Ethyl 5-bromopyridine-3-carboxylate → Ethyl 5-(3,4,5-trimethoxyphenyl)nicotinate

HRID 1937686Notes

Reaction equation

HRID 1937686 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5](B(O)O)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].Br[C:17]1[CH:18]=[N:19][CH:20]=[C:21]([CH:27]=1)[C:22]([O:24][CH2:25][CH3:26])=[O:23]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:17]2[CH:18]=[N:19][CH:20]=[C:21]([CH:27]=2)[C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10]

Participants

3

Reactant 2

HCID 140785Ethyl 5-bromopyridine-3-carboxylateHCID 27343903,4,5-Trimethoxybenzeneboronic acid

Product 1

HCID 22557861Ethyl 5-(3,4,5-trimethoxyphenyl)nicotinate

Procedure

3,4,5-Trimethoxyphenylboronic acid (6.36 g) and ethyl 5-bromonicotinate (6.90 g) were reacted in the same manner as described in Preparation Example 1 to give the title compound.

Workup

  1. customas described in Preparation Example 1

Sources & evidence

ORD record
ord-58b0d8227f0f40988368b6f62b4b42f7
Source dataset
uspto-grants-2002_05
Patent number
US06395753B1

Reaction notes

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