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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451473Generated: October 30, 2026

Iodine → 8-(3,4-Difluorophenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-amine

https://huagongshe.com/reaction/451473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTetrahydrofuranHCID 8028—
ReactantMagnesiumHCID 5462224—
Reactant8-(3,4-Difluorophenyl)-[1,2,4]triazolo[1,5-A]pyridin-2-amineHCID 67337204—
SolventMethanolHCID 887—
Product8-(3,4-Difluorophenyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 67342682—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 8-(3,4-difluorophenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine (prepared in analogy to example 66a-c, 500 mg, 2.03 mmol) in methanol (60 mL) and THF (30 mL) magnesium (395 mg, 16.2 mmol) and iodine (3 mg) were added. After 1.5 hours at room temperature further magnesium (395 mg, 16.2 mmol) was added and the reaction mixture was stirred at 50° C. for 1 hour. Further magnesium (148 mg, 6.09 mmol) was added again and stirred at room temperature for 4 hours. The solvent was evaporated, the residue was dissolved in THF and dried over Na2SO4. The solvent was evaporated and the residue was purified by flash chromatography (silica gel, 100 g, 0% to 15% MeOH/NH3 (9:1) in dichloromethane, 45 minutes). The title compound was obtained as white solid (226 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486967B2
Source datasetuspto-grants-2013_07
ORD IDord-942b9ae4a8f74b55890205aacf304a5f
Source noteuspto-grants-2013_07