HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968727Generated: October 29, 2026
HCID 178418247, compound → HCID 178510291, compound
https://huagongshe.com/reaction/968727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418247 | HCID 178418247 | — |
| Reactant | HCID 178458707 | HCID 178458707 | — |
| Reactant | HCID 178510297 | HCID 178510297 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178510291 | HCID 178510291 | 21.5% |
Reaction Steps
To a mixture of 2-(trans)-phenylcyclopylamino-thiazol-4-one (38.0 mg, 0.16 mmol) (see Example 3), AcONa (160 mg, 1.95 mmol), and 6-formyl-[1,5]naphthyridine-3-carbonitrile (38.5 mg, 0.21 mmol) (see Example 11), in a sealed tube was added AcOH (0.3 mL). The reaction mixture was heated to 100° 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 acetone and ether to give 6-[4-oxo-2-(2-phenyl-cyclopropylamino)-4H-thiazol-5-ylidenemethyl]-[1,5]naphthyridine-3-carbonitrile as a yellowish solid (13.7 mg, 18.3%). HR-ES (+) m/e calcd for C22H15N5OS (M+H)+ 398.1070. found 398.1071.
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-891a2a24a8ba4ebbb77373ae20b30341 |
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| Source note | uspto-grants-2007_12 |
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