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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889429Generated: October 26, 2026

Water → (3R,4S)-4-azido-1-(3-nitro-5-(4H-1,2,4-triazol-4-yl)phenyl)piperidin-3-ol

https://huagongshe.com/reaction/889429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Azidopiperidin-3-olHCID 21874366—
Reactant4-(3-fluoro-5-nitrophenyl)-4H-1,2,4-triazoleHCID 67377342—
SolventDimethyl SulfoxideHCID 679—
Product(3R,4S)-4-azido-1-(3-nitro-5-(4H-1,2,4-triazol-4-yl)phenyl)piperidin-3-olHCID 5931395743%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-(3-fluoro-5-nitrophenyl)-4H-1,2,4-triazole (200 mg, 0.96 mmol), 4-azidopiperidin-3-ol (164 mg, 1.15 mmol) and K2CO3 (199 mg, 1.44 mmol) in DMSO was heated at 100° C. for 4 hours. The reaction mixture was poured into water and extracted with EtOAc (two times). The combined extracts were washed with water and brine, dried over MgSO4, filtered and concentrated. The crude material was purified by flash chromatography, (SiO2, 24 g column, 0-12% MeOH/DCM) to give Intermediate 33A (135 mg, 43%) as a yellow solid. HPLC: Rt=1.722 min. (CHROMOLITH® column 4.6×50 mm eluting with 10-90% aqueous methanol over 4 min. containing 0.1% TFA, 4 mL/min., monitoring at 220 nm). MS (ES): m/z=331 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252795B2
Source datasetuspto-grants-2012_08
ORD IDord-838c8cb8d3aa4c3f8b54f7bcc037daa2
Source noteuspto-grants-2012_08