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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410308Generated: October 26, 2026

2-Cyclopentene-1-ol → HCID 59327086, compound

https://huagongshe.com/reaction/410308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyclopentene-1-olHCID 220164—
ReactantPotassium AcetateHCID 517044—
ReactantN-(4-(3-Iodopyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amineHCID 59327141—
CatalystTetrabutylammonium ChlorideHCID 70681—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 59327086HCID 59327086—

Reaction Conditions

Temperature90 °C

Reaction Steps

A suspension of N-(4-(3-iodopyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine (493 mg, 1.107 mmol), cyclopent-2-enol (373 mg, 4.43 mmol), potassium acetate (217 mg, 2.214 mmol), tetrabutylammonium chloride (338 mg, 1.218 mmol) and Palladium (II) acetate (24.86 mg, 0.111 mmol) in acetonitrile (3 mL) and water (0.300 mL) was degassed and backfilled with argon. The reaction was heated to 90° C. for 18 h. Palladium (II) acetate (24.86 mg, 0.111 mmol) was added, and the reaction was capped, degassed and filled with argon, and heated to 135° C. in a microwave for 1 h. The crude reaction mixture was diluted with dichloromethane (75 mL) and washed with brine (75 mL), dried over MgSO4, concentrated in vacuo and purified by silica gel chromatography (eluant: 35-50% EtOAc/hexane), affording a white solid. It was further purified on a prep HPLC system (and free-based by partitioning between dichloromethane and saturated sodium bicarbonate solution), affording the product as a white solid. MS (ESI, pos. ion) m/z: 402.1 (M+1). IC50 (uM) +++++.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-a4ce46ecd9f643ca9ce6ff91411bf380
Source noteuspto-grants-2014_06