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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 494710생성일: 2026년 10월 26일

2-tert-Butyl-1,3-diisopropylisourea → 4-(4-Bromo-2-chlorophenylamino)-6-chloronicotinic acid tert-butyl ester

https://huagongshe.com/reaction/494710

반응식

참여 물질

역할이름HCID투입량
반응물2-tert-Butyl-1,3-diisopropylisoureaHCID 11041782—
반응물4-(4-Bromo-2-chlorophenylamino)-6-chloronicotinic acid hydrochloride saltHCID 86596777—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-(4-Bromo-2-chlorophenylamino)-6-chloronicotinic acid tert-butyl esterHCID 86596778107.3%

반응 단계

2-tert-Butyl-1,3-diisopropylisourea (8.04 g, 40.1 mmol) was added to a mixture of 4-(4-bromo-2-chlorophenylamino)-6-chloronicotinic acid hydrochloride salt (24) (2.91 g, 7.31 mmol) in THF (165 mL). After stirring for 2 hours at room temperature and 30 minutes at reflux, the reaction mixture was cooled to room temperature and diluted with EtOAc. The organic layer was washed with 10% K2CO3 and brine, dried (Na2SO4) and concentrated. The resulting residue was dissolved in CH2Cl2 and filtered. The filtrate was concentrated and purified by flash column chromatography using the Biotage system (CH2Cl2) to give the desired product (40) (3.28 g, 78%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07538120B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-b9925329c8134f9fbab4bddce9e963e1
출처 메모uspto-grants-2009_05