Ammonia → 6-Chloro-2-methylpyrimidine-4,5-diamine

HRID 1255883Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1255883
[NH2:1][C:2]1[C:3](Cl)=[N:4][C:5]([CH3:9])=[N:6][C:7]=1[Cl:8].[NH3:11]>C(O)(C)C>[Cl:8][C:7]1[N:6]=[C:5]([CH3:9])[N:4]=[C:3]([NH2:11])[C:2]=1[NH2:1]

Komponenten

4

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

A 200 mL stainless steel Parr vessel was loaded with 5-amino-4,6-dichloro-2-methylpyrimidine (7.2 g, 40 mmol) and 2 M ammonia in isopropanol (100 mL), and then was sealed and heated at 150° C. for 16 h. HPLC analysis indicated complete conversion. The mixture was concentrated in vacuo, and the residue was suspended in a mixture of H2O (10 mL) and isopropanol (35 mL). This was stirred at 50° C. for 1 h and then was cooled to room temperature. The precipitate was collected by suction filtration, washed sparingly with isopropanol, then air dried on the filter to afford 6-chloro-4,5-diamino-2-methylpyrimidine (5.8 g, 91%) as a brown powder, which was used without further purification in the next step.

Aufarbeitung

  1. customwas sealed
  2. concentrationThe mixture was concentrated in vacuo
  3. additionthe residue was suspended in a mixture of H2O (10 mL) and isopropanol (35 mL)
  4. temperaturewas cooled to room temperature
  5. filtrationThe precipitate was collected by suction filtration
  6. washwashed sparingly with isopropanol
  7. customair dried on the
  8. filtrationfilter

Quellen und Nachweise

ORD-Eintrag
ord-174415b6b2094838afba2611bf0c7800
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08461164B2

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