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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406174Generated: October 30, 2026

1,3-Dimethyl-2-imidazolidinone → HCID 66665632, compound

https://huagongshe.com/reaction/406174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantLithium BromideHCID 82050—
ReactantHCID 86681846HCID 86681846—
ReactantHCID 178471412HCID 178471412—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66665632HCID 66665632—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture comprising lithium bromide (307 mg, 3.54 mmol) and PEPPSi-iPr catalyst (75 mg, 0.110 mmol) in THF (2 ml) was stirred at room temperature for 15 minutes until a solution formed. (6-Ethoxy-6-oxohexyl)zinc(II) bromide (13.26 ml of a 0.5M solution in THF, 6.62 mmol) was added and the mixture was cooled to 0° C. A solution of 7-chloro-2,3-diphenyl-1,8-naphthyridine (step 1) (350 mg, 1.105 mmol) in THF (3 ml)/DMI (1 ml) was added and the resulting mixture was stirred at room temperature for 24 h. The reaction mixture was partitioned between EtOAc and water and the organic portion was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. Purification of the crude product by chromatography on silica eluting with 0-50% EtOAc in iso-hexane afforded the title product as a yellow oil; LC-MS Rt=1.54 mins; [M+H]+425.3, Method 2minLC_v002

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754085B2
Source datasetuspto-grants-2014_06
ORD IDord-933372fc2c32482e8f3bcaefdd54857b
Source noteuspto-grants-2014_06