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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968720Generated: October 29, 2026

6-Formyl-4-isopropoxy-[1,5]naphthyridine-3-carbonitrile → HCID 178458711, compound

https://huagongshe.com/reaction/968720

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Formyl-4-isopropoxy-[1,5]naphthyridine-3-carbonitrileHCID 58724311—
ReactantHCID 178418247HCID 178418247—
ReactantHCID 178516943HCID 178516943—
SolventAcetic AcidHCID 176—
ProductHCID 178458711HCID 17845871141.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-[2-(3-fluoro-phenyl)-ethylamino]-thiazol-4-one (38.1 mg, 0.16 mmol) (prepared as described below), AcONa (160 mg, 1.95 mmol), and 6-formyl-4-isopropoxy-[1,5]naphthyridine-3-carbonitrile (50.2 mg, 0.21 mmol) (see Example 1) in a sealed tube was added AcOH (0.3 mL). The reaction mixture was heated to 80° C. (oil bath) for 5 hrs. The reaction mixture was then cooled to r.t. and triturated with water. The solid was collected by filtration and washed with water. The solid was then suspended in AcOEt (20 mL) and filtered through a glass filter. The solid was washed with AcOEt and dried to give 6-{2-[2-(3-fluoro-phenyl)-ethylamino]-4-oxo-4H-thiazol-5-ylidenemethyl}-4-isopropoxy-[1,5]naphthyridine-3-carbonitrile as a light green solid (30.7 mg, 41.6%). HR-ES (+) m/e calcd for C24H20FN5O2S (M+H)+ 462.1395. found 462.1395.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304074B2
Source datasetuspto-grants-2007_12
ORD IDord-77f6e892fa994b5f929a4109589a5fe0
Source noteuspto-grants-2007_12