돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41554생성일: 2026년 10월 24일

Diisopropylethylamine → 9-(Quinoxalin-2-yl)-2,9-diazaspiro[5.5]undecan-1-one

https://huagongshe.com/ko/reaction/41554

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-ChloroquinoxalineHCID 238938—
반응물2,9-Diazaspiro[5.5]undecan-1-one trifluoroacetateHCID 46861535—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매EthanolHCID 702—
생성물9-(Quinoxalin-2-yl)-2,9-diazaspiro[5.5]undecan-1-oneHCID 6725174578.1%

반응 조건

온도160 °C

반응 단계

The mixture of 2,9-diazaspiro[5.5]undecan-1-one TFA salt ([1190586-22-1], 1.0 g, 3.5 mmol), 2-chloroquinoxaline ([1448-87-9], 0.77 g, 4.6 mmol), DIPEA (3.7 ml, 21 mmol) and DMAP (22 mg, 0.18 mmol) in ethanol (10 ml) was placed in a microwave tube. The tube was sealed and the suspension was heated at 160° C. for 2 h under microwave conditions. The mixture was filtered and the residue washed with ethanol. The filtrate was concentrated and the precipitate filtered and washed with ethanol. The combined solid material was dissolved in ethyl acetate, washed with water and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford 0.81 g (77%) of the title compound as a pale yellow solid which was not further purified. [1H NMR (400 MHz, DMSO-d6) ♀ ppm 8.79 (s, 1H), 7.78 (d, J=7.8 Hz, 1H), 7.53-7.58 (m, 2H), 7.31-7.39 (m, 2H), 4.22 (dt, J=13.5, 4.4 Hz, 2H), 3.37-3.49 (m, 2H), 3.06-3.15 (m, 2H), 1.91-2.05 (m, 2H), 1.75-1.83 (m, 2H), 1.65-1.75 (m, 2H), 1.44-1.55 (m, 2H); LCMS RtB=2.80 min, [M+H]+=297.2].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530648B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-2c3365bfdad04b4d927b0e6172fba61b
출처 메모uspto-grants-2013_09