Benzoyl chloride, 3-chloro- → HCID 67307651, 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:63]=[C:64]([CH:68]=[CH:69][CH:70]=1)[C:65](Cl)=[O:66]>>[Cl:61][C:62]1[CH:63]=[C:64]([CH:68]=[CH:69][CH:70]=1)[C:65]([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]([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:39][CH:40]=1)=[O:66]Participants
4
Procedure
The compound of example 546 was prepared analogous to compound of example 97 by reaction of compound of example 543 with 3-chloro benzoyl chloride.
Sources & evidence
- ORD record
- ord-a3b66f80f4b446b281ecc2e554709485
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08748426B2
Reaction notes
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