3-Phenyl-4-(trifluoromethyl)-5-(7-vinyl-4,5-dihydronaphtho[2,1-d]thiazol-2-yl)isoxazole → 5-(7-(Oxiran-2-yl)-4,5-dihydronaphtho[2,1-d]thiazol-2-yl)-3-phenyl-4-(trifluoromethyl)isoxazole
Reaction equation
[O:1]1CC1C1C=C2C(=CC=1)C1=NOC(C3C(C(F)(F)F)=C(C4C=CC=CC=4)ON=3)=C1CC2.[C:32]1([C:38]2[C:42]([C:43]([F:46])([F:45])[F:44])=[C:41]([C:47]3[S:48][C:49]4[C:59]5[C:54](=[CH:55][C:56]([CH:60]=[CH2:61])=[CH:57][CH:58]=5)[CH2:53][CH2:52][C:50]=4[N:51]=3)[O:40][N:39]=2)[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>>[O:1]1[CH2:61][CH:60]1[C:56]1[CH:55]=[C:54]2[C:59](=[CH:58][CH:57]=1)[C:49]1[S:48][C:47]([C:41]3[O:40][N:39]=[C:38]([C:32]4[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=4)[C:42]=3[C:43]([F:46])([F:44])[F:45])=[N:51][C:50]=1[CH2:52][CH2:53]2Participants
3
Reactant 2
Product 1
Procedure
This compound was prepared according to the procedure described for Preparation 13A, employing 100 mgs of 3-phenyl-4-(trifluoromethyl)-5-(7-vinyl-4,5-dihydronaphtho[2,1-d]thiazol-2-yl)isoxazole (82E). Yield: 100 mgs (96%)
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-d8d50049eb45474399c9d1f355ddca99
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09216972B2
Reaction notes
Loading…