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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914938Generated: October 31, 2026

Dichloromethane → 5-[2-(5-Chloro-2-fluoro-phenyl)-[1,8]naphthyridin-4-yl]-pyridin-2-ylamine

https://huagongshe.com/reaction/1914938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCesium carbonateHCID 10796—
Reactant2-Amino-5-bromopyridineHCID 70622—
ReactantHCID 53344730HCID 53344730—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-[2-(5-Chloro-2-fluoro-phenyl)-[1,8]naphthyridin-4-yl]-pyridin-2-ylamineHCID 67364075—

Reaction Conditions

Temperature100 °C

Reaction Steps

A slurry of 352 mg (2.04 mmol) 2-amino-5-bromo-pyridine, 678 mg (2.24 mmol) 2-(5-chloro-2-fluoro-phenyl)-[1,8]naphthyridine-4-boronic acid and 1.33 g (4.07 mmol) cesium carbonate in 10 ml dioxane and 2 ml water was heated to 80° C. under nitrogen. Then 118 mg (0.10 mmol) tetrakis-(triphenylphosphine)-palladium(0) were added and the reaction mixture was stirred for 1 hour at 100° C. The reaction mixture was cooled to room temperature and water and dichloromethane were added. The resulting precipitate was filtered off, washed with water and dried in vacuo yielding 5-[2-(5-chloro-2-fluoro-phenyl)-[1,8]naphthyridin-4-yl]-pyridin-2-ylamine as brown crystals; HPLC-MS: 1.43 min, [M+H] 351.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614226B2
Source datasetuspto-grants-2013_12
ORD IDord-fdaafda817134e7c8e3803f216d9782b
Source noteuspto-grants-2013_12