2-羟基-3-甲基苯硼酸

反应条件: temp:0.00; pressure:0.00; stir:

反应条件: temp:0.00; pressure:0.00; stir:

反应条件: temp:0.00; pressure:0.00; stir:

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: 6-(2-Hydroxy-3-methoxyphenyl)-6′-(2-hydroxy-3-methylphenyl)-2,2′-bipyridine was prepared from 6-bromo-6′-(2-hydroxy-3-methoxyphenyl)-2,2′-bipyridine and 2-hydroxy-3-methylphenylboronic acid in 59% yield using method F; δH [2H6]-DMSO 13.28,(1H, s), 8.37,(1H, d), 8.35,(1H, d), 8.29,(2H, t), 8.18,(1H, d), 8.10,(1H, d), 7.97,(1H, d), 7.71,(1H, d), 7.29,(1H, d), 7.10,(1H, d), 6.97-6.87,(2H, m), 3.84,(3H, s), 2.29,(3H, s); MS 385 (MH)+; HPLC retention time (system 1) 4.27 minutes. HPLC retention time (system 1) 4.27 minutes

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: 6-(2-Hydroxy-3-methylphenyl)-6′-(2-hydroxy-4-methylphenyl)-2,2′-bipyridine was prepared from 6-bromo-6′-(2-hydroxy-4-methylphenyl)-2,2′-bipyridine and 2-hydroxy-3-methylphenylboronic acid in 84% yield using method F; δH [2H6]-DMSO 13.38,(1H, b), 8.41-8.22,(4H, m), 8.13,(1H, d), 8.09-8.01,(2H, m), 7.96,(1H, d), 7.28,(1H, d), 6.90,(1H, t), 6.80,(2H, m), 2.33,(3H, s), 2.26,(3H s); MS 369 (MH)+; HPLC retention time (system 1) 4.53 minutes. HPLC retention time (system 1) 4.53 minutes

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: 6-(2-Hydroxy-5-methoxyphenyl)-6′-(2-hydroxy-3-methylphenyl)-2,2′-bipyridine was prepared from 6-bromo-6′-(2-hydroxy-5-methoxyphenyl)-2,2′-bipyridine and 2-hydroxy-3-methylphenylboronic acid in 65% yield using method F; δH [2H6]-DMSO 12.35,(1H, s), 8.37,(2H, m), 8.24,(2H, m), 8.17,(1H, d), 7.96,(1H, d), 7.65,(1H, s), 7.27,(1H, d), 7.02-6.86,(3H, m), 3.83,(3H, s), 8.09,(1H, s); MS 385 (MH)+; HPLC retention time (system 1) 4.31 minutes. HPLC retention time (system 1) 4.31 minutes

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: 6-(2-Hydroxy-5-methoxyphenyl)-6′-(2-hydroxy-3-methylphenyl)-2,2′-bipyridine was prepared from 6-bromo-6′-(2-hydroxy-5-methoxyphenyl)-2,2′-bipyridine and 2-hydroxy-3-methylphenylboronic acid in 65% yield using method F; δH [2H6]-DMSO 12.35,(1H, s), 8.37,(2H, m), 8.24,(2H, m), 8.17,(1H, d), 7.96,(1H, d), 7.65,(1H, s), 7.27,(1H, d), 7.02-6.86,(3H, m), 3.83,(3H, s), 8.09,(1H, s); MS 385 (MH)+; HPLC retention time (system 1) 4.31 minutes. HPLC retention time (system 1) 4.31 minutes

反应条件: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: To a solution of 3.0 g (20 mmol) of 2,4-dichloro-pyrimidine in a 10:1 mixture of dioxane:water (220 mL) is added 3.3 g (22 mmol) of 2-hydroxy-3-methyl-phenyl boronic acid followed by 6.0 g (57 mmol) of sodium carbonate. Argon is bubbled through the solution for 15 min then 2.4 g (2.1 mmol) of tetrakis(triphenylphosphine)palladium (0) is added. The reaction is heated overnight at 100° C. then cooled to ambient temperature and filtered through diatomaceous earth. The filter pad is washed with EtOAc then placed on a new receiving flask and washed with a 1:1 mixture of MeOH:DCM. The filtrate is concentrated under reduced pressure to B-16 (1.60 g, 36.0%) Argon is bubbled through the solution for 15 min then cooled to ambient temperature filtered through diatomaceous earth The filter pad is washed with EtOAc washed with a 1:1 mixture of MeOH The filtrate is concentrated under reduced pressure to B-16 (1.60 g, 36.0%)

反应条件: temp:0.00; pressure:0.00; stir:

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: 6-(2-Hydroxy-3-methoxyphenyl)-6′-(2-hydroxy-3-methylphenyl)-2,2′-bipyridine was prepared from 6-bromo-6′-(2-hydroxy-3-methoxyphenyl)-2,2′-bipyridine and 2-hydroxy-3-methylphenylboronic acid in 59% yield using method F; δH [2H6]-DMSO 13.28,(1H, s), 8.37,(1H, d), 8.35,(1H, d), 8.29,(2H, t), 8.18,(1H, d), 8.10,(1H, d), 7.97,(1H, d), 7.71,(1H, d), 7.29,(1H, d), 7.10,(1H, d), 6.97-6.87,(2H, m), 3.84,(3H, s), 2.29,(3H, s); MS 385 (MH)+; HPLC retention time (system 1) 4.27 minutes. HPLC retention time (system 1) 4.27 minutes

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: 6-(2-Hydroxy-3-methylphenyl)-6′-(2-hydroxy-4-methylphenyl)-2,2′-bipyridine was prepared from 6-bromo-6′-(2-hydroxy-4-methylphenyl)-2,2′-bipyridine and 2-hydroxy-3-methylphenylboronic acid in 84% yield using method F; δH [2H6]-DMSO 13.38,(1H, b), 8.41-8.22,(4H, m), 8.13,(1H, d), 8.09-8.01,(2H, m), 7.96,(1H, d), 7.28,(1H, d), 6.90,(1H, t), 6.80,(2H, m), 2.33,(3H, s), 2.26,(3H, s); MS 369 (MH)+; HPLC retention time (system 1) 4.53 minutes. HPLC retention time (system 1) 4.53 minutes

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: 6-(2-Hydroxy-5-methoxyphenyl)-6′-(2-hydroxy-3-methylphenyl)-2,2′-bipyridine was prepared from 6-bromo-6′-(2-hydroxy-5-methoxyphenyl)-2,2′-bipyridine and 2-hydroxy-3-methylphenylboronic acid in 65% yield using method F; δH [2H6]-DMSO 12.35,(1H, s), 8.37,(2H, m), 8.24,(2H, m), 8.17,(1H, d), 8.09,(1H, d), 7.96,(1H, d), 7.65,(1H, s), 7.27,(1H, d), 7.02-6.86,(3H, m), 3.83,(3H, s), 2.26,(3H, s); MS 385 (MH)+; HPLC retention time (system 1) 4.31 minutes. HPLC retention time (system 1) 4.31 minutes