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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956450Generated: November 2, 2026

Ethyl 5-amino-2-hydroxybenzoate → Ethyl 5-(6-ethoxy-3-ethoxycarbonyl-7-methyl-1,8-naphthyridin-4-ylamino)salicylate hydrochloride

https://huagongshe.com/reaction/1956450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-amino-2-hydroxybenzoateHCID 13445456—
ReactantEthyl 4-chloro-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylateHCID 23198600—
SolventEthanolHCID 702—
ProductEthyl 5-(6-ethoxy-3-ethoxycarbonyl-7-methyl-1,8-naphthyridin-4-ylamino)salicylate hydrochlorideHCID 23209207—

Reaction Steps

A mixture of ethyl 4-chloro-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylate (2.0 g), absolute ethanol (30 ml) and ethyl 5-aminosalicylate (1.23 g) was boiled under reflux for 1 hour. The mixture was cooled to ambient temperature and filtered to give a solid which was recrystallised from IMS to give ethyl 5-(6-ethoxy-3-ethoxycarbonyl-7-methyl-1,8-naphthyridin-4-ylamino)salicylate hydrochloride, m.p. 208°-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780482
Source datasetuspto-grants-1998_07
ORD IDord-d22229dcbc8c43fa98ad409a0d4469cd
Source noteuspto-grants-1998_07