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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220123Generated: October 28, 2026

3-Chloro-4-(2-pyridylmethoxy)aniline → 4-(3-Chloro-4-(pyridin-2-ylmethoxy)phenylamino)-quinazoline-6-carboxylic acid methoxymethylamide

https://huagongshe.com/reaction/220123

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-(2-pyridylmethoxy)anilineHCID 16781212—
Reactant4-Chloroquinazoline-6-carboxylic acid methoxymethylamideHCID 86630923—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Chloro-4-(pyridin-2-ylmethoxy)phenylamino)-quinazoline-6-carboxylic acid methoxymethylamideHCID 6875379076.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Chloroquinazoline-6-carboxylic acid methoxymethylamide (XIV-1, 5.78 g) was dissolved in tetrahydrofuran (100 ml), and 5.39 g of 3-chloro-4 (pyridin-2-ylmethoxy)aniline was added, followed by stirring at 60° C. for 1 hour. A precipitate was filtered, and washed with tetrahydrofuran to obtain 4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)-quinazoline-6-carboxylic acid methoxymethylamide (XI-2, 7.87 g) as a white solid. The filtrate was allowed to stand at room temperature, and the resulting precipitate was collected by filtration, to newly obtain 2.21 g of XI-2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202879B2
Source datasetuspto-grants-2012_06
ORD IDord-8ded8dd40a514f9387d69b4c64f5bd37
Source noteuspto-grants-2012_06