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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255888Generated: November 3, 2026

Sodium Bicarbonate → HCID 58174067, compound

https://huagongshe.com/reaction/1255888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(6-Fluoropyridin-3-yl)boronic acidHCID 2783397—
ReactantHCID 58174271HCID 58174271—
CatalystHCID 178418476HCID 178418476—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 58174067HCID 581740679.5%

Reaction Steps

To a round bottom flask was added [2-(4-bromophenyl)-ethyl]-pteridin-4-yl-amine (200 mg, 0.61 mmol), 2-fluoro-5-pyridineboronic acid (102 mg, 0.73 mmol), NaHCO3 (102 mg, 1.21 mmol), PdCl2(PPh3)2 (213 mg) and 50% aqueous ethylene glycol dimethyl ether (DME; 3.0 mL). The reaction was heated to reflux for 4.5 h, after which the reaction was cooled and the resulting orange precipitate filtered. The filtered material was washed with EtOAc and the filtrate washed with H2O. The organic fractions were pooled and concentrated in vacuo. The residue (229 mg) was purified by preparative RP-HPLC to afford {2-[4-(6-fluoropyridin-3-yl)-phenyl]-ethyl}-pteridin-4-yl-amine (20 mg) as an orange solid: mp 184-186° C.; EIMS m/z 346 ([M]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461164B2
Source datasetuspto-grants-2013_06
ORD IDord-f170e2938a23448db8aa9f2515c66d66
Source noteuspto-grants-2013_06