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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538085Generated: October 27, 2026

Water → 2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester

https://huagongshe.com/reaction/538085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-(methylsulfonyl)pyrimidine-5-carboxylateHCID 254889—
Reactant1-(Naphthalene-2-sulfonyl)-piperazineHCID 703957—
SolventTetrahydrofuranHCID 8028—
Product2-[4-(2-Naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl esterHCID 5884497784%

Reaction Steps

NaH 60% (0.0217 mol) was added portionwise at room temperature to a solution of 1-(2-naphtalenesulfonyl)-piperazine (0.011 mol) in THF (50 ml) under N2 flow. The mixture was stirred at room temperature for 1 hour, then cooled to 0° C. A solution of 2-(methylsulfonyl)-5-pyrimidinecarboxylic acid, ethyl ester (0.014 mol) in THF (30 ml) was added quickly. The mixture was stirred at room temperature for 2 hours, poured out into water and extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered, and the solvent was evaporated. The residue was taken up in diethyl ether. The precipitate was filtered off and dried, yielding 3.92 g (84%) of 2-[4-(2-naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester (interm. 8), melting point>260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865720B2
Source datasetuspto-grants-2014_10
ORD IDord-04ddf9950e6b470aa8729598a55cb8aa
Source noteuspto-grants-2014_10