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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644344Generated: October 30, 2026

Tetrahydrofuran → ethyl (R)-2-{[4-(5-oxo-3-phenyl-4,5-dihydro-[1,2,4]triazol-1-yl)-piperidine-1-carbonyl]-amino}-3-(5,6,7,8-tetrahydro-naphthalen-2-yl)-propionate

https://huagongshe.com/reaction/644344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactantethyl (R)-2-amino-3-(5,6,7,8-tetrahydro-naphthalen-2-yl)-propionateHCID 69720392—
Reactant5-Phenyl-2-piperidin-4-YL-2,4-dihydro-[1,2,4]triazol-3-oneHCID 135627598—
Productethyl (R)-2-{[4-(5-oxo-3-phenyl-4,5-dihydro-[1,2,4]triazol-1-yl)-piperidine-1-carbonyl]-amino}-3-(5,6,7,8-tetrahydro-naphthalen-2-yl)-propionateHCID 136388296—

Reaction Steps

A mixture of 15 mL THF, 0.830 g (3.4 mmol) ethyl (R)-2-amino-3-(5,6,7,8-tetrahydro-naphthalen-2-yl)-propionate and 0.63 g (3.8 mmol) CDT was stirred for 1 h in the ice bath and for 1 h at RT. Then 0.83 g (3.4 mmol) 5-phenyl-2-piperidin-4-yl-2,4-dihydro-[1,2,4]triazol-3-one was added and the mixture was refluxed for 3 h. The reaction mixture was evaporated down under reduced pressure, the residue was combined with 15% K2CO3 solution, the precipitate was suction filtered and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700589B2
Source datasetuspto-grants-2010_04
ORD IDord-1f13717b011447658f30078d335eb336
Source noteuspto-grants-2010_04