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HRID 243625作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物octanedioic acid [4-(3-Nitro-phenyl)-thiazol-2-yl]-amide methyl esterHCID 44550802—
触媒PalladiumHCID 23938—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
生成物octanedioic acid [4-(3-Amino-phenyl)-thiazol-2-yl]-amide methyl esterHCID 4455093072.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653278B2
出典データセットuspto-grants-2014_02
ORD IDord-7d7cc4d73072448797ac305437d34c6e
出典メモuspto-grants-2014_02