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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28Generated: October 23, 2026

2-Amino-N-methylbenzamide → 2-[(2,5-Dichloro-4-pyridinyl)amino]-N-methylbenzamide

https://huagongshe.com/en/reaction/28

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-N-methylbenzamideHCID 308072—
Reactant2,5-Dichloro-4-iodopyridineHCID 53400965—
ReagentCesium carbonateHCID 10796—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,4-DioxaneHCID 31275—
Product2-[(2,5-Dichloro-4-pyridinyl)amino]-N-methylbenzamideHCID 5751689169.36%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-amino-N-methylbenzamide (110 mg, 0.73 mmol), 2,5-dichloro-4-iodopyridine (200 mg, 0.73 mmol), diacetoxypalladium (8.20 mg, 0.04 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (42.3 mg, 0.07 mmol) and cesium carbonate (357 mg, 1.10 mmol) suspended in 1,4-dioxane (4 mL) was weighed out in a microwave vial and sealed. argon was let to bubble into the mixture for 5 minutes at rt then the resulting mixture was stirred at 100 °C for 1 hour. The reaction mixture was allowed to cool to room temperature under stirring and diluted with dichloromethane. Insolubles were removed by filtration and the filtrate was concentrated. The residue was triturated in DCM, collected by filtration and dried to afford 2-(2,5-dichloropyridin-4-ylamino)-N-methylbenzamide (150 mg, 69.4 %) as a off- white solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-b94a4cbc1fbd4100843834a92096e35b
Source note750 AstraZeneca ELN dataset