反応 #325831

ord-1794439bd43c4443a22a56ee45e8677f

反応方程式

COC(C)=O
acetic acid methyl ester
CCS(=O)(=O)c1cnc(Cl)c(Br)c1
3-bromo-2-chloro-5-ethanesulfonyl-pyridine
COC(=O)C(=Cc1ccc(F)cc1)C(C)C(=O)O
methyl ester
COC(=O)C(=Cc1ccc(F)cc1)C(C)C(=O)O
2-(4-fluoro-benzylidene)-3-methyl-succinic acid 1-methyl ester
CCS(=O)(=O)c1cnc(Oc2c(C)c(CC(=O)OC)cc3ccc(F)cc23)c(Br)c1
[4-(3-bromo-5-ethanesulfonyl-pyridin-2-yloxy)-6-fluoro-3-methyl-naphthalen-2-yl]-acetic acid methyl ester
収率 73.9%

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

Starting with 6-fluoro-4-hydroxy-3-methyl-naphthalen-2-yl)-acetic acid methyl ester (124 mg, 0.50 mmol) and 3-bromo-2-chloro-5-ethanesulfonyl-pyridine (157 mg, 0.55 mmol), using a method analogous to the one described for the methyl ester of example 2-1, [4-(3-bromo-5-ethanesulfonyl-pyridin-2-yloxy)-6-fluoro-3-methyl-naphthalen-2-yl]-acetic acid methyl ester (183 mg, 73.9%) was obtained as a white solid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08642629B2uspto-grants-2014_02