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HRID 1857742作成日:2026年10月25日

Hydrochloric Acid → 1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-((2-nitrophenyl)methyl)-

https://huagongshe.com/reaction/1857742

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物2-Nitrobenzyl chlorideHCID 11921—
反応物HCID 178491401HCID 178491401—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-((2-nitrophenyl)methyl)-HCID 47403447.1%

反応手順

To dimethylformamide was added 237 mg of o-nitrobenzyl chloride and 228 mg of potassium iodide under ice-cooling, the mixture was allowed to warm up to room temperature and stirred for 20 minutes. Then, 400 mg of 5-(3,5-dichlorophenylthio)-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazole (101b) was added, followed by addition of 152 mg of potassium carbonate. Then, the mixture was warmed up to 50° C., and allowed to react for 6 hours. After completion of the reaction, the mixture was diluted with water, extracted with diethyl ether, the extract was dried over sodium sulfate, and the solvent was distilled off under reduced pressure. To thus-obtained oil were added 10 ml of ethanol and 20 ml of 36% hydrochloric acid, and the mixture was stirred at 90° C. for 2 hours. After completion of the reaction, the solvent was distilled off under reduced pressure, an aqueous sodium hydrogen carbonate solution was added, extracted with ethyl acetate, the extract was dried over sodium sulfate, and the solvent was distilled off under reduced pressure. The crystals were washed with diethyl ether, filtered, and 195 mg of 5-(3,5-dichlorophenylthio)-2-hydroxymethyl-4-isopropyl-1-(o-nitrobenzyl)-1H-imidazole (103c) was obtained (yield 47%). mp 160-166° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06147097
出典データセットuspto-grants-2000_11
ORD IDord-09f04a4a2f2246b880c961467dee9a15
出典メモuspto-grants-2000_11