Benzoyl chloride, 3-chloro- → HCID 59643196, compound
Reaction equation
[NH2:1]/[C:2](/[N:5]([CH2:23][C:24]1[CH:29]=[CH:28][C:27]([C:30]([F:33])([F:32])[F:31])=[CH:26][CH:25]=1)[CH2:6][CH2:7][C:8]1[CH:22]=[CH:21][C:11]([O:12][C:13]([CH3:20])([CH3:19])[C:14]([O:16]CC)=[O:15])=[CH:10][CH:9]=1)=[N:3]\[OH:4].[Cl:34][C:35]1[CH:36]=[C:37]([CH:41]=[CH:42][CH:43]=1)[C:38](Cl)=O>>[Cl:34][C:35]1[CH:36]=[C:37]([C:38]2[O:4][N:3]=[C:2]([N:5]([CH2:23][C:24]3[CH:29]=[CH:28][C:27]([C:30]([F:31])([F:32])[F:33])=[CH:26][CH:25]=3)[CH2:6][CH2:7][C:8]3[CH:22]=[CH:21][C:11]([O:12][C:13]([CH3:19])([CH3:20])[C:14]([OH:16])=[O:15])=[CH:10][CH:9]=3)[N:1]=2)[CH:41]=[CH:42][CH:43]=1Participants
3
Procedure
Similarly prepared from ethyl 2-[4-(2-{[(E)-amino(hydroxyimino)methyl][4-(trifluoromethyl)benzyl]amino}ethyl)phenoxy]-2-methylpropanoate and 3-chlorobenzoyl chloride.
Sources & evidence
- ORD record
- ord-76b69e51a9d74841b21490dd16925a4a
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07319104B2
Reaction notes
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