Butanoic acid, 2-bromo-, methyl ester → HCID 86709158, compound
Reaction equation
[CH3:1][C:2]1[NH:3][C:4]2[C:9]([CH:10]=1)=[C:8]([C:11]([F:14])([F:13])[F:12])[C:7]([C:15]#[N:16])=[CH:6][CH:5]=2.Br[CH:18]([CH2:23][CH3:24])[C:19]([O:21][CH3:22])=[O:20]>>[C:15]([C:7]1[C:8]([C:11]([F:12])([F:14])[F:13])=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]([CH:18]([CH2:23][CH3:24])[C:19]([O:21][CH3:22])=[O:20])[C:2]([CH3:1])=[CH:10]2)#[N:16]Participants
3
Procedure
Synthesized in a manner similar to Example 1 using 2-methyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile and methyl 2-bromobutanoate: MS (ESI): m/z 325 (MH+).
Sources & evidence
- ORD record
- ord-ecd86bafc8ab4a23980f7fef49c2c17a
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957104B2
Reaction notes
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