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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025546Generated: October 31, 2026

1,1'-Carbonyldiimidazole → HCID 67293127, compound

https://huagongshe.com/reaction/1025546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant8-Hydroxyquinoline-7-carboxylic AcidHCID 231363—
Reactant1224640-26-9HCID 55212074—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67293127HCID 6729312713.3%

Reaction Steps

A mixture of 8-hydroxyquinoline-7-carboxylic acid (100 mg, 0.53 mmol) and di(1H-imidazol-1-yl)methanone (86 mg, 0.53 mmol) in THF (6 mL) was heated to reflux for 4 h, under nitrogen. The reaction mixture was allowed to cool to RT and 7-fluoro-1,2,3,4-tetrahydroquinoline hydrochloride (84.4 mg, 0.45 mmol) and TEA (0.062 mL, 0.45 mmol) were added. The resulting mixture was heated in a MW oven at 120° C. for 90 min and then at 140° C. for 2 h. The reaction mixture was then quenched with H2O and an aqueous saturated solution of sodium hydrogen carbonate, and twice extracted with DCM. The separated organics were dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by preparative HPLC. Product-containing fractions were combined, made basic with a saturated aqueous solution of sodium hydrogen carbonate and CH3CN was removed under reduced pressure. The aqueous phase was extracted with DCM and the separated organics dried over Na2SO4, filtered and concentrated to dryness, affording the title compound (19 mg, 0.06 mmol) as a off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729098B2
Source datasetuspto-grants-2014_05
ORD IDord-0cfef7f8bce04a838ca3ccdea869d94d
Source noteuspto-grants-2014_05