Sodium borohydride → HCID 70359449, compound
Reaction equation
[CH3:1][C@@:2]1([F:22])[CH2:7][C@H:6]2[C@H:8]3[C@H:18]([CH2:19][CH2:20][C@:4]2([CH3:5])[C:3]1=[O:21])[C@:16]1([CH3:17])[C:11]([CH2:12][CH2:13][CH2:14][CH2:15]1)=[CH:10][CH2:9]3.[BH4-].[Na+]>[Pd]>[CH3:1][C@@:2]1([F:22])[CH2:7][C@H:6]2[C@H:8]3[C@H:18]([CH2:19][CH2:20][C@:4]2([CH3:5])[C@@H:3]1[OH:21])[C@:16]1([CH3:17])[C@H:11]([CH2:12][CH2:13][CH2:14][CH2:15]1)[CH2:10][CH2:9]3.[CH3:1][C@@:2]1([F:22])[CH2:7][C@H:6]2[C@H:8]3[C@H:18]([CH2:19][CH2:20][C@:4]2([CH3:5])[C@H:3]1[OH:21])[C@:16]1([CH3:17])[C@H:11]([CH2:12][CH2:13][CH2:14][CH2:15]1)[CH2:10][CH2:9]3Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
Similary, catalytic hydrogenation over 5% palladium on carbon of the 16β-methyl-16α-fluoro-5-androsten-17-one produced in Example 5 followed by treatment with sodium borohydrid affords 16β-methyl-16α-fluoro-5α-androstan-17α-ol and 16β-methyl-16α-fluoro-5α-androstan-17β-ol.
Sources & evidence
- ORD record
- ord-590f97440b794b82b453c1c5d7c4490f
- Source dataset
- uspto-grants-1990_02
- Patent number
- US04898694
Reaction notes
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