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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1808248생성일: 2026년 10월 27일

Dimethylformamide → 4-Amino-3-fluoro-N-[2-(4-fluorophenoxy)-2-methylpropyl]benzamide

https://huagongshe.com/reaction/1808248

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물4-Amino-3-fluorobenzoic acidHCID 9971—
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물2-(4-Fluorophenoxy)-2-methylpropan-1-amineHCID 28917627—
생성물4-Amino-3-fluoro-N-[2-(4-fluorophenoxy)-2-methylpropyl]benzamideHCID 57732241—

반응 단계

To a mixture of 4-amino-3-fluorobenzoic acid (200.0 mg, 1.289 mmol) and HBTU (490 mg, 1.3 mmol) in DMF (2 mL, 20 mmol) at 0° C. were added N,N-diisopropylethylamine (0.67 mL, 3.9 mmol) and 2-(4-fluorophenoxy)-2-methylpropan-1-amine (Preparation 91, 280 mg, 1.5 mmol). The reaction mixture was slowly warmed to ambient temperature. The reaction mixture was quenched with an equal volume of saturated aqueous sodium bicarbonate and extracted with ethyl acetate (3×). The combined organic layers were washed successively with water, aqueous lithium chloride, and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified on the Isco (120 g cartridge, chloroform to 12% MeOH in chloroform).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08357711B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-a21d075e470f4516997390ef108200d2
출처 메모uspto-grants-2013_01