Boron tribromide → HCID 69896758, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:27])[C:4]1[C:9]([NH:10][CH:11]([CH2:14][CH3:15])[CH2:12][CH3:13])=[CH:8][C:7]([CH3:16])=[N:6][C:5]=1[O:17][C:18]1[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:19]=1[O:25]C.B(Br)(Br)Br>C(Cl)Cl>[CH3:1][O:2][C:3](=[O:27])[C:4]1[C:9]([NH:10][CH:11]([CH2:12][CH3:13])[CH2:14][CH3:15])=[CH:8][C:7]([CH3:16])=[N:6][C:5]=1[O:17][C:18]1[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:19]=1[OH:25]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared by reacting 2-(4-chloro-2-methoxy-phenoxy)-4-(1-ethyl-propylamino)-6-methyl-nicotinic acid methyl ester with BBr3 in methylene chloride at rt until all starting material was consumed. Standard work-up procedure gave the title compound.
Workup
- customThe title compound was prepared
- customat rt
- customwas consumed
Sources & evidence
- ORD record
- ord-19081d4188de4ca79c950726a5b98985
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06833378B2
Reaction notes
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