HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509656Generated: October 29, 2026
Sodium Carbonate → 5-(6-Morpholino-1,5-naphthyridin-3-yl)benzo[d]oxazol-2-amine
https://huagongshe.com/reaction/509656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Aminobenzo[d]oxazol-5-ylboronic acid | HCID 46199574 | — |
| Reactant | 7-Bromo-2-morpholino-1,5-naphthyridine | HCID 67993057 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-(6-Morpholino-1,5-naphthyridin-3-yl)benzo[d]oxazol-2-amine | HCID 54675302 | 67.2% |
Reaction Steps
A mixture of 7-bromo-2-morpholino-1,5-naphthyridine (F-32) (180 mg, 0.6 mmol, 1.0 eq), 2-aminobenzo[d]oxazol-5-ylboronic acid (131 mg, 0.73 mmol, 1.2 eq), Pd(PPh3)4 (71 mg, 0.06 mmol, 0.1 eq), and Na2CO3 (195 mg, 1.8 mmol, 3.0 eq) were dissolved in a mixture of 1,4-dioxane (10 mL) and water (10 mL). The resulting mixture was degassed and back-filled with argon three times and heated at reflux under an argon atmosphere for 2 h. The reaction was complete based on TLC analysis. The mixture was concentrated in vacuo and the residue was purified by column chromatography on silica gel (3-5% MeOH-DCM) to afford 5-(6-morpholino-1,5-naphthyridin-3-yl)benzo[d]oxazol-2-amine (73) (140 mg, 67.2% yield). 1H NMR (400 MHz, DMSO-d6) δ: 8.93 (s, 1H), 8.10 (m, 2H), 7.66 (s, 1H), 7.53 (s, 2H), 7.45 (m, 3H), 3.74 (m, 8H); ESI-MS m/z: 348.11 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09096590B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-eaace88260a44c7eaa5ce3eeabfc323b |
|---|
| Source note | uspto-grants-2015_08 |
|---|