반응 #366778

ord-87027db21fb54e789cd8687809145b7e

반응 방정식

OCc1ccnc(Cl)c1
2-chloro-4-hydroxymethylpyridine
O=S(Cl)Cl
thionyl chloride
Cl.ClCc1ccnc(Cl)c1
2-chloro-4-chloromethylpyridine hydrochloride

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The volatiles were removed by evaporation

실험 절차

A mixture of 2-chloro-4-hydroxymethylpyridine (180 mg, 1.25 mmol), thionyl chloride (0.2 ml) in toluene (10 ml) was stirred at ambient temperature for 1 hour. The volatiles were removed by evaporation to give 2-chloro-4-chloromethylpyridine hydrochloride (180 mg, 0.9 mmol). A mixture of 7-hydroxy-6-methoxy-4-phenoxyquinazoline (268 mg, 1 mmol), (prepared as described for the starting material in Example 13), potassium carbonate (680 mg, 5 mmol) and DMF (10 ml) was added to this crude product and the mixture was heated at 90° C. for 1 hour. The mixture was allowed to cool, diluted with water and extracted with ethyl acetate (3×70 ml). The extracts were combined, washed with water (×3) and brine, dried (MgSO4) and the solvent removed by evaporation to give 7-((2-chloro-4-pyridyl)methoxy)-6-methoxy-4-phenoxyquinazoline (260 mg, 66%) as a solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06362336B1uspto-grants-2002_03