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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060632Generated: November 1, 2026

Ethanol → Ethyl 5-amino-2-(6-morpholin-4-ylpyridin-3-yl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/2060632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1,4-DioxaneHCID 31275—
ReactantEthyl 5-[(tert-butoxycarbonyl)amino]-2-(6-morpholin-4-ylpyridin-3-yl)-1,3-thiazole-4-carboxylateHCID 67305664—
SolventHydrochloric AcidHCID 313—
ProductEthyl 5-amino-2-(6-morpholin-4-ylpyridin-3-yl)-1,3-thiazole-4-carboxylateHCID 58335250—

Reaction Steps

Ethyl 5-[(tert-butoxycarbonyl)amino]-2-(6-morpholin-4-ylpyridin-3-yl)-1,3-thiazole-4-carboxylate (634 mg, 1.46 mmol) was taken up in 4 N HCl in dioxane (7.3 ml, 29.2 mmol) and ethanol (5 ml) and stirred at ambient temperature for 20 hours. The mixture was then partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The aqueous layer was extracted twice with ethyl acetate. Combined organics were dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting residue was purified via flash chromatography (silica, 0-100% ethyl acetate/hexanes) to afford the title compound. LRMS (APCI) calc'd for (C15H19N4O3S) [M+H]+, 335.1; found 335.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278335B2
Source datasetuspto-grants-2012_10
ORD IDord-a9a3fb1173344194995455918e56a668
Source noteuspto-grants-2012_10