[CH3:1][C:2]([CH:4]=[N+]=[N-])=[CH2:3].[F:7][C@:8]12[C@@H:28]([OH:29])[CH2:27][C@@:26]3([CH3:30])[C@@H:18]([CH2:19][C@@H:20]([OH:32])[C@:21]3([OH:31])[C:22](=[O:25])[CH2:23][OH:24])[C@@H:17]1[CH2:16][CH2:15][C:14]1[C@:9]2([CH3:34])[CH2:10][CH2:11][C:12](=[O:33])[CH:13]=1>CCOCC.CO>[F:7][C@:8]12[C@@H:28]([OH:29])[CH2:27][C@@:26]3([CH3:30])[C@@H:18]([CH2:19][C@@H:20]([O:32][CH2:3][C:2]([CH3:4])=[CH2:1])[C@:21]3([OH:31])[C:22](=[O:25])[CH2:23][OH:24])[C@@H:17]1[CH2:16][CH2:15][C:14]1[C@:9]2([CH3:34])[CH2:10][CH2:11][C:12](=[O:33])[CH:13]=1A solution of 2-methyl-3-diazo-1-propene in 250 ml of ether (prepared from 0.2 mole of N-(2-methyl-2-propenyl)ethyl carbamate by the method of J. L. Brewbaker and H. Hart, J. Am. Chem. Soc., 91, 711 (1969) is diluted with 300 ml of methanol and cooled to 0°C. A total of 6.5 g of 9-fluoro-11β ,16α ,17,21-tetrahydroxypregn-4-ene-3,20-dione, 16,17-cycloborate is added in portions until the initial red color fades and nitrogen evolution ceases. The solvent is evaporated in vacuo and the residue dissolved in chloroform and chromatographed on a 100 g - silica gel column. Elution with chloroform and chloroform-ethyl acetate gives TLC homogeneous material which crystallizes from acetone-hexane to give 3.73 g of 9-fluoro-11β ,17,21-trihydroxy-16α-[(2-methyl-2-propenyl)oxy]pregn-4-ene-3,20-dione, melting point 213°-215°C, softening at 198°-200°C.
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