m-Chloroperbenzoic acid → HCID 69506712、化合物
反応式
[N:1]1([CH2:14][C:15]([CH3:22])([CH3:21])[C:16]([O:18][CH2:19]C)=[O:17])[C:13]2[C:12]3[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=3[N:6]=[CH:5][C:4]=2[N:3]=[CH:2]1.C1C=C(Cl)C=C(C(OO)=O)C=1.ClC(Cl)(Cl)C([N:38]=C=O)=O.[N-]=C=O.C[O-].[Na+]>>[NH2:38][C:5]1[C:4]2[N:3]=[CH:2][N:1]([CH2:14][C:15]([CH3:22])([CH3:21])[C:16]([O:18][CH3:19])=[O:17])[C:13]=2[C:12]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[N:6]=1参加物
反応条件
- 温度
- 0 °C
実験手順
A modification of the methods described in Part B of Example 60 was used to treat ethyl 3-(1H-imidazo[4,5-c]quinolin-1-yl)-2,2-dimethylpropanoate (4.3 g, 14 mmol) with mCPBA (6.3 g of 77% pure material), followed by trichloroacetyl isocyanate (2.0 mL, 17 mmol). The reaction with the isocyanate was stirred for two hours before the addition of additional trichloroacetyl isocyanate (1.0 mL) and stirring for an additional two hours. After the reaction with sodium methoxide (11 mL of 25% in methanol), the solvent was removed under reduced pressure. The residue was mixed with methanol (25 mL), and the mixture was cooled to 0° C. and filtered to isolate 1.61 g of methyl 3-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)-2,2-dimethylpropanoate as a solid. The filtrate was concentrated under reduced pressure, and the residue was mixed with saturated aqueous sodium bicarbonate (100 mL). A precipitate formed, was isolated by filtration, and was mixed with concentrated hydrochloric acid to adjust to pH 7. The precipitate was again isolated by filtration and dissolved in dichloromethane. The resulting solution was dried over potassium carbonate, filtered, and concentrated under reduced pressure to provide an additional 1.51 g of methyl 3-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)-2,2-dimethylpropanoate as an oil.
後処理
- customthe solvent was removed under reduced pressure
- additionThe residue was mixed with methanol (25 mL)
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-228d0061b48a44ce82c3c7340d891e63
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08697873B2
反応ノート
読み込み中…