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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2422317생성일: 2026년 10월 27일

Hydrochloric Acid → Methyl 3-{4-[(4-{[(4-isopropyl-1,3-thiazol-2-yl)(3-methylbutyl)amino]methyl}benzyl)oxy]phenyl}propanoate

https://huagongshe.com/reaction/2422317

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물Methyl 3-(4-([4-(chloromethyl)benzyl]oxy)phenyl)propanoateHCID 23082857—
반응물4-isopropyl-N-(3-methylbutyl)-1,3-thiazol-2-amineHCID 23083099—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Methyl 3-{4-[(4-{[(4-isopropyl-1,3-thiazol-2-yl)(3-methylbutyl)amino]methyl}benzyl)oxy]phenyl}propanoateHCID 5754185830.4%

반응 단계

A mixture of 4-isopropyl-N-(3-methylbutyl)-1,3-thiazol-2-amine (313 mg), sodium hydride (60% oil, 50 mg) and N,N-dimethylformamide (5 mL) was stirred at room temperature for 1 hr. Methyl 3-(4-{[4-(chloromethyl)benzyl]oxy}phenyl)propanoate (318 mg) was added to the reaction mixture, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water, acidified with 1N aqueous hydrochloric acid solution, and extracted with ethyl acetate. The ethyl acetate layer was dried using Presep Dehydration tube (manufactured by Wako Pure Chemical Industries, Ltd.), and concentrated. The residue was purified by preparative HPLC (gradient cycle A) to give the title compound (150 mg, yield 28%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07960369B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-8f63154f9215437d896ab3bd116e09bb
출처 메모uspto-grants-2011_06