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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024910Generated: October 31, 2026

N-[2-[[(2,3-difluorophenyl)methyl]thio]-6-[2-hydroxy-1-(hydroxymethyl)ethoxy]-4-pyrimidinyl]-1-azetidinesulfonamide → HCID 86619881, compound

https://huagongshe.com/reaction/1024910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[2-[[(2,3-difluorophenyl)methyl]thio]-6-[2-hydroxy-1-(hydroxymethyl)ethoxy]-4-pyrimidinyl]-1-azetidinesulfonamideHCID 11698344—
Reactant(R)-1-((S)-2,2-Dimethyl-1,3-dioxolan-4-yl)ethanolHCID 53628362—
Reactant4,6-Dichloro-2-((2,3-difluorobenzyl)thio)pyrimidineHCID 85928037—
SolventTetrahydrofuranHCID 8028—
SolventSodium hydrideHCID 24758—
ProductHCID 86619881HCID 86619881—

Reaction Steps

The subtitle compound was prepared according to the procedure outlined in example 1 step (iii) using (1R)-1-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethanol (prepared according to Liebigs, Ann. Chem. 1987, 7-14) (0.25 g) and 4,6-Dichloro-2-[(2,3-difluorobenzyl)thio]pyrimidine (the product of example 1 step (0.53 g) in THF (20 mL) and 60% sodium hydride (80 mg). Crude material was purified by column chromatography on silica gel using EtOAc/isohexane (1:3) as eluent to give the subtitle compound as a clear, colourless oil. Yield: 0.37 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722883B2
Source datasetuspto-grants-2014_05
ORD IDord-8029fddd1f9a4860bc314dfbb6f0f9a8
Source noteuspto-grants-2014_05