Reaction equation
[Br:1]C1C=C(C(F)(F)F)C=CC=1N1CCOC2C=C(S(Cl)(=O)=O)C=CC1=2.Cl[C:27]1[CH:32]=[C:31]([C:33]([F:36])([F:35])[F:34])[CH:30]=[CH:29][C:28]=1[N:37]1[CH2:42][CH2:41][O:40][C:39]2[CH:43]=[C:44]([S:47]([O:50][C:51]3[C:56]([F:57])=[C:55]([F:58])[C:54]([F:59])=[C:53]([F:60])[C:52]=3[F:61])(=[O:49])=[O:48])[CH:45]=[CH:46][C:38]1=2>>[Br:1][C:27]1[CH:32]=[C:31]([C:33]([F:36])([F:35])[F:34])[CH:30]=[CH:29][C:28]=1[N:37]1[CH2:42][CH2:41][O:40][C:39]2[CH:43]=[C:44]([S:47]([O:50][C:51]3[C:56]([F:57])=[C:55]([F:58])[C:54]([F:59])=[C:53]([F:60])[C:52]=3[F:61])(=[O:49])=[O:48])[CH:45]=[CH:46][C:38]1=2Participants
3
Reactant 2
Product 1
Procedure
Perfluorophenyl 4-(2-bromo-4-(trifluoromethyl)phenyl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-sulfonate was prepared from INTERMEDIATE C according to the procedure used to prepare INTERMEDIATE F. MS (ESI, positive) m/z: 625.8 (M+Na).
Sources & evidence
- ORD record
- ord-af89dbf0860848f69e2dc1d0c8ac38ea
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09346798B2
Linked notes
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