3-(1,3,2-Dioxaborinan-2-yl)pyridine → HCID 18007545, compound
Reaction equation
Br[C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][N:8]2[CH2:11][CH2:12][N:13]([CH2:16][CH3:17])[CH2:14][CH3:15])=[CH:4][CH:3]=1.B1([C:24]2[CH:29]=[CH:28][CH:27]=[N:26][CH:25]=2)OCCCO1>>[CH2:14]([N:13]([CH2:12][CH2:11][N:8]1[C:9]2[C:5](=[CH:4][CH:3]=[C:2]([C:24]3[CH:25]=[N:26][CH:27]=[CH:28][CH:29]=3)[CH:10]=2)[CH:6]=[CH:7]1)[CH2:16][CH3:17])[CH3:15]Participants
3
Procedure
(16.6 mg , 56%); from 6-bromo-1-(2-(N,N-diethylamino)ethyl) indole (30.7 mg, 0.101 mmol) and pyridine-3-boronic acid 1,3-propanediol cyclic ester (33.0 mg,0.202 mmol).
Sources & evidence
- ORD record
- ord-e3d3b93cd49e4ddcb26bced1ac6f529e
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06380242B1
Reaction notes
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