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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1617생성일: 2026년 10월 23일

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → N-Carboxy-[1-butyl-4-piperidinylmethyl]-carbazole

https://huagongshe.com/ko/reaction/1617

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물N-Carboxy-[1-butyl-4-piperidinylmethyl]-1,2,3,4,4a,9a-hexahydrocarbazoleHCID 67817506—
용매ChloroformHCID 6212—
생성물N-Carboxy-[1-butyl-4-piperidinylmethyl]-carbazoleHCID 19691861—

반응 단계

N-Carboxy-[1-butylpiperidin-4-ylmethyl]-1,2,3,4,4a,9a-hexahydrocarbazole (0.530 g, 1.32 mmol) was dissolved in chloroform (25 ml) and treated with 2,3-dichloro-5,6-dicyano-1, 4-benzoquinone (0.329 g, 1.58 mmol) with stirring. The mixture was heated to reflux for 12 hours, cooled, and more 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (0.329 g 1.58 mmol) added with stirring. The mixture was heated to reflux for 12 hours, cooled and evaporated under reduced pressure. The residue was purified by Silica-gel chromatography, eluting with 2%MeOH/CHCl3 to give the title compounds as 3:1 mixture. The mixture was separated by preparative HPLC using a Waters Micro Bondapak C18 (300 mm×7.8 mm) column and eluting with 75:25 MeCN: 0.1M Ammonium Acetate (pH 5.0).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726187
출처 데이터셋uspto-grants-1998_03
ORD IDord-4f6016db03934931aac4c3c4d6a66417
출처 메모uspto-grants-1998_03