HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968734Generated: October 29, 2026
8-Isopropoxy-[1,5]naphthyridine-2-carbaldehyde → HCID 178458598, compound
https://huagongshe.com/reaction/968734
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Isopropoxy-[1,5]naphthyridine-2-carbaldehyde | HCID 58724302 | — |
| Reactant | HCID 178418247 | HCID 178418247 | — |
| Reactant | HCID 178458707 | HCID 178458707 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178458598 | HCID 178458598 | 73.7% |
Reaction Steps
To a mixture of 2-(trans)-phenylcyclopylamino-thiazol-4-one (76.0 mg, 0.32 mmol) (see Example 3) AcONa (160 mg, 1.95 mmol), and 8-isopropoxy-[1,5]naphthyridine-2-carbaldehyde (77.8 mg, 0.36 mmol) (prepared as described below) in a sealed tube was added AcOH (0.4 mL). The reaction mixture was heated to 100° C. (oil bath) for 4 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-(2-phenyl-cyclopropylamino)-thiazol-4-one as a yellowish solid (101.5 mg, 73.7%). HR-ES (+) m/e calcd for C24H22N4O2S (M+H)+ 431.1536. found 431.1537.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304074B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-22ac91824a834d7784e61cd90de76eab |
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| Source note | uspto-grants-2007_12 |
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