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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395958Generated: November 1, 2026

Sodium hydride → HCID 9904880, compound

https://huagongshe.com/reaction/2395958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Hydroxy-2,2-dimethylpropane-1-sulfonamideHCID 10329687—
ReactantHCID 15271015HCID 15271015—
SolventDimethylformamideHCID 6228—
ProductHCID 9904880HCID 990488039.3%

Reaction Steps

0.59 g of 60% oily sodium hydride was suspended in 21 ml of dimethylformamide. To this suspension, 1.18 g of 3-hydroxy-2,2-dimethyl-1-propanesulfonamide was added, followed by stirring at room temperature (15° to 20° C.) under reduced pressure for 1 hour. To this mixture was added 1.28 g of 6-chloro-7,8-dimethylimidazo[1,2-b]pyridazine, followed by stirring at 60° C. for 40 minutes. After dimethylformamide was distilled off under reduced pressure, ice water was added to the residue, which was subsequently adjusted to pH 6 by the addition of 5 N hydrochloric acid andthen extracted with ethyl acetate-tetrahydrofuran (2:1). The extract was washed with 20 ml of saturated saline and then dried over magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was subjected to silica gel column chromatography and eluted with dichloromethane-ethyl acetate-methanol (10:10:1). The fraction containing the desired product was concentrated and recrystallized from ethanol to yield 0.866 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491145
Source datasetuspto-grants-1996_02
ORD IDord-ab34d232b0b94a96a395b979e82beb94
Source noteuspto-grants-1996_02