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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Aminobenzo[d]oxazol-5-ylboronic acidHCID 46199574—
Reactant7-Bromo-2-morpholino-1,5-naphthyridineHCID 67993057—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-(6-Morpholino-1,5-naphthyridin-3-yl)benzo[d]oxazol-2-amineHCID 5467530267.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096590B2
Source datasetuspto-grants-2015_08
ORD IDord-eaace88260a44c7eaa5ce3eeabfc323b
Source noteuspto-grants-2015_08