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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880156Generated: October 26, 2026

2,5-Dihydrofuran → N-(4-(3-(2,3-Dihydrofuran-2-YL)pyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amine

https://huagongshe.com/reaction/1880156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DihydrofuranHCID 15570—
ReactantN-Methyl dicyclohexylamineHCID 24210—
ReactantN-(4-(3-Iodopyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amineHCID 59327141—
CatalystHCID 178418851HCID 178418851—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-(3-(2,3-Dihydrofuran-2-YL)pyridin-2-yloxy)phenyl)benzo[D]thiazol-2-amineHCID 59326959—

Reaction Steps

A mixture of N-(4-(3-iodopyridin-2-yloxy)phenyl)benzo[d]thiazol-2-amine (0.403 g, 0.905 mmol), N-methyldicyclohexylamine (0.400 mL, 1.886 mmol, Aldrich), bis(tri-tert-butylphosphine)palladium (0) (0.045 g, 0.088 mmol, Strem) and 2,5-dihydrofuran (0.500 mL, 6.78 mmol, Aldrich) in 5 mL of dioxane was capped under an atmosphere of argon and stirred at rt for 3 h and then heated at 45° C. overnight. The reaction mixture was diluted with MeOH, evaporated onto silica gel and purified by flash chromatography (Isco, (40 gram)) eluting with 2M NH3 in MeOH:CH2Cl2 (0:1→3:97) to give a white amorphous solid. MS (ESI, pos. ion) m/z: 386.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318718B2
Source datasetuspto-grants-2012_11
ORD IDord-0b75d648e2394da9a601f999ad6e9a57
Source noteuspto-grants-2012_11