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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183724Generated: November 1, 2026

Urea → HCID 9913280, compound

https://huagongshe.com/reaction/2183724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantSodiumHCID 5360545—
ReactantHCID 69705675HCID 69705675—
SolventEthanolHCID 702—
ProductHCID 9913280HCID 9913280—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a flame dried flask is added ethanol (6 mL) and freshly cut sodium metal (62.4 mg, 2.71 mmol). The solution is stirred until homogenous. Recrystallized urea (98 mg, 1.63 mmol) is added and the solution is stirred at room temperature for 5 minutes. 1-{6-[1-(4-Fluoro-phenyl)-1H-indazol-5-yloxy]-pyridin-3-yl}-pyrrolidine-2,2-dicarboxylic acid diethyl ester (0.54 mmol) is added, and the solution is heated to 80° C. for 30 minutes, then cooled to 50° C. and stirred for 16 hours. The reaction is then quenched by the addition of 10 mL water, and 1N hydrochloric acid is added to adjust the pH to 5. The aqueous layer is extracted with ethyl acetate (3×20 mL). The combined ethyl acetate layers are washed with saturated sodium chloride, dried with magnesium sulfate, filtered, and concentrated under vacuum to produce crude product. This material is chromatographed on silica gel (ISCO MPLC purification, 30 minutes, 50-100% ethyl acetate gradient, Biotage flash 40s column) to provide 1-{6-[1-(4-Fluoro-phenyl)-1H-indazol-5-yloxy]-pyridin-3-yl}-1,7,9-triaza-spiro[4.5]decane-6,8,10-trione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900201B2
Source datasetuspto-grants-2005_05
ORD IDord-679d36473bc24968b35b083474dc1155
Source noteuspto-grants-2005_05