Isobutylamine → HCID 86609792, compound
Reaction equation
[Br:1][C:2]1[N:7]=[CH:6][C:5]([C:8]([CH3:13])([CH3:12])[C:9]([OH:11])=O)=[CH:4][CH:3]=1.[CH2:14]([NH2:18])[CH:15]([CH3:17])[CH3:16]>>[Br:1][C:2]1[N:7]=[CH:6][C:5]([C:8]([CH3:13])([CH3:12])[C:9]([NH:18][CH2:14][CH:15]([CH3:17])[CH3:16])=[O:11])=[CH:4][CH:3]=1Participants
3
Procedure
Prepared in a similar manner to Example 35a from 2-(6-Bromopyridin-3-yl)-2-methylpropanoic acid (example 40b) and isobutyl amine. Yield: 93%. MS+H (300).
Sources & evidence
- ORD record
- ord-39e14bfa3d3d4789ad2b6fde4e2543e4
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07842324B2
Reaction notes
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