6-Desamino 6-Chloro Etravirine → Etravirine

HRID 41369Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 41369
[Br:1][C:2]1[C:3]([O:18][C:19]2[C:24]([CH3:25])=[CH:23][C:22]([C:26]#[N:27])=[CH:21][C:20]=2[CH3:28])=[N:4][C:5]([NH:9][C:10]2[CH:17]=[CH:16][C:13]([C:14]#[N:15])=[CH:12][CH:11]=2)=[N:6][C:7]=1Cl.[NH3:29].O1CCOCC1>O>[NH2:29][C:7]1[C:2]([Br:1])=[C:3]([O:18][C:19]2[C:24]([CH3:25])=[CH:23][C:22]([C:26]#[N:27])=[CH:21][C:20]=2[CH3:28])[N:4]=[C:5]([NH:9][C:10]2[CH:17]=[CH:16][C:13]([C:14]#[N:15])=[CH:12][CH:11]=2)[N:6]=1

Komponenten

4

Edukt 2

HCID 117514166-Desamino 6-Chloro EtravirineHCID 66648793Ammonia dioxane

Produkt 1

HCID 193962EtravirineAusbeute 40,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

4-[[5-bromo-4-(4-cyano-2,6-dimethylphenoxy)-6-chloro-2-pyrimidinyl]amino]benzonitrile (0.00250 mol) and NH3/1,4-dioxane 0.5M (0.015 mol) were heated in a pressure vessel at 150° C. for 4 days. The sample was allowed to sit at ambient conditions for 2 days. Water was added slowly to the mixture until a precipitate formed. The mixture was stirred for 2 hours and filtered. The solid was recrystallized from CH3CN to obtain 0.58 g (fraction 1). The filtrate was evaporated (fraction 2). Both fractions were combined and purified by column chromatography, eluting with CH2Cl2. The resulting residue of the desired fraction was recrystallized from CH3CN to yield 0.44 g of 4-[[4-amino-5-bromo-6-(4-cyano-2,6-dimethylphenyloxy)-2-pyrimidinyl]amino]benzonitrile (40.5%). The sample was dried at 80° C. for 16 hours at 0.2 mm Hg (comp. 46).

Aufarbeitung

  1. customformed
  2. filtrationfiltered
  3. customThe solid was recrystallized from CH3CN
  4. customto obtain 0.58 g (fraction 1)
  5. customThe filtrate was evaporated (fraction 2)
  6. custompurified by column chromatography
  7. washeluting with CH2Cl2
  8. customThe resulting residue of the desired fraction was recrystallized from CH3CN

Quellen und Nachweise

ORD-Eintrag
ord-a571e09baa8c4edfa080376dad7e16dc
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08530655B2

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