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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 605682생성일: 2026년 10월 24일

Bromoacetic Acid → 2-bromo-N-[1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-yl]acetamide

https://huagongshe.com/ko/reaction/605682

반응식

참여 물질

역할이름HCID투입량
반응물Bromoacetic AcidHCID 6227—
반응물DiisopropylethylamineHCID 81531—
반응물PyBOPHCID 2724699—
반응물1-({3,4-Difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amineHCID 16221889—
용매DimethylformamideHCID 6228—
생성물2-bromo-N-[1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-yl]acetamideHCID 6705159382%

반응 단계

A solution of 1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amine (100 mg, 0.22 mmol), PyBOP (131 mg, 0.25 mmol), N,N-diisopropylethylamine (80 μL, 0.44 mol) and bromoacetic acid (35 mg, 0.25 mmol) in dimethylformamide (1 mL) was stirred at room temperature for 15 hours. The reaction mixture was concentrated in vacuo and the resultant residue was purified by column chromatography eluting with 80% ethyl acetate in hexanes to afford 2-bromo-N-[1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-yl]acetamide (102 mg, 82% yield) as a white foam. MS (EI) for C18H14BrF3IN3O2: 568.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915250B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-d50041f524db4061b8c456d72ffa5b13
출처 메모uspto-grants-2011_03