4-Amino-2-(ethylthio)-5-(hydroxymethyl)pyrimidine → 4-Pyrimidinamine, 2-(ethylthio)-

HRID 2354141

Reaktionsgleichung

Reaktionsgleichung von HRID 2354141
[NH2:1][C:2]1[C:7](CO)=[CH:6][N:5]=[C:4]([S:10][CH2:11][CH3:12])[N:3]=1>C(Cl)(Cl)Cl.O=[Mn]=O>[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([S:10][CH2:11][CH3:12])[N:3]=1

Komponenten

4

Edukt 1

HCID 2254334-Amino-2-(ethylthio)-5-(hydroxymethyl)pyrimidine

Produkt 1

HCID 5657304-Pyrimidinamine, 2-(ethylthio)-

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 14801Manganese dioxideKatalysatorHCID 6212ChloroformLösungsmittel

Versuchsvorschrift

To a solution of 4-amino-5-hydroxymethyl-2-(ethylthio)pyrimidine (5-1a) (9.6 g, 51.89 mmol) in CHCl3 (1 L) was added MnO2 (86.9 g, 415 mmol, 8 equiv). The suspension was stirred at rt overnight. The mixture was filtered through celite and washed with CHCl3. The combined filtrate was concentrated to give the titled compound (5-2a). 1H-NMR (500 MHz, CDCl3) δ 9.78 (s, 1H), 8.42 (s, 1H), 8.20 (broad, 1H), 5.74 (broad, 1H), 2.55 (q, 2H), 1.38 (t, 3H). LRMS m/z (M+H) Calcd. 184.24, found 184.16.

Aufarbeitung

  1. filtrationThe mixture was filtered through celite
  2. washwashed with CHCl3
  3. concentrationThe combined filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-1973106fc9044484a5cab37b74b97786
Quelldatensatz
uspto-grants-2010_07
Patentnummer
US07750151B2

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