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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219568Generated: October 27, 2026

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

https://huagongshe.com/reaction/219568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-Azido-2-fluorobenzeneHCID 11607924—
ReactantEthyl 3-(oxan-4-yl)-3-oxopropanoateHCID 23144053—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-(2-fluorophenyl)-5-(tetrahydro-2H-pyran-4-yl)-1H-1,2,3-triazole-4-carboxylateHCID 68648996—

Reaction Steps

DBU (1.32 ml; 8.82 mmol; 1.10 eq.) was dissolved in DMF (16.5 ml) and put under nitrogen atmosphere. 3-Oxo-3-(tetrahydro-pyran-4-yl)-propionic acid ethyl ester (Pharmacore, 1.767 g; 8.82 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, (1.1 g; 8.02 mmol; 1 eq.) in DMF (15 mL) was added dropwise to the solution at room temperature. The reaction mixture was stirred at 70° C. for 2 hours. Water (40 mL) was added to the reaction mixture. The aqueous layer was extracted with EtOAc (3×40 mL). Combined organic layers were washed with HCl 0.1N, brine, dried over MgSO4 and concentrated under vacuum giving the title compound as a yellow oil. It was used in the next step without further purification. LC/MS (Method B): 320.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202856B2
Source datasetuspto-grants-2012_06
ORD IDord-dbcf062b0b8744c8aed5f5d246ac469f
Source noteuspto-grants-2012_06