Oxalyl chloride → 2-(4-Fluorophenyl)acetyl isocyanate

HRID 2117063Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2117063
FC1C=CC(CC(N)=O)=CC=1.C(Cl)(=O)C(Cl)=O.[F:18][C:19]1[CH:24]=[CH:23][C:22]([CH2:25][C:26]([NH:28][C:29](=O)[O:30]C)=[O:27])=[CH:21][CH:20]=1>ClC(Cl)C>[F:18][C:19]1[CH:20]=[CH:21][C:22]([CH2:25][C:26]([N:28]=[C:29]=[O:30])=[O:27])=[CH:23][CH:24]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

To a solution/suspension of 4-fluorophenylacetamide (77 mg, 0.50 mmol, see generally, J. Med. Chem. 2003, 46, 4333-4341, the disclosure of which is herein incorporated by referene) in dichloroethane (2 mL) was added oxalyl chloride (0.175 mL, 2.00 mmol). The reaction was heated at 80° C. for 24 h and then 70° C. for two days. By this time, most of the solids had dissolved and the reaction was yellow. LC/MS analysis found a peak with a molecular weight of 211 corresponding to methyl 2-(4-fluorophenyl)acetylcarbamate, resulting from quenching of the isocyanate with methanol. The reaction was concentrated in vacuo to give a yellow slurry. The slurry was redissolved in dichloroethane (2 mL) and again concentrated in vacuo. The resulting residue was redissolved again in dichloroethane (2 mL) to give a 0.25 M solution of 2-(4-fluorophenyl)acetyl isocyanate in dichloroethane, which was used directly in subsequent reactions.

Aufarbeitung

  1. dissolutionBy this time, most of the solids had dissolved
  2. customresulting
  3. customfrom quenching of the isocyanate with methanol
  4. concentrationThe reaction was concentrated in vacuo
  5. customto give a yellow slurry
  6. concentrationagain concentrated in vacuo
  7. dissolutionThe resulting residue was redissolved again in dichloroethane (2 mL)

Quellen und Nachweise

ORD-Eintrag
ord-1364d466808840128cf17b0c78d0a9cd
Quelldatensatz
uspto-grants-2008_10
Patentnummer
US07439246B2

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