Thionyl Chloride → n-[2-[1-(2-Chlorophenyl)-3-(trifluoromethyl)-1h-pyrazol-5-yl]-8-methyl-4h-3,1-benzoxazin-4-ylidene]-2-propanamine

HRID 857857Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 857857
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:12]([C:13]([NH:15][C:16]2[C:21]([C:22]([NH:24][CH:25]([CH3:27])[CH3:26])=[O:23])=[CH:20][CH:19]=[CH:18][C:17]=2[CH3:28])=O)=[CH:11][C:10]([C:29]([F:32])([F:31])[F:30])=[N:9]1.S(Cl)(Cl)=O>ClCCl>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:12]([C:13]2[O:23][C:22](=[N:24][CH:25]([CH3:26])[CH3:27])[C:21]3[CH:20]=[CH:19][CH:18]=[C:17]([CH3:28])[C:16]=3[N:15]=2)=[CH:11][C:10]([C:29]([F:32])([F:31])[F:30])=[N:9]1

Komponenten

4

Edukt 2

HCID 24386Thionyl ChlorideHCID 444044961-(2-Chlorophenyl)-n-[2-methyl-6-[[(1-methylethyl)amino]carbonyl]phenyl]-3-(trifluoromethyl)-1h-pyrazole-5-carboxamide

Produkt 1

HCID 69183093n-[2-[1-(2-Chlorophenyl)-3-(trifluoromethyl)-1h-pyrazol-5-yl]-8-methyl-4h-3,1-benzoxazin-4-ylidene]-2-propanamineAusbeute 58 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To the title compound of Step D (1.2 g, 2.7 mmol) dissolved in 8 mL of dichloromethane, 5 mL of thionyl chloride was added and the solution heated at reflux for 8 hours. The solvent was removed in vacuo aid remaining residue partitioned between 70 mL of ethyl acetate and water. The organic layer was separated, washed with water, saturated aqueous sodium bicarbonate and brine. The organic phase was dried over magnesium sulfate and the solvent was removed in vacuo to give a crude oily solid residue. Purification by flash chromatography on silica gel (2:1 hexane/ethyl acetate) and filtering from hexane afforded 700 mg of the title compound, a compound of the invention, isolated as a white solid melting at 133–135° C.

Aufarbeitung

  1. temperaturethe solution heated
  2. temperatureat reflux for 8 hours
  3. customThe solvent was removed in vacuo aid
  4. custompartitioned between 70 mL of ethyl acetate and water
  5. customThe organic layer was separated
  6. washwashed with water, saturated aqueous sodium bicarbonate and brine
  7. dry with materialThe organic phase was dried over magnesium sulfate
  8. customthe solvent was removed in vacuo
  9. customto give a crude oily solid residue
  10. customPurification by flash chromatography on silica gel (2:1 hexane/ethyl acetate)
  11. filtrationfiltering from hexane

Quellen und Nachweise

ORD-Eintrag
ord-7c26ed9e3bb149298cedbc3e4a396378
Quelldatensatz
uspto-grants-2006_12
Patentnummer
US07148217B2

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