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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922301Generated: November 2, 2026

N,N-Dimethylglycine → N-[(2S)-5-(2-pyridinyloxy)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide

https://huagongshe.com/reaction/1922301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
Reactant2-BromopyridineHCID 7973—
ReactantCesium carbonateHCID 10796—
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—
ProductN-[(2S)-5-(2-pyridinyloxy)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamideHCID 4412472032.4%

Reaction Conditions

Temperature190 °C

Reaction Steps

A reaction mixture of N-[(2S)-5-hydroxy-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide (100 mg, 0.39 mmol, Description 3), 2-bromopyridine (62 mg, 0.39 mmol), caesium carbonate (382 mg, 1.17 mmol), copper(I) iodide (82 mg, 0.43 mmol) and N,N-dimethylglycine (49 mg, 0.47 mmol) in DMSO (1.5 ml) was heated in a microwave at 190° C. for 30 minutes. The resulting mixture was then partitioned between dichloromethane and water and the organic solution was dried (MgSO4) and evaporated under reduced pressure to yield the crude product. The crude product was purified using MDAP. The resulting solution was diluted with saturated aqueous sodium bicarbonate solution and extracted with dichloromethane. The organic solution was dried (MgSO4) and evaporated under reduced pressure to obtain the title compound as a yellow gum (42 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173820B2
Source datasetuspto-grants-2012_05
ORD IDord-b3067db738094521aab945ce0fb4d209
Source noteuspto-grants-2012_05