Picolinic acid → HCID 53241439, compound
Reaction equation
C(OC(=O)[NH:7][C:8]1[O:9][CH2:10][CH2:11][C@:12]([C:16]2[CH:21]=[C:20]([NH2:22])[CH:19]=[CH:18][C:17]=2[F:23])([CH2:14][CH3:15])[N:13]=1)(C)(C)C.[N:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[C:31](O)=[O:32]>>[NH2:7][C:8]1[O:9][CH2:10][CH2:11][C@:12]([C:16]2[CH:21]=[C:20]([NH:22][C:31]([C:26]3[CH:27]=[CH:28][CH:29]=[CH:30][N:25]=3)=[O:32])[CH:19]=[CH:18][C:17]=2[F:23])([CH2:14][CH3:15])[N:13]=1Participants
3
Procedure
The coupling of [(S)-4-(5-amino-2-fluoro-phenyl)-4-ethyl-5,6-dihydro-4H-[1,3]oxazin-2-yl]-carbamic acid tert-butyl ester from experiment F2 (R3=Et) and pyridine-2-carboxylic acid followed by deprotection using procedure H yielded the title compound.
Sources & evidence
- ORD record
- ord-d45d8b84d1c344ab9139d21642fd69d2
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964594B1
Reaction notes
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