4-Chlorobenzoyl chloride → HCID 67307112, 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]([CH:51]4[CH2:56][CH2:55][CH2:54][CH:53]([C:57]([O:59][CH3:60])=[O:58])[CH2:52]4)[C:47]3=[O:50])=[CH:43][CH:42]=2)=[CH:37][CH:36]=1.[Cl:61][C:62]1[CH:70]=[CH:69][C:65]([C:66](Cl)=[O:67])=[CH:64][CH:63]=1>>[Cl:61][C:62]1[CH:70]=[CH:69][C:65]([C:66]([NH:34][C:35]2[CH:36]=[CH:37][C:38]([C:41]3[CH:49]=[C:48]4[C:44]([CH2:45][N:46]([CH:51]5[CH2:56][CH2:55][CH2:54][CH:53]([C:57]([O:59][CH3:60])=[O:58])[CH2:52]5)[C:47]4=[O:50])=[CH:43][CH:42]=3)=[CH:39][CH:40]=2)=[O:67])=[CH:64][CH:63]=1Participants
4
Procedure
The compound of example 548 was prepared analogous to compound of example 97 by reaction of compound of example 543 with 4-chloro benzoyl chloride.
Sources & evidence
- ORD record
- ord-db18d892b279401da0d3dad353e22766
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08748426B2
Reaction notes
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