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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 460536생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/460536

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl iodideHCID 6328—
반응물Ammonium ChlorideHCID 25517—
반응물Propyl IsothiocyanateHCID 69403—
반응물6-(3-Phenylamino-4-aminophenyl)oxyhexanoic acid methyl esterHCID 12043085—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물6-[[1-Phenyl-2-propylamino-1H-benzimidazol-6-yl]oxy]Hexanoic Acid Methyl EsterHCID 10200735—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196202B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-f98b9b517ccf4f888b9a125c52b6dba9
출처 메모uspto-grants-2007_03