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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2302245Generated: October 31, 2026

6-Quinolinecarboxylic acid → HCID 9867182, compound

https://huagongshe.com/reaction/2302245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Quinolinecarboxylic acidHCID 82571—
ReactantHCID 16793499HCID 16793499—
ProductHCID 9867182HCID 986718218%

Reaction Steps

Using an analogous procedure to that described in Example 3, quinoline-6-carboxylic acid was reacted with N-(3-amino-4-chlorophenyl)-4-cyanobenzamide. The crude reaction product was purified by column chromatography on silica using a 97:3 mixture of methylene chloride and methanol as eluent. There was thus obtained the title compound in 18% yield; NMR Spectrum: (DMSOd6) 7.58 (d, 1H), 7.62 (m, 1H), 7.77 (m, 1H), 8.01 (d, 2H), 8.12 (t, 4H), 8.28 (d, 2H), 8.56 (d, 1H), 8.67 (s, 1H), 9.01 (d, 1H), 10.34 (s, 1H), 10.67 (s, 1H); Mass Spectrum: M−H− 425.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432949B1
Source datasetuspto-grants-2002_08
ORD IDord-57854f18c84c4cd38e705f744149f2e2
Source noteuspto-grants-2002_08