Dimethyl bromomalonate → HCID 18598656, Verbindung

HRID 370845

Reaktionsgleichung

Reaktionsgleichung von HRID 370845
Br[CH:2]([C:7]([O:9][CH3:10])=[O:8])[C:3]([O:5][CH3:6])=[O:4].[C:11]([O:15][C:16](=[O:27])[C@@H:17]1[CH2:21][CH2:20][CH2:19][N:18]1[C:22](=[O:26])[C@H:23]([CH3:25])[NH2:24])([CH3:14])([CH3:13])[CH3:12]>ClCCl>[C:11]([O:15][C:16](=[O:27])[C@@H:17]1[CH2:21][CH2:20][CH2:19][N:18]1[C:22](=[O:26])[C@H:23]([CH3:25])[NH:24][CH:2]([C:7]([O:9][CH3:10])=[O:8])[C:3]([O:5][CH3:6])=[O:4])([CH3:13])([CH3:12])[CH3:14]

Komponenten

4

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Dimethyl bromomalonate (6.6 ml.) was added to a stirred solution of L-alanyl-L-proline t-butyl ester (22.9 g.) in dichloromethane (40 ml.) which was cooled to 0° C., and the mixture was allowed to warm up to laboratory temperature and stirred at that temperature for 16 hours, then diluted with dichloromethane (150 ml.). The solution was washed successively twice with aqueous 0.5N-citric acid solution (150 ml. each time), water (200 ml.) and saturated aqueous sodium chloride solution (200 ml.), dried over magnesium sulphate and evaporated to dryness. The residue was purified by chromatography on a silica gel column using a 4:1 v/v mixture of dichloromethane and ethyl acetate as eluant, and there was thus obtained as an oil N-(dimethoxycarbonylmethyl)-L-alanyl-L-proline t-butyl ester.

Aufarbeitung

  1. temperatureto warm up to laboratory temperature
  2. washThe solution was washed successively twice with aqueous 0.5N-citric acid solution (150 ml
  3. dry with materialeach time), water (200 ml.) and saturated aqueous sodium chloride solution (200 ml.), dried over magnesium sulphate
  4. customevaporated to dryness
  5. customThe residue was purified by chromatography on a silica gel column
  6. additiona 4:1 v/v mixture of dichloromethane and ethyl acetate as eluant

Quellen und Nachweise

ORD-Eintrag
ord-9d1472b862584287938396040f14e3cd
Quelldatensatz
uspto-grants-1985_07
Patentnummer
US04528282

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