Cyanamide → 4-(4-Fluorophenoxy)phenethyl carbamimidate

HRID 705881Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 705881
[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][OH:17])=[CH:11][CH:10]=2)=[CH:4][CH:3]=1.[N:18]#[C:19][NH2:20].FC(F)(F)S(O)(=O)=O>C1COCC1>[C:19](=[NH:18])([O:17][CH2:16][CH2:15][C:12]1[CH:13]=[CH:14][C:9]([O:8][C:5]2[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=2)=[CH:10][CH:11]=1)[NH2:20]

Komponenten

5

Edukt 3

HCID 9864CyanamideHCID 62406Trifluoromethanesulfonic acidHCID 677754954-(4-Fluorophenoxy)phenethyl alcohol

Produkt 1

HCID 679525344-(4-Fluorophenoxy)phenethyl carbamimidateAusbeute 32,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 2-{4-[(4-fluorophenyl)oxy]phenyl}ethanol (750 mg, 3.23 mmol) and cyanamide (149 mg, 3.55 mmol) in THF (15 mL) was added trifluoromethanesulfonic acid (0.344 mL, 3.88 mmol) at 0° C. The reaction mixture was stirred at room temperature overnight. After removing the solvent, the residue was diluted with water, extracted with DCM. The organic phase was dried over sodium sulfate, filtered, and concentrated. Purification via reverse phase flash chromatography then afforded the title compound (290 mg, 1.057 mmol, 32.7% yield).

Aufarbeitung

  1. customAfter removing the solvent
  2. additionthe residue was diluted with water
  3. extractionextracted with DCM
  4. dry with materialThe organic phase was dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customPurification via reverse phase flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-8e43322c0f444268bf352fb3cd7e10bb
Quelldatensatz
uspto-grants-2015_11
Patentnummer
US09174968B2

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