Reaktion #8699

ord-1651722f46a94c749ccc1cc5a9bbb235

Reaktionsgleichung

[H-].[Na+]
NaH
OCCO
ethylene glycol
[H-].[Na+]
NaH
COc1ccccc1Oc1c(Cl)nc(-c2ccncc2)nc1NS(=O)(=O)CCc1ccccc1
2-phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide
COc1ccccc1Oc1c(NS(=O)(=O)CCc2ccccc2)nc(-c2ccncc2)nc1OCCO
2-phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide

Lösungsmittel

Reaktionsbedingungen

Temperatur
90°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGstirring
  2. 2
    workup.WAITwas continued at 90° C. for 4 d
  3. 3
    Waschenwashed once with 10% aq. citric acid and 3 times with water
  4. 4
    SonstigeThe organic phase was evaporated
  5. 5
    SonstigeThe solid material was collected
  6. 6
    Waschenwashed with diethyl ether
  7. 7
    Sonstigedried

Vorschrift

To a suspension of NaH (644 mg, 60% in mineral oil) in DME (15 ml) was added ethylene glycol (15 ml). After evolution of gas had ceased, 2-phenyl-ethanesulfonic acid [6-chloro-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide (800 mg) was added and the resulting solution was stirred at 90° C. for 16 h. A further portion of NaH (322 mg) was added and stirring was continued at 90° C. for 4 d. The mixture was diluted with EA (200 ml) and washed once with 10% aq. citric acid and 3 times with water. The organic phase was evaporated and the residue was suspended in diethyl ether. The solid material was collected, washed with diethyl ether and dried to give 2-phenyl-ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-(2-methoxy-phenoxy)-2-pyridin-4-yl-pyrimidin-4-yl]-amide (513 mg) as a beige solid. LC-MS: tR=4.05 min, [M+1]+=523.10, [M−1]−=521.24.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091201B2uspto-grants-2006_08