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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19046생성일: 2026년 10월 26일

3-(2,3-dichloro-phenoxy)-4-{(1S,3S)-3-ethoxy-1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-butylamino}-but-2-enoic acid ethyl ester → HCID 44252315, 화합물

https://huagongshe.com/reaction/19046

반응식

참여 물질

역할이름HCID투입량
반응물3-(2,3-dichloro-phenoxy)-4-{(1S,3S)-3-ethoxy-1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-butylamino}-but-2-enoic acid ethyl esterHCID 67504248—
용매TetrahydrofuranHCID 8028—
생성물HCID 44252315HCID 4425231536.3%

반응 조건

온도160 °C

반응 단계

3-(2,3-Dichloro-phenoxy)-4-{(1S,3S)-3-ethoxy-1-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-ylcarbamoyl]-butylamino}-but-2-enoic acid ethyl ester (120 mg) was dissolved in tetrahydrofuran (2 mL). The sealed tube was heated in a microwave at 160° C. for 4 h. The resulting solution was concentrated and the residue was purified by reverse phase column chromatography (acetonitrile in water 25% to 100%) to give (2S,4S)-2-[4-(2,3-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-ethoxy-pentanoic acid [1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-amide (40 mg) as a white powder: HR-ES-MS m/z calculated for C24H30Cl2N4O5 [M+H]+ 525.1666, observed 525.1669; 1H NMR (300 MHz, CDCl3) δ ppm 1.14 (br. s., 6H), 1.19-1.30 (m, 6H), 1.88-2.09 (m, 1H), 2.18 (ddd, J=14.7, 9.3, 5.9 Hz, 1H), 3.30-3.46 (m, 1H), 3.54 (br. s., 1H), 3.61-3.77 (m, 1H), 3.94 (s, 2H), 4.14 (d, J=17.8 Hz, 1H), 4.47 (d, J=17.8 Hz, 1H), 4.92 (s, 1H), 5.01 (t, J=6.2 Hz, 1H), 6.68 (d, J=1.5 Hz, 1H), 7.16-7.33 (m, 4H), 7.42 (d, J=7.8 Hz, 1H), 9.35 (br. s., 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f4afa48db1a246a9b0296b29ac2b75a1
출처 메모uspto-grants-2010_06