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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335513Generated: October 29, 2026

Ammonium Chloride → Rufinamide

https://huagongshe.com/reaction/335513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
ReactantCgp-47292HCID 10014469—
SolventTetrahydrofuranHCID 8028—
ProductRufinamideHCID 12922856.2%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

3.74 ml (45.65 mmol) of oxalyl chloride were added drop wise to a suspension of 10 g (41.8 mmol) of 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxylic acid in ml of anhydrous THF, at 20-25° C. and under nitrogen atmosphere. When the addition of oxalyl chloride was concluded, the mixture was stirred at 20-25° C. for 4 h. Afterwards, the resulting mixture was diluted with 50 ml of anhydrous THF, followed by the distillation of 15 ml at 35-40° C. under vacuum, in order to remove the remaining HCl. The reaction was cooled to 20-25° C. and 8 g (149.57 mmol) of ammonium chloride were added followed by addition of 20 ml of 8% aqueous solution of sodium bicarbonate. After further addition of 8.8 g (104.97 mmol) of sodium bicarbonate, the mixture was left under powerful stirring over 4 h at 20-25° C. To conclude with, the suspension was filtered and washed twice with 50 ml of a saturated aqueous sodium bicarbonate solution and twice with 50 ml of water The solid was dried on a vacuum drier at 50° C. to yield 5.6 g (56.2%) of 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide as Form R-5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08884026B2
Source datasetuspto-grants-2014_11
ORD IDord-c76100d850494e598273b8dfb09aaa8c
Source noteuspto-grants-2014_11