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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415723Generated: October 26, 2026

Quinoline-6-carbonyl chloride → 4-methyl-N-(3-morpholinophenyl)-3-(6-quinolylcarbonylamino)benzamide

https://huagongshe.com/reaction/2415723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoline-6-carbonyl chlorideHCID 12391963—
Reactant3-amino-4-methyl-N-(3-morpholinophenyl)benzamideHCID 22636145—
Product4-methyl-N-(3-morpholinophenyl)-3-(6-quinolylcarbonylamino)benzamideHCID 22636159—

Reaction Steps

Using an analogous procedure to that described in Example 1, 6-quinolylcarbonyl chloride was reacted with 3-amino-4-methyl-N-(3-morpholinophenyl)benzamide to give the title compound; NMR Spectrum: (DMSOd6) 2.35 (s, 3H), 3.0-3.1 (m, 4H), 3.65-3.75 (m, 4H), 6.65-6.7 (m, 1H), 7.17 (t, 1H), 7.3-7.35 (m, 1H), 7.38-7.48 (m, 2H), 7.6-7.7 (m, 1H), 7.8-7.85 (m, 1H), 8.0 (s, 1H), 8.1-8.15 (m, 1H), 8.3-8.35 (m, 1H), 8.5-8.55 (m, 1H), 8.7 (s, 1H), 8.98-9.02 (m, 1H), 10.0-10.1 (br s, 1H), 10.25-10.35 (br s, 1H); Mass Spectrum: M+H+ 467.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06821965B1
Source datasetuspto-grants-2004_11
ORD IDord-5baacfec9bc24301994773a051051e87
Source noteuspto-grants-2004_11