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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577424Generated: October 28, 2026

Ethyl Acetate → Ethyl 5-((5-fluoropyridin-3-yl)amino)-3-(methylthio)-1,2,4-triazine-6-carboxylate

https://huagongshe.com/reaction/577424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Fluoro-3-pyridinamineHCID 574450—
ReactantEthyl 5-Chloro-3-(Methylthio)-1,2,4-Triazine-6-CarboxylateHCID 11557703—
SolventDimethylformamideHCID 6228—
ProductEthyl 5-((5-fluoropyridin-3-yl)amino)-3-(methylthio)-1,2,4-triazine-6-carboxylateHCID 86706418—

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethyl 5-chloro-3-(methylthio)-1,2,4-triazine-6-carboxylate (300 mg, 1.29 mmol) was dissolved in 10 mL dry DMF. To it was added 3-amino-5-fluoropyridine (728 mg, 6.50 mmol) and then DIEA (0.45 mL, 2.60 mmol). The mixture was stirred at 100° C. for 1.5 h. To the mixture were poured 200 mL EtOAc. The mixture was washed with brine twice and water twice, dried in MgSO4, and concentrated in vacuo to afford crude ethyl 5-((5-fluoropyridin-3-yl)amino)-3-(methylthio)-1,2,4-triazine-6-carboxylate. It was stirred in 30 mL “7.0 N ammonia in methanol” (Acros, #133710010) as a slurry for overnight. The solid was isolated by filtration, washed with hexane and dried in vacuum oven. It was very pure 5-((5-fluoropyridin-3-yl)amino)-3-(methylthio)-1,2,4-triazine-6-carboxamide. Yield was 189 mg (52% for 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040530B2
Source datasetuspto-grants-2015_05
ORD IDord-08d6695a8b7e48fb83509069f9e2ed10
Source noteuspto-grants-2015_05