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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369035Generated: October 26, 2026

Sodium Carbonate → 6-(4-Carboxyphenyl)-8-methoxy-1,7-naphthyridine

https://huagongshe.com/reaction/369035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Carboxyphenylboronic AcidHCID 312183—
Reactant6-Trifluoromethylsulfonyloxy-8-methoxy-1,7-naphthyridineHCID 23284635—
CatalystTri-o-tolylphosphineHCID 80271—
Catalyst1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
SolventDimethylformamideHCID 6228—
Product6-(4-Carboxyphenyl)-8-methoxy-1,7-naphthyridineHCID 2328464280.8%

Reaction Steps

To a solution of 6-trifluoromethylsulfonyloxy-8-methoxy-1,7-napthyridine (1.5 g, 4.86 mmol) in DMF (40 ml) is added 4-carboxy-phenylboronic acid (0.866 g, 5.34 mmol), bis(dibenzylidenacetone) palladium (112 mg, 0.167 mmol), tri-o-tolylphosphine (96 mg, 0.32 mmol) and aqueous Na2CO3 (14.6 ml, 2N,). The reaction mixture is stirred at 110° for 3 h. The hot solution is filtred through cellit and the solution evaporated to dryness. The crude product is dissolved in hot water (60 ml) and the water phase washed with ethyl acetate (3×50 ml). The product is precipitated from the water phase by carefully adding aqueous HCl (2N, 6 ml). The suspension is filtered and the crude product is stirred again in hot ethyl acetate (50 ml). The cold suspension is filtered to yield the title compound (1.10 g). M+280; Melting point >300°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136821
Source datasetuspto-grants-2000_10
ORD IDord-449fc1ba55304cbb90163e63a52ba620
Source noteuspto-grants-2000_10