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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956442Generated: November 3, 2026

6-Ethoxy-2-pyridinamine → 3-Ethoxy-5-(6-ethoxy-2-pyridylamino)-2-methyl-1,8-naphthyridine hydrochloride

https://huagongshe.com/reaction/1956442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Ethoxy-2-pyridinamineHCID 586710—
Reactant5-Chloro-3-ethoxy-2-methyl-1,8-naphthyridineHCID 19374266—
CatalystHydrochloric AcidHCID 313—
Product3-Ethoxy-5-(6-ethoxy-2-pyridylamino)-2-methyl-1,8-naphthyridine hydrochlorideHCID 23209288—

Reaction Steps

A mixture of 5-chloro-3-ethoxy-2-methyl-1,8 naphthyridine (0.98 g), 6-amino-2-ethoxypyridine (0.6 g), IMS (25 ml) and concentrated hydrochloric acid (2 drops) was boiled under reflux for 18 hours. The mixture was cooled and filtered to give 3-ethoxy-5-(6-ethoxy-2-pyridylamino)-2-methyl-1,8-naphthyridine hydrochloride, m.p. >250° C. Active (1/1) at 30 mg/kg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780482
Source datasetuspto-grants-1998_07
ORD IDord-9df1d179ccc64a039946b9f7b5eecca5
Source noteuspto-grants-1998_07