(4-Methoxyphenyl)boronic acid → HCID 131729209, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([C:9]([F:12])([F:11])[F:10])[CH:5]=[C:6](Br)[CH:7]=1.[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18](B(O)O)=[CH:17][CH:16]=1>CCCCCC.CCOC(C)=O>[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([C:6]2[CH:5]=[C:4]([C:9]([F:12])([F:11])[F:10])[CH:3]=[C:2]([NH2:1])[CH:7]=2)=[CH:17][CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared as described in Example 13 but using 3-amino-5-bromobenzotrifluoride (RYAN SCIENTIFIC) and 4-methoxyphenylboronic acid (Aldrich). Title compound: ES-MS: 266.0 [M-H]−; single peak at tR=4.61 min (System 1); Rf=0.20 (Hexane/EtOAc, 3:1).
Workup
- customThe title compound is prepared
Sources & evidence
- ORD record
- ord-7dea5d4e3d6f4941ba3b47c1e1d59f11
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08030311B2
Reaction notes
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