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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410865Generated: November 1, 2026

Sodium Carbonate → Methyl 3-amino-6-bromo-2-(4-(morpholinosulfonyl)phenyl)isonicotinate

https://huagongshe.com/reaction/2410865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-(Morpholin-4-ylsulphonyl)benzeneboronic acidHCID 44119546—
ReactantMethyl 3-amino-2,6-dibromoisonicotinateHCID 53419616—
ProductMethyl 3-amino-6-bromo-2-(4-(morpholinosulfonyl)phenyl)isonicotinateHCID 8666306776%

Reaction Steps

A flask containing mixture of 4-(morpholinosulfonyl)-phenylboronic acid (0.920 g, 3.39 mmol), methyl 3-amino-2,6-dibromoisonicotinate (0.877 g, 2.83 mmol), tetrakistriphenylphosphine palladium(0) (0.196 g, 0.170 mmol), sodium carbonate (0.719 g, 6.79 mmol) was flushed with nitrogen. Toluene (7 mL), and MeOH (2.4 mL) were added and the reaction was heated at reflux under nitrogen for 24 hr. The reaction was partitioned between EtOAc and water. The organic phase was washed with brine, dried with sodium sulfate, and the solvent removed. Radial silica gel chromatography (step gradient elution with DCM containing 0 to 20% EtOAc) afforded methyl 3-amino-6-bromo-2-(4-(morpholinosulfonyl)phenyl)isonicotinate (982 mg, 2.15 mmol, 76% yield) as a yellow solid. MS (ESI) m/z 457.9 (M+H). 1H NMR (500 MHz, chloroform-d) δ ppm 7.80-7.91 (5H, m), 5.94 (2H, br. s.), 3.94 (3H, s), 3.68-3.79 (4H, m), 2.98-3.07 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815840B2
Source datasetuspto-grants-2014_08
ORD IDord-ce1ee12ffc114a08a19175026a6c2050
Source noteuspto-grants-2014_08