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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383234Generated: November 2, 2026

Acetic Acid → 2-Amino-7-chloro-1-ethyl-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamide

https://huagongshe.com/reaction/2383234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2-Cyano-N-methylacetamideHCID 80622—
Reactant2-(Aminoethyl)-6-chloronicotinic acid fluorideHCID 87400373—
SolventWaterHCID 962—
Product2-Amino-7-chloro-1-ethyl-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamideHCID 8664233694%

Reaction Steps

0.394 g (9.95 mmol) of 60% sodium hydride in mineral oil is added in small amounts to a solution, cooled to 0-5° C., of 0.483 g (4.93 mmol) of N-methylcyanoacetamide in 7 ml of anhydrous dimethylformamide. Stirring is continued at this temperature for 10 minutes and then a solution of 1.0 g (4.93 mmol) of 2-(aminoethyl)-6-chloronicotinic acid fluoride in 5 ml of dimethylformamide is added. The medium is stirred overnight at ambient temperature and then a further 0.197 g (4.93 mmol) of 60% sodium hydride is added in small amounts. Stirring is continued at this temperature for 10 minutes and then 0.56 ml (9.78 mmol) of acetic acid is added. 60 ml of water are subsequently added and the solid is filtered off, rinsed with water and then dried in an oven. 1.30 g of the expected product are obtained. Melting point: 283-284° C. MH+=281. Yield=94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263614B2
Source datasetuspto-grants-2012_09
ORD IDord-d12c346c3c8a416d95df19a9f0b5c742
Source noteuspto-grants-2012_09