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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 7-Cyclobutyl-5-iodo-imidazo[5,1-f][1,2,4]triazin-4-ylamine | HCID 53328624 | — |
| Reactant | 1,3,2-Dioxaborolane,2-[2-fluoro-3-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl- | HCID 59344877 | — |
| Catalyst | Palladium--triphenylphosphane (1/1) | HCID 15220664 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 5-(3-Benzyloxy-2-fluoro-phenyl)-7-cyclobutyl-imidazo[5,1-f][1,2,4]triazin-4-ylamine | HCID 11552840 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07741324B2 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-b6ef54b351c34423871cddc28de58fba |
|---|
| Source note | uspto-grants-2010_06 |
|---|