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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1622554생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1622554

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물4-BromoanisoleHCID 7730—
반응물MagnesiumHCID 5462224—
반응물(NE,S)-2-methyl-N-[[3-(trifluoromethyl)pyridin-2-yl]methylidene]propane-2-sulfinamideHCID 89310312—
용매TetrahydrofuranHCID 8028—
생성물(S)-N-((S)-(4-methoxyphenyl)(3-(trifluoromethyl)pyridin-2-yl)methyl)-2-methylpropane-2-sulfinamideHCID 71143955—

반응 단계

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 resulting mixture was stirred for 2 hours. Next, (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 were mixed and separated. The organic layer was dried with magnesium sulfate 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08778941B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-5ed0fed17c6145f59a64afee3a38e652
출처 메모uspto-grants-2014_07