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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818705Generated: October 30, 2026

Triethylamine → HCID 11706696, compound

https://huagongshe.com/reaction/1818705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant9H-Fluoren-2-yl isocyanateHCID 4118622—
ReactantHCID 58960949HCID 58960949—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11706696HCID 1170669644%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of N-[2-(2-methylbenzothiazol-5-yloxy)-1-(piperazinylmethyl)ethyl]-acetamide (18.4 mg) in tetrahydrofuran (1 ml) was added triethylamine (25.6 μl) and 2-fluorenyl isocyanate (9.5 mg). The reaction mixture was stirred at 55° C. for 4 hours, producing a white precipitate. The precipitate was filtered off, and solvent removed from the filtrate under reduced pressure. The residue was purified by thin layer chromatography, developing with 4% methanol/methylene chloride, to provide N-{2-[4-(N-fluoren-2-ylcarbamoyl)piperazinyl]-1-[(2-methylbenzothiazol-5-yloxy)methyl]ethyl}acetamide (11.2 mg), a compound of Formula I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601721B2
Source datasetuspto-grants-2009_10
ORD IDord-4b0d3c9bd079434cafa2b586a664c2e8
Source noteuspto-grants-2009_10