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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1045972생성일: 2026년 10월 25일

1,1'-Carbonyldiimidazole → 2-amino-N,6-dimethoxybenzamide

https://huagongshe.com/reaction/1045972

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물DiisopropylethylamineHCID 81531—
반응물2-Amino-6-methoxybenzoic AcidHCID 2735357—
용매TetrahydrofuranHCID 8028—
생성물2-amino-N,6-dimethoxybenzamideHCID 5695165933.9%

반응 조건

온도21 °C

반응 단계

A mixture of 2-amino-6-methoxybenzoic acid (4.6 g, 27.52 mmol) and carbonyl-1,1′-dimidazole (5.35 g, 33.02 mmol) in THF (70 ml) was stirred at 21° C. under nitrogen for 3 days. N,N-diisopropyl-N-ethyl-amine (1.667 ml, 9.57 mmol) and O-methylhydroxylaminehydrochloride (0.545 ml, 7.18 mmol) were added. The solution was heated to 50° C. for 3 hours. After cooling and concentration under vacuum, the reaction mixture was diluted with EtOAc, washed with a saturated aqueous solution of sodium hydrogencarbonate, water and brine, dried over magnesium sulfate, concentrated under vacuum. The residue was purified by flash chromatography on silica gel eluting with 10 to 20% EtOAc in DCM to afford 2-amino-N,6-dimethoxybenzamide (318 mg, 33.9%) as a white solid. Mass spectrum: MH+ 197; NMR Spectrum: (DMSOd6) 3.67 (s, 3H), 3.71 (s, 3H), 5.57 (bs, 2H), 6.19 (d, 1H), 6.31 (d, 1H), 7.02 (dd, 1H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569298B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-4eeda08fd5ba448a9af5234e19039102
출처 메모uspto-grants-2013_10