Methyl 2-((S)-6-((R)-7-fluoro-4-(4-((4-hydroxytetrahydro-2H-pyran-4-yl)methoxy)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate → 2-((S)-6-((R)-7-Fluoro-4-(4-((4-hydroxytetrahydro-2H-pyran-4-yl)methoxy)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetic acid
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:26]2[C:31]([CH3:32])=[CH:30][C:29]([O:33][CH2:34][C:35]3([OH:41])[CH2:40][CH2:39][O:38][CH2:37][CH2:36]3)=[CH:28][C:27]=2[CH3:42])=[C:6]2[C:10]=1[C@H:9]([O:11][C:12]1[CH:25]=[CH:24][C:15]3[C@H:16]([CH2:19][C:20]([O:22]C)=[O:21])[CH2:17][O:18][C:14]=3[CH:13]=1)[CH2:8][CH2:7]2>C(OCC)(=O)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:26]2[C:31]([CH3:32])=[CH:30][C:29]([O:33][CH2:34][C:35]3([OH:41])[CH2:36][CH2:37][O:38][CH2:39][CH2:40]3)=[CH:28][C:27]=2[CH3:42])=[C:6]2[C:10]=1[C@H:9]([O:11][C:12]1[CH:25]=[CH:24][C:15]3[C@H:16]([CH2:19][C:20]([OH:22])=[O:21])[CH2:17][O:18][C:14]=3[CH:13]=1)[CH2:8][CH2:7]2Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared from methyl 2-((S)-6-((R)-7-fluoro-4-(4-((4-hydroxytetrahydro-2H-pyran-4-yl)methoxy)-2,6-dimethylphenyl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate following a procedure analogous to that described in example 4. TLC: rf=0.2 (silicagel, ethyl acetate); Mass spectrum (ESI+): m/z=563 [M+H]+.
Sources & evidence
- ORD record
- ord-32cc8482d21d4c1ba1a69908daa1821c
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642585B2
Reaction notes
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