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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60440생성일: 2026년 10월 24일

Triethylamine → 5-Bromo-2-(3-(3-methoxy-3-oxopropyl)ureido)nicotinic acid

https://huagongshe.com/ko/reaction/60440

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물monoMethyl succinateHCID 77487—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물2-Amino-5-bromonicotinic acidHCID 737445—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물5-Bromo-2-(3-(3-methoxy-3-oxopropyl)ureido)nicotinic acidHCID 11887545658.9%

반응 단계

To a solution of 4-methoxy-4-oxobutanoic acid (14.6 g, 110.6 mmol) in toluene (530 mL) was added diphenylphosphoryl azide (30.4 g, 110.5 mmol) followed by triethylamine (18.3 g, 181.2 mmol). The reaction was stirred at RT for 30 min then 2-amino-5-bromonicotinic acid (15.9 g, 73.61 mmol) was added. The reaction was refluxed for 6 h, cooled to RT then diluted with EA (530 mL) and washed with brine (2×300 mL). The combined aqueous layers were acidified to PH 5 by adding aq. 2N HCl and a solid formed which was filtered off. The solid was dried to give 5-bromo-2-(3-(3-methoxy-3-oxopropyl)ureido)nicotinic acid (15 g, 39.3% yield) as pale yellow solid. LCMS: MH+ 347 and TR=1.047 min. Used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440972B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-8209793ed19746dea5047f1b9397dc90
출처 메모uspto-grants-2016_09