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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1469729생성일: 2026년 10월 25일

Diisopropylethylamine → N-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amine

https://huagongshe.com/reaction/1469729

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물(4,4-Difluorocyclohexyl)amineHCID 3847030—
반응물4-Chloro-8-nitroquinazolineHCID 11458471—
용매IsopropanolHCID 3776—
생성물N-(4,4-difluorocyclohexyl)-8-nitroquinazolin-4-amineHCID 7167805061.2%

반응 단계

A solution of 4-chloro-8-nitroquinazoline (Intermediate-7, step 2, 200 mg, 0.954 mmol), 4,4-difluorocyclohexanamine (491 mg, 2.86 mmol) and DIPEA (367 mg, 2.86 mmol) in iPrOH (2 mL) was heated in a sealed tube at 80° C. for 2 h. Then the reaction mixture was quenched with water at rt and was extracted with CHCl3. The organic layer was separated, dried, filtered and concentrated. The concentrate was purified by column chromatography using 3-5% EtOAc in CHCl3 to afford 180 mg of the title product. 1H NMR (300 MHz, DMSO d6): δ 8.59-8.55 (m, 2H), 8.43-8.40 (d, J=7.2 Hz, 1H), 8.27-8.25 (d, J=7.8 Hz, 1H), 7.69-7.63 (t, J=7.8 Hz, 1H), 4.41 (m, 1H), 2.26-2.00 (m, 6H), 1.75-1.71 (m, 2H); MS (m/z): 309.18 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09006257B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-0921096d044e42d59ec9c1b94892f827
출처 메모uspto-grants-2015_04