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HRID 509314作成日:2026年10月26日

Iodine → (S)-N-((S)-(4-methoxyphenyl)(3-(trifluoromethyl)pyridin-2-yl)methyl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/509314

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物4-BromoanisoleHCID 7730—
反応物MagnesiumHCID 5462224—
反応物(NE,S)-2-methyl-N-[[3-(trifluoromethyl)pyridin-2-yl]methylidene]propane-2-sulfinamideHCID 89310312—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-N-((S)-(4-methoxyphenyl)(3-(trifluoromethyl)pyridin-2-yl)methyl)-2-methylpropane-2-sulfinamideHCID 71143955—

反応手順

Magnesium metal (0.095 g, 3.91 mmol) was activated using a crystal of iodine prior to addition of THF (1 mL). 1-Bromo-4-methoxybenzene (0.400 g, 2.139 mmol) was added, and the reaction was left without stirring for 5 minutes after which initiation was observed. Additional THF (15 mL) was added and the mixture was stirred for 2 hours. (S,E)-2-Methyl-N-((3-(trifluoromethyl)pyridin-2-yl)methylene)propane-2-sulfinamide (0.500 g, 1.797 mmol) was added, and the mixture was stirred for 10 minutes. The reaction was quenched by addition of saturated aqueous NH4Cl (10 mL). H2O (100 mL) and EtOAc (150 mL) were added, and the phases mixed and separated. The organic layer was dried with MgSO4 and evaporated to dryness under reduced pressure. Purification using silica chromatography (hexane to EtOAc gradient) gave (S)—N—((S)-(4-methoxyphenyl)-(3-(trifluoromethyl)pyridin-2-yl)methyl)-2-methylpropane-2-sulfinamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096527B2
出典データセットuspto-grants-2015_08
ORD IDord-c5de1539f0fa4e2780c2099c8bd46eaf
出典メモuspto-grants-2015_08