2-(4-Bromo-3,5-dimethylphenoxy)acetonitrile → Methyl 2-((S)-6-((R)-4-(4-(cyanomethoxy)-2,6-dimethylphenyl)-7-fluoro-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate
Reaction equation
[F:1][C:2]1[CH:3]=[CH:4][C:5](B2OC(C)(C)C(C)(C)O2)=[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][CH3:23])=[O:21])[CH2:17][O:18][C:14]=3[CH:13]=1)[CH2:8][CH2:7]2.Br[C:36]1[C:45]([CH3:46])=[CH:44][C:39]([O:40][CH2:41][C:42]#[N:43])=[CH:38][C:37]=1[CH3:47]>>[C:42]([CH2:41][O:40][C:39]1[CH:38]=[C:37]([CH3:47])[C:36]([C:5]2[CH:4]=[CH:3][C:2]([F:1])=[C:10]3[C:6]=2[CH2:7][CH2:8][C@H:9]3[O:11][C:12]2[CH:25]=[CH:24][C:15]3[C@H:16]([CH2:19][C:20]([O:22][CH3:23])=[O:21])[CH2:17][O:18][C:14]=3[CH:13]=2)=[C:45]([CH3:46])[CH:44]=1)#[N:43]Participants
3
Reactant 2
Product 1
Procedure
The title compound is prepared from methyl 2-((S)-6-((R)-7-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydrobenzofuran-3-yl)acetate and 2-(4-bromo-3,5-dimethylphenoxy)acetonitrile following a procedure analogous to that described in Step 5 of Intermediate 1. LC (method 8): tR=0.71 min; Mass spectrum (ESI+): m/z=502 [M+H]+.
Sources & evidence
- ORD record
- ord-358d464fc1be403d86c6bcabc6dd5273
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642585B2
Reaction notes
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