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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510109Generated: November 2, 2026

Sodium Carbonate → HCID 20099815, compound

https://huagongshe.com/reaction/1510109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-5-bromopyridineHCID 70622—
Reactant2-Chlorophenylboronic acidHCID 2734322—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
ProductHCID 20099815HCID 2009981598%

Reaction Steps

A suspension of 70 mg (0.06 mmol) of tetrakis(triphenylphosphine) palladium(0) in benzene (4 ml) was treated at RT under an argon atmosphere successively with 0.35 g (2 mmol) of 2-amino-5-bromo-pyridine, 2.2 ml (4.4 mmol) of 2 M aqueous Na2CO3 solution, 0.34 g (2.2 mmol) of 2-chlorophenylboronic acid in ethanol (1 ml) and heated to reflux for 24 h. The reaction mixture was cooled and partitioned between EtOAc and water. The layers were separated, the organic layer dried over sodium sulphate and concentrated in vacuo. The residue was applied to a silica gel column with EtOAc as eluent. Combination of the purified fractions and concentration in vacuo gave 0.4 g (98%) of the desired 5-(2-chloro-phenyl)-pyridin-2-ylamine as white crystalline solid. ISP mass spectrum, m/e: 205.1 (M+1 calculated for C11H9ClN2: 205).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211913B2
Source datasetuspto-grants-2012_07
ORD IDord-68551a7fa8584d18b278bc82ab17156a
Source noteuspto-grants-2012_07