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HRID 460536作成日:2026年10月27日

Hydrochloric Acid → 6-[[1-Phenyl-2-propylamino-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl Ester

https://huagongshe.com/reaction/460536

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Methyl iodideHCID 6328—
反応物Ammonium ChlorideHCID 25517—
反応物Propyl IsothiocyanateHCID 69403—
反応物6-(3-Phenylamino-4-aminophenyl)oxyhexanoic acid methyl esterHCID 12043085—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物6-[[1-Phenyl-2-propylamino-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl EsterHCID 10200735—

反応手順

200 mg of 6-(3-phenylamino-4-aminophenyl)oxyhexanoic acid methyl ester was dissolved in 2 ml of methanol, the solution was mixed with 90 μl of propylisothiocyanate, and the mixture was heated for 3 hours to 50° C. After cooling, it was mixed with saturated ammonium chloride solution, diluted with water, extracted three times with ethyl acetate, the combined organic phases were washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 140 mg of a thiourea derivative, which was dissolved in 1.5 ml of methanol, was obtained. 0.16 ml of iodomethane was added to this solution, and it was refluxed for 4 hours. After cooling, it was mixed with IN aqueous hydrochloric acid, extracted three times with ethyl acetate, the combined organic phases were washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 72 mg was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196202B2
出典データセットuspto-grants-2007_03
ORD IDord-f98b9b517ccf4f888b9a125c52b6dba9
出典メモuspto-grants-2007_03