![659742-21-9](/CAS/GIF/659742-21-9.gif)
6-Methylpyridine-3-boronic Acid synthesis
- Product Name:6-Methylpyridine-3-boronic Acid
- CAS Number:659742-21-9
- Molecular formula:C6H8BNO2
- Molecular Weight:136.94
![2-METHYL-5-PYRIDINETRIFLUOROMETHANESULF&](/CAS/GIF/111770-91-3.gif)
111770-91-3
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$41.29/1g
![Bis(pinacolato)diboron](/CAS/20180808/GIF/73183-34-3.gif)
73183-34-3
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$6.00/5g
![6-Methylpyridine-3-boronic Acid](/CAS/GIF/659742-21-9.gif)
659742-21-9
222 suppliers
$12.00/250mg
Yield:659742-21-9 92%
Reaction Conditions:
with potassium acetate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride in acetonitrile at 160; for 0.333333 h;Microwave;
Steps:
1b
The INFLATE (4. 6MMOL) was dissolved in acetonitrile (30MOL) and placed into A 5M . microwave vessel. To the solution was added 1. 5 EQ of bis (PINACOLATO) DIBORON (6. 9MMOL ; 1. 71 G). The mixture was stirred on A magnetic stir plate until dissolution. To the mixture was added KOAC (13. 8MMOL ; 1. 35g) and 98mg of [1,1'-bis (DIPHENYLPHOSPHINO)- FERROCENE] DICHLOROPALLADIUM (II) (0. 03MOI%). The reaction mixture was heated at 160°C for 2 X 600s. After completion (monitored by LC-MS), the acetonitrile was evaporated to give a black solid. The solid was dissolved in DMSO, ms and purified by HPLC to give the boronic acid (580mg, 92%; 4. 2MMOL). MS: MH+= 138
References:
RENOVIS, INC. WO2005/32493, 2005, A2 Location in patent:Page/Page column 40-41
![5-Bromo-2-methylpyridine](/CAS/GIF/3430-13-5.gif)
3430-13-5
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![6-Methylpyridine-3-boronic Acid](/CAS/GIF/659742-21-9.gif)
659742-21-9
222 suppliers
$12.00/250mg
![5-Bromo-2-methylpyridine](/CAS/GIF/3430-13-5.gif)
3430-13-5
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![Triisopropyl borate](/CAS/GIF/5419-55-6.gif)
5419-55-6
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![6-Methylpyridine-3-boronic Acid](/CAS/GIF/659742-21-9.gif)
659742-21-9
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$12.00/250mg
![3-Hydroxy-6-methylpyridine](/CAS/GIF/1121-78-4.gif)
1121-78-4
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![6-Methylpyridine-3-boronic Acid](/CAS/GIF/659742-21-9.gif)
659742-21-9
222 suppliers
$12.00/250mg