تفاعل #838023

ord-8afdae1b7b9e477bb0a34c9dfbb90332

معادلة التفاعل

CS(=O)(=O)c1ncc(-c2ccc(Cl)cc2)c(-c2ccc(Cl)cc2Cl)n1
2-methylsulfonyl-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine
Oc1ccc(F)cc1
4-fluorophenol
O=C([O-])[O-].[K+].[K+]
K2CO3
COCCOCCN(CCOCCOC)CCOCCOC
tris[2-(2-methoxyethoxy)-ethyl]amine
Fc1ccc(Oc2ncc(-c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3Cl)n2)cc1
desired product
Fc1ccc(Oc2ncc(-c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3Cl)n2)cc1
2-(4-Fluorophenyloxy)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine

المذيبات

ظروف التفاعل

درجة الحرارة
70°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a 5 mL round bottom flask fitted with a stirrer bar

الإجراء التجريبي

To a 5 mL round bottom flask fitted with a stirrer bar and septum was added 2 mL CH3CN and 2-methylsulfonyl-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine from from Reference Example 3 (100 mg, 0.24 mmol). Then 4-fluorophenol (10 eq., 269 mg, 2.4 mmol), K2CO3 (2 eq., 66.3 mg, 0.48 mmol) and a drop of tris[2-(2-methoxyethoxy)-ethyl]amine were added via syringe and the mixture heated at 70° C. for 2 h. By HPLC/MS, the starting material was converted to the desired product. The product was extracted from 10 mL water with 20 mL ethyl acetate, dried over anhydrous MgSO4, filtered and the solvent removed under reduced pressure. Flash column chromatography on silica gel (eluted with 90/10 hexanes/ethyl acetate) afforded 2-(4-fluorophenyloxy)-4-(2,4-dichlorophenyl)-5-(4-chlorophenyl)pyrimidine: HPLC/MS: m/e=445 (M++1); Rt=4.53 min; 1H-NMR 400 MHz (CDCl3): δ 7.02 (d, J=9 Hz, 2H), 7.20-7.40 (m, 9H), 8.80 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07405221B2uspto-grants-2008_07