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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82890Generated: October 26, 2026

Acetonitrile → HCID 66740793, compound

https://huagongshe.com/reaction/82890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(2-(2-amino-3-benzyl-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamideHCID 56837046—
CatalystWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 66740793HCID 66740793—

Reaction Steps

To N-(2-(2-amino-3-benzyl-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide (35.4 mg, 0.083 mmol; see example 193), 1,3-dibromopropane and potassium carbonate(12.62 mg, 0.091 mmol) in water (1 mL)+1 drop acetonitrile were added. Microwave at 120° C. for 20 min. Evaporated acetonitrile, re-dissolved in dichloromethane and extracted with water and brine, dried over sodium bicarbonate, filtered and evaporated to obtain the crude product and was purified by flash silica gel chromatography on 4 g SiO2-cartridge using 10% methanol in dichloromethane to obtain N-(2-(2-(azetidin-1-yl)-3-benzyl-2,3-dihydro-1H-inden-5-yloxy)ethyl)-1-methyl-1H-imidazole-4-sulfonamide as a clear glass. m=3.1 mg (8%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846743B2
Source datasetuspto-grants-2014_09
ORD IDord-93a4b76f0fb844658395d28745c952c7
Source noteuspto-grants-2014_09