HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968728Generated: October 29, 2026
6-[[2-[(3-methylthiophen-2-yl)methylamino]-4-oxo-1,3-thiazol-5-ylidene]methyl]-4-propan-2-yloxy-1,5-naphthyridine-3-carbonitrile → HCID 178429645, compound
https://huagongshe.com/reaction/968728
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-[[2-[(3-methylthiophen-2-yl)methylamino]-4-oxo-1,3-thiazol-5-ylidene]methyl]-4-propan-2-yloxy-1,5-naphthyridine-3-carbonitrile | HCID 178429646 | — |
| Reactant | HCID 178429647 | HCID 178429647 | — |
| Reactant | HCID 178510297 | HCID 178510297 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178429645 | HCID 178429645 | 35.8% |
Reaction Steps
To a mixture of 2-[(3-methyl-thiophen-2-ylmethyl)-amino]-thiazol-4-one (21.7 mg, 0.10 mmol), AcONa (160 mg, 1.95 mmol) (see Example 5), and 6-formyl-[1,5]naphthyridine-3-carbonitrile (22.0 mg, 0.12 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 1.5 hrs. The reaction mixture was then cooled to r.t. and triturated with water. The solid was collected by filtration and washed with water, AcOEt and ether to give 6-{2-[(3-methyl-thiophen-2-ylmethyl)-amino]-4-oxo-4H-thiazol-5-ylidenemethyl}-[1,5]naphthyridine-3-carbonitrile as a light brown solid (14.0 mg, 35.8%). HR-ES (+) m/e calcd for C19H13N5OS2 (M+H)+ 414.0454. found 414.0452.
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-9c409334352143518122fe0675cb3c19 |
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| Source note | uspto-grants-2007_12 |
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