Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366314Generated: October 26, 2026

1,4-Dioxane → HCID 66801881, compound

https://huagongshe.com/reaction/2366314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant3,5-Difluoropyridin-4-amineHCID 2737654—
Reactant2,6-Dichloro-4-iodobenzoyl chlorideHCID 86648958—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 66801881HCID 6680188183%

Reaction Steps

A suspension of 2,6-dichloro-4-iodobenzoyl chloride (24.2 g, 72.1 mmol) in THF (25 mL), was added drop-wise over 10 minutes, to a solution of 3,5-difluoropyridin-4-ylamine (10.37 g, 79.7 mmol) in pyridine (100 mL) at a temperature of between 3 and 5° C., under nitrogen. The reaction mixture was allowed to warm to room temperature over 1 hour and then stirred overnight. The volatiles were removed under reduced pressure and the resultant residue was treated with HCl (1 N, 90 mL). The resultant suspension was stirred at room temperature for 45 minutes and the precipitate obtained was collected by filtration, washing with water before drying. The resultant solid obtained was suspended in 1N NaOH (124 mL) and MeOH (124 mL), and heated at 65° C. for 5 hours then slowly cooled to room temperature. Further MeOH (50 mL) and dioxane (100 mL) were added and the reaction mixture was heated at 75° C. overnight. The resultant mixture was cooled to room temperature and the organic solvents removed under reduced pressure. The pH of the aqueous mixture was adjusted to 4-5 by drop-wise addition of 12 N HCl, controlling the exotherm by the use of an ice-bath. The residue was left standing at room temperature for 18 hours and then the resultant solid was collected by filtration, washing with water and dried under vacuum to afford the title compound as an off-white solid (21.3 g, 83% yield). LCMS (Method D): RT=3.46 min, m/z: 429 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697708B2
Source datasetuspto-grants-2014_04
ORD IDord-6af8a049921e4fccac5d3e08912e95f4
Source noteuspto-grants-2014_04