Ammonia → HCID 70626912, Verbindung
Reaktionsgleichung
[FH:1].[C:2]([O:5][C@:6]1([C@:26]2([CH3:27])[C@H:12]([C@H:13]3[C:23](=[CH:24][CH2:25]2)[C@:21]2([CH3:22])[C:16](=[CH:17][C:18](=[O:28])[CH2:19][CH2:20]2)[CH2:15][CH2:14]3)[CH2:11][CH2:10]1)[C:7](=[O:9])[CH3:8])(=[O:4])[CH3:3].[Br:29]N1C(=O)CCC1=O.N>O.CN(C)C=O>[C:2]([O:5][C@:6]1([C@:26]2([CH3:27])[C@H:12]([C@H:13]3[C@:23]([Br:29])([C@@H:24]([F:1])[CH2:25]2)[C@:21]2([CH3:22])[C:16](=[CH:17][C:18](=[O:28])[CH2:19][CH2:20]2)[CH2:15][CH2:14]3)[CH2:11][CH2:10]1)[C:7](=[O:9])[CH3:8])(=[O:4])[CH3:3]Komponenten
7
Versuchsvorschrift
At -78° C., 20 ml. of hydrogen fluoride is combined with 8 ml. of dimethylformamide, and 6 g. of 17-acetoxy-4,9(11)-pregnadiene-3,20-dione (J. Org. Chem. 26 1961!: 866) and 4 g. of N-bromosuccinimide are added to the reaction mixture. The latter is allowed to stand for 3 hours at -30° C. and then introduced into a mixture of water, ice, and a 25% ammonia solution. The precipitate is filtered off, washed with water, taken up in ethyl acetate, and dried over sodium sulfate. After chromatography of the crude product on silica gel with 19-21.6% acetone/hexane, the yield is 3.0 g. of 17-acetoxy- 9-bromo-11β -fluoro-4-pregnene-3,20-dione; m.p. 180°-182° C. (under decomposition).
Aufarbeitung
- customAt -78° C.
- filtrationThe precipitate is filtered off
- washwashed with water
- dry with materialdried over sodium sulfate
Quellen und Nachweise
- ORD-Eintrag
- ord-62706be1eec24027b8b0a08515d82635
- Quelldatensatz
- uspto-grants-1978_02
- Patentnummer
- US04073900
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