(3S,3aR,6aR)-5,5-difluoro-3-fluoromethyl-3-(2-fluoro-phenyl)-hexahydro-cyclopenta[d]isoxazole → (3R,3aS,6aS)-5,5-difluoro-3-fluoromethyl-3-(2-fluoro-phenyl)-hexahydro-cyclopenta[d]isoxazole

HRID 444802

反応式

[F:1][C:2]1([F:19])[CH2:18][C@@H:5]2[C@@:6]([CH2:16][F:17])([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[F:15])[NH:7][O:8][C@@H:4]2[CH2:3]1>CCCCCCC.C(O)C>[F:19][C:2]1([F:1])[CH2:18][C@H:5]2[C@:6]([CH2:16][F:17])([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[F:15])[NH:7][O:8][C@H:4]2[CH2:3]1

参加物

実験手順

Intermediate XXII-1: The racemate of (3S,3aR,6aR)-5,5-difluoro-3-fluoromethyl-3-(2-fluoro-phenyl)-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-fluoromethyl-3-(2-fluoro-phenyl)-hexahydro-cyclopenta[d]isoxazole as the faster eluting enantiomer and the desired (3S,3aR,6aR)-5,5-difluoro-3-fluoromethyl-3-(2-fluoro-phenyl)-hexahydro-cyclopenta[d]isoxazole as the slower eluting enantiomer. MS: m/z=276.1 [M+H]+.

出典と根拠

ORDレコード: ord-0e7203762e73418fb6d7a0f9c459c84a
出典データセット: uspto-grants-2013_07
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US08476264B2

反応式

参加物

反応物 1

生成物 1

試薬・触媒・溶媒 1

実験手順

出典と根拠

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