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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956443Generated: November 2, 2026

6-Ethoxy-2-pyridinamine → Ethyl 6-ethoxy-4-(6-ethoxy-2-pyridylamino)-7-methyl-1,8-naphthyridine-3-carboxylate sesquihydrochloride hydrate

https://huagongshe.com/reaction/1956443

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Ethoxy-2-pyridinamineHCID 586710—
ReactantEthyl 4-chloro-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylateHCID 23198600—
CatalystHydrochloric AcidHCID 313—
ProductEthyl 6-ethoxy-4-(6-ethoxy-2-pyridylamino)-7-methyl-1,8-naphthyridine-3-carboxylate sesquihydrochloride hydrateHCID 131720767—

Reaction Steps

A mixture of ethyl 4-chloro-6-ethoxy-7-methyl-1,8-naphthyridine-3-carboxylate (1.3 g), 6-amino-2-ethoxy pyridine (0.68 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 ethyl 6-ethoxy-4-(6-ethoxy-2-pyridylamino)-7-methyl-1,8-naphthyridine-3-carboxylate sesquihydrochloride hydrate, m.p. 195°-200° 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-745f2b90cee9427da243b8cfd4480318
Source noteuspto-grants-1998_07