Phenylboronic Acid → 2-(3-Methoxyphenyl)-5-nitro-3-phenylpyridine

HRID 41992Notes

Reaction equation

HRID 41992 reaction equation
Br[C:2]1[C:3]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=2)=[N:4][CH:5]=[C:6]([N+:8]([O-:10])=[O:9])[CH:7]=1.[C:19]1(B(O)O)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[CH3:18][O:17][C:13]1[CH:12]=[C:11]([C:3]2[C:2]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)=[CH:7][C:6]([N+:8]([O-:10])=[O:9])=[CH:5][N:4]=2)[CH:16]=[CH:15][CH:14]=1

Participants

3

Reactant 2

HCID 66827Phenylboronic AcidHCID 673943393-Bromo-2-(3-methoxyphenyl)-5-nitropyridine2×

Product 1

HCID 673943592-(3-Methoxyphenyl)-5-nitro-3-phenylpyridine

Procedure

Obtained (0.257 g, 87% of yield) following the procedure described in Intermediate 2 (step A) starting with 3-bromo-2-(3-methoxyphenyl)-5-nitropyridine (0.97 mmol, 0.300 g) and phenylboronic acid (1.07 mmol, 0.130 g).

Workup

  1. customObtained
  2. custom(0.257 g, 87% of yield)

Sources & evidence

ORD record
ord-e6a3441e82224c6c8c01402c96b952db
Source dataset
uspto-grants-2013_09
Patent number
US08536165B2

Reaction notes

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