Triethylamine → HCID 131717864、化合物

HRID 1590962ノート

反応式

HRID 1590962 の反応式
[NH2:1][C@H:2]([C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:9])[CH2:3][CH2:4][C:5](=[O:7])[OH:6].C(N(CC)CC)C.[NH:25]([C:47]([O:49][C:50]([CH3:53])([CH3:52])[CH3:51])=[O:48])[C@H:26]([C:37]([O:39]N1C(=O)CCC1=O)=[O:38])[C@@H:27]([CH3:36])[O:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1>C(#N)C>[CH3:36][C@@H:27]([O:28][CH2:29][C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)[C@H:26]([NH:25][C:47]([O:49][C:50]([CH3:52])([CH3:53])[CH3:51])=[O:48])[C:37]([OH:39])=[O:38].[NH2:1][C@H:2]([C:8]([O:10][CH2:11][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)=[O:9])[CH2:3][CH2:4][C:5](=[O:6])[OH:7]

参加物

5

実験手順

To a solution of 2.83 g of H-Glu-OBzl dissolved in 40 ml of acetonitrile were added 3.3 ml of triethylamine and 5.00 g of Boc-Thr(Bzl)-OSu under ice-cooling. The mixture was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in 50 ml of ethyl acetate and the resulting solution was washed with 30 ml of water twice. The ethyl acetate layer was dried with anhydrous magnesium sulfate. The solvent was removed by distillation to dry the ethyl acetate layer, whereby 5.50 g (yield: 87.2%) of the above objective compound was obtained as a powder form product.

後処理

  1. temperaturecooling
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. dissolutionThe residue was dissolved in 50 ml of ethyl acetate
  4. washthe resulting solution was washed with 30 ml of water twice
  5. dry with materialThe ethyl acetate layer was dried with anhydrous magnesium sulfate
  6. customThe solvent was removed by distillation
  7. dry with materialto dry the ethyl acetate layer

出典と根拠

ORDレコード
ord-0c5d9703500a43a5b5b338648344c05e
出典データセット
uspto-grants-1993_04
特許番号
US05204326

反応ノート

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