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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712725Generated: November 1, 2026

Tetrahydrofuran → HCID 117667705, compound

https://huagongshe.com/reaction/712725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantDiphenylphosphoryl azideHCID 123414—
ReactantHCID 86305760HCID 86305760—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 117667705HCID 11766770582.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-[5-Fluoro-4-((S)-1-hydroxy-ethyl)-pyridin-3-yl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide (100 mg, 0.32 mmol), THF (1.4 mL) and phosphorazidic acid diphenyl ester (0.088 mL, 0.41 mmol) are combined and cooled to 0° C. DBU (0.061 mL, 0.41 mmol) is added dropwise. After 10 minutes, the reaction is warmed to room temperature for 18 hrs. The reaction mixture is diluted with EtOAc and water. The layers are separated. The aqueous layer is extracted with EtOAc. The combined organic layers are washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo to the crude product. Purification by flash column chromatography affords 90 mg of 6-[4-((R)-1-azido-ethyl)-5-fluoro-pyridin-3-yl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-bba2048360944c9eb1ed0f6b96fe727a
Source noteuspto-grants-2015_11