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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395963Generated: October 30, 2026

Sodium hydride → HCID 10782939, compound

https://huagongshe.com/reaction/2395963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Hydroxy-2,2-dimethylpropane-1-sulfonamideHCID 10329687—
ReactantHCID 15271019HCID 15271019—
SolventDimethylformamideHCID 6228—
ProductHCID 10782939HCID 1078293966.6%

Reaction Steps

0.293 g of 60% oily sodium hydride was suspended in 10 ml of dimethylformamide. To this suspension, 0.577 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 30 minutes. To this mixture was added 0.703 g of 6-chloroimidazo[2,1-a]phthalazine, followed by stirring at room temperature for 3 hours. After dimethylformamide was distilled off under reduced pressure, ice water was added to the residue, which was subsequently adjusted to pH 5.0 by the addition of 5 N hydrochloric acid and then extracted with ethyl acetate-tetrahydrofuran (1:1). 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 (20:20:1). The fraction containing the desired product was concentrated and ethyl ether was added to separate a crystal, which was collected by filtration, to yield 0.769 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491145
Source datasetuspto-grants-1996_02
ORD IDord-2b0b0a46671d43a2b1e681061374a688
Source noteuspto-grants-1996_02