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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876077Generated: November 2, 2026

6-Methoxy-3-pyridinylamine → 2-Chloro-N-(6-methoxypyridin-3-yl)quinazolin-4-amine

https://huagongshe.com/reaction/1876077

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-3-pyridinylamineHCID 81121—
Reactant2,4-DichloroquinazolineHCID 252886—
ReactantSodium AcetateHCID 517045—
SolventEthyl AcetateHCID 8857—
Product2-Chloro-N-(6-methoxypyridin-3-yl)quinazolin-4-amineHCID 5793878198%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2,4-dichloroquinazoline (61 mg, 0.31 mmol), 5-amino-2-methoxy pyridine (40 mg, 0.32 mmol) and sodium acetate (38 mg, 0.46 mmol) in 3 mL of solvent (THF:water/1:1) was stirred at 60° C. for 45 min. The reaction mixture was diluted with 25 mL of ethyl acetate. It was washed with saturated NaCl, dried over anhydrous MgSO4, filtered and concentrated. The crude product was purified by chromatography (40% ethyl acetate/hexanes) on silica gel to give the title compound (86 mg, 0.30 mmol, 98%). 1H NMR (CDCl3): 8.38 (d, J=3.0 Hz, 1H), 8.07 (dd, J=8.7 and 3.0 Hz, 1H), 7.89-7.79 (d, J=8.4 Hz, 1H), 7.86 (m, 2H), 7.59-7.53 (m, 2H), 6.84 (d, J=8.7 Hz, 1H), 3.96 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309562B2
Source datasetuspto-grants-2012_11
ORD IDord-11e788fb1e8f46d5ac3b94d63d775ce4
Source noteuspto-grants-2012_11