Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043222Generated: October 26, 2026

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

https://huagongshe.com/reaction/1043222

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 numberUS08557983B2
Source datasetuspto-grants-2013_10
ORD IDord-ed0df36af5d547f7b09908022f217309
Source noteuspto-grants-2013_10