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HRID 1808939作成日:2026年10月26日

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

https://huagongshe.com/reaction/1808939

反応式

関与物質

役割名称HCID仕込み量
反応物Bromoacetic AcidHCID 6227—
反応物DiisopropylethylamineHCID 81531—
反応物PyBOPHCID 2724699—
反応物1-({3,4-Difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-amineHCID 16221889—
溶媒DimethylformamideHCID 6228—
生成物2-bromo-N-[1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)azetidin-3-yl]acetamideHCID 6705159382%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08362002B2
出典データセットuspto-grants-2013_01
ORD IDord-3389bb29b7a14c288ce2a4358d6b1f3f
出典メモuspto-grants-2013_01