反応式
[CH3:1][N:2]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][C:6](=[O:7])[N:5]([CH3:14])[C:3]1=[O:4].FC(F)(F)C(O)=O.FC(F)(F)C(OC(=O)C(F)(F)F)=O.C1C(=O)N([I:42])C(=O)C1.S([O-])([O-])=S.[Na+].[Na+]>C(=O)([O-])[O-].[K+].[K+]>[CH3:1][N:2]1[C:9]([C:10]([F:13])([F:11])[F:12])=[C:8]([I:42])[C:6](=[O:7])[N:5]([CH3:14])[C:3]1=[O:4]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 1
実験手順
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.
後処理
- temperaturewas refluxed for 5 min
- temperaturereflux
- waitwas continued for another 5 h
- customto remove the excess iodine color
- filtrationThe resulting solids were collected by filtration
- washwashed with water
- customAfter air drying
出典と根拠
- ORDレコード
- ord-93837f21262b4ec49dfe9dd9dc9a902d
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06380387B1
関連ノート
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