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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080234Generated: November 3, 2026

Quinoline → HCID 58387874, compound

https://huagongshe.com/reaction/2080234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
ReactantHCID 67119620HCID 67119620—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58387874HCID 5838787492%

Reaction Steps

To a mixture of quinoline-6-carboxylic acid 4-phenylethenyl-benzylamide described in Preparation Example E+-5 (48 mg, 0.13 mmol), quinoline (26 mg, 0.20 mmol) and tetrahydrofuran (2 mL) was added Linear catalyst (5.0 mg), and the solution was stirred under hydrogen atmosphere at room temperature for 1 hour. The interior of the reaction system was changed to nitrogen atmosphere, then, filtration was carried out through Celite pad. The filtrate was evaporated in vacuo, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:4), and the title compound (45 mg, 0.12 mmol, 92%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-93ac92695b624efeb73bd9e589f9ca52
Source noteuspto-grants-2011_04