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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922311Generated: November 2, 2026

N,N-Dimethylglycine → HCID 44124829, compound

https://huagongshe.com/reaction/1922311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantCesium carbonateHCID 10796—
Reactant2-Bromo-5-methylpyridineHCID 564216—
Reactant(S)-N-(5-hydroxy-2,3-dihydro-1H-inden-2-yl)propane-2-sulfonamideHCID 66857149—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 44124829HCID 44124829—

Reaction Steps

N-[(2S)-5-hydroxy-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide (50 mg, 0.196 mmol, Description 3), copper(I) iodide (41.0 mg, 0.215 mmol), 2-bromo-5-methylpyridine (33.7 mg, 0.196 mmol), Cs2CO3 (191 mg, 0.587 mmol) and N,N-dimethylglycine (24.23 mg, 0.235 mmol), in dimethyl sulfoxide (2 ml) were heated under microwave conditions for 30 minutes at 190° C. The reaction mixture was partitioned between EtOAc (10 ml) and water (5 ml). Aqueous was further extracted with DCM (10 ml). The organic solution was dried (Na2SO4) and evaporated under reduced pressure to yield the impure product as a dark brown oil. The product was purified by reverse phase chromatography using MDAP to give the title compound as a solid (17 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173820B2
Source datasetuspto-grants-2012_05
ORD IDord-7bc4ba6ea00049af9d1db61274f5c28d
Source noteuspto-grants-2012_05