Methyl 3-(bromomethyl)benzoate → 4-Bromo-1-(3-methoxybenzyl)-1H-pyrazole
Reaction equation
[Br:1][C:2]1[CH:3]=[N:4][N:5]([CH2:7][C:8]2[CH:9]=[C:10]([CH:15]=[CH:16][CH:17]=2)C(OC)=O)[CH:6]=1.BrCC1C=C(C=CC=1)[C:23](OC)=[O:24].BrCC1C=CC=C(OC)C=1>>[Br:1][C:2]1[CH:3]=[N:4][N:5]([CH2:7][C:8]2[CH:17]=[CH:16][CH:15]=[C:10]([O:24][CH3:23])[CH:9]=2)[CH:6]=1Participants
4
Procedure
The title compound was prepared using a procedure analogous to methyl 3-((4-bromo-1H-pyrazol-1-yl)methyl)benzoate except that methyl 3-(bromomethyl)benzoate was replaced with 1-(bromomethyl)-3-methoxybenzene. LCMS, [M+H]+=267.1.
Sources & evidence
- ORD record
- ord-bd6674d54962448983920e40ece8e267
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062028B2
Reaction notes
Loading…