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HRID 728836作成日:2026年10月26日

Hydrochloric Acid → 1-[[[4-(1H-Imidazol-1-yl)phenyl]methyl]amino]-3-(2-methylphenoxy)-2-propanol dihydrochloride

https://huagongshe.com/reaction/728836

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HexamethyldisilazaneHCID 13838—
反応物Sodium HydroxideHCID 14798—
反応物o-CRESYL GLYCIDYL ETHERHCID 16640—
反応物4-(Imidazol-1-yl)benzylamineHCID 14739888—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物1-[[[4-(1H-Imidazol-1-yl)phenyl]methyl]amino]-3-(2-methylphenoxy)-2-propanol dihydrochlorideHCID 67689907—

反応手順

Dissolve 1.74 g (10.04 mmol) of 4-(1H-imidazol-1-yl)-benzenemethanamine in 20 mL of dry DMSO under nitrogen. Add 2.44 mL (11.55 mmol) of hexamethyldisilazane and stir at room temperature for 30 min. After this time, add a solution of 1.73 g (10.54 mmol) of 1,2-epoxy-3-(2-methylphenoxy)propane in 10 mL of DMSO and heat in an oil bath at 60° C. for 42 h. Follow the progress of the reaction by thin-layer chromatography on silica gel (acetonitrile: ammonia (aq), 90:10). At the completion of the reaction, add 6 N hydrochloric acid to pH=1 and then add 4 N sodium hydroxide to pH=12. Dilute this basic mixturewith 20 mL of water and extract with 3×75 mL of methylene chloride. Remove the solvent on the rotary evaporator. Purify this residue by flash chromatography using flash silica gel (Baker) and eluting with a solution of acetonitrile: ammonia hydroxide 98:2. Combine pure fractions and removethe solvent on the rotary evaporator. Dissolve this residue in 50 mL of acetonitrile and remove the solvent on the rotary evaporator. Dissolve this residue in 10 mL of methanol and bubble hydrogen chloride through thesolution until pH=1 is reached. Remove the solvent on the rotary evaporatorand recrystallize the solid from 20 mL of isopropanol to provide the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05051423
出典データセットuspto-grants-1991_09
ORD IDord-7714465f0331494c892e535d29bba125
出典メモuspto-grants-1991_09