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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036773Generated: October 25, 2026

Triethylamine → 2-chloro-5-phenyl-N-(pyridin-2-ylmethyl)quinazolin-4-amine

https://huagongshe.com/reaction/2036773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-PyridinemethanamineHCID 19509—
ReactantHCID 71741791HCID 71741791—
SolventTetrahydrofuranHCID 8028—
Product2-chloro-5-phenyl-N-(pyridin-2-ylmethyl)quinazolin-4-amineHCID 8667061375.7%

Reaction Steps

2,4-Dichloro-5-phenylquinazoline (1.38 g, 5.03 mmol) was dissolved in THF (80 mL) and triethylamine (1.33 mL, 9.56 mmol) was added dropwise. The mixture was stirred for 5 min at room temperature and then pyridin-2-ylmethanamine (0.57 mL, 5.53 mmol) was added dropwise. The resulting mixture was stirred at ambient temperature for 14 hours. After this time, the mixture was filtered through a medium porosity glass frit, concentrated to dryness under reduced pressure and then purified by ISCO flash column chromatography (80 g silica gel column) eluting with 0-100% ethyl acetate/hexanes over 30 min to provide 2-chloro-5-phenyl-N-(pyridin-2-ylmethyl)quinazolin-4-amine (1.32 g, 75%). LCMS Method A [M+1] observed 347.1. HPLC Method B: Purity 99.1% retention time 6.66 min. 1H NMR (400 MHz, chloroform-d) δ ppm 8.16 (1H, d, J=4.77 Hz), 7.79 (1H, d, J=7.28 Hz), 7.70 (1H, t, J=7.78 Hz), 7.59 (1H, dt, J=7.53, 1.51 Hz), 7.40-7.55 (5H, m), 7.08-7.25 (4H, m), 4.66 (2H, d, J=4.02 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575184B2
Source datasetuspto-grants-2013_11
ORD IDord-7716253c92b2408dbd1801fb5e933477
Source noteuspto-grants-2013_11