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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 430949생성일: 2026년 10월 24일

Anthranilic Acid → 2-(3-chlorophenylamino)-6-octyl-4H-3,1-benzoxazin-4-one

https://huagongshe.com/ko/reaction/430949

반응식

참여 물질

역할이름HCID투입량
반응물Anthranilic AcidHCID 227—
반응물UreaHCID 1176—
반응물Benzene, 1-chloro-3-isocyanato-HCID 17968—
반응물2H-1,2-Benzoxazin-3(4H)-oneHCID 19937448—
용매TetrahydrofuranHCID 8028—
생성물2-(3-chlorophenylamino)-6-octyl-4H-3,1-benzoxazin-4-oneHCID 18762630—

반응 단계

The anthranilic acid (200 mg, 0.8 mmol) was dissolved in anhydrous THF (1 ml), and to this was added 3-chlorophenylisocyanate (117 μl, 0.96 mmol). The mixture was stirred for 3 h before being concentrated. The residue was partitioned between water and ethyl acetate. The organic layer was washed with 5% aqueous citric acid, saturated aqueous sodium bicarbonate and brine then dried (MgSO4) and concentrated to give an orange solid. This was purified by flash chromatography on silica (15% EtOAc/hexane to 100% EtOAc, then 10% EtOH/EtOAc) which gave, in order of elution, the benzoxazinone (18 mg, 0.05 mmol); δH (400 MHz, CDCl3) 0.77-0.82 (3H, m, Me), 1.19-1.24 (10H, m, 5×CH2), 1.55-1.57 (2H, m, ArCH2CH2), 2.56-2.62 (2H, m, ArCH2), 7.00-7.32 (4H, m, 3×ArH, NH), 7.40-7.49 (2H, m, 2×ArH), 7.81-7.83 (2H, m, ArH); m/z (ES+) 385 (MH+) and the urea (160 mg, 0.4 mmol); m/z (ES−) 401 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06656934B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-4003d3bed4964987a4570d398919c426
출처 메모uspto-grants-2003_12