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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67Generated: October 24, 2026

2-Amino-N-methylbenzamide → 2-[2-Chloro-5-(trifluoromethyl)pyridin-4-ylamino]-N-methylbenzamide

https://huagongshe.com/en/reaction/67

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-N-methylbenzamideHCID 308072—
Reactant2-Chloro-4-iodo-5-(trifluoromethyl)pyridineHCID 2773791—
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-Chloro-5-(trifluoromethyl)pyridin-4-ylamino]-N-methylbenzamideHCID 5665532873.43%

Reaction Conditions

Temperature90 °C

Reaction Steps

2-chloro-4-iodo-5-(trifluoromethyl)pyridine (4.305 g, 14.00 mmol), 2-amino-N- methylbenzamide (2.103 g, 14.00 mmol), diacetoxypalladium (0.251 g, 1.12 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (1.296 g, 2.24 mmol) and cesium carbonate (5.47 g, 16.80 mmol) were mixed together in dioxane (80 mL). Reaction was degassed with argon and was stirred at 90 °C overnight (15 hours) under argon. Reaction was filtered, washed with CH2Cl2 and filtrate was concentrated to dryness. The crude product was purified by flash chromatography on silica gel eluting with 10 to 40% ethyl acetate in petroleum ether. The solvent was evaporated to dryness to afford 2-(2-chloro-5-(trifluoromethyl)pyridin-4-ylamino)-N-methylbenzamide (3.39 g, 73.4 %) as a white crystalline solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-f216b4e86bcc4a2b8660bf0c5e130be5
Source note750 AstraZeneca ELN dataset