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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497429Generated: October 30, 2026

1,10-Phenanthroline → HCID 86759850, compound

https://huagongshe.com/reaction/497429

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl [(1H-imidazol-2-yl)methyl]methylcarbamateHCID 12125407—
ReactantHCID 86759851HCID 86759851—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86759850HCID 8675985066.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

Benzyl 1H-imidazol-2-ylmethyl(methyl)carbamat (1.17 g, 4.76 mmol) from Part E, 1-[2-trifluoroacetamidomethyl-phenyl]-3-trifluoromethyl-6-[4-Iodo-2-fluorophenyl]-1,4,5,6-tetrahydropyrazolo-[3,4-c]-pyridin-7-one from Part D (1.63 g, 3.18 mmol), CuI (0.12 9, 20%), K2CO3 (0.66 g, 4.76 mmol), 1,10-phenanthroline (56 mg, 20%) were added together with 100 mL of DMSO. The mixture was degassed and then heated at 130° C. under N2 for 12 h. The mixture was cooled and aqueous NH4OH (200 mL of of 10% NH4OH) was added. The mixture was filtered through Celite® and washed with EtOAc. The two layers were separated and the aqueous layer was extracted with EtOAc. The combined EtOAc mixture was washed with brine, dried over MgSO4, concentrated, and chromatographed with EtOAc to give 1.34 g of the desired product (66.9%). MS (ES+): 631.3, (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949550B2
Source datasetuspto-grants-2005_09
ORD IDord-8373de6249c24b8faf730d386b505b64
Source noteuspto-grants-2005_09