Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968742Generated: October 30, 2026

HCID 178418247, compound → 5-[(8-propan-2-yloxy-1,5-naphthyridin-2-yl)methylidene]-2-(thiophen-2-ylmethylamino)-1,3-thiazol-4-one

https://huagongshe.com/reaction/968742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418247HCID 178418247—
ReactantHCID 178458598HCID 178458598—
ReactantHCID 178458710HCID 178458710—
SolventAcetic AcidHCID 176—
Product5-[(8-propan-2-yloxy-1,5-naphthyridin-2-yl)methylidene]-2-(thiophen-2-ylmethylamino)-1,3-thiazol-4-oneHCID 17845860245.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 2-[(thiophen-2-ylmethyl)-amino]-thiazol-4-one one (34.0 mg, 0.16 mmol) (see Example 4), AcONa (160 mg, 1.95 mmol), and 8-isopropoxy-[1,5]naphthyridine-2-carbaldehyde (38.9 mg, 0.18 mmol) (see Example 20) in a sealed tube was added AcOH (0.3 mL). The reaction mixture was heated to 100° C. (oil bath) for 4.5 hrs. The reaction mixture was then cooled to r.t. and triturated with water. The solid was collected by filtration and washed with water, acetone and ether to give 5-(8-isopropoxy-[1,5]naphthyridin-2-ylmethylene)-2-[(thiophen-2-ylmethyl)-amino]-thiazol-4-one as a light brown solid (29.8 mg, 45.4%). HR-ES (+) m/e calcd for C20H18N4O2S2 (M+H)+ 411.0944. found 411.0945.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304074B2
Source datasetuspto-grants-2007_12
ORD IDord-74be7b53c5df494cbe8a414eb0377e3d
Source noteuspto-grants-2007_12