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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956436Generated: November 2, 2026

P-Anisidine → 3-Ethoxy-5-(4-methoxyanilino)-2-methyl-1,8-naphthyridine hydrate

https://huagongshe.com/reaction/1956436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantSodium HydroxideHCID 14798—
Reactant5-Chloro-3-ethoxy-2-methyl-1,8-naphthyridineHCID 19374266—
SolventWaterHCID 962—
Product3-Ethoxy-5-(4-methoxyanilino)-2-methyl-1,8-naphthyridine hydrateHCID 23209235—

Reaction Steps

The mixture of 5-chloro-3-ethoxy-2-methyl-1,8-naphthyridine (5.0 g), 4-methoxyaniline (2.77 g) and IMS (40 ml) was boiled under reflux for 2.5 hours. The mixture was cooled and filtered. The solid obtained was dissolved in boiling IMS (50 ml) and 5M sodium hydroxide solution (4.0 ml) was added. The mixture was heated under reflux for 1 hour and then cooled and water (100 ml) was added. The mixture was filtered to give 3-ethoxy-5-(4-methoxyanilino)-2-methyl-1,8-naphthyridine hydrate, m.p. 228°-231° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780482
Source datasetuspto-grants-1998_07
ORD IDord-8eabe4fb124348e4bc8c9fd6fcf6d758
Source noteuspto-grants-1998_07