Isoamylamine → HCID 59730350, compound
Reaction equation
[F:1][C:2]1[CH:17]=[C:16]([CH:18]=O)[CH:15]=[CH:14][C:3]=1[O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([NH2:11])=[O:10])=[CH:7][N:6]=1.[CH3:20][CH:21]([CH3:25])[CH2:22][CH2:23][NH2:24]>>[F:1][C:2]1[CH:17]=[C:16]([CH2:18][NH:24][CH2:23][CH2:22][CH:21]([CH3:25])[CH3:20])[CH:15]=[CH:14][C:3]=1[O:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([NH2:11])=[O:10])=[CH:7][N:6]=1Participants
3
Procedure
Using the compound of Example 223, step 1, and using 3-methylbutylamine, the title compound was prepared by reductive amination as described previously.
Sources & evidence
- ORD record
- ord-c4c971771780439a921d06f9270a3a46
- Source dataset
- uspto-grants-2008_06
- Patent number
- US07381719B2
Reaction notes
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