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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112816Generated: November 2, 2026

2-Chloro-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinoline → {6-[5-(4-Chlorophenyl)pyridin-2-ylethynyl]-4-methylquinolin-2-yl} methylamine

https://huagongshe.com/reaction/2112816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinolineHCID 86079850—
Reactant2-Bromo-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinolineHCID 86079852—
SolventDimethylformamideHCID 6228—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product{6-[5-(4-Chlorophenyl)pyridin-2-ylethynyl]-4-methylquinolin-2-yl} methylamineHCID 69064008—

Reaction Steps

Analogously to Example 1k, the following Examples may be prepared starting from 2-chloro-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinoline (Example 1h) or 2-bromo-6-[5-(4-chlorophenyl)pyridin-2-ylethynyl]-4-methylquinoline (Example 1i) and the corresponding amines: Examples 1.8-1.9, 1.11, 1.15-1.21, 1.23 and 1.28 were prepared by heating in NMP in the microwave (300 W, 190° C.; 30-60 min); Example 1.13 was prepared by heating in DMF in the microwave (150 W, 170° C.; 10 min); and Example 1.51 was obtained as a by-product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524862B2
Source datasetuspto-grants-2009_04
ORD IDord-2e4afacdc5e44c009b05356c39df2ea5
Source noteuspto-grants-2009_04