1187917-12-9 → HCID 44230180, compound
Reaction equation
ClC1C=C(C2N(C3C=CC=C(Cl)C=3)N=C(C(O)=O)C=2)C=C(F)C=1.[Cl:24][C:25]1[CH:26]=[C:27]([N:32]2[C:36]([C:37]3[CH:42]=[C:41]([F:43])[CH:40]=[C:39]([Cl:44])[CH:38]=3)=[CH:35][C:34]([C:45]([N:47]3[CH2:51][C:50](=[O:52])[NH:49][CH2:48]3)=[O:46])=[N:33]2)[CH:28]=[CH:29][C:30]=1F>>[Cl:44][C:39]1[CH:38]=[C:37]([C:36]2[N:32]([C:27]3[CH:28]=[CH:29][CH:30]=[C:25]([Cl:24])[CH:26]=3)[N:33]=[C:34]([C:45]([N:47]3[CH2:51][C:50](=[O:52])[NH:49][CH2:48]3)=[O:46])[CH:35]=2)[CH:42]=[C:41]([F:43])[CH:40]=1Participants
3
Procedure
The preparation of the title compound takes place starting from the compound of Example 72A in analogy to the synthesis of the compound of Example 1. 50 mg (84% of theory) of the title compound are obtained.
Sources & evidence
- ORD record
- ord-6eca6c7a952847028d52a3a91234227b
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399682B2
Reaction notes
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