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HRID 12257作成日:2026年10月26日

2-Methyl-2-thiopseudourea → HCID 178473458、化合物

https://huagongshe.com/reaction/12257

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-thiopseudoureaHCID 5142—
反応物Ethyl chloroformateHCID 10928—
反応物Sodium HydroxideHCID 14798—
反応物1-(2,3-Diamino-5-pyridin-3-yl-phenyl)-propan-1-oneHCID 17984912—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178473458HCID 178473458—

反応条件

温度90 °C

反応手順

To a mixture of 2-methyl-2-thiopseudourea (109 mg, 0.39 mmol) and ethyl chloroformate (75 μL, 0.78 mmol) in water (2 mL) at 5° C. was added over 40 minutes a 6N aqueous NaOH solution until pH stabilized to 8. The pH was then adjusted to 5 with glacial AcOH. A suspension of 1-(2,3-diamino-5-pyridin-3-yl-phenyl)-propan-1-one (0.30 mmol) in water (5 mL) was subsequently added to the reaction mixture. The reaction was heated at 90° C. for 18 hours, cooled to ambient temperature, and diluted with water (10 mL) and EtOAc (20 mL). The phases were separated and the aqueous layer extracted with EtOAc (3×). The combined organic extracts were washed with brine, dried (MgSO4), filtered, and the filtrate concentrated in vacuo. The crude residue was taken up in DMSO, purified by preparative HPLC, and by flash column chromatography (SiO2; CH2Cl2:MeOH, 1:0 to 19:1). The residue was then converted to the bis-HCl salt to afford the title compound as an off white solid (5.0 mg): HPLC (10 to 90% CH3CN, 8 min.): Rt=3.90 minutes; 1H NMR (CD3OD, 500 MHz) δ 9.39 (d, 1H), 9.07 (d, 1H), 8.93 (d, 1H), 8.48 (d, 1H), 8.28 (d, 1H), 8.25 (dd, 1H), 4.46 (q, 2H), 3.35 (q, 2H), 1.43 (t, 3H), 1.29 (t, 3H); MS (ES+) m/z (M++1) 339.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07727992B2
出典データセットuspto-grants-2010_06
ORD IDord-7c5490cbc6894f5eace522a61c214842
出典メモuspto-grants-2010_06