Ethyl Acetate → HCID 86608383, Verbindung

HRID 882750Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 882750
[NH:1]([C:3]1[N:8]=[C:7]([N:9]2[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[N:6]=[C:5]([O:15][CH2:16][C:17]([CH3:20])([OH:19])[CH3:18])[CH:4]=1)[NH2:2].[N:21]([O-])=O.[Na+].C(OCC)(=O)C>C(O)(=O)C.O>[N:1]([C:3]1[N:8]=[C:7]([N:9]2[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[N:6]=[C:5]([O:15][CH2:16][C:17]([CH3:20])([OH:19])[CH3:18])[CH:4]=1)=[N+:2]=[N-:21]

Komponenten

6

Versuchsvorschrift

1-(6-hydrazino-2-morpholin-4-yl-pyrimidin-4-yloxy)-2-methyl-propan-2-ol was dissolved in glacial acetic acid (30 mL). To this solution was added a solution of sodium nitrite (700 mg) in water (4 mL). The reaction was stirred for ten minutes, and poured into ethyl acetate (100 mL). The organic layer was then washed with water (100 mL) and 10% sodium carbonate (2×100 mL). The organic layer was dried over magnesium sulfate and evaporated to give 1-(6-Azido-2-morpholin-4-yl-pyrimidin-4-yloxy)-2-methyl-propan-2-ol, which was used without purification in the next reaction.

Aufarbeitung

  1. washThe organic layer was then washed with water (100 mL) and 10% sodium carbonate (2×100 mL)
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-94c5e64fbf0e4a82ac3d783ff8f5e7dd
Quelldatensatz
uspto-grants-2012_08
Patentnummer
US08236795B2

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