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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219563Generated: October 25, 2026

Water → Ethyl 5-cyclopentyl-1-(2-fluorophenyl)-1H-1,2,3-triazole-4-carboxylate

https://huagongshe.com/reaction/219563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantEthyl 3-cyclopentyl-3-oxopropanoateHCID 11159709—
Reactant1-Azido-2-fluorobenzeneHCID 11607924—
SolventDimethylformamideHCID 6228—
ProductEthyl 5-cyclopentyl-1-(2-fluorophenyl)-1H-1,2,3-triazole-4-carboxylateHCID 67969121—

Reaction Steps

DBU (2.99 ml; 20.06 mmol; 1.10 eq.) was dissolved in DMF (25 ml) and put under nitrogen atmosphere. 3-Cyclopentyl-3-oxo-propionic acid ethyl ester (Pharmacore, 3.695 g; 20.06 mmol; 1.10 eq.) was added to the mixture and it was stirred for 15 min. Then a solution of 1-azido-2-fluorobenzene, prepared according to Platz, M. S. et al. J. Org. Chem. 1989, 54, 5938-5945, (2.5 g; 18.23 mmol; 1 eq.) in DMF (5 mL) was added dropwise to the solution at room temperature. The mixture was stirred at 90° C. for 2 hours. Water (50 mL) was added to the cooled reaction mixture and the aqueous layer was extracted with EtOAc (3×50 mL). Combined organics were washed with water and brine, dried over MgSO4 and concentrated under vacuum affording the title compound as a yellow oil. It was used in the next step without further purification. LC/MS (Method B): 304.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202856B2
Source datasetuspto-grants-2012_06
ORD IDord-1265a8aa4ec24b1c82bdda4769ce40cf
Source noteuspto-grants-2012_06