Ammonia → HCID 178450371, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][CH2:14][CH3:15])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([O:23]C)[N:6]2[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.N>Cl>[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][CH2:14][CH3:15])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([OH:23])[N:6]2[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
6-Amino-9-benzyl-2-butoxy-8-methoxypurine (20 mg, 0.061 mmol) in concentrated hydrochloric acid (5 ml) was stirred for 3 hours at room temperature. The reaction mixture was made basic with 28% aqueous ammonia. The resulting crystals were filtered, washed with water, and the crude product was purified by silica gel chromatography (3% methanol/chloroform) to give the subject compound (13 mg, yield 68%).
Aufarbeitung
- filtrationThe resulting crystals were filtered
- washwashed with water
- customthe crude product was purified by silica gel chromatography (3% methanol/chloroform)
Quellen und Nachweise
- ORD-Eintrag
- ord-ee2430c7a49b4b0895fb247b963887dc
- Quelldatensatz
- uspto-grants-2001_12
- Patentnummer
- US06329381B1
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