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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869082Generated: October 30, 2026

Pyridine → HCID 18925013, compound

https://huagongshe.com/reaction/1869082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Chloro-6,7-bis(2-methoxyethoxy)quinazolineHCID 11289942—
Reactant5-Ethynyl-2-methylanilineHCID 18925060—
SolventDimethylformamideHCID 6228—
ProductHCID 18925013HCID 1892501319%

Reaction Steps

4-Chloro-6,7-bis-(2-methoxy-ethoxy)-quinazoline (153 mg, 0.49 mmol), pyridine (40 μL) and 3-ethynyl-6-methylaniline (71 mg, 0.54 mmol) were reacted in DMF (3 mL) at 110° C. under an atmosphere of N2 for 36 hours. The solvent was removed in vacuo and the residue was partitioned between CHCl3 and saturated aqueous NaHCO3. The organic extracts were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was chromatographed on silica using 40% acetone/CH2Cl2 to provide 40 mg (19%) of pure product as its free base. This oil was dissolved in a minimum volume of CHCl3, diluted with several volumes of ether, and triturated with 1M HCl in ether to precipitate the title product as a white solid (M.P. 170°-185° C. (dec); LC-MS: 408 (MH+); anal. RP18-HPLC RT: 3.93 min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE041065E1
Source datasetuspto-grants-2009_12
ORD IDord-8018fffc136b4a88a48ffd6b2c0b0e07
Source noteuspto-grants-2009_12