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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213110Generated: October 31, 2026

2-Aminothiazole → HCID 11723599, compound

https://huagongshe.com/reaction/2213110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant2-Bromo-1-(3-methoxy-4-pyridin-2-ylphenyl)propan-1-oneHCID 21956519—
SolventEthanolHCID 702—
ProductHCID 11723599HCID 11723599—

Reaction Steps

A solution of 2-bromo-1-(3-methoxy-4-pyridin-2-ylphenyl)propan-1-one (153 mg, 0.50 mmol) and 2-aminothiazole (50 mg, 0.50 mmol) in ethanol (1 mL) was heated to reflux for 12 h, then concentrated. The residue was dissolved in ethyl acetate (25 mL) and washed with saturated aqueous NaHCO3 (10 mL) and brine (10 mL). The organic layer was dried (MgSO4), concentrated and purified by flash column chromatography on silica gel eluting with EtOAc:hexanes (2:1 to 1:0) to afford 6-(3-methoxy-4-pyridin-2-ylphenyl)-5-methylimidazo[2,1-b][1,3]thiazole. 1H NMR (CDCl3, 500 MHz) δ 8.73 (m, 1H), 7.94 (d, 1H), 7.88 (d, 1H), 7.73 (dt, 1H), 7.52 (s, 1H), 7.35 (dd, 1H), 7.34 (dd, 1H), 7.22 (m, 1H), 6.86 (dd, 1H), 3.98 (s, 3H), 2.66 (s, 3H) ppm. MS (ESI) 322 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105533B2
Source datasetuspto-grants-2006_09
ORD IDord-fbe28aef313741ad8dca150a599a7cc7
Source noteuspto-grants-2006_09