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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34773생성일: 2026년 10월 24일

1-Methylthio-1-methylamino-2-nitroethylene → 1-(2-[4-(2-[2,2,2-Trifluoroethyl]guanidino)pyrimid-2-yl-methylthio]ethylamino)-1-methylamino-2-nitroethylene

https://huagongshe.com/ko/reaction/34773

반응식

참여 물질

역할이름HCID투입량
반응물1-Methylthio-1-methylamino-2-nitroethyleneHCID 123549—
반응물4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-(2-aminoethyl)thiomethylpyrimidineHCID 21298720—
용매AcetonitrileHCID 6342—
생성물1-(2-[4-(2-[2,2,2-Trifluoroethyl]guanidino)pyrimid-2-yl-methylthio]ethylamino)-1-methylamino-2-nitroethyleneHCID 7041864663.3%

반응 단계

A mixture of 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[(2-aminoethyl)thiomethyl]pyrimidine (0.31 g.) 1-methylamino-1-methylthio-2-nitroethylene (0.15 g.) and acetonitrile (5 ml.) was heated under reflux for 6 hours and then left at room temperature for 18 hours. The yellow crystalline precipitate was collected to give 1-(2-[4-(2-[2,2,2-trifluoroethyl]guanidino)pyrimid-2-ylmethylthio]ethylamino)-1-methylamino-2-nitroethylene (0.26 g.), m.p. 154°-157° after recrystallisation from ethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04762932
출처 데이터셋uspto-grants-1988_08
ORD IDord-ed279f94630a4ea5b86684ffc48f68de
출처 메모uspto-grants-1988_08