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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468841Generated: November 1, 2026

N,N'-Dimethylethylenediamine → 2-{4-[(1R,2R)-2-({[4-(cyclopropylsulfonyl)benzyl]oxy}methyl)cyclopropyl]piperidin-1-yl}-5-ethylpyrimidine

https://huagongshe.com/reaction/1468841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantSodium cyclopropanesulfinateHCID 42643363—
Reactant2-[4-((1R,2R)-2-{[(4-bromobenzyl)oxy]methyl}cyclopropyl)piperidin-1-yl]-5-ethyl pyrimidineHCID 71135272—
SolventDimethyl SulfoxideHCID 679—
Product2-{4-[(1R,2R)-2-({[4-(cyclopropylsulfonyl)benzyl]oxy}methyl)cyclopropyl]piperidin-1-yl}-5-ethylpyrimidineHCID 86717791—

Reaction Conditions

Temperature120 °C

Reaction Steps

The product of example 54 (step A) (100 mg, 0.2 mmol), sodium cyclopropanesulfinate (36 mg, 0.28 mmol), copper (I) trifluoromethanesulfonate benzene complex (6 mg, 0.012 mmol), and N,N′-dimethylethylenediamine (2 mg, 0.02 mmol) were dissolved in DMSO (1 mL), and the solution was heated at 120° C. The solution was partitioned between water and Et2O. The aqueous layer was extracted with Et2O. The combined organic layers were washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. The residue was purified via silica gel column chromatography (2/1 EtOAc/hexanes) to provide the title compound. MS (ESI) m/z 456 [M+H]+. GPR119 Human EC50: 1.2 nM

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006228B2
Source datasetuspto-grants-2015_04
ORD IDord-95f3e728e20540ef9b914e06b1247593
Source noteuspto-grants-2015_04