1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3,4,5-Trifluoro-N-({1-[4-hydroxy-4-(6-methoxy-pyridin-3-yl)-cyclohexyl]-azetidin-3-ylcarbamoyl}-methyl)-benzamide
Reaction equation
[NH2:1][CH2:2][C:3]([NH:5][CH:6]1[CH2:9][N:8]([CH:10]2[CH2:15][CH2:14][C:13]([OH:24])([C:16]3[CH:17]=[N:18][C:19]([O:22][CH3:23])=[CH:20][CH:21]=3)[CH2:12][CH2:11]2)[CH2:7]1)=[O:4].[F:25][C:26]1[CH:27]=[C:28]([CH:32]=[C:33]([F:36])[C:34]=1[F:35])[C:29](O)=[O:30].CCN=C=NCCCN(C)C>>[F:25][C:26]1[CH:27]=[C:28]([CH:32]=[C:33]([F:36])[C:34]=1[F:35])[C:29]([NH:1][CH2:2][C:3](=[O:4])[NH:5][CH:6]1[CH2:9][N:8]([CH:10]2[CH2:15][CH2:14][C:13]([OH:24])([C:16]3[CH:17]=[N:18][C:19]([O:22][CH3:23])=[CH:20][CH:21]=3)[CH2:12][CH2:11]2)[CH2:7]1)=[O:30]Participants
4
Reactant 3
Product 1
Procedure
The title compound was prepared from 2-amino-N-{1-[4-hydroxy-4-(6-methoxy-pyridin-3-yl)-cyclohexyl]-azetidin-3-yl}-acetamide, as prepared in Step D of Example 16, and 3,4,5-trifluorobenzoic acid by EDCI coupling using the procedure described in Step C of Example 16.
Sources & evidence
- ORD record
- ord-a3a2e7f3cd5a4701b2a05434f428353b
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08450304B2
Reaction notes
Loading…