HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968741Generated: October 29, 2026
HCID 178418247, compound → HCID 178458603, compound
https://huagongshe.com/reaction/968741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418247 | HCID 178418247 | — |
| Reactant | HCID 178458598 | HCID 178458598 | — |
| Reactant | HCID 178458711 | HCID 178458711 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178458603 | HCID 178458603 | 65.8% |
Reaction Steps
To a mixture of 2-[2-(3-fluoro-phenyl)-ethylamino]-thiazol-4-one (38.1 mg, 0.16 mmol) (see Example 7), 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 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 2-[2-(3-fluoro-phenyl)-ethylamino]-5-(8-isopropoxy-[1,5]naphthyridin-2-ylmethylene)-thiazol-4-one as a light green solid (45.9 mg, 65.8%). HR-ES (+) m/e calcd for C23H21FN4O2S (M+H)+ 437.1442. found 437.1443.
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-f8fdfb2269dd46038b11e11908c3a6ec |
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| Source note | uspto-grants-2007_12 |
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