HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968733Generated: October 30, 2026
HCID 178418247, compound → HCID 178510296, compound
https://huagongshe.com/reaction/968733
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418247 | HCID 178418247 | — |
| Reactant | HCID 178510297 | HCID 178510297 | — |
| Reactant | HCID 178516941 | HCID 178516941 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178510296 | HCID 178510296 | 45.1% |
Reaction Steps
To a mixture of 2-(3-chloro-4-fluoro-benzylamino)-thiazol-4-one (41.4 mg, 0.16 mmol) (prepared as described below) AcONa (160 mg, 1.95 mmol), and 6-formyl-[1,5]naphthyridine-3-carbonitrile (33.6 mg, 0.18 mmol) (see Example 11) in a sealed tube was added AcOH (0.3 mL). The reaction mixture was heated to 120° C. (oil bath) for 3 hrs. The reaction mixture was then cooled to r.t. and triturated with water. The solid was collected by filtration and washed with water, AcOEt and ether to give 6-[2-(3-chloro-4-fluoro-benzylamino)-4-oxo-4H-thiazol-5-ylidenemethyl]-[1,5]naphthyridine-3-carbonitrile as a light brown solid (30.6 mg, 45.1%). HR-ES (+) m/e calcd for C20H11FClN5OS (M+H)+ 424.0430. found 424.0431.
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-72531deee3564b4c8e28ef1ce1d2bbc0 |
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| Source note | uspto-grants-2007_12 |
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