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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574975Generated: October 31, 2026

Sodium hydride → 5-Chloro-6-((2-oxo-1-oxa-3-azaspiro[4.5]decan-8-yl)methoxy)pyridine-3-sulfonamide

https://huagongshe.com/reaction/574975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5,6-Dichloropyridine-3-sulfonamideHCID 4730921—
Reactant8-(Hydroxymethyl)-1-oxa-3-azaspiro[4.5]decan-2-oneHCID 57576531—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-6-((2-oxo-1-oxa-3-azaspiro[4.5]decan-8-yl)methoxy)pyridine-3-sulfonamideHCID 67126698—

Reaction Steps

To a solution of EXAMPLE 385C (325 mg, 1.755 mmol) in a mixture of tetrahydrofuran (16 mL) and N,N-dimethylformamide (8 mL) was added sodium hydride (281 mg, 7.02 mmol) and the mixture was stirred for 30 minutes. 5,6-Dichloropyridine-3-sulfonamide (389 mg) was added and the reaction was stirred for 42 hours. The reaction was quenched with water (5 mL) and concentrated. The residue was diluted with 75% brine (200 mL) and extracted with methylene chloride (3×200 mL). The organics were dried over sodium sulfate, filtered, and concentrated. The residue was purified on silica gel and eluted with a 1, 5, and 10% methanol in methylene chloride step gradient to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034875B2
Source datasetuspto-grants-2015_05
ORD IDord-af37d3b9bacf41fb93960001a1ffa98c
Source noteuspto-grants-2015_05