HCID 66687731, compound → HCID 86574659, compound
Reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([C:14]2[N:18]([C:19]3[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=3)[N:17]=[C:16]([C:25](O)=[O:26])[CH:15]=2)[CH:6]=[C:7]([O:9][C:10]([F:13])([F:12])[F:11])[CH:8]=1)#[N:2].ClC1C=C(C2N(C3C=CC=CN=3)N=C(C([N:49]3[CH2:53][C:52](=[O:54])[NH:51][CH2:50]3)=O)C=2)C=C(F)C=1.Cl.N1C=CNC1=O>>[O:54]=[C:52]1[CH2:53][N:49]([C:25]([C:16]2[CH:15]=[C:14]([C:5]3[CH:4]=[C:3]([CH:8]=[C:7]([O:9][C:10]([F:11])([F:13])[F:12])[CH:6]=3)[C:1]#[N:2])[N:18]([C:19]3[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=3)[N:17]=2)=[O:26])[CH2:50][NH:51]1Participants
4
Procedure
98 mg (0.26 mmol) of the compound of Example 58A is reacted analogously to the synthesis of the compound of Example 1 with 35 mg (0.29 mmol) of 4-imidazolinone-hydrochloride. 80 mg (69% of theory) of the title compound is obtained.
Sources & evidence
- ORD record
- ord-c0ddd52331404284a57be2111c9fe27d
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09296720B2
Reaction notes
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