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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12257생성일: 2026년 10월 25일

2-Methyl-2-thiopseudourea → HCID 178473458, 화합물

https://huagongshe.com/reaction/12257

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-thiopseudoureaHCID 5142—
반응물Ethyl chloroformateHCID 10928—
반응물Sodium HydroxideHCID 14798—
반응물1-(2,3-Diamino-5-pyridin-3-yl-phenyl)-propan-1-oneHCID 17984912—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물HCID 178473458HCID 178473458—

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727992B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-7c5490cbc6894f5eace522a61c214842
출처 메모uspto-grants-2010_06