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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1012872생성일: 2026년 10월 26일

Hydrogen Peroxide → 8-(trifluoromethyl)-7H-purine-2,6-diamine

https://huagongshe.com/reaction/1012872

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물TrifluoroiodomethaneHCID 16843—
반응물2,6-DiaminopurineHCID 30976—
촉매Ferrous SulfateHCID 24393—
용매Dimethyl SulfoxideHCID 679—
생성물8-(trifluoromethyl)-7H-purine-2,6-diamineHCID 363540740%

반응 단계

0.12 g (0.8 mmol) of 2,6-diaminopurine was weighed and placed in a two-neck flask and the atmosphere in the flask was replaced with argon. The following materials were added thereinto: 3.0 ml of dimethyl sulfoxide, 0.8 ml of a 3.0 mol/l dimethyl sulfoxide solution of trifluoromethyl iodide, 0.25 ml of a 1.0 mol/l aqueous solution of iron(II) sulfate and 0.15 ml of a 30% hydrogen peroxide aqueous solution, and the mixture was stirred for 20 minutes. During the stirring, the temperature of the reaction system rose up in the range of from 40° C. to 50° C. Thereafter, the resulting solution was cooled to room temperature. Formation of 2,6-diamino-8-trifluoromethylpurine (19F-NMR yield: 40%) was confirmed by 19F-NMR with 2,2,2-trifluoroethanol as an internal standard. Water was added to the resulting solution, sodium hydrogen carbonate was added thereto to neutralize, and the desired product was extracted with ethyl acetate. The extract was passed through column chromatography and concentrated under reduced pressure to obtain 2,6-diamino-8-trifluoromethylpurine as a white solid (0.043 g, yield: 20%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07981318B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-c48c95f2c6d1432caa5693517c218c98
출처 메모uspto-grants-2011_07