Sodium hydride → (2R,5S)-4-Benzyl-2-methyl-5-(3-oxo-morpholin-4-ylmethyl)-piperazine-1-carboxylic acid tert-butyl ester

HRID 1475473ノート

反応式

HRID 1475473 の反応式
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][C:2]1=[O:7].[H-].[Na+].[C:10]([O:14][C:15]([N:17]1[CH2:22][C@H:21]([CH2:23]Cl)[N:20]([CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH2:19][C@H:18]1[CH3:32])=[O:16])([CH3:13])([CH3:12])[CH3:11]>CN(C=O)C>[C:10]([O:14][C:15]([N:17]1[CH2:22][C@H:21]([CH2:23][N:1]2[CH2:6][CH2:5][O:4][CH2:3][C:2]2=[O:7])[N:20]([CH2:25][C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH2:19][C@H:18]1[CH3:32])=[O:16])([CH3:11])([CH3:12])[CH3:13]

参加物

5

実験手順

Morpholin-3-one (896 mg, 8.87 mmol) was added to a slurry of NaH (60% in mineral oil, 355 mg, 8.87 mmol) in DMF (10 mL) under N2. The suspension was stirred for 30 minutes at room temperature and then a solution of (2R,5R)-4-benzyl-5-chloromethyl-2-methyl-piperazine-1-carboxylic acid tert-butyl ester (2.0 g, 5.9 mmol) in DMF (10 mL) was slowly added. The resulting mixture was stirred at 65° C. for 2 h. The reaction was cooled to room temperature and partitioned between EtOAc and saturated aqueous NaHCO3. The organic phase was dried over MgSO4 and concentrated in vacuo. Chromatography (50% EtOAc in petrol) gave the title compound (1.76 g) as a pale yellow gum. MS: [M+H]+=404.

後処理

  1. stirringThe resulting mixture was stirred at 65° C. for 2 h
  2. temperatureThe reaction was cooled to room temperature
  3. custompartitioned between EtOAc and saturated aqueous NaHCO3
  4. dry with materialThe organic phase was dried over MgSO4
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-eb6113c5aef741abab9fbcc34ca8eda6
出典データセット
uspto-grants-2015_04
特許番号
US09018214B2

反応ノート

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