4-Ethynyl-1-methylpiperidin-4-ol → 4-(6'-Cyclopropylamino-[2,2';4',3'']terpyridin-5''-ylethynyl)-1-methyl-piperidin-4-ol
Reaction equation
CNC1N=C(C2C=CC=CN=2)C=C(C2C=NC=C(C#CC3N(C)C=NC=3)C=2)C=1.Br[C:30]1[CH:31]=[C:32]([C:36]2[CH:41]=[C:40]([NH:42][CH:43]3[CH2:45][CH2:44]3)[N:39]=[C:38]([C:46]3[CH:51]=[CH:50][CH:49]=[CH:48][N:47]=3)[CH:37]=2)[CH:33]=[N:34][CH:35]=1.[C:52]([C:54]1([OH:61])[CH2:59][CH2:58][N:57]([CH3:60])[CH2:56][CH2:55]1)#[CH:53]>>[CH:43]1([NH:42][C:40]2[N:39]=[C:38]([C:46]3[CH:51]=[CH:50][CH:49]=[CH:48][N:47]=3)[CH:37]=[C:36]([C:32]3[CH:33]=[N:34][CH:35]=[C:30]([C:53]#[C:52][C:54]4([OH:61])[CH2:59][CH2:58][N:57]([CH3:60])[CH2:56][CH2:55]4)[CH:31]=3)[CH:41]=2)[CH2:45][CH2:44]1Participants
4
Reactant 3
Product 1
Procedure
is prepared analogously to Methyl-[5″-(3-methyl-3H-imidazol-4-ylethynyl)-[2,2′;4′,3″]terpyridin-6′-yl]-amine (Example 2.182) by replacing (5″-Bromo-[2,2′;4′,3″]terpyridin-6′-yl)-methyl-amine (Example 2.1; step1) with (5″-Bromo-[2,2′;4′,3″]terpyridin-6′-yl)-cyclopropyl-amine (Example 1.26) and by replacing 1-methyl-5-((trimethylsilyl)ethynyl)-1H-imidazole with 4-ethynyl-1-methylpiperidin-4-ol.
Sources & evidence
- ORD record
- ord-bd6f1aeb9e37488297296ff82f24e3d4
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08343966B2
Reaction notes
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