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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640690Generated: October 31, 2026

Trifluoroacetic acid → Methyl 6-iodo-5-methyl-3-oxo-4-[3-(trifluoromethyl)phenyl]-3,4-dihydropyrazine-2-carboxylate

https://huagongshe.com/reaction/1640690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-IodosuccinimideHCID 120273—
ReactantAluminumHCID 5359268—
ReactantAZ-32S-methyl-esterHCID 58432791—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-iodo-5-methyl-3-oxo-4-[3-(trifluoromethyl)phenyl]-3,4-dihydropyrazine-2-carboxylateHCID 6673877746%

Reaction Steps

Methyl 5-methyl-3-oxo-4-[3-(trifluoromethyl)phenyl]-3,4-dihydropyrazine-2-carboxylate (described in the synthesis of SM2, 1.5 g, 4.8 mmol), dry DCM (7.0 mL), trifluoroacetic acid (3.0 mL) and N-iodosuccinimide (1.0 g, 4.5 mmol) were mixed and stirred at RT in the dark (flask covered with aluminum foil). After 5 h, water (5 mL) was added and the mixture was concentrated by rotary evaporation. Water (3 mL) was added once more and the mixture was concentrated as described above. The resulting mixture was diluted with acetonitrile to a total volume of 50 mL. Purification by preparative HPLC with acetonitrile-water as eluent (neutral eluent) gave 0.905 g (46% yield) of the title compound as a yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114881B2
Source datasetuspto-grants-2012_02
ORD IDord-0552440ecc5247378cb8dbaca0e5397a
Source noteuspto-grants-2012_02