2,4-Dichlorobenzoyl chloride → HCID 123277878, compound
Reaction equation
C(NC1C=CC(C2C=C3C(CN([C@@H](C(C)C)C(OC)=O)C3=O)=CC=2)=CC=1)(=O)C1C=CC=CC=1.[NH2:34][C:35]1[CH:40]=[CH:39][C:38]([C:41]2[CH:49]=[C:48]3[C:44]([CH2:45][N:46]([C@@H:51]([CH:56]([CH3:58])[CH3:57])[C:52]([O:54][CH3:55])=[O:53])[C:47]3=[O:50])=[CH:43][CH:42]=2)=[CH:37][CH:36]=1.[Cl:59][C:60]1[CH:68]=[C:67]([Cl:69])[CH:66]=[CH:65][C:61]=1[C:62](Cl)=[O:63]>>[Cl:59][C:60]1[CH:68]=[C:67]([Cl:69])[CH:66]=[CH:65][C:61]=1[C:62]([NH:34][C:35]1[CH:36]=[CH:37][C:38]([C:41]2[CH:49]=[C:48]3[C:44]([CH2:45][N:46]([C@@H:51]([CH:56]([CH3:58])[CH3:57])[C:52]([O:54][CH3:55])=[O:53])[C:47]3=[O:50])=[CH:43][CH:42]=2)=[CH:39][CH:40]=1)=[O:63]Participants
4
Procedure
The compound of example 133 was prepared analogous to compound of example 97 by reaction of compound of example 6 with 2,4-dichloro benzoyl chloride.
Sources & evidence
- ORD record
- ord-d36611d854644fe1ac48c268ab375bab
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08748426B2
Reaction notes
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