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Iodine → Methyl 4-amino-6-chloro-5-fluoro-3-iodopicolinate

HRID 75097
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 75097
[NH2:1][C:2]1[C:7]([F:8])=[C:6]([Cl:9])[N:5]=[C:4]([C:10]([O:12][CH3:13])=[O:11])[CH:3]=1.[I:14](O)(=O)(=O)=O.II>CO>[NH2:1][C:2]1[C:7]([F:8])=[C:6]([Cl:9])[N:5]=[C:4]([C:10]([O:12][CH3:13])=[O:11])[C:3]=1[I:14]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 807IodineHCID 65185Metaperiodic acidHCID 86668302Methyl 4-amino-6-chloro-5-fluoropicolinate

Produkt 1

HCID 86668303Methyl 4-amino-6-chloro-5-fluoro-3-iodopicolinateAusbeute 194 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

Methyl 4-amino-6-chloro-5-fluoropicolinate (2.2 g, 10.8 mmol) was dissolved in methyl alcohol (20 mL). The solution was treated with periodic acid (880 mg, 3.9 mmol) and iodine (2.2 g, 8.6 mmol) and then heated at reflux for 20 h. The mixture was cooled, and the volatiles were removed under vacuum. The residue was dissolved in EtOAc (50 mL) and then stirred with 10% NaHSO3 solution (20 mL) for 10 min. The organic phase was separated and washed with satd aq NaCl (10 mL), dried (Na2SO4) and evaporated. The residue was purified by silica gel chromatography (5-50% EtOAc-hexane gradient) to give the title compound as a light orange solid (2.5 g, 70%): mp 149-151° C.; ESIMS m/z 330 ([M]+); 1H NMR (400 MHz, CDCl3) δ 5.17 (s, 2H, NH2), 3.97 (s, 3H, OMe); 19F NMR (376 MHz, CDCl3) δ −135.79 (s).

Aufarbeitung

  1. temperatureheated
  2. temperatureat reflux for 20 h
  3. temperatureThe mixture was cooled
  4. customthe volatiles were removed under vacuum
  5. dissolutionThe residue was dissolved in EtOAc (50 mL)
  6. customThe organic phase was separated
  7. washwashed with satd aq NaCl (10 mL)
  8. dry with materialdried (Na2SO4)
  9. customevaporated
  10. customThe residue was purified by silica gel chromatography (5-50% EtOAc-hexane gradient)

Quellen und Nachweise

ORD-Eintrag
ord-2712a8aeddff4f0b972d1f42640d4120
Quelldatensatz
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08835409B2

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