Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 62044생성일: 2026년 10월 24일
m-Tolylisothiocyanate → N-(m-tolylcarbamothioyl)-N-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)acetamide
https://huagongshe.com/ko/reaction/62044
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | m-Tolylisothiocyanate | HCID 69304 | — |
| 반응물 | N-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)acetamide | HCID 118675042 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(m-tolylcarbamothioyl)-N-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)acetamide | HCID 118675189 | 55% |
반응 단계
To N-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)acetamide in tetrahydrofuran (1.1 mL) cooled to −78° C. was added n-butyllithium (2.5 M, 0.13 mL). The reaction was stirred for 1 hour. 1-Isothiocyanato-3-methylbenzene was added and the solution was slowly warmed to 0° C. over 1 hour. The mixture was quenched with aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated. The residue was purified via radial chromatography using a 97:3 chloroform/methanol mixture as eluent providing the title compound as a tan solid (0.062 g, 55%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09445594B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-a1c8ac62b26b460c9c80443c7658ff7d |
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| 출처 메모 | uspto-grants-2016_09 |
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