Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1245632생성일: 2026년 10월 25일
2,4,6-Trichlorobenzenesulfonyl chloride → 2,4,6-trichloro-N-[4-methyl-5-(2,2,2-trichloroethyl)-1,3-thiazol-2-yl]benzenesulfonamide
https://huagongshe.com/reaction/1245632
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2,4,6-Trichlorobenzenesulfonyl chloride | HCID 521335 | — |
| 반응물 | 4-Methyl-5-(2,2,2-trichloroethyl)-1,3-thiazol-2-ylamine | HCID 15648825 | — |
| 생성물 | 2,4,6-trichloro-N-[4-methyl-5-(2,2,2-trichloroethyl)-1,3-thiazol-2-yl]benzenesulfonamide | HCID 11409207 | 46% |
반응 단계
The title compound was prepared according to METHOD A from 4-methyl-5-(2,2,2-trichloroethyl)-1,3-thiazol-2-ylamine (123 mg, 0.5 mmol, prepared according to Dodinov, A. A et al (1993) Chem. Heterocycl. Comp (Eng. Transl.) 29(8): 955-958) and 2,4,6-trichlorobenzenesulfonyl chloride (140 mg, 0.5 mmol). The solution was allowed to stand at room temperature overnight. The solution was directly loaded on a silica gel column for flash column chromatography, eluted with a mixed solvent of ethyl acetate and hexane (up to 40% v/v) to give a solid product. Crystallization of the product from ethyl acetate and hexane gave the title compound as a white solid (112 mg, 46% yield): mp 228-229° C.; MS m/e 487, 489, 491, 493; Anal. Calcd. (found) for C12H8Cl6N2O2S2: C 29.5 (29.7) % H 1.7 (2.1) % N 5.7 (5.8) %.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07125900B2 |
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| 출처 데이터셋 | uspto-grants-2006_10 |
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| ORD ID | ord-31c77c55b0174d7482390a1008b0753a |
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| 출처 메모 | uspto-grants-2006_10 |
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