Dimethyl Sulfoxide → 2-(methoxymethoxy)-3-(6-methoxy-3-oxopyrido[2,3-b]pyrazin-4(3H)-yl)propanal
反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[OH:11][CH2:12][CH:13]([O:28][CH2:29][O:30][CH3:31])[CH2:14][N:15]1[C:20](=[O:21])[CH:19]=[N:18][C:17]2[CH:22]=[CH:23][C:24]([O:26][CH3:27])=[N:25][C:16]1=2.C(N(CC)CC)C>ClCCl>[CH3:31][O:30][CH2:29][O:28][CH:13]([CH2:14][N:15]1[C:20](=[O:21])[CH:19]=[N:18][C:17]2[CH:22]=[CH:23][C:24]([O:26][CH3:27])=[N:25][C:16]1=2)[CH:12]=[O:11]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- -78 °C
実験手順
Oxalyl chloride (0.022 ml, 0.260 mmol) was dissolved in dichloromethane (1 ml), a solution of dimethyl sulfoxide (0.037 ml, 0.521 mmol) in dichloromethane (0.5 ml) was added to the solution at −78° C. and mixed for 30 minutes. While maintaining at −78° C., a solution of 4-[3-hydroxy-2-(methoxymethoxy)propyl]-6-methoxypyrido[2,3-b]pyrazin-3(4H)-one (64 mg, 0.217 mmol) in dichloromethane (3 ml) was added to the reaction solution and the mixture was stirred for 1 hour. While maintaining the temperature at −78° C., triethylamine (0.181 ml, 1.302 mmol) was added to the reaction solution and the mixture was stirred for 30 minutes. The temperature was raised to 0° C., the reaction solution was stirred for 1 hour, then diluted with dichloromethane and washed with water. The organic layer was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure to yield 67 mg (quantitative) of the title compound in the form of a yellow-orange oily product. The product was used as such for next reaction without purification.
後処理
- additionmixed for 30 minutes
- temperatureWhile maintaining the temperature at −78° C.
- stirringthe mixture was stirred for 30 minutes
- temperatureThe temperature was raised to 0° C.
- stirringthe reaction solution was stirred for 1 hour
- washwashed with water
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- customthe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-c58e5549790e4c0ba7043c213edbb547
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08952010B2
反応ノート
読み込み中…