反応式
[F:1][C:2]1([F:18])[CH2:17][C@@H:5]2[C@:6]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[F:16])([CH3:9])[NH:7][O:8][C@@H:4]2[CH2:3]1>CCCCCCC.C(O)C>[F:18][C:2]1([F:1])[CH2:17][C@H:5]2[C@@:6]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[F:16])([CH3:9])[NH:7][O:8][C@H:4]2[CH2:3]1参加物
3
実験手順
Intermediate IX-1: The racemate of (3S,3aR,6aR)-5,5-difluoro-3-(2-fluoro-phenyl)-3-methyl-hexahydro-cyclopenta[d]isoxazole was resolved on a chiral high-performance liquid chromatography (HPLC) column (Chiralpak AD) using n-heptane/ethanol (85:15) to give (3R,3aS,6aS)-5,5-difluoro-3-(2-fluoro-phenyl)-3-methyl-hexahydro-cyclopenta[d]isoxazole as the faster eluting enantiomer and the desired (3S,3aR,6aR)-5,5-difluoro-3-(2-fluoro-phenyl)-3-methyl-hexahydro-cyclopenta[d]isoxazole as the slower eluting enantiomer. MS: m/z=258.2 [M+H]+.
出典と根拠
- ORDレコード
- ord-5b81d7fc022f4c268535d27a448701c5
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08476264B2
関連ノート
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