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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350409생성일: 2026년 10월 25일

Water → ethyl 3-[N'-(2-bromophenyl)ureido]-2-methoxy-6-pyridylacetate

https://huagongshe.com/reaction/350409

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Bromophenyl isocyanateHCID 137097—
반응물Ethyl 3-amino-2-methoxy-6-pyridylacetateHCID 69334098—
용매TetrahydrofuranHCID 8028—
생성물ethyl 3-[N'-(2-bromophenyl)ureido]-2-methoxy-6-pyridylacetateHCID 6933326893.1%

반응 단계

To a stirred solution of ethyl 3-amino-2-methoxy-6-pyridylacetate (1.61 g, 7.66 mmol) in THF (10 ml) were added 2-bromophenylisocyanate (948 ml, 7.66 mmol) and Et3 N (107 ml, 0.776 mmol). After stirring overnight, the mixture was poured into H2O (100 ml) and extracted with CHCl3-MeOH (4:1, 2×200 ml). The combined extracts were dried over MgSO4 and evaporated. The residue was recrystallized from CHCl3-MeOH-hexane to give ethyl 3-[N′-(2-bromophenyl)ureido]-2-methoxy-6-pyridylacetate (2.91 g, 93%) as a colorless crystalline powder. mp 160–163° C.; 1H-NMR (DMSO-d6) δ 1.19 (dt, J=7.1, 0.7 Hz, 3 H), 3.69 (s, 2 H), 3.95 (s, 3 H), 4.07–4.13 (m, 2 H), 6.90 (d, J=7.8 Hz, 1 H), 6.99 (t, J=7.8 Hz, 1 H), 7.33 (t, J=7.8 Hz, 1 H), 7.61 (d, J=7.8 Hz, 1 H), 7.96 (dd, J=7.8, 1.5 Hz, 1 H), 8.31 (d, J=7.8 Hz, 1 H), 8.82 (s, 1 H), 9.12 (s, 1 H); MS (FAB) m/z 408 (M+), 410 (M++2); Anal. Calcd for C17H18BrN3O4.0.25 H2O: C, 49.47; H, 4.52; 9.96. Found: C, 49.34; H, 4.48; N, 9.96.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179819B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-ea157780ba05440c85acfde2ec47048b
출처 메모uspto-grants-2007_02