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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279093생성일: 2026년 10월 25일

Methyl iodide → 2-(4-Chlorophenylsulfonyl)-3-methylsulfanyl-3-(pyridin-3-ylamino)-2-propenenitrile

https://huagongshe.com/reaction/279093

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물2-(4-Chlorobenzenesulfonyl)acetonitrileHCID 735829—
반응물3-Pyridyl isothiocyanateHCID 2737242—
용매AcetoneHCID 180—
생성물2-(4-Chlorophenylsulfonyl)-3-methylsulfanyl-3-(pyridin-3-ylamino)-2-propenenitrileHCID 7015017717.5%

반응 단계

To a solution of 4-chlorophenylsulfonylacetonitrile (1.00 g, 4.6 mmol) in dry acetone (10 ml) first dry potassium carbonate (1.28 g, 9.3 mmol) and then pyridin-3-yl isothiocyanate (0.663 g, 4.9 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 4 h, and then filtered. To the filtrate methyl iodide (0.315 ml, 5.1 mmol) was added. The mixture was stirred at room temperature for 16 h. The reaction mixture was concentrated and the residue was taken up into ethyl acetate and water. The organic layer was washed with 1N aqueous HCl (2×). The organic phase was dried (sodium sulfate) and concentrated. The residue was purified by flash chromatography using heptane/ethyl acetate 1:2 as eluent and recrystallisation in ethyl acetate to give 294 mg (16%) of the title compound. Mp 181-182° C. 1H NMR (300 MHz, CDCl3): δ=2.20 (s, 3H), 7.36 (dd, 1H), 7.54 (dm, 2H), 7.6 (m, 1H), 7.88 (dm, 2H), 8.55 (m, 2H), 9.85 (br s, 1H); EI SP/MS: 365 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362205B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-6d1fe10259b544d98becbfeb1471f09e
출처 메모uspto-grants-2002_03