تفاعل #8743

ord-a6ff9daab63b4b308f667c53494f9a38

معادلة التفاعل

BrCCCOc1cccc(-c2noc3ccsc23)c1
3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole
ClCCCOc1cccc(-c2noc3ccsc23)c1
3-[3-(3-chloro-propoxy)-phenyl]-thieno[2,3-d]isoxazole
COc1ccc(CN)cc1
4-methoxybenzylamine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
title compound
المردود 100.0%
COc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
(4-methoxy-benzyl)-[3-(3-thieno[2,3-d]isoxazol-3-yl-phenoxy)-propyl]-amine
المردود 100.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزCombine the appropriate fractions and concentrate

الإجراء التجريبي

The title compound is prepared from a mixture of 3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole, 3-[3-(3-chloro-propoxy)-phenyl]-thieno[2,3-d]isoxazole, 4-methoxybenzylamine and potassium carbonate essentially as described above in example 4. Combine the appropriate fractions and concentrate to give the title compound (0.44 g, 100% Yield) as a solid. Purity by LC/MS (APCI)=100% area, [M+H]+=395 m/e.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091199B1uspto-grants-2006_08