참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Peroxide | HCID 784 | — |
| 반응물 | Trifluoroiodomethane | HCID 16843 | — |
| 반응물 | 2,6-Diaminopurine | HCID 30976 | — |
| 촉매 | Ferrous Sulfate | HCID 24393 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 8-(trifluoromethyl)-7H-purine-2,6-diamine | HCID 3635407 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07981318B2 |
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| 출처 데이터셋 | uspto-grants-2011_07 |
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| ORD ID | ord-c48c95f2c6d1432caa5693517c218c98 |
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| 출처 메모 | uspto-grants-2011_07 |
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