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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053971Generated: October 29, 2026

Bromobenzene → HCID 178513764, compound

https://huagongshe.com/reaction/1053971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantDi-tert-butyl[3,4,5,6-tetramethyl-2',4',6'-tris(propan-2-yl)-[1,1'-biphenyl]-2-yl]phosphaneHCID 11953610—
ReactantHCID 178513763HCID 178513763—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 178513764HCID 178513764—

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Amino-1H-pyrazole-4-carboxamide (19.8 g, 157 mmol), K3PO4 (66.7 g, 314 mmol), bromobenzene (23.2 mL, 220 mmol) and 2-propanol (785 mL) were combined in a round bottom flask and purged with a stream of N2 gas for 40 minutes. Pd2(dba)3 (1.80 g, 1.96 mmol) and 2-di-t-butylphosphino-3,4,5,6-tetramethyl-2′,4′,6′-tri-i-propylbiphenyl(3.77 g, 7.85 mmol) were added and the reaction was purged for an additional 5 minutes. The reaction mixture was then heated to 80° C. and allowed to stir under a N2 atmosphere for 12 hours. The mixture was then allowed to cool to ambient temperature for an additional 16 hours. The reaction mixture was diluted with EtOAc (300 mL) and filtered through celite (slowly). The celite was washed with EtOAc (300 mL) and the combined filtrates were concentrated in vacuo to afford an oil which was purified by MPLC on silica gel (using a gradient elution of 0-10% MeOH/DCM). The major, low rf product, was isolated to afford a reddish-brown oily solid. The brown solid was suspended in 40 mL of warm MeOH, cooled to ambient temperature, and water (40 mL) was added. The mixture was stirred for 30 minutes and filtered. The solid was suction dried for 16 hours to afford the title compound as a peach-colored solid. LRMS (ESI) calc'd for C10H10N4O [M+H]+: 203. Found: 203.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394282B2
Source datasetuspto-grants-2016_07
ORD IDord-e132d6ecc6a441f3b8814eff4bead8b7
Source noteuspto-grants-2016_07