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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-(4-Chlorobenzenesulfonyl)acetonitrile | HCID 735829 | — |
| 반응물 | 3-Pyridyl isothiocyanate | HCID 2737242 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2-(4-Chlorophenylsulfonyl)-3-methylsulfanyl-3-(pyridin-3-ylamino)-2-propenenitrile | HCID 70150177 | 17.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06362205B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-6d1fe10259b544d98becbfeb1471f09e |
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| 출처 메모 | uspto-grants-2002_03 |
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