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HRID 1178069作成日:2026年10月27日

3-(4-Hydroxyphenyl)propionic acid → 2-[3-(4-Hydroxyphenyl)propionylamino]acetic acid ethyl ester

https://huagongshe.com/reaction/1178069

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4-Hydroxyphenyl)propionic acidHCID 10394—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物DiisopropylethylamineHCID 81531—
反応物Glycine ethyl ester, hydrochlorideHCID 2723640—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-[3-(4-Hydroxyphenyl)propionylamino]acetic acid ethyl esterHCID 10264158130%

反応手順

DIPEA (390 mg, 0.52 mL, 3.02 mmol) was added to a stirred solution of 3-[4-hydroxy phenyl]propionic acid (100 mg, 0.60 mmol) in DMF (10 mL). HOBT (90 mg, 0.67 mmol) and EDCI.HCl (290 mg, 1.51 mmol) were added at room temperature. After 2 minutes glycine ethyl ester hydrochloride (100 mg, 0.72 mmol) was added. The resulting mixture was stirred at room temperature for 48 hours. Water was then added, and the product was extracted with EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure to afford 196 mg of [3-(4-hydroxy-phenyl) propionylamino]-acetic acid ethyl ester. 1H NMR (CDCL3): δ 7 (d, 2H), 6.65 (d, 2H), 6.0 (bs, 1H), 4.15 (q, 2H), 4.0 (d, 2H), 3.5 (s, 2H), 2.8 (t, 2H), 2.45 (t, 2H), 1.2 (t, 3H), LC-MS purity: 68.23%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07842696B2
出典データセットuspto-grants-2010_11
ORD IDord-d37264a6fbb144a8a5e7942dea211699
出典メモuspto-grants-2010_11