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HRID 885159作成日:2026年10月26日

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/885159

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazineHCID 736066—
反応物(3-Iodo-1-trifluoromethylpropyl)-benzeneHCID 67178112—
反応物HCID 178418306HCID 178418306—
溶媒TetrahydrofuranHCID 8028—
生成物(2R,5S)-2-Isopropyl-3,6-dimethoxy-5-(4,4,4-trifluoro-3-phenyl-butyl)-2,5-dihydro-pyrazineHCID 67177689—

反応手順

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-trifluoromethyl-propyl)-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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08242153B2
出典データセットuspto-grants-2012_08
ORD IDord-8b979149bfaf420d84f4f17b56e20eb0
出典メモuspto-grants-2012_08