تفاعل #2155100

ord-d138d451690b412ba96a850638e4d9ef

معادلة التفاعل

CCOC(=O)c1cn(Cc2ccc(Br)cn2)c2c(F)ccc(F)c2c1=O
ethyl 1-[(5-bromopyridin-2-yl)methyl]-5,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate
CC(C)(C)OC(=O)n1cc(B2OC(C)(C)C(C)(C)O2)cn1
tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CCOC(C)=O
Ethyl acetate
CCOC(=O)c1cn(Cc2ccc(-c3cn[nH]c3)cn2)c2c(F)ccc(F)c2c1=O
ethyl 5,8-difluoro-4-oxo-1-{[5-(1H-pyrazol-4-yl)pyridin-2-yl]methyl}-1,4-dihydroquinoline-3-carboxylate

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled to room temperature
  2. 2
    أخرىthe resultant brown solid was collected

الإجراء التجريبي

To a solution of ethyl 1-[(5-bromopyridin-2-yl)methyl]-5,8-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate (3.00 g, 7.09 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-carboxylate (5.42 g, 18.4 mmol), and 1 N cesium carbonate (14.2 mL, 14.2 mmol) in 50 mL of THF under nitrogen was added bis(tri-tert-butylphosphoranyl)palladium (10 mol %). The reaction mixture was heated to 100° C. for 20 hours, then cooled to room temperature. Ethyl acetate (100 mL) and water (100 mL) were added, and the resultant brown solid was collected to provide ethyl 5,8-difluoro-4-oxo-1-{[5-(1H-pyrazol-4-yl)pyridin-2-yl]methyl}-1,4-dihydroquinoline-3-carboxylate that gave a proton NMR spectra consistent with theory and a mass ion (ES+) of 411.0 for M+H+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08293914B2uspto-grants-2012_10