Potassium Carbonate → 1-[2-benzoylthio-3-methoxybutanoyl]L-proline

HRID 1252829ノート

反応式

HRID 1252829 の反応式
[NH:1]1[CH2:8][CH2:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4].Br[CH:10]([CH:14]([O:16][CH3:17])[CH3:15])[C:11](Cl)=[O:12].[C:18]([OH:26])(=[S:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(=O)([O-])[O-].[K+].[K+]>[OH-].[Na+]>[C:18]([S:25][CH:10]([CH:14]([O:16][CH3:17])[CH3:15])[C:11]([N:1]1[CH2:8][CH2:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4])=[O:12])(=[O:26])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1

参加物

6

実験手順

To a solution of L-proline (5.75 g) in N sodium hydroxide (50 ml) chilled in an ice bath, 2N sodium hydroxide (25 ml) and 2-bromo-3-methoxybutyric acid chloride [obtained from 2-bromo-3-methoxybutyric acid [J. Am. Chem. Soc., 71, 1096, (1949)] and thionyl chloride] (10.7 g) are added, with vigorous stirring. After three hours, thiobenzoic acid (7.5 g) and potassium carbonate (4.8 g) are added and the mixture is stirred at room temperature overnight. The reaction mixture is acidified and extracted with ethyl acetate. The organic layer is concentrated to dryness and the residue is chromatographed on a column of silica gel with benzene-acetic acid to yield N-[2-benzoylthio-3-methoxybutanoyl]-L-proline.

後処理

  1. extractionextracted with ethyl acetate
  2. concentrationThe organic layer is concentrated to dryness
  3. customthe residue is chromatographed on a column of silica gel with benzene-acetic acid

出典と根拠

ORDレコード
ord-387804414a1645e685a15f0cb260fcc1
出典データセット
uspto-grants-1988_05
特許番号
US04745124

反応ノート

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