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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843784Generated: November 2, 2026

Thiourea → HCID 58442382, compound

https://huagongshe.com/reaction/1843784

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, 1 H), 9.00 (brs, 1 H), 6.64 (s, 2 H), 6.22 (s, 1 H), 4.04-4.05 (m, 2 H), 3.54-3.56 (m, 2 H), 3.37 (s, 3 H), 2.19 (s, 6 H), 2.03-2.06 (m, 2 H); ESI-MS m/z 293.8 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946268B2
Source datasetuspto-grants-2015_02
ORD IDord-f3bcd1b943bf48e1bfdbbb342f1cac16
Source noteuspto-grants-2015_02