HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880165Generated: October 31, 2026
2-Cyclopenten-1-one → 3-(2-(4-(Benzo[D]thiazol-2-ylamino)phenoxy)pyridin-3-YL)cyclopent-2-enone
https://huagongshe.com/reaction/1880165
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Cyclopenten-1-one | HCID 13588 | — |
| Reactant | N-Methyl dicyclohexylamine | HCID 24210 | — |
| Reactant | N-(4-(3-bromopyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine | HCID 59326883 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(2-(4-(Benzo[D]thiazol-2-ylamino)phenoxy)pyridin-3-YL)cyclopent-2-enone | HCID 46214873 | — |
Reaction Steps
A solution of N-(4-(3-bromopyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine (600 mg, 1.506 mmol), 2-cyclopenten-1-one (0.609 mL, 7.53 mmol), n-methyldicyclohexylamine (0.959 mL, 4.52 mmol) and bis(tri-tert-butylphosphine)palladium (0) (77 mg, 0.151 mmol) in Dioxane (4 mL) was capped, degassed and backfilled with argon. The reaction was heated to 90° C. After 6 h, the reaction was heated to 110° C. After 36 h, the reaction was cooled to 23° C., diluted with EtOAc (150 mL) and washed with water (100 mL) and brine (100 mL), dried over MgSO4, concentrated in vacuo and purified by silica gel chromatography (eluant: 0.5-3% methanol/dichloromethane), affording the product as a yellow solid. MS (ESI, pos. ion) m/z: 400.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318718B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-cbfc0db826d742eb8a537d1203cba941 |
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| Source note | uspto-grants-2012_11 |
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