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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262300Generated: November 2, 2026

Water → HCID 86761891, compound

https://huagongshe.com/reaction/1262300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Formylphenylboronic acidHCID 2734356—
Reactant(7-Bromo-pyrrolo[2,1-f][1,2,4]triazin-2-yl)-(4-morpholin-4-yl-phenyl)-amineHCID 54578326—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 86761891HCID 86761891—

Reaction Steps

Into a 8-dram vial, Palladium Acetate (0.021 g, 0.000094 mol) and Triphenylphosphine (0.069 g, 0.00026 mol) were added. The mixture was purged under an atmosphere of Nitrogen for 10 minutes. 1,4-Dioxane (7.10 mL) was added and stirred for 10 minutes at room temperature. (7-Bromo-pyrrolo[2,1-f][1,2,4]triazin-2-yl)-(4-morpholin-4-yl-phenyl)-amine (0.35 g, 0.00094 mol), 3-Formylphenyl boronic acid (0.280 g, 0.00187 mol), N,N-Dimethylformamide (14 mL), and 1.50 M of Sodium carbonate in Water (5.61 mL, 8.42 mmol) were added. The reaction was heated at 90° C. for 3 hours. The reaction was partitioned with water and EtOAc. The organic was separated, washed with Brine, and dried over magnesium sulfate. The solid was filtered and washed with EtOAc. The solvent was removed under vacuum. The product was isolated via column chromatography with DCM and Methanol as eluant (0 to 10% MeOH). The collected fractions afforded a solid. The solid was triturated with Et2O and filtered to give 3-[2-(4-Morpholin-4-yl-phenylamino)-pyrrolo[2,1-f][1,2,4]triazin-7-yl]-benzaldehyde as a yellow (0.20 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-178aecbe617846bdb290b734aa9ddc3a
Source noteuspto-grants-2013_06