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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480706Generated: November 3, 2026

Thiourea → HCID 58442382, compound

https://huagongshe.com/reaction/1480706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
ReactantHCID 58442430HCID 58442430—
SolventEthanolHCID 702—
ProductHCID 58442382HCID 5844238271%

Reaction Steps

A reaction mixture containing 2-bromo-1-(4-(3-methoxypropoxy)-2,6-dimethylphenyl)ethanone (500.0 mg, 1.6 mmol, 1.0 equiv) and thiourea (126.8 mg, 1.6 mmol, 1.0 equiv) in EtOH (10.0 mL) was heated at reflux for 16 h. The solution was concentrated under reduced pressure, and the residue was re-dissolved in EtOAc (50 mL). The solution was washed with saturated aqueous NaHCO3 (30 mL), dried over MgSO4, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (30% EtOAc in hexanes as eluant) to provide 4-(4-(3-methoxypropoxy)-2,6-dimethylphenyl)thiazol-2-amine (328.9 mg, 1.1 mmol) as yellow solids in 71% yield: 1H NMR (CDCl3, 500 MHz) δ 9.35 (brs, 1H), 9.00 (brs, 1H), 6.64 (s, 2H), 6.22 (s, 1H), 4.04-4.05 (m, 2H), 3.54-3.56 (m, 2H), 3.37 (s, 3H), 2.19 (s, 6H), 2.03-2.06 (m, 2H); ESI-MS m/z 293.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409902B2
Source datasetuspto-grants-2016_08
ORD IDord-48035cd2a1fb429a83a0b37dae5a74da
Source noteuspto-grants-2016_08