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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605599Generated: November 2, 2026

Sodium Chloride → HCID 11655616, compound

https://huagongshe.com/reaction/605599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
Reactant3-(Dimethylamino)-1-propanolHCID 76646—
ReactantHCID 11523767HCID 11523767—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 11655616HCID 1165561651.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 7-chloro-N-(2,2,2-trifluoroethyl)-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidin-5-amine (19 mg, 0.05 mmol) and 3-dimethylamino-1-propanol (51 m g, 0.5 mmol) in 0.5 mL of dimethylsulfoxide at room temperature is added sodium hydride (60% in mineral oil, 20 mg, 0.5 mmol). The mixture is heated at 50° C. for 30 minutes, and cooled to room temperature. A saturated sodium chloride solution is added, and the product is extracted with ethyl acetate. The organic solution is washed with saturated sodium chloride (×3), dried over magnesium sulfate, and concentrated. The residue is chromatographed over silica gel, eluting with a gradient of ethyl acetate to 30% methyl alcohol in ethyl acetate. Concentration provides 7-chloro-6-{4-[3-(dimethylamino)propoxy]-2,6-difluorophenyl}-N-(2,2,2-trifluoroethyl)imidazo[1,2-a]pyrimidin-5-amine as a tan solid (12 mg, mp 52-55° C.). MS: m/z 464.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915266B2
Source datasetuspto-grants-2011_03
ORD IDord-18ec533a86b048c68e42518284d13d9d
Source noteuspto-grants-2011_03