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HRID 239773作成日:2026年10月24日

2-Amino-2-phenylacetamide → 3-{[(1S)-2-Amino-2-oxo-1-phenylethyl]amino}propane-1-sulfonic acid

https://huagongshe.com/ja/reaction/239773

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-2-phenylacetamideHCID 12791—
反応物Propane sultoneHCID 14264—
溶媒TetrahydrofuranHCID 8028—
溶媒1,4-DioxaneHCID 31275—
生成物3-{[(1S)-2-Amino-2-oxo-1-phenylethyl]amino}propane-1-sulfonic acidHCID 1603606038.9%

反応手順

To a solution of D-Phenylglycine amide (850 mg, 7.5 mmol) in tetrahydrofuran (10 mL) and 1,4-dioxane (4 mL) was added 1,3-propanesultone (818 mg, 6.8 mmol). The solution stirred at reflux for 2 hours. The reaction was cooled to room temperature. The solid was collected by filtration and washed with acetone (2×20 mL). The solid was dissolved in 50% water/EtOH mL). Dowex Marathon C ion exchange resin (strongly acidic) was added to the solution. The suspension was stirred for 15 minutes before the resin was removed by filtration. The filtrate was evaporated under reduced pressure. The solid was suspended in acetone (50 mL), filtered and dried in the vacuum oven (50° C.), affording the title compound (720 mg, 34%). 1H NMR (D2O, 500 MHz) δ ppm 7.38 (m, 5H), 4.92, (s, 1H), 3.00 (m, 1H), 2.90 (m, 1H), 2.78 (m, 2H), 1.97 (m, 2H). 13C (D2O, 125 MHz) δ ppm 170.14, 130.95, 130.24, 129.94, 128.74, 63.40, 47.99, 44.92, 21.27. [α]D=+106° (c=0.0016 in water), ES-MS 273 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642801B2
出典データセットuspto-grants-2014_02
ORD IDord-497ddc527a5543ecacbd5f8fdb4364ff
出典メモuspto-grants-2014_02