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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968717Generated: October 29, 2026

6-Formyl-4-isopropoxy-[1,5]naphthyridine-3-carbonitrile → HCID 178458710, compound

https://huagongshe.com/reaction/968717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Formyl-4-isopropoxy-[1,5]naphthyridine-3-carbonitrileHCID 58724311—
ReactantHCID 178418247HCID 178418247—
ReactantHCID 178516942HCID 178516942—
SolventAcetic AcidHCID 176—
ProductHCID 178458710HCID 17845871050.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-[(thiophen-2-ylmethyl)-amino]-thiazol-4-one (34.0 mg, 0.16 mmol, (prepared as described below), AcONa (160 mg, 1.95 mmol), and 6-formyl-4-isopropoxy-[1,5]naphthyridine-3-carbonitrile (57.9 mg, 0.24 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. The solid was washed with AcOEt and dried to give 4-isopropoxy-6-{4-oxo-2-[(thiophen-2-ylmethyl)-amino]-4H-thiazol-5-ylidenemethyl}-[1,5]naphthyridine-3-carbonitrile as a light brown solid (35.4 mg, 50.8%). HR-ES (+) m/e calcd for C21H17N5O2S2 (M+H)+ 436.0897. found 436.0895.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304074B2
Source datasetuspto-grants-2007_12
ORD IDord-d4ce85bc08af42538acb3aeea76f94d5
Source noteuspto-grants-2007_12