Реакция #1906407

ord-37fd63391e3b4c82af897ec9c452f83a

Уравнение реакции

O=C(O)c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1
4-{1-[5-chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}benzoic acid
c1ccc(CCN2CCNCC2)nc1
1-piperazinyl-2-(2-pyridinyl)ethane
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1)N1CCN(CCc2ccccn2)CC1
title compound
O=C(c1ccc(-c2cnc3c(c2)N(Cc2cc(Cl)ccc2C(F)(F)F)CCN3)cc1)N1CCN(CCc2ccccn2)CC1
(4-{1-[5-Chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}phenyl)-[4-(2-pyridin-2-yl-ethyl)piperazin-1-yl]methanone

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

4-{1-[5-chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}benzoic acid was reacted with 1-piperazinyl-2-(2-pyridinyl)ethane as in General Procedure 10 to give the title compound. LCMS: m/z=620.98 (M+H+); retention time=0.53 minutes.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07601716B2uspto-grants-2009_10