Methylamine → 1-(6-Bromo-pyridin-2-yl)-cyclopropanecarboxylic acid methylamide
Reaction equation
[Br:1][C:2]1[N:7]=[C:6]([C:8]2([C:11]([OH:13])=O)[CH2:10][CH2:9]2)[CH:5]=[CH:4][CH:3]=1.[CH3:14][NH2:15]>>[CH3:14][NH:15][C:11]([C:8]1([C:6]2[CH:5]=[CH:4][CH:3]=[C:2]([Br:1])[N:7]=2)[CH2:10][CH2:9]1)=[O:13]Participants
3
Procedure
The title compound was prepared from 1-(6-bromo-pyridin-2-yl)-cyclopropanecarboxylic acid and methylamine (2 mol/L in tetrahydrofuran) following a procedure analogous to that described in Step 2 for Intermediate 5. Yield: 70% of theory; LC (method 3): tR=2.27 min; Mass spectrum (ESI+): m/z=255/257 (Br) [M+H]+.
Sources & evidence
- ORD record
- ord-6808309e2e1b487592bec2f7e380d903
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08933072B2
Reaction notes
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