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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 243625생성일: 2026년 10월 26일

octanedioic acid [4-(3-Nitro-phenyl)-thiazol-2-yl]-amide methyl ester → octanedioic acid [4-(3-Amino-phenyl)-thiazol-2-yl]-amide methyl ester

https://huagongshe.com/reaction/243625

반응식

참여 물질

역할이름HCID투입량
반응물octanedioic acid [4-(3-Nitro-phenyl)-thiazol-2-yl]-amide methyl esterHCID 44550802—
촉매PalladiumHCID 23938—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
생성물octanedioic acid [4-(3-Amino-phenyl)-thiazol-2-yl]-amide methyl esterHCID 4455093072.4%

반응 단계

A suspension of compound 14 (0.391 g, 1 mmol) and Pd/C (10 wt. %, 50 mg) in EtOH and AcOH (20 ml+1 ml) was reacted under hydrogen atmosphere at 50° C. for 2 hours. The catalyst was removed by filtration through a pad of Celite. After removal of the solvent in vacuo, the crude material was dissolved in EtOAc and washed with NaHCO3 solution and brine and dried over Na2SO4. The solvent was removed by rotary evaporation. The crude solid was purified by flash chromatography (EtOAc/hexane, 2:1) to give compound 20 (0.261 g, 72.4%). 1H NMR (300 MHz, CDCl3) δ 11.2 (1H, s), 7.22 (1H, s), 7.20 (1H, s), 7.16 (1H, brs), 7.10 (1H, s), 6.70-6.66 (1H, m), 3.69 (3H, s), 2.28 (2H, t, J=7.4 Hz), 2.06 (2H, dd, J=7.3, 4.7 Hz), 1.61-1.45 (4H, m), 1.22-1.08 (4H, m). 13C NMR (75 MHz, CDCl3) δ 174.6, 171.8, 159.6, 150.1, 147.3, 135.7, 130.2, 116.9, 115.3, 113.0, 108.1, 51.9, 36.1, 34.3, 29.07, 29.01, 25.09, 25.00, 21.4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653278B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-7d7cc4d73072448797ac305437d34c6e
출처 메모uspto-grants-2014_02