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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436303Generated: November 3, 2026

4-Aminopyridine → 2-Methyl-N-(pyridin-4-yl)quinazolin-4-amine

https://huagongshe.com/reaction/1436303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
Reactant4-Chloro-2-methylquinazolineHCID 2785421—
Product2-Methyl-N-(pyridin-4-yl)quinazolin-4-amineHCID 57938810—

Reaction Steps

The title compound was prepared from 4-chloro-2-methyl-quinazoline and 4-amino-pyridine by a procedure similar to examples 100. 1H NMR (CDCl3): 8.58 (m, 1H), 7.79-7.93 (m, 5H), 7.70 (s, broad, 1H), 7.55 (ddd, J=1.2, 6.9, 8.1, 1H), 2.79 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618975B2
Source datasetuspto-grants-2009_11
ORD IDord-4341317c505248b9bc66d65c6feec8ba
Source noteuspto-grants-2009_11