4-tert-Butyl-N-{5-fluoro-3-[6-(4-hydroxy-cyclohex-1-enyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-2-methyl-phenyl}-benzamide → 4-tert-Butyl-N-{3-[6 (4 hydroxy-cyclohex-1-enyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-2-methyl-phenyl}-benzamide
Reaction equation
[C:1]([C:5]1[CH:37]=[CH:36][C:8]([C:9]([NH:11][C:12]2[CH:17]=[C:16](F)[CH:15]=[C:14]([C:19]3[C:20]4[CH:27]=[C:26]([C:28]5[CH2:33][CH2:32][CH:31]([OH:34])[CH2:30][CH:29]=5)[NH:25][C:21]=4[N:22]=[CH:23][N:24]=3)[C:13]=2[CH3:35])=[O:10])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].C(C1C=CC(C(NC2C=CC=C(C3C4C=C(C5CCC(=O)CC=5)NC=4N=CN=3)C=2C)=O)=CC=1)(C)(C)C>>[C:1]([C:5]1[CH:6]=[CH:7][C:8]([C:9]([NH:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:19]3[C:20]4[CH:27]=[C:26]([C:28]5[CH2:33][CH2:32][CH:31]([OH:34])[CH2:30][CH:29]=5)[NH:25][C:21]=4[N:22]=[CH:23][N:24]=3)[C:13]=2[CH3:35])=[O:10])=[CH:36][CH:37]=1)([CH3:4])([CH3:2])[CH3:3]Participants
3
Reactant 2
Product 1
Procedure
Example 66 was prepared analogue to Example 28 step 2 by replacing Intermediate 19 in with Intermediate 55.
Workup
- customExample 66 was prepared analogue to Example 28 step 2
Sources & evidence
- ORD record
- ord-a5d4e241992444f98de87d53a542cfe8
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09233111B2
Reaction notes
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