6-(Ethylimino)-1,6-dihydropyridin-3-amine → HCID 59301326, compound
Reaction equation
[C:1]1([C:7]2[O:8][C:9]([C:15]([F:18])([F:17])[F:16])=[C:10]([C:12]([OH:14])=O)[N:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:19]([NH:21][C:22]1[CH:27]=[CH:26][C:25]([NH2:28])=[CH:24][N:23]=1)[CH3:20]>>[CH2:19]([NH:21][C:22]1[N:23]=[CH:24][C:25]([NH:28][C:12]([C:10]2[N:11]=[C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[O:8][C:9]=2[C:15]([F:18])([F:17])[F:16])=[O:14])=[CH:26][CH:27]=1)[CH3:20]Participants
3
Procedure
With a procedure similar to example 16 above, 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (6-ethylamino-pyridin-3-yl)-amide was prepared from 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid and N2-ethyl-pyridine-2,5-diamine. LCMS calcd for C18H15F3N4O2 (m/e) 376, obsd 377 (M+H).
Sources & evidence
- ORD record
- ord-0c01a62268a24d8da4bd45d62f17cbde
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07714126B2
Reaction notes
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