反应 #48122
ord-92edc8facad94061b468a8aadbad725c
反应方程式
(4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone
(4,4-Difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone
intermediate 1
(4,4-Difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone
4-fluorobenzyl bromide
→
title compound
(4,4-Difluoro-piperidin-1-yl)-[1-(4-fluoro-benzyl)-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone
反应物
(4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone
(4,4-Difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone
intermediate 1
(4,4-Difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone
4-fluorobenzyl bromide
试剂
无
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1其他In analogy to the procedure described for the synthesis of example 1
实验过程
In analogy to the procedure described for the synthesis of example 1, the title compound was synthesized from (4,4-difluoro-piperidin-1-yl)-[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-methanone (intermediate 1) and 4-fluorobenzyl bromide. The title compound was obtained in 5% yield as yellow oil. MS (m/e): 514.3 (MH+, 100%).