6-(4-Fluorobenzyl)picolinic acid → HCID 71105686, compound
Reaction equation
[F:1][C:2]1[CH:17]=[CH:16][C:5]([CH2:6][C:7]2[N:12]=[C:11]([C:13]([OH:15])=O)[CH:10]=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.Cl.[F:19][C:20]([F:30])([F:29])[C@@H:21]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][N:24]=1)[NH2:22]>>[F:30][C:20]([F:19])([F:29])[C@H:21]([NH:22][C:13]([C:11]1[CH:10]=[CH:9][CH:8]=[C:7]([CH2:6][C:5]2[CH:4]=[CH:3][C:2]([F:1])=[CH:17][CH:16]=2)[N:12]=1)=[O:15])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][N:24]=1Participants
3
Procedure
The title compound was synthesized in analogy to Example 1, using 6-(4-fluorobenzyl)picolinic acid (Example 277 a) and (R)-2,2,2-trifluoro-1-(pyridin-2-yl)ethanamine hydrochloride (CAN 1228565-87-4) as starting materials. MS (EI): m/e=390.1 [M+H]+.
Sources & evidence
- ORD record
- ord-374a086d28684074acc585ce6d9b7d43
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321727B2
Reaction notes
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