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HRID 31395作成日:2026年10月24日

Ammonium Hydroxide → Methyl 3-[3-(2-methyl-4,5-dihydro-1H-imidazol-1-yl)phenyl]isonicotinate

https://huagongshe.com/ja/reaction/31395

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物Phosphorus pentachlorideHCID 24819—
反応物N-(2-Chloroethyl)acetamideHCID 81815—
反応物Methyl 3-(3-aminophenyl)isonicotinateHCID 11368161—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 3-[3-(2-methyl-4,5-dihydro-1H-imidazol-1-yl)phenyl]isonicotinateHCID 1144930648.3%

反応条件

温度0 °C

反応手順

N-(2-chloroethyl)acetamide (0.32 g) in ethyl acetate (5 ml) was added over 10 min. to a stirred suspension of phosphorus pentachloride (0.55 g) in ethyl acetate (2 ml) at 0° C. under nitrogen to give a clear pale straw solution. After 45 min. at 0° C. a solution of methyl 3-(3-aminophenyl)isonicotinate (0.4 g) in dichloromethane (10 ml) was added over 15 min. at 0-5° C. The mixture was stirred at 0° C. for 10 min. and then allowed to warm up to 20° C. After 3 h the mixture was treated with ammonium hydroxide solution (28%, 5 ml) over 10 min. and stirring continued for ca. 1 h. The layers were allowed to separate, the organic layer was collected, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (dichloromethane:methanol:ammonia=100:10:1, v/v/v) to give 0.25 g (48%) of yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425639B2
出典データセットuspto-grants-2008_09
ORD IDord-507e9c0a8a6647cfa5a69d6b4dee8230
出典メモuspto-grants-2008_09