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Ammonium Hydroxide → 4-Iodo-6-methoxypyridin-2-amine

HRID 1253563
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1253563
F[C:2]1[CH:7]=[C:6]([I:8])[CH:5]=[C:4]([O:9][CH3:10])[N:3]=1.[OH-].[NH4+:12]>C(O)CCC>[I:8][C:6]1[CH:5]=[C:4]([O:9][CH3:10])[N:3]=[C:2]([NH2:12])[CH:7]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14923Ammonium Hydroxide3×HCID 672052392-Fluoro-4-iodo-6-methoxypyridine

Produkt 1

HCID 672046804-Iodo-6-methoxypyridin-2-amine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 2631-ButanolLösungsmittel

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

To a solution of 2-fluoro-4-iodo-6-methoxypyridine (7.1 g, 28 mmol) in n-butanol (64 ml) was added 28% solution of ammonium hydroxide (20 ml, 140 mmol). The reaction mixture was heated to 120° C. After 16 hours LRMS indicated incomplete conversion to product. Additional 28% solution of ammonium hydroxide (20 ml, 140 mmol) was added and the reaction mixture was reheated to 120° C. After 16 h LRMS indicated incomplete conversion to product. Additional 28% solution of ammonium hydroxide (8.0 ml, 56 mmol) was added and the reaction mixture was reheated to 120° C. After 24 h the reaction mixture was cooled, partially concentrated, diluted with ethyl ether, washed with water, then dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (ethyl ether/isohexane gradient) to give 4-iodo-6-methoxypyridin-2-amine LRMS (ESI) calculated for C6H8IN2O [M+H]+, 251.0 found 250.9.

Aufarbeitung

  1. customwas reheated to 120° C
  2. waitAfter 16 h LRMS indicated incomplete conversion to product
  3. customwas reheated to 120° C
  4. temperatureAfter 24 h the reaction mixture was cooled
  5. concentrationpartially concentrated
  6. additiondiluted with ethyl ether
  7. washwashed with water
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe residue was purified by column chromatography on silica gel (ethyl ether/isohexane gradient)

Quellen und Nachweise

ORD-Eintrag
ord-b22167b834ff4131999638bf330d5d54
Quelldatensatz
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08455477B2

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