돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1043785생성일: 2026년 10월 25일

Triethylamine → 3-Amino-6-(2-(pyrrolidin-1-yl)ethoxy)quinoline

https://huagongshe.com/reaction/1043785

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Nitro-6-(2-(pyrrolidin-1-yl)ethoxy)quinolineHCID 59507599—
촉매PalladiumHCID 23938—
용매Ethyl AcetateHCID 8857—
생성물3-Amino-6-(2-(pyrrolidin-1-yl)ethoxy)quinolineHCID 59507982—

반응 단계

3-Nitro-6-(2-(pyrrolidin-1-yl)ethoxy)quinoline (134 mg, 0.46 mmol) was dissolved in EtOAc (10 mL) and the solution was sparged with N2 for several minutes. Triethylamine (0.065 mL, 0.46 mmol) was then added followed by a catalytic amount of 10% Pd/C. Sparging with N2 was repeated after each addition. A balloon of H2 was connected to the reaction flask and the reaction mixture was stirred at room temperature under H2 atmosphere for 48 hours. The mixture was then filtered through a Celite pad and concentrated to obtain crude 3-amino-6-(2-(pyrrolidin-1-yl)ethoxy)quinoline, which was used as is in the next reaction. LC/MS (m/z): 258.1 (MH+), Rt 0.33 minutes.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08563549B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-1260b52ca94a471592548e362ef93802
출처 메모uspto-grants-2013_10