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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2248827생성일: 2026년 10월 25일

Methyl isothiocyanate → N-[2-[4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidinyl]ethyl]-N'-methylthiourea

https://huagongshe.com/reaction/2248827

반응식

참여 물질

역할이름HCID투입량
반응물Methyl isothiocyanateHCID 11167—
반응물N-[1-(2-aminoethyl)-4-piperidinyl]-9-[(4-fluorophenyl)methyl]-9H-purin-8-amineHCID 19785318—
용매TetrahydrofuranHCID 8028—
생성물N-[2-[4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidinyl]ethyl]-N'-methylthioureaHCID 1978523429%

반응 단계

A mixture of 0.7 parts of isothiocyanatomethane, 3.7 parts of N-[1-(2-aminoethyl)-4-piperidinyl]-9-[(4-fluorophenyl)methyl]-9H-purin-8-amine and 90 parts of tetrahydrofuran was stirred for 4 hours at room temperature. After evaporation, the residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95:5 by volume) as eluent. The first fraction was collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 1.3 parts (29%) of N-[2-[4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]amino]-1-piperidinyl]ethyl]-N'-methylthiourea; mp. 205.5° C. (compound 179).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05041448
출처 데이터셋uspto-grants-1991_08
ORD IDord-0a76f5d407534870a4b0570913640445
출처 메모uspto-grants-1991_08