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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17976Generated: October 30, 2026

Sodium Carbonate → 5-(3-Benzyloxy-2-fluoro-phenyl)-7-cyclobutyl-imidazo[5,1-f][1,2,4]triazin-4-ylamine

https://huagongshe.com/reaction/17976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant7-Cyclobutyl-5-iodo-imidazo[5,1-f][1,2,4]triazin-4-ylamineHCID 53328624—
Reactant1,3,2-Dioxaborolane,2-[2-fluoro-3-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl-HCID 59344877—
CatalystPalladium--triphenylphosphane (1/1)HCID 15220664—
CatalystHCID 178418397HCID 178418397—
Product5-(3-Benzyloxy-2-fluoro-phenyl)-7-cyclobutyl-imidazo[5,1-f][1,2,4]triazin-4-ylamineHCID 11552840—

Reaction Conditions

Temperature75 °C

Reaction Steps

A flask was charged with 7-cyclobutyl-5-iodo-imidazo[5,1-f][1,2,4]triazin-4-ylamine (30 mg, 0.095 mmol), 2-(3-benzyloxy-2-fluoro-phenyl)-4,4,5,5- tetramethyl [1,3,2]dioxaborolane (62.5 mg, 0.158 mmol), and sodium carbonate (30 mg, 0.286 mmol) and was evacuated and charged with N2 (3×). This mixture was charged with tetrakis(triphenylphosphine palladium (0) (Pd(PPh3)4 (0)) (36 mg, 0.0318 mmol) and the tube was re-evacuated and charged with N2 (2×). This mixture was then charged with a previously degassed solvent DME/H2O (5:1)(3 mL) and heated to 75° C. for 16 h. The reaction mixture was concentrated in vacuo and dissolved in MeOH/CH3CN (1:1) (5 mL), filtered though a 0.45 μM fritted autovial and submitted for mass directed purification (MDP) resulting in the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741324B2
Source datasetuspto-grants-2010_06
ORD IDord-b6ef54b351c34423871cddc28de58fba
Source noteuspto-grants-2010_06