돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43154생성일: 2026년 10월 25일

Water → 8-(3,5-Dimethoxy-phenyl)-quinoxaline-5-carboxylic acid [5-(4-ethyl-piperazin-1-ylmethyl)-pyridin-2-yl]-amide

https://huagongshe.com/reaction/43154

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TrimethylaluminumHCID 16682925—
반응물5-[(4-Ethyl-1-piperazinyl)methyl]-2-pyridinamineHCID 45489910—
반응물8-(3,5-Dimethoxy-phenyl)-quinoxaline-5-carboxylic acid ethyl esterHCID 66914690—
용매TolueneHCID 1140—
생성물8-(3,5-Dimethoxy-phenyl)-quinoxaline-5-carboxylic acid [5-(4-ethyl-piperazin-1-ylmethyl)-pyridin-2-yl]-amideHCID 5929295835.1%

반응 단계

Trimethyl aluminum (2 M in toluene, 0.37 mL, 0.74 mmol, 2.5 equiv) was added to a mixture of 8-(3,5-dimethoxy-phenyl)-quinoxaline-5-carboxylic acid ethyl ester (Step 115.1) (100 mg, 0.30 mmol) and 5-(4-ethyl-piperazin-1-ylmethyl)-pyridin-2-ylamine (Step 26.1; purified by column chromatography) (78 mg, 0.36 mmol, 1.2 equiv) in toluene (2 mL). The reaction mixture was stirred for 1 h at rt, heated to reflux, stirred for 3 h, allowed to cool, poured onto EtOAc and H2O, and filtered through a pad of celite. The filtrate was extracted with EtOAc. The organic phase was washed with H2O and brine, dried (Na2SO4), filtered and concentrated. The residue was purified by silica gel column chromatography (DCM/MeOH/NH3aq, 94:5:1) followed by reverse-phase preparative HPLC to afford 54 mg of the title compound as a pale yellow solid. Title compound: ESI-MS: 513.2 [M+H]+; tR=3.54 min (System 1); TLC: Rf=0.29 (DCM/MeOH/NH3aq, 94:5:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536175B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-33d127c707d948e392fb565b48665bab
출처 메모uspto-grants-2013_09