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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049915Generated: October 31, 2026

Potassium Carbonate → 3-(4-Aminopyrido[3,2-d]pyrimidin-6-yl)-5-fluorobenzaldehyde

https://huagongshe.com/reaction/1049915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluoro-5-formylphenylboronic acidHCID 22279193—
Reactant6-(3-Fluorophenyl)pyrido[3,2-d]pyrimidin-4-amineHCID 86703914—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-(4-Aminopyrido[3,2-d]pyrimidin-6-yl)-5-fluorobenzaldehydeHCID 8670391890%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 6-chloropyrido[3,2-d]pyrimidin-4-amine (1) (3.61 g, 20 mmol), 3-fluoro-5-formylphenylboronic acid (CAS 328956-60-1) (4.03 g, 24 mmol, 1.2 eq), Pd(PPh3)4 (1.16 g, 1.0 mmol, 0.05 eq), and K2CO3 (5.53 g, 40 mmol, 2.0 eq) in a mixture of dioxane (100 mL) and H2O (10 mL) was heated at 100° C. for 3 h. After it was cooled to r.t., the reaction was extracted with EtOAc (100 mL) and water (60 mL). The organic layer were washed with water and concentrated. The yellow solid was recrystallized in MeCN to give the titled product (4.8 g, yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382241B2
Source datasetuspto-grants-2016_07
ORD IDord-14d458fa545b4fc5a9defba99da2bef3
Source noteuspto-grants-2016_07