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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023308Generated: November 1, 2026

Potassium Carbonate → 7-chloro-5-(4-(hydroxymethyl)thiazol-2-ylamino)-3-methylpyrido[4,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/1023308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Amino-1,3-thiazol-4-yl)methanolHCID 16766621—
Reactant5,7-dichloro-3-methylpyrido[4,3-d]pyrimidin-4(3H)-oneHCID 58092948—
Solvent1,4-DioxaneHCID 31275—
Product7-chloro-5-(4-(hydroxymethyl)thiazol-2-ylamino)-3-methylpyrido[4,3-d]pyrimidin-4(3H)-oneHCID 86667981—

Reaction Conditions

Temperature80 °C

Reaction Steps

(2-aminothiazol-4-yl)methanol (70.0 mg, 0.54 mmol) and K2CO3 (148.6 mg, 1.08 mmol) were added to a solution of 5,7-dichloro-3-methylpyrido[4,3-d]pyrimidin-4(3H)-one (123.7 mg, 0.54 mmol) in 1,4-dioxane (2.7 mL). The reaction mixture was heated at 80° C. overnight, cooled down, quenched with H2O (20 mL) and extracted with ethyl acetate (3×5 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered, concentrated, and purified by silica gel chromatography (10% methanol/dichloromethane) to give 7-chloro-5-(4-(hydroxymethyl)thiazol-2-ylamino)-3-methylpyrido[4,3-d]pyrimidin-4(3H)-one as a white solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722692B2
Source datasetuspto-grants-2014_05
ORD IDord-517d9d400b8349ce8496b034e21a2a6c
Source noteuspto-grants-2014_05