Benzylamine → N-Benzyl-2-chloro-9-isopropyl-9H-purin-6-amine

HRID 48184

Reaktionsgleichung

Reaktionsgleichung von HRID 48184
[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH:11]([CH3:13])[CH3:12])=[C:4](Cl)[N:3]=1.[CH2:15]([NH2:22])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(O)CCC>[CH2:15]([NH:22][C:4]1[N:3]=[C:2]([Cl:1])[N:10]=[C:9]2[C:5]=1[N:6]=[CH:7][N:8]2[CH:11]([CH3:13])[CH3:12])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

Komponenten

4

Versuchsvorschrift

2,6-dichloro-9-isopropylpurine (1 mmol) and benzylamine (3.5 mmol) were heated with stirring in 3 ml of n-butanol (3 hour, 110° C.). The reaction mixture (after evaporation of n-butanol) was worked up as above for the compound 2, yield 85-90%.

Aufarbeitung

  1. customThe reaction mixture (after evaporation of n-butanol)

Quellen und Nachweise

ORD-Eintrag
ord-d2bcde2ca2704df1811ca52f0c53f035
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06703395B2

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