反応 #1111884

ord-95e5569b5d6a408a88df5a689d5cfcb0

反応方程式

N#Cc1ccc(Oc2nc(Oc3ccc(OC(F)(F)F)cc3)ccc2C(=O)O)cc1
2-(4-cyano phenoxy)-6-(4-trifluoromethoxy phenoxy)nicotinic acid
CC(C)(C)OC(=O)NCCC1CCNCC1
(2-Piperidin-4-yl-ethyl)-carbamic acid tert-butyl ester
CC(C)(C)OC(=O)NCCC1CCN(C(=O)c2ccc(Oc3ccc(OC(F)(F)F)cc3)nc2Oc2ccc(C#N)cc2)CC1
required product
収率 69.8%
CC(C)(C)OC(=O)NCCC1CCN(C(=O)c2ccc(Oc3ccc(OC(F)(F)F)cc3)nc2Oc2ccc(C#N)cc2)CC1
(2-{1-[2-(4-cyanophenoxy)-6-(4-trifluoromethoxyphenoxy)pyridine-3-carbonyl]piperidin-4-yl}ethyl)carbamic Acid Tert-butyl Ester
収率 69.8%

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

2-(4-cyano phenoxy)-6-(4-trifluoromethoxy phenoxy)nicotinic acid (0.2 g, 0.48 mmol) and (2-Piperidin-4-yl-ethyl)-carbamic acid tert-butyl ester (0.11 g, 0.48 mmol) were coupled using the procedure of Example 5(c) to afford 0.21 g of the required product. Percentage purity (LCMS): 68.11%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08722930B2uspto-grants-2014_05