Acetoprole → HCID 178420101, compound
Reaction equation
CC(C1C(S(C)=O)=C(N)N([C:13]2[C:18](Cl)=[CH:17][C:16]([C:20](F)(F)F)=[CH:15][C:14]=2Cl)N=1)=O.CC[S+]([O-])[C:28]1[C:29](C#N)=[N:30][N:31](C2C(Cl)=CC(C(F)(F)F)=CC=2Cl)C=1N.C1C(C(F)(F)F)=CC(Cl)=C(N2N=C(C#N)C([S+]([O-])C(F)(F)F)=C2N)C=1Cl.COC1C(=O)C=C/C(=C\NC2N(C3C(Cl)=CC(C(F)(F)F)=CC=3Cl)N=C(C#N)C=2SC(F)(F)F)/C=1.C1C=C(CNC2N(C3C(Cl)=CC(C(F)(F)F)=CC=3Cl)N=C(C#N)C=2SC(F)F)N=CC=1.C1N=CC(CNC2N(C3C(Cl)=CC(C(F)(F)F)=CC=3Cl)N=C(C#N)C=2SCF)=NC=1>>[C:16]1([C:20]2[CH:28]=[CH:29][NH:30][N:31]=2)[CH:15]=[CH:14][CH:13]=[CH:18][CH:17]=1Participants
7
Procedure
acetoprole, ethiprole, fipronil, vaniliprole, pyriprole, and pyrafluprole.
Sources & evidence
- ORD record
- ord-23a155b8e30245539f7184b628a6506c
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09120792B2
Reaction notes
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