تفاعل #69447

ord-60e44a26519f419db7b74f7c8a9c59d3

معادلة التفاعل

COC(=O)c1cc(C2CCCN2)c2oc(N3CCOCC3)cc(=O)c2c1
methyl 2-morpholino-4-oxo-8-(pyrrolidin-2-yl)-4H-chromene-6-carboxylate
Fc1cc(F)cc(Br)c1
1-bromo-3,5-difluorobenzene
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
methyl 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate
المردود 58.4%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe resulting suspension was degassed with argon
  2. 2
    درجة الحرارةto cool to room temperature
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe crude product was purified by flash chromatography on silica gel eluting with 0 to 6% MeOH in EtAc
  6. 6
    أخرىThe solvent was evaporated to dryness

الإجراء التجريبي

Palladium complex (33 mg, 0.04 mmol, see below) was added to a stirred mixture of methyl 2-morpholino-4-oxo-8-(pyrrolidin-2-yl)-4H-chromene-6-carboxylate (270 mg, 0.75 mmol), 1-bromo-3,5-difluorobenzene (0.095 ml, 0.83 mmol) and cesium carbonate (368 mg, 1.13 mmol) dissolved in 1,4-dioxane (5 mL). The resulting suspension was degassed with argon and then stirred at 80° C. for 23 h. The reaction mixture was allowed to cool to room temperature, filtered and concentrated. The crude product was purified by flash chromatography on silica gel eluting with 0 to 6% MeOH in EtAc. The solvent was evaporated to dryness to afford methyl 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate (206 mg, 58%) as a clear yellow foam.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08530470B2uspto-grants-2013_09