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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133745생성일: 2026년 10월 26일

n-(2-Fluoro-4-hydroxyphenyl)acetamide → 3-(4-Acetylamino-3-fluorophenoxy)-N-(4-cyano-3-methylphenyl)-2-hydroxy-2-methylpropionamide

https://huagongshe.com/reaction/133745

반응식

참여 물질

역할이름HCID투입량
반응물n-(2-Fluoro-4-hydroxyphenyl)acetamideHCID 190616—
반응물2-Methyl-oxirane-2-carboxylic acid (4-cyano-3-methylphenyl)amideHCID 45097465—
생성물3-(4-Acetylamino-3-fluorophenoxy)-N-(4-cyano-3-methylphenyl)-2-hydroxy-2-methylpropionamideHCID 67526297—

반응 단계

3-(4-Acetylamino-3-fluorophenoxy)-N-(4-cyano-3-methylphenyl)-2-hydroxy-2-methylpropionamide was prepared as described in Example 1 starting from N-(2-fluoro-4-hydroxyphenyl)acetamide and 2-methyl-oxirane-2-carboxylic acid (4-cyano-3-methylphenyl)amide. 1H NMR (DMSO-d6): 1.41 (3H, s), 2.02 (3H, s), 2.44 (3H, s), 3.95 (1H, d, J=9.8 Hz), 4.26 (1H, d, J=9.8 Hz), 6.21 (1H, bs), 6.72 (1H, m), 6.86 (1H, m),7.56 (1H, m,) 7.69 (1H, d, J=9.0 Hz), 7.78 (1H, dd, J=9.0 Hz and 2.2 Hz), 7.93 (1H, d, J=2.2 Hz), 9.51 (1H, s), 9.99 (1H, bs).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390923B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-e16f61a13d404482b6839223858d160a
출처 메모uspto-grants-2008_06