돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1876800생성일: 2026년 10월 27일

1,4-Diiodobutane → (4aRS,5SR,8aRS)-1-benzyl-5-(pyrrolidin-1-yl)perhydroquinoxaline-2,3-dione

https://huagongshe.com/reaction/1876800

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DiiodobutaneHCID 12337—
반응물Sodium BicarbonateHCID 516892—
반응물(4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dioneHCID 68777664—
용매AcetonitrileHCID 6342—
생성물(4aRS,5SR,8aRS)-1-benzyl-5-(pyrrolidin-1-yl)perhydroquinoxaline-2,3-dioneHCID 68777117—

반응 단계

(4aRS,5SR,8aRS)-5-Amino-1-benzylperhydroquinoxaline-2,3-dione (3.06 g, 11.2 mmol) was dissolved in CH3CN (300 ml). NaHCO3 (6.4 g, 76.2 mmol) and 1,4-diiodobutane (13.9 g, 44.8 mmol, 5.9 ml) were added and the mixture was heated under reflux for 18 hours. NaHCO3 was separated off with a blue-band filter (Schleicher&Schuell) and the yellow solution was concentrated in vacuo. The solid was taken up in CH2Cl2 and the mixture was extracted by shaking three times with HCl (1 N). The aqueous phase was then brought to pH 8 with NaOH (2 N) and extracted by shaking three times with CH2Cl2. The organic phases were dried over Na2SO4 and evaporated in vacuo. A pale yellow solid was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309725B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-f8523a2b440a489c84e2be6a3be9cf77
출처 메모uspto-grants-2012_11