2,4-Difluoroaniline → N-(2,4-Difluoro-phenyl)-2-(3-dodecyl-isoxazol-5-yl)-2-phenyl-acetamide
Reaction equation
[CH2:1]([C:13]1[CH:17]=[C:16]([CH:18]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:19]([OH:21])=O)[O:15][N:14]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C(C1ON=C(C(C2C=CC=CC=2)C(O)=O)C=1)CCCCCCCCCCC.[F:55][C:56]1[CH:62]=[C:61]([F:63])[CH:60]=[CH:59][C:57]=1[NH2:58]>>[F:55][C:56]1[CH:62]=[C:61]([F:63])[CH:60]=[CH:59][C:57]=1[NH:58][C:19](=[O:21])[CH:18]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:16]1[O:15][N:14]=[C:13]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[CH:17]=1Participants
4
Procedure
In a manner similar to Example 128, a mixture of 3-dodecyl-α-phenyl-5-isoxazole acetic acid and 5-dodecyl-α-phenyl-3-isoxazole acetic acid was condensed with 2,4-difluoroaniline to give, after chromatography, pure title compound; mp 68°-70° C.
Workup
- customto give
Sources & evidence
- ORD record
- ord-a778c5437b15428499706c54478b31d6
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05646170
Reaction notes
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