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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1927610생성일: 2026년 10월 25일

2-Ethylbutyric acid → {4-[4-(2-Ethyl-butyrylamino)-2-fluoro-phenyl]-piperazin-1-yl}-phenyl-acetic acid methyl ester

https://huagongshe.com/reaction/1927610

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethylbutyric acidHCID 6915—
반응물Carbonate IonHCID 19660—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물CarbodiimideHCID 160435—
반응물[4-(4-Amino-2-fluoro-phenyl)-piperazin-1-yl]-phenyl-acetic acid methyl esterHCID 69304062—
용매DichloromethaneHCID 6344—
생성물{4-[4-(2-Ethyl-butyrylamino)-2-fluoro-phenyl]-piperazin-1-yl}-phenyl-acetic acid methyl esterHCID 1666733157%

반응 단계

A mixture of 2-ethylbutyric acid (32 μL, 0.22 mmol), polymer-supported carbodiimide (240 mg, 0.29 mmol), and HOBt (33 mg, 0.25 mmol) in DCM (5 mL) was stirred at rt for 15 min. A solution of [4-(4-amino-2-fluoro-phenyl)-piperazin-1-yl]-phenyl-acetic acid methyl ester (50 mg, 0.15 mmol) in DCM (1 mL) was added and the mixture was stirred for 16 h. Polymer-bound tetraalkylammonium carbonate (PB-carbonate; 250 mg, 0.77 mmol) was added and the mixture was stirred for 2 h. The resins were removed by filtration and the filtrate was concentrated to give an oil, which was purified by PTLC to give a peach solid (37 mg, 57%). MS (ESI): mass calcd. for C25H32FN3O3, 441.54; m/z found, 442.5 [M+H]+. 1H NMR (CDCl3): 7.46-7.44 (m, 3H), 7.36-7.33 (m, 3H), 7.19-7.12 (m, 1H), 7.00 (br s, 1H), 6.87 (t, J=9.0, 1H), 4.06 (s, 1H), 3.70 (s, 3H), 3.09-3.08 (m, 4H), 2.64-2.62 (m, 4H), 2.02-1.95 (m, 1H), 1.70-1.67 (m, 2H), 1.56-1.53 (m, 2H), 0.94 (t, J=7.4, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08183239B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-60c4ddcbd4fd4ce590b4c39fd8a1f2f9
출처 메모uspto-grants-2012_05