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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049900Generated: October 30, 2026

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

https://huagongshe.com/reaction/1049900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Carboxyphenylboronic acidHCID 2733957—
Reactant6-Chloropyrido[3,2-d]pyrimidin-4-amineHCID 86703896—
CatalystHCID 178477754HCID 178477754—
SolventAcetonitrileHCID 6342—
Product3-(4-Aminopyrido[3,2-d]pyrimidin-6-yl)benzoic acidHCID 86703903—

Reaction Conditions

Temperature80 °C

Reaction Steps

6-chloropyrido[3,2-d]pyrimidin-4-amine 3-A (500 mg, 2.8 mmol) in acetonitrile (5 mL) was treated with 3-borono-benzoic acid (CAS 269404-73-6) (560 mg, 3 mL), PDCL2(DPPF) (202 mg, 0.28 mmol) and 1 M POTASSIUM CARBONATE solution (8 mL). The reaction vial was purged with nitrogen, and heated to 80° C. for 1 hour. LCMS showed 100% conversion to desired product. Yellow ppt. was filtered and LCMS indicated it is pure product 3-(4-aminopyrido[3,2-d]pyrimidin-6-yl)benzoic acid 14. The filtrate was concentrate and purified with reverse phase C-18 column to provide more product. LC/MS (ESI+): m/z 267 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382241B2
Source datasetuspto-grants-2016_07
ORD IDord-9d755f0f67e04d329a3f5a7e43c5ed6b
Source noteuspto-grants-2016_07