Reaktion #69458

ord-cf80b1b2cc91478aa981d2ca01c97ae6

Reaktionsgleichung

CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[B-](F)(F)F
TBTU
O=C(O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid
CN1CCOCC1
4-methylmorpholine
CNCCO
2-(methylamino)ethanol
CN(CCO)C(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-N-(2-hydroxyethyl)-N-methyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide
Ausbeute 71.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethen purified by preparative HPLC
  2. 2
    SonstigeThe fractions were evaporated to dryness
  3. 3
    Sonstigetriturated in diethyl ether
  4. 4
    Sonstigeto afford a solid
  5. 5
    FiltrationThis material was collected by filtration
  6. 6
    Waschenwashed with diethyl ether
  7. 7
    Sonstigedried under vacuum at 50° C.

Vorschrift

TBTU (102 mg, 0.32 mmol) was added to a stirred solution of 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylic acid (105 mg, 0.21 mmol), 4-methylmorpholine (0.070 mL, 0.63 mmol) and 2-(methylamino)ethanol (0.022 mL, 0.28 mmol) dissolved in NMP (1.5 mL). The resulting solution was stirred at room temperature for 16 h then purified by preparative HPLC. The fractions were evaporated to dryness and triturated in diethyl ether to afford a solid. This material was collected by filtration, washed with diethyl ether and dried under vacuum at 50° C. to afford 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-N-(2-hydroxyethyl)-N-methyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide (77 mg, 71%) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08530470B2uspto-grants-2013_09