Citric Acid → HCID 67490916、化合物

HRID 1917307ノート

反応式

HRID 1917307 の反応式
[CH:1]([N-]C(C)C)(C)C.[Li+].[C:9]([O:13][C:14]([C@@:16]1([CH2:30][CH2:31][O:32][Si:33]([C:36]([CH3:39])([CH3:38])[CH3:37])([CH3:35])[CH3:34])[CH2:20][C:19](=[O:21])[N:18]([C@@H:22]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[CH3:23])[CH2:17]1)=[O:15])([CH3:12])([CH3:11])[CH3:10].CI.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>O1CCCC1.C(OCC)(=O)C>[C:9]([O:13][C:14]([C@@:16]1([CH2:30][CH2:31][O:32][Si:33]([C:36]([CH3:38])([CH3:37])[CH3:39])([CH3:35])[CH3:34])[CH:20]([CH3:1])[C:19](=[O:21])[N:18]([C@@H:22]([C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=2)[CH3:23])[CH2:17]1)=[O:15])([CH3:12])([CH3:11])[CH3:10]

参加物

7

反応物 4

HCID 311Citric Acid2 回HCID 6328Methyl iodideHCID 2724682Lithium diisopropylamideHCID 67490763(3S)-3-[2-(tert-Butyldimethylsilyloxy)ethyl]-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carboxylic acid tert-butyl ester

生成物 1

HCID 67490916HCID 67490916、化合物

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒2 回HCID 8857Ethyl Acetate溶媒

反応条件

温度
-10 °C

実験手順

A 1.8 M solution of lithium diisopropylamide in tetrahydrofuran (3.10 mL) was added dropwise to a solution of (3S)-3-[2-(tert-butyldimethylsilyloxy)ethyl]-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carboxylic acid tert-butyl ester (2.24 g, 5.00 mmol) in tetrahydrofuran (20 mL) in a nitrogen atmosphere at −72° C. over five minutes. After stirring at the same temperature for 10 minutes, methyl iodide (0.34 mL, 5.50 mmol) was added. The mixture was stirred at the same temperature for 15 minutes and then heated to −10° C. over 10 minutes. Thereafter, a 10% citric acid aqueous solution (5 mL) was added. The reaction solution was poured into a mixture of ethyl acetate (100 mL) and 10% citric acid solution (50 mL), followed by extraction with ethyl acetate (200 mL). The organic layer was washed with brine (50 mL×2), dried over anhydrous sodium sulfate, and filtered. The filtrate was then concentrated under reduced pressure. The resulting dark brown residue was used for the next reaction without further purification.

後処理

  1. stirringThe mixture was stirred at the same temperature for 15 minutes
  2. extractionfollowed by extraction with ethyl acetate (200 mL)
  3. washThe organic layer was washed with brine (50 mL×2)
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationThe filtrate was then concentrated under reduced pressure
  7. customThe resulting dark brown residue was used for the next reaction without further purification

出典と根拠

ORDレコード
ord-e5d63454f6a74429adbefccb433a1bbd
出典データセット
uspto-grants-2013_12
特許番号
US08618094B2

反応ノート

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