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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031362Generated: November 1, 2026

2,6-Difluoroaniline → HCID 14155228, compound

https://huagongshe.com/reaction/1031362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DifluoroanilineHCID 79647—
ReactantHCID 14155106HCID 14155106—
SolventPyridineHCID 1049—
ProductHCID 14155228HCID 1415522855.6%

Reaction Steps

The starting 2,6-difluoroaniline (1.7 g, 13 mmol) was dissolved in 3.5 ml of pyridine and 3.5 g (14 mmol) of 6-chloro-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonyl chloride was added. After an exothermic reaction subsided the reaction mixture was heated at 60°-70° C. overnight. The solvent was removed by evaporation at reduced pressure and the residue was taken up in aqueous sodium bicarbonate. The aqueous solution was washed with ether, and acidified with aqueous HCl. The solid which separated upon acidification was collected by filtration, dried and recrystallized from methanol to afford 2.5 g (55%) of the desired product as a crystalline solid, m.p. 224°-226° C. IR and 1H NMR spectra were in agreement with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954163
Source datasetuspto-grants-1990_09
ORD IDord-5c75e5bd1e5a4a7380a3fec0886d5433
Source noteuspto-grants-1990_09