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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

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물1,1,1-Trifluoro-2-isothiocyanatoethaneHCID 13883777—
반응물HCID 178485067HCID 178485067—
생성물4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-[2-(3-cyano-2-methylguanidino)ethylthiomethyl]pyrimidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04762932
출처 데이터셋uspto-grants-1988_08
ORD IDord-fde28169ae7b4666a018551f7f1d8772
출처 메모uspto-grants-1988_08