HCID 67168162, compound → 7-Iodo-3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazole
Reaction equation
C1(N2C(C(F)(F)F)=C(C3ON=C4C5C(CCC=34)=CC(C=C)=CC=5)C=N2)C=CC=CC=1.[I:31][C:32]1[CH:33]=[C:34]2[C:39](=[CH:40][CH:41]=1)/[C:38](=[N:42]/[OH:43])/[CH2:37][CH2:36][CH2:35]2.[C:44]1([C:50]2[O:54][N:53]=[C:52]([C:55](OC)=O)[C:51]=2[C:59]([F:62])([F:61])[F:60])[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1>>[I:31][C:32]1[CH:33]=[C:34]2[C:39](=[CH:40][CH:41]=1)[C:38]1=[N:42][O:43][C:55]([C:52]3[C:51]([C:59]([F:60])([F:61])[F:62])=[C:50]([C:44]4[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=4)[O:54][N:53]=3)=[C:37]1[CH2:36][CH2:35]2Participants
4
Reactant 3
Product 1
Procedure
The titled compound was prepared using the experimental protocol described for Preparation 89A employing (E)-6-iodo-3,4-dihydronaphthalen-1(2H)-one oxime (121A) and methyl 5-phenyl-4-(trifluoromethyl)isoxazole-3-carboxylate (Intermediate I-5) as starting materials. The compound had an HPLC retention time=4.42 min. (condition C); LC/MS M+1=509.0.
Sources & evidence
- ORD record
- ord-8b415f84974f471fa71953461d3b0ef1
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09216972B2
Reaction notes
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