2-(Dimethylamino)ethanol → HCID 67392175, compound
Reaction equation
[CH3:1][N:2]([CH3:6])[CH2:3][CH2:4][OH:5].[F:7][C:8]1[CH:9]=[C:10]([B:15]([CH:17]([O:24][CH:25]([B:32]([C:34]2[CH:39]=[CH:38][C:37]([F:40])=[C:36]([F:41])[CH:35]=2)[OH:33])[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)O)[CH:11]=[CH:12][C:13]=1[F:14]>C(O)C>[F:7][C:8]1[CH:9]=[C:10]([B:15]([CH:17]([O:24][CH:25]([B:32]([C:34]2[CH:39]=[CH:38][C:37]([F:40])=[C:36]([F:41])[CH:35]=2)[O:33][CH2:4][CH2:3][N:2]([CH3:6])[CH3:1])[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[O:5][CH2:4][CH2:3][N:2]([CH3:6])[CH3:1])[CH:11]=[CH:12][C:13]=1[F:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The entitled compound (15 mg) was obtained by allowing 20 mg of dimethylethanolamine to act on 49 mg of bis(4,4′-(3,4-difluorophenyl-hydroxyboryl)benzyl) ether in 0.6 mL of ethanol.
Sources & evidence
- ORD record
- ord-5320f6bd210c44a690b965a7341cb510
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08017809B2
Reaction notes
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