Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573201Generated: October 26, 2026

Cyano-borohydride → 4-((4-Fluoro-1-(oxetan-3-yl)piperidin-4-yl)methoxy)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/573201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyano-borohydrideHCID 498716—
Reactant3-OxetanoneHCID 15024254—
Reactant4((4-Fluoropiperidin-4-yl)methoxy)-3-nitrobenzenesulfonamideHCID 67126502—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product4-((4-Fluoro-1-(oxetan-3-yl)piperidin-4-yl)methoxy)-3-nitrobenzenesulfonamideHCID 67127155—

Reaction Steps

To a solution of EXAMPLE 341C (72 mg) in tetrahydrofuran (1.5 mL) and acetic acid (0.5 mL) was added oxetan-3-one (14 mg) and MP-cyanoborohydride (2.38 mmol/g, 162 mg). The mixture was stirred at room temperature overnight. The reaction was then filtered and the filtrate was concentrated under vacuum. The residue was slurried in ether and the product was collected by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029404B2
Source datasetuspto-grants-2015_05
ORD IDord-e7b29ce207654796a5a686b34844e679
Source noteuspto-grants-2015_05