참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Trifluoroacetic anhydride | HCID 9845 | — |
| 반응물 | N-Iodosuccinimide | HCID 120273 | — |
| 반응물 | 1,3-Dimethyl-6-(trifluoromethyl)uracil | HCID 2758669 | — |
| 반응물 | sodium thiosulfite anhydrous | HCID 15847209 | — |
| 용매 | Potassium Carbonate | HCID 11430 | — |
| 생성물 | 1,3-Dimethyl-5-iodo-6-(trifluoromethyl)uracil | HCID 22613714 | 66% |
반응 단계
A mixture of 1,3-dimethyl-6-(trifluoromethyl)uracil (16.91 mmol, 3.52 g), trifluoroacetic acid (20 mL) and trifluoroacetic anhydride (5 mL) was refluxed for 5 min. Then, NIS (16.91 mmol, 3.8 g) was added and the resulting mixture was stirred for 15 h at which time the TLC analysis of the reaction mixture indicated the presence of some starting material. Another portion of NIS (8.45 mmol, 1.9 g) was added and reflux was continued for another 5 h. The reaction mixture was cooled to room temperature and was poured slowly into a saturated potassium carbonate solution (100 mL). Then, sodium thiosulfite solution was added to remove the excess iodine color. The resulting solids were collected by filtration and washed with water. After air drying, 3.73 g (66% yield) of 1,3-dimethyl-5-iodo-6-(trifluoromethyl)uracil was obtained as a white solid: mp 149-151° C. EI-HRMS m/e calcd for C7H6F3IN2O2 (M+) 333.9426, found 333.9436.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06380387B1 |
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| 출처 데이터셋 | uspto-grants-2002_04 |
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| ORD ID | ord-93837f21262b4ec49dfe9dd9dc9a902d |
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| 출처 메모 | uspto-grants-2002_04 |
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