature overnight, then diluted into brine (330 ml) and extracted three times with EA (70 ml). The combined organic phases were washed with water (300 ml), filtered over diatomaceous earth, dried over sodium sulfate, filtered and evaporated to dryness under reduced pressure. The product was dissolved in EA and extracted three times with a 1 N solution of sodium hydroxide. The combined aqueous phases were acidified to pH 1 with 6 N hydrochloric acid, extracted with EA and the combined extracts were washed with water and brine, dried over sodium sulfate, filtered and evaporated to dryness. 2.226 g of the title compound were obtained as a thick colorless oil.

後処理

  1. extractionextracted three times with EA (70 ml)
  2. washThe combined organic phases were washed with water (300 ml)
  3. filtrationfiltered over diatomaceous earth
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. customevaporated to dryness under reduced pressure
  7. dissolutionThe product was dissolved in EA
  8. extractionextracted three times with a 1 N solution of sodium hydroxide
  9. extractionextracted with EA
  10. washthe combined extracts were washed with water and brine
  11. dry with materialdried over sodium sulfate
  12. filtrationfiltered
  13. customevaporated to dryness

出典と根拠

ORDレコード
ord-3ca8ff02171d46f5b1da326048603521
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08415336B2

反応ノート

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