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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746405Generated: October 31, 2026

4-Hydroxymethylpyridine → N-(2,4-dimethylphenyl)-N-isobutyl-4-(pyridine-4-ylmethoxy)benzenesulfonamide

https://huagongshe.com/reaction/1746405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxymethylpyridineHCID 11472—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantN-(2,4-dimethylphenyl)-4-hydroxy-N-isobutylbenzenesulfonamideHCID 71543523—
SolventTetrahydrofuranHCID 8028—
ProductN-(2,4-dimethylphenyl)-N-isobutyl-4-(pyridine-4-ylmethoxy)benzenesulfonamideHCID 71543524—

Reaction Steps

N-(2,4-dimethylphenyl)-4-hydroxy-N-isobutylbenzenesulfonamide (33 mg, 0.099 mmol), pyridine-4ylmethanol (2.52 mg, 0.148 mmol), triphenylphosphine (39 mg, 0.149 mmol) were pre-weighed into a 4 mL glass vial. Tetrahydrofuran (THF) (0.6 mL) was added followed by diisopropyl diazene-1,2-dicarboxylate (DIAD) (0.029 mL, 0.148 mmol). The vial was capped and stirred at RT for 2 days. The reaction mixture was filtered to remove any insoluble materials. The sample was purified by mass directed autoprep on an Xbridge column using acetonitrile:water with an ammonium carbonate modifier. The solvent was dried under a stream of nitrogen in the Radleys blowdown apparatus to give the required product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150508B2
Source datasetuspto-grants-2015_10
ORD IDord-f943437f7d684f46837b27bcd0da421e
Source noteuspto-grants-2015_10