Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34774생성일: 2026년 10월 24일
Pyridine → 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-[2-(3-cyano-2-methylguanidino)ethylthiomethyl]pyrimidine
https://huagongshe.com/ko/reaction/34774
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 1,1,1-Trifluoro-2-isothiocyanatoethane | HCID 13883777 | — |
| 반응물 | HCID 178485067 | HCID 178485067 | — |
| 생성물 | 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-[2-(3-cyano-2-methylguanidino)ethylthiomethyl]pyrimidine | HCID 21298820 | — |
반응 단계
A mixture of 4-amino-2-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]pyrimidine (0.5 g.), 2,2,2-trifluoroethylisothiocyanate (0.55 g.) and pyridine (10 ml.) was heated at 70° for 18 hours and then evaporated to dryness. The residue was dissolved in ethyl acetate and the solution washed with 2N aqueous acetic acid, dried and evaporated to dryness. The residue was dissolved in ethanolic ammonia (15 ml.), treated with yellow mercuric oxide (0.4 g.) and the mixture stirred at room temperature for 4 hours. The mixture was filtered and the filtrate evaporated to dryness. The residue was purified by preparative thin layer chromatography using ethyl acetate/methanol/ammonia 6:1:0.5 v/v/v as developing solvent to give 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[2-(3-cyano-2-methylguanidino)ethylthiomethyl]pyrimidine (0.2 g.) characterised as the hydrogen maleate, m.p. 111°-114° (decomp.) after recrystallisation from acetonitrile.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04762932 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-fde28169ae7b4666a018551f7f1d8772 |
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| 출처 메모 | uspto-grants-1988_08 |
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