1,2-Dimethylhydrazine → (7-alpha)-3-Methoxy-7-propylestra-1,3,5(10)-trien-17-one dimethylhydrazone

HRID 1421557

Reaktionsgleichung

Reaktionsgleichung von HRID 1421557
[CH3:1][O:2][C:3]1[CH:20]=[CH:19][C:18]2[C@@H:17]3[C@H:8]([C@H:9]4[C@@:13]([CH2:15][CH2:16]3)([CH3:14])[C:12](=O)[CH2:11][CH2:10]4)[C@H:7]([CH2:22][CH2:23][CH3:24])[CH2:6][C:5]=2[CH:4]=1.C[NH:26][NH:27][CH3:28].F[C:30](F)(F)C(O)=O.C([O-])(O)=O.[Na+]>C1(C)C=CC=CC=1>[CH3:30][N:27]([CH3:28])[N:26]=[C:12]1[CH2:11][CH2:10][C@H:9]2[C@H:8]3[C@H:17]([CH2:16][CH2:15][C@:13]12[CH3:14])[C:18]1[CH:19]=[CH:20][C:3]([O:2][CH3:1])=[CH:4][C:5]=1[CH2:6][C@H:7]3[CH2:22][CH2:23][CH3:24]

Komponenten

6

Versuchsvorschrift

To a solution of 11.2 g. of 7a-propyl-3-O-methylestrone 5 in 60 ml of toluene were added 6 ml of dimethylhydrazine and 0.5 ml. of trifluoroacetic acid. The mixture was refluxed for 1.5 hr. After cooling to r.t. the reaction mixture was neutralized with 5% NaHCO3 and the organic layer was washed several times with water and dried over sodium sulfate. After concentration and chromatography 11.4 g of the hydrazone 6 remained as an oil; Rf 030 (hept/ethylac. 7/3).

Aufarbeitung

  1. temperatureThe mixture was refluxed for 1.5 hr
  2. washthe organic layer was washed several times with water
  3. dry with materialdried over sodium sulfate
  4. concentrationAfter concentration and chromatography 11.4 g of the hydrazone 6

Quellen und Nachweise

ORD-Eintrag
ord-3e54e0df0bbd4eee9818d67738ee763e
Quelldatensatz
uspto-grants-2000_06
Patentnummer
US06077873

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