Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyclopenten-1-oneHCID 13588—
ReactantN-Methyl dicyclohexylamineHCID 24210—
ReactantN-(4-(3-bromopyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amineHCID 59326883—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
Product3-(2-(4-(Benzo[D]thiazol-2-ylamino)phenoxy)pyridin-3-YL)cyclopent-2-enoneHCID 46214873—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318718B2
Source datasetuspto-grants-2012_11
ORD IDord-cbfc0db826d742eb8a537d1203cba941
Source noteuspto-grants-2012_11