Sodium hydride → 1-{3-[3-({2-[(E)-2-(2,4-difluorophenyl)ethenyl]-1,3-oxazol-4-yl}methoxy)phenyl]propyl}-1H-1,2,3-triazole
Reaction equation
[N:1]1([CH2:6][CH2:7][CH2:8][C:9]2[CH:10]=[C:11]([OH:15])[CH:12]=[CH:13][CH:14]=2)[CH:5]=[CH:4][N:3]=[N:2]1.[H-].[Na+].Cl[CH2:19][C:20]1[N:21]=[C:22](/[CH:25]=[CH:26]/[C:27]2[CH:32]=[CH:31][C:30]([F:33])=[CH:29][C:28]=2[F:34])[O:23][CH:24]=1>>[F:34][C:28]1[CH:29]=[C:30]([F:33])[CH:31]=[CH:32][C:27]=1/[CH:26]=[CH:25]/[C:22]1[O:23][CH:24]=[C:20]([CH2:19][O:15][C:11]2[CH:10]=[C:9]([CH2:8][CH2:7][CH2:6][N:1]3[CH:5]=[CH:4][N:3]=[N:2]3)[CH:14]=[CH:13][CH:12]=2)[N:21]=1Participants
4
Procedure
Using 3-[3-(1H-1,2,3-triazol-1-yl)propyl]phenol (143 mg), 65% oily sodium hydride (28 mg) and 4-(chloromethyl)-2-[(E)-2-(2,4-difluorophenyl)ethenyl]-1,3-oxazole (188 mg), the same reaction as Example 2 was carried out to yield the titled compound (257 mg).
Workup
- customthe same reaction as Example 2
Sources & evidence
- ORD record
- ord-d213f13622dd4b1695d6edce07fbf8e6
- Source dataset
- uspto-grants-2004_04
- Patent number
- US06716863B2
Reaction notes
Loading…