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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Fluoro-5-formylphenylboronic acid | HCID 22279193 | — |
| Reactant | 6-(3-Fluorophenyl)pyrido[3,2-d]pyrimidin-4-amine | HCID 86703914 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(4-Aminopyrido[3,2-d]pyrimidin-6-yl)-5-fluorobenzaldehyde | HCID 86703918 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09382241B2 |
|---|
| Source dataset | uspto-grants-2016_07 |
|---|
| ORD ID | ord-14d458fa545b4fc5a9defba99da2bef3 |
|---|
| Source note | uspto-grants-2016_07 |
|---|