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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404281생성일: 2026년 10월 25일

3-Methoxyaniline → Ethyl 5-(2-Hydroxy-3-(3-methoxyphenylamino)propyl)-8-methyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate

https://huagongshe.com/reaction/404281

반응식

참여 물질

역할이름HCID투입량
반응물3-MethoxyanilineHCID 10824—
반응물Lithium BromideHCID 82050—
반응물ethyl 8-Methyl-5-(oxiran-2-ylmethyl)-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylateHCID 58097199—
생성물Ethyl 5-(2-Hydroxy-3-(3-methoxyphenylamino)propyl)-8-methyl-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylateHCID 4685121067.2%

반응 단계

Following a literature procedure (Chakraborti, A. K.; Rudrawar, S.; Kondaskar, A. Eur. J. Org. Chem. 2004, 3597-3600) LiBr (0.001 g, 0.010 mmol) and m-anisidine (0.011 mL, 0.102 mmol) were added to ethyl 8-Methyl-5-(oxiran-2-ylmethyl)-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylate (0.032 g, 0.102 mmol) and stirred vigorously at ambient temperature overnight. Upon completion the reaction was partitioned between EtOAc/H2O, and the organic layer was concentrated to an orange oil. The crude residue was purified by chromatography (SiO2, 0-50% EtOAc/Hexane) to afford the desired product (30 mg, 67%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748473B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-49c4f447ed0a4164b04535d119e5a848
출처 메모uspto-grants-2014_06