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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402480Generated: November 2, 2026

Nitrogen → 2-Chloro-N-(3-nitrophenyl)pyridine-4-amine

https://huagongshe.com/reaction/1402480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant3-NitroanilineHCID 7423—
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Chloro-4-iodopyridineHCID 1516511—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product2-Chloro-N-(3-nitrophenyl)pyridine-4-amineHCID 5816790791%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a degassed (15 min, N2) suspension of 2-chloro-4-iodopyridine (3.0 g, 12.53 mmol), 3-nitroaniline (1.82 g, 13.18 mmol), BINAP (0.39 g, 0.626 mmol) and Cs2CO3 (8.16 g, 25.04 mmol) in toluene (72 mL) was added Pd(OAc)2 (0.084 g, 0.374 mmol). The reaction tube was sealed and the mixture stirred at 90° C. for 18 h. The mixture was cooled to rt and filtered, washing with EtOAc. The orange/yellow solid collected was washed with CH2Cl2 until all the product washed through into the filtrate. The filtrate was concentrated to afford 2-Chloro-N-(3-nitrophenyl)pyridine-4-amine as a bright yellow solid. Additional product was collected from the solid collected upon concentration of the previous filtrate, after washing with CH2Cl2. No further purification. Total amount of product collected was 2.85 g (91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906944B2
Source datasetuspto-grants-2014_12
ORD IDord-e41336eb5668465ebb2a9179796fef04
Source noteuspto-grants-2014_12