Reaktion #359814

ord-840b4cd1819e43acb5e41b8f14a7d16d

Reaktionsgleichung

Clc1ncc(I)c(Cl)n1
2,4-Dichloro-5-iodo-pyrimidine
CCN(CC)CC
triethylamine
CC(C)[C@@H](N)CO
(R)-2-Amino-3-methyl-butan-1-ol
CC(C)[C@H](CO)Nc1nc(Cl)ncc1I
(R)-2-(2-Chloro-5-iodo-pyrimidin-4-ylamino)-3-methyl-butan-1-ol

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe batch is filtered
  2. 2
    Waschenthe solid is washed with small amounts of acetonitrile and water
  3. 3
    SonstigeThe solid is dried
  4. 4
    Sonstige10.24 g (30.0 mmol, corresponding to 82% of theory) of the product is obtained

Vorschrift

A solution of 10.05 g (36.6 mmol) of 2,4-Dichloro-5-iodo-pyrimidine and 5.6 ml (40.0 mmol) triethylamine in 30 ml of acetonitrile is mixed with 4.85 g (47.0 mmol) of (R)-2-Amino-3-methyl-butan-1-ol. The batch is stirred at room temperature for 16 hours and is finally diluted with water. The batch is filtered and the solid is washed with small amounts of acetonitrile and water. The solid is dried. 10.24 g (30.0 mmol, corresponding to 82% of theory) of the product is obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07456191B2uspto-grants-2008_11