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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802487Generated: November 1, 2026

2-Chloro-4,6-difluoroaniline → HCID 59436014, compound

https://huagongshe.com/reaction/1802487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4,6-difluoroanilineHCID 2734083—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 59436091HCID 59436091—
ReactantHCID 59436097HCID 59436097—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59436014HCID 59436014—
ProductHCID 59436106HCID 59436106—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 1.5:1 mixture of 6-chloro-10-ethoxypyrido[4,3-c]-1,6-naphthyridine and 6,10-dichloropyrido[4,3-c]-1,6-naphthyridine (1.5 g) in THF (25 mL) was added 2-chloro-4,6 difluoro aniline (945 mg, 5.78 mmol) and sodium tert-butoxide (1.65 g, 17 mmol). The solution was heated to 85° C. for 40 min then cooled to room temperature and extracted with EtOAc and brine. The organic layers were dried with MgSO4, filtered, and concentrated under reduced pressure. The crude residue was purified on silica gel (100% hexanes to 100% EtOAc, gradient elution) which provided N-(2-chloro-4,6-difluorophenyl)-10-ethoxypyrido[4,3-c]-1,6-naphthyridin-6-amine and 10-chloro-N-(2-chloro-4,6-difluorophenyl)pyrido[4,3-c]-1,6-naphthyridin-6-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349865B2
Source datasetuspto-grants-2013_01
ORD IDord-d4a4e8bfa27e41ac9cc1803335175697
Source noteuspto-grants-2013_01