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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926611Generated: November 2, 2026

Tetrahydrofuran → HCID 118006303, compound

https://huagongshe.com/reaction/926611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 118006217HCID 118006217—
ReactantHCID 178478191HCID 178478191—
SolventDiethyl EtherHCID 3283—
ProductHCID 118006303HCID 118006303—

Reaction Steps

A solution of LaCl3-2LiCl in THF (0.36 mL, 0.22 mmol, 0.6 M in THF) was added to a solution of 3-(4-(1H-pyrazol-1-yl)benzyl)-6-(1-methyl-1H-imidazole-5-carbonyl)quinoline-2,4-dicarbonitrile (50 mg, 0.08 mmol, Intermediate 14: step e) in THF (1.8 mL) at room temperature. After 15 minutes of stirring, a solution of 4-chlorophenyl magnesium bromide (0.32 mL, 0.32 mmol) in diethylether was added dropwise at 0° C. After stirring for 30 minutes, the reaction mixture was quenched with a saturated aqueous solution of NH4Cl and the mixture was partitioned between water and DCM. The layers were separated and the aqueous phase was further extracted with DCM. The organic layers were combined, washed with saturated aqueous NaCl solution, dried (MgSO4), filtered, and concentrated to dryness. The crude product was purified by flash column chromatography (silica gel, 0-7% MeOH-DCM) to provide the title compound. MS m/e 570.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-f2d2743f70f84358b72e54094030f321
Source noteuspto-grants-2016_03