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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711414Generated: November 1, 2026

Dichloromethane → HCID 86732562, compound

https://huagongshe.com/reaction/711414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCesium carbonateHCID 10796—
ReactantThiophene-3-boronic acidHCID 581760—
ReactantHCID 86732561HCID 86732561—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86732562HCID 8673256254.2%

Reaction Steps

To a solution of tert-butyl(2-{6-iodo-1-oxo-7-[3-(trifluoromethoxy)phenyl]-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl}ethyl)carbamate (100 mg, 0.177 mmol) in 3 ml of 1,4-dioxane and 1 ml of water, under argon atmosphere, (67.9 mg, 0.531 mmol) of 3-thienylboronic acid, 7.2 mg (0.009 mmol) of 1,1′-bis(diphenylphosphino)ferrocenepalladium, complex with dichloromethane and 172 mg (0.531 mmol) of cesium carbonate, were subsequently added. The mixture was heated at 80° for 1 hour in a sealed vial. The reaction was filtered through a celite pad and the solvent evaporated to dryness. The crude was then portioned between ethyl acetate and water, the organic layer dried over sodium sulphate and the solvent removed in vacuo. After purification by flash chromatography on silica gel column (DCM/EtOAc/EtOH 6/4/0.5), and further purification by HPLC/MS preparative method 1, 50 mg (54%) of tert-butyl(2-{1-oxo-6-(thiophen-3-yl)-7-[3-(trifluoromethoxy)phenyl]-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-4-yl}ethyl)carbamate were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181258B2
Source datasetuspto-grants-2015_11
ORD IDord-ed8ad42661774de99ce074922af53043
Source noteuspto-grants-2015_11