4-(4-{2-(tert-Butyl-diphenyl-silanyloxymethyl)-3-[2-fluoro-4-(1-hydroxy-1-methyl-ethyl)-benzoylamino]-phenyl}-7H-pyrrolo[2,3-d]pyrimidin-6-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid dimethylamide → HCID 178455414, compound
Reaction equation
CN(C)C(N1C[CH:9]=[C:8]([C:11]2[NH:58][C:14]3[N:15]=[CH:16][N:17]=[C:18]([C:19]4[CH:24]=[CH:23][CH:22]=[C:21]([NH:25][C:26](=[O:38])[C:27]5[CH:32]=[CH:31][C:30]([C:33]([OH:36])([CH3:35])[CH3:34])=[CH:29][C:28]=5[F:37])[C:20]=4[C:39]([C:52]4[CH:57]=[CH:56][CH:55]=[CH:54][CH:53]=4)([C:46]4[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=4)[O:40][SiH2:41][C:42]([CH3:45])([CH3:44])[CH3:43])[C:13]=3[CH:12]=2)[CH2:7][CH2:6]1)=O.C([SiH2][O:65][C:66](C1C=CC=CC=1)(C1C=CC=CC=1)C1C(C2C3C=C(C4CCOCC=4)NC=3N=CN=2)=CC=CC=1N)(C)(C)C>>[C:42]([SiH2:41][O:40][C:39]([C:46]1[CH:47]=[CH:48][CH:49]=[CH:50][CH:51]=1)([C:52]1[CH:53]=[CH:54][CH:55]=[CH:56][CH:57]=1)[C:20]1[C:19]([C:18]2[C:13]3[CH:12]=[C:11]([C:8]4[CH2:9][CH2:66][O:65][CH2:6][CH:7]=4)[NH:58][C:14]=3[N:15]=[CH:16][N:17]=2)=[CH:24][CH:23]=[CH:22][C:21]=1[NH:25][C:26](=[O:38])[C:27]1[CH:32]=[CH:31][C:30]([C:33]([OH:36])([CH3:35])[CH3:34])=[CH:29][C:28]=1[F:37])([CH3:44])([CH3:45])[CH3:43]Participants
3
Reactant 2
Product 1
Procedure
Intermediate 14 was prepared analogue to Intermediate 9 by replacing Intermediate 7 with Intermediate 13.
Sources & evidence
- ORD record
- ord-a45aa55c929a43c388727d2c31258b2f
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09233111B2
Reaction notes
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