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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395962Generated: October 30, 2026

Sodium hydride → 6-(2,2-Dimethyl-3-sulfamoyl-1-propoxy)-7,8,9,10-tetrahydroimidazo[2,1-a]phthalazine

https://huagongshe.com/reaction/2395962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Hydroxy-2,2-dimethylpropane-1-sulfonamideHCID 10329687—
Reactant6-Chloro-7,8,9,10-tetrahydroimidazo[2,1-a]phthalazineHCID 13178975—
SolventDimethylformamideHCID 6228—
Product6-(2,2-Dimethyl-3-sulfamoyl-1-propoxy)-7,8,9,10-tetrahydroimidazo[2,1-a]phthalazineHCID 1080694930%

Reaction Steps

0.59 g of 60% oily sodium hydride was suspended in 20 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 30 minutes. To this mixture was added 1.35 g of 6-chloro-7,8,9,10-tetrahydroimidazo[2,1-a]phthalazine, followed by stirring at 60° C. for 1.5 hours. 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 and then 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 (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 0.66 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491145
Source datasetuspto-grants-1996_02
ORD IDord-a33ac3ffa4204888ba6dd273f478077d
Source noteuspto-grants-1996_02