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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968688Generated: October 26, 2026

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

https://huagongshe.com/reaction/1968688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-thiopseudoureaHCID 5142—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
Reactant1-(2,3-Diamino-5-pyridin-3-yl-phenyl)-propan-1-oneHCID 17984912—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 178473458HCID 178473458—

Reaction Conditions

Temperature90 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426426B2
Source datasetuspto-grants-2013_04
ORD IDord-dff4534d09ba48e6a504acca5ec03f4e
Source noteuspto-grants-2013_04