Hydrochloric Acid → Z-Phe-pro-OH

HRID 1722879ノート

反応式

HRID 1722879 の反応式
COS([O-])(=O)=O.C[S+](C)C1C=CC(O[C:16](=[O:36])[C@H:17]([CH2:29][C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[NH:18][C:19]([O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[O:20])=CC=1.[NH:38]1[CH2:45][CH2:44][CH2:43][C@H:39]1[C:40]([OH:42])=[O:41].C(N(CC)CC)C.Cl>O>[CH2:22]([O:21][C:19]([NH:18][C@H:17]([C:16]([N:38]1[CH2:45][CH2:44][CH2:43][C@H:39]1[C:40]([OH:42])=[O:41])=[O:36])[CH2:29][C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)=[O:20])[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1

参加物

6

実験手順

In 30 ml of water was dissolved 5.47 g of benzyloxycarbonylphenylalanine p-dimethylsulfoniophenyl ester methylsulfate obtained by a synthesizing method according to Synthetic Example 5, and 20 ml of an aqueous solution of 1.15 g of proline and 1.4 ml of triethylamine was dropwise added thereto under stirring. The reaction mixture was further stirred for 12 hours at room temperature, adjusted to pH 2 by adding 2% HCl, and extracted twice with 50 ml of ethyl acetate. The ethyl acetate layer was washed with water, dried, and concentrated under reduced pressure, and the obtained residue was recrystallized by adding ether. This crystalline product indicated only the peak of the desired product by HPLC.

後処理

  1. customobtained by a synthesizing method
  2. additionwas dropwise added
  3. stirringThe reaction mixture was further stirred for 12 hours at room temperature
  4. extractionextracted twice with 50 ml of ethyl acetate
  5. washThe ethyl acetate layer was washed with water
  6. customdried
  7. concentrationconcentrated under reduced pressure
  8. customthe obtained residue was recrystallized
  9. additionby adding ether

出典と根拠

ORDレコード
ord-2ed9e91d970143dd9b26efcc38ce2ddb
出典データセット
uspto-grants-1989_08
特許番号
US04857656

反応ノート

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