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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807894Generated: October 26, 2026

Ammonium Chloride → (2R,5S)-2-Isopropyl-3,6-dimethoxy-5-(4,4,4-trifluoro-3-phenyl-butyl)-2,5-dihydro-pyrazine

https://huagongshe.com/reaction/1807894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazineHCID 736066—
Reactant(3-Iodo-1-trifluoromethylpropyl)-benzeneHCID 67178112—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product(2R,5S)-2-Isopropyl-3,6-dimethoxy-5-(4,4,4-trifluoro-3-phenyl-butyl)-2,5-dihydro-pyrazineHCID 67177689—

Reaction Steps

A solution of (R)-(−)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine (1.1 g) in tetrahydrofuran (25 ml) was cooled to −70° C., then tert.butyllithium (1.7 M in pentane, 3.88 ml) was added and the mixture was stirred for 1 hour. A solution of (3-iodo-1-trifluoromethylpropyl)-benzene (1.98 g) in tetrahydrofuran (7 ml) was added slowly and the mixture was stirred overnight at −70° C. At room temperature saturated ammonium chloride solution was added and the mixture was extracted three times with ether. The combined organic layers were dried (MgSO4), filtered and evaporated. The residue was purified by column chromatography (SiO2, heptane/EtOAc=9:1 to yield a yellow liquid, (1.86 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357712B2
Source datasetuspto-grants-2013_01
ORD IDord-1db39d056f0c41f7926bddf8f45ec9e0
Source noteuspto-grants-2013_01