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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711415Generated: November 1, 2026

Dichloromethane → HCID 178466069, compound

https://huagongshe.com/reaction/711415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCesium carbonateHCID 10796—
Reactant(4-Ethoxy-3-fluorophenyl)boronic acidHCID 2782821—
Reactant4-({(4S)-6-iodo-1-oxo-7-[3-(trifluoromethoxy)phenyl]-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl}methyl)-N,N-dimethyl-1H-imidazole-1-sulfonamideHCID 86732564—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178466069HCID 178466069—

Reaction Conditions

Temperature75 °C

Reaction Steps

(4-ethoxy-3-fluorophenyl)boronic acid (0.072 g, 0.39 mmol), cesium carbonate (0.096 g, 0.3 mmol) and 1,1′-bis(diphenylphosphino)ferrocenepalladium (0.008 g, 0.010 mmol) complex with dichloromethane, were subsequently added to a degassed solution of 4-({(4S)-6-iodo-1-oxo-7-[3-(trifluoromethoxy)phenyl]-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl}methyl)-N,N-dimethyl-1H-imidazole-1-sulfonamide (0.06 g, 0.1 mmol) in 3 ml of 1,4-dioxane and 1 ml of water, under argon. The mixture was heated at 100° for 3 hours in a sealed vial. The reaction was portioned between ethyl acetate and water, the organic layer dried over sodium sulphate and the solvent removed in vacuo. 4-({(4S)-6-(4-ethoxy-3-fluorophenyl)-1-oxo-7-[3-(trifluoromethoxy)phenyl]-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl}methyl)-N,N-dimethyl-1H-imidazole-1-sulfonamide was submitted to the next step without purification. The crude was dissolved in a mixture 1:1 of water (2 ml) and 4N HCl in dioxane (2 ml) and heated at 75° C. until deprotection was completed. After evaporation under vacuo, purification by RP-HPLC afforded the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181258B2
Source datasetuspto-grants-2015_11
ORD IDord-7ae1ac74f46a4c81bfb5c976df801189
Source noteuspto-grants-2015_11