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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870536Generated: October 30, 2026

Sodium hydride → HCID 53341128, compound

https://huagongshe.com/reaction/870536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(4R)-4-(hydroxyMethyl)-2-PyrrolidinoneHCID 51669743—
ReactantHCID 58072085HCID 58072085—
ProductHCID 53341128HCID 53341128—

Reaction Conditions

Temperature70 °C

Reaction Steps

50.7 mg (R)-4-Hydroxymethyl-pyrrolidine-2-one (2.2) was placed in 1.5 mL of dimethylacetamaide at ambient temperature under nitrogen before 20.5 mg sodium hydride (60% dispersion in oil) was added. The reaction was stirred for 10 min and then 150 mg 5-chloro-7-[4-(tetrahydro-pyran-4-yloxy)-3-trifluoromethyl-phenyl]-[1,6]naphthyridine (6.23) was introduced and the reaction was heated to 70° C. and stirred overnight. After this time the mixture was cooled to ambient temperature and partitioned between ethyl acetate, water and some saturared sodium chloride solution. The organic layer was separated, dried over sodium sulfate, filtered and the solvent was removed from the filtrate under reduced pressure. Purification by chromatography on silica provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969568B2
Source datasetuspto-grants-2015_03
ORD IDord-150ab42ad4844ccc89ce142c9962256f
Source noteuspto-grants-2015_03